start-ver=1.4
cd-journal=joma
no-vol=59
cd-vols=
no-issue=
article-no=
start-page=143
end-page=163
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2025
dt-pub=20250328
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=An Analysis of the Function of “1Gja軍” in the Tangut Military System ―Positions of “1Gja軍” and its Relationship with “1Tśju職”―
kn-title=西夏軍制における「軍」の機能 ―「軍」に属する地位名称および「職」との関係―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=ONOHiroko
en-aut-sei=ONO
en-aut-mei=Hiroko
kn-aut-name=小野裕子
kn-aut-sei=小野
kn-aut-mei=裕子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=15
cd-vols=
no-issue=1
article-no=
start-page=6666
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2025
dt-pub=20250224
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Microfluidic fabrication of rattle shaped biopolymer microcapsules via sequential phase separation in oil droplets
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Multilayer microcapsules containing a small particle within a larger capsule have recently attracted considerable attention owing to their potential applications in diverse fields, including drug delivery, active ingredient storage, and chemical reactions. These complex capsules have been fabricated using interfacial polymerization or seeded emulsion polymerization. However, these methods often require complex and lengthy polymerization processes, limiting their utility, particularly in biopolymer systems. This study introduces a simple and efficient approach for preparing rattle-shaped cellulose acetate (CA) microcapsules through sequential phase separation in droplets. We systematically examine the effects of various preparation parameters, including the amount of co-solvent, initial droplet size, and flow rates, and reveal that the incorporation of a co-solvent-ethyl acetate (EA)- in the dispersed phase significantly impacts the microcapsule morphology. Our findings demonstrate a transition from a core-shell to a rattle-shaped structure as the EA concentration increases. Furthermore, the initial droplet diameter and flow rates influence microcapsule formation-larger droplets and reduced continuous-phase flow rates favor the development of multi-layered structures. These results indicate that the formation mechanism of these rattle-shaped microcapsules arises from the establishment of a radial solvent concentration gradient and subsequent phase separation within the droplets, driven by kinetic rather than thermodynamic factors.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=SakaiYuko
en-aut-sei=Sakai
en-aut-mei=Yuko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=MoriKurumi
en-aut-sei=Mori
en-aut-mei=Kurumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Environmental, Life, Natural Science and Technology
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Environmental, Life, Natural Science and Technology
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Environmental, Life, Natural Science and Technology
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Environmental, Life, Natural Science and Technology
kn-affil=
en-keyword=Microfluidics
kn-keyword=Microfluidics
en-keyword=Phase separation
kn-keyword=Phase separation
en-keyword=Nucleation
kn-keyword=Nucleation
en-keyword=Multi-core
kn-keyword=Multi-core
en-keyword=Rattle-shaped
kn-keyword=Rattle-shaped
END
start-ver=1.4
cd-journal=joma
no-vol=2024
cd-vols=
no-issue=
article-no=
start-page=8836103
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20241028
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=A Rare Case of Multiple Myeloma Identified Following the Diagnosis of Amyloidosis of the Tongue
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Amyloidosis is a disease in which amyloid protein is deposited in organs and tissues, resulting in functional impairment. Amyloidosis occurs in 12%-30% of patients with multiple myeloma, but in rare cases, amyloidosis may precede the diagnosis of multiple myeloma. Our patient was a 76-year-old Japanese male on dialysis. Multiple nodules accompanied by ulcers were observed on his tongue. He had no subjective symptoms or clinical findings associated with multiple myeloma. The histopathological findings suggested amyloidosis. We suspected both systemic and localized amyloidosis and performed a comprehensive systemic examination. Since the patient had been on dialysis for only a short period of time (similar to 3 months), dialysis-related amyloidosis was ruled out. After blood and urine tests, a diagnosis of multiple myeloma was made. Chemotherapy treatment was started, but the patient's multiple myeloma could not be suppressed and the tongue amyloidosis worsened, leading to his death 2 years and 2 months after the initial diagnosis.
en-copyright=
kn-copyright=
en-aut-name=KanemotoHideka
en-aut-sei=Kanemoto
en-aut-mei=Hideka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KadoyaKoichi
en-aut-sei=Kadoya
en-aut-mei=Koichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=YaoMayumi
en-aut-sei=Yao
en-aut-mei=Mayumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=5
en-affil=Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Tsuyama Chuo Hospital
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=21
cd-vols=
no-issue=5
article-no=
start-page=464
end-page=473
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240827
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Terrein Exhibits Anti-tumor Activity by Suppressing Angiogenin Expression in Malignant Melanoma Cells
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Background/Aim: Malignant melanoma is a tumor with a poor prognosis that can metastasize distally at an early stage. Terrein, a metabolite produced by Aspergillus terreus, suppresses the expression of angiogenin, an angiogenic factor. However, the pharmacological effects of natural terrein have not been elucidated, because only a small amount of terrein can be extracted from large fungal cultures. In this study, we investigated the antineoplastic effects of terrein on human malignant melanoma cells and its underlying mechanisms. Materials and methods: Human malignant melanoma cell lines were cultured in the presence of terrein and analyzed. Angiogenin production was evaluated using ELISA. Ribosome biosynthesis was evaluated using silver staining of the nucleolar organizer region. Intracellular signaling pathways were analyzed using western blotting. Malignant melanoma cells were transplanted subcutaneously into the backs of nude mice. The tumors were removed at 5 weeks and analyzed histopathologically. Results: Terrein inhibited angiogenin expression, proliferation, migration, invasion, and ribosome biosynthesis in malignant melanoma cells. Terrein was shown to inhibit tumor growth and angiogenesis in animal models. Conclusion: This study demonstrated that terrein has anti-tumor effects against malignant melanoma. Furthermore, chemically synthesized non-natural terrein can be mass-produced and serve as a novel potential anti-tumor drug candidate.
en-copyright=
kn-copyright=
en-aut-name=HIROSETAIRA
en-aut-sei=HIROSE
en-aut-mei=TAIRA
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KUNISADAYUKI
en-aut-sei=KUNISADA
en-aut-mei=YUKI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KADOYAKOICHI
en-aut-sei=KADOYA
en-aut-mei=KOICHI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=MANDAIHIROKI
en-aut-sei=MANDAI
en-aut-mei=HIROKI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=SAKAMOTOYUMI
en-aut-sei=SAKAMOTO
en-aut-mei=YUMI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OBATAKYOICHI
en-aut-sei=OBATA
en-aut-mei=KYOICHI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=ONOKISHO
en-aut-sei=ONO
en-aut-mei=KISHO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=TAKAKURAHIROAKI
en-aut-sei=TAKAKURA
en-aut-mei=HIROAKI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=OMORIKAZUHIRO
en-aut-sei=OMORI
en-aut-mei=KAZUHIRO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=TAKASHIBASHOGO
en-aut-sei=TAKASHIBA
en-aut-mei=SHOGO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=SUGASEIJI
en-aut-sei=SUGA
en-aut-mei=SEIJI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=IBARAGISOICHIRO
en-aut-sei=IBARAGI
en-aut-mei=SOICHIRO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=4
en-affil=Department of Pharmacy, Faculty of Pharmacy, Gifu University of Medical Science
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=9
en-affil=Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=11
en-affil=Division of Applied Chemistry, Graduate School of Natural Sciences and Technology, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
en-keyword=Head and neck cancer
kn-keyword=Head and neck cancer
en-keyword=oral cancer
kn-keyword=oral cancer
en-keyword=malignant melanoma
kn-keyword=malignant melanoma
en-keyword=angiogenin
kn-keyword=angiogenin
en-keyword=terrein
kn-keyword=terrein
END
start-ver=1.4
cd-journal=joma
no-vol=24
cd-vols=
no-issue=1
article-no=
start-page=341
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240813
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Pathological findings in enucleated eyes of patients with neurofibromatosis type 1: report of a case with 15-year follow-up and review of 14 patients in the literature
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Backgrounds Iris nodules are frequently noted as clinical manifestations of neurofibromatosis type 1 but the other intraocular manifestations are rare. The purpose of this study is to present a patient with a phthisic eye who underwent enucleation for a cosmetic reason after 15-year follow-up and also to review 14 patients with enucleation described in the literature.
Case presentation A 17-year-old man with neurofibromatosis type 1 from infancy underwent the enucleation of phthisic left eye and also had the resection of eyelid subcutaneous mass lesions on the left side for a cosmetic reason. He had undergone four-time preceding surgeries for eyelid and orbital mass reduction on the left side in childhood and had developed total retinal detachment 10 years previously. Pathologically, the enucleated eye showed massive retinal gliosis positive for both S-100 and glial fibrillary acidic protein (GFAP) in the area with involvement of the detached retinal neuronal layer, together with a more fibrotic lesion along the choroid which were, in contrast, negative for both S-100 and GFAP. The choroid, ciliary body, and iris did not show apparent neurofibroma while episcleral neurofibroma was present.
Literature review In review of enucleated eyes of 14 patients in the literature, buphthalmic eyes with early-onset glaucoma on the unilateral side was clinically diagnosed in 9 patients who frequently showed varying extent of hemifacial neurofibromatosis which involved the eyelid and orbit on the same side. Pathologically, neurofibromas in varying extent were found in the choroid of 12 patients. One patient showed choroidal malignant melanoma on the left side and fusiform enlargement of the optic nerve on the right side suspected of optic nerve glioma. The phthisic eye in another patient showed massive retinal gliosis similar to the present patient.
Conclusions In summary of the 15 patients with neurofibromatosis type 1, including the present patient, buphthalmic or phthisic eyes with no vision were enucleated for cosmetic reasons and showed choroidal neurofibroma in most patients and massive retinal gliosis in two patients including the present patient.
en-copyright=
kn-copyright=
en-aut-name=MatsuoToshihiko
en-aut-sei=Matsuo
en-aut-mei=Toshihiko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=NishidaKenji
en-aut-sei=Nishida
en-aut-mei=Kenji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=TanakaTakehiro
en-aut-sei=Tanaka
en-aut-mei=Takehiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=SenoTakaya
en-aut-sei=Seno
en-aut-mei=Takaya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=YamadaKiyoshi
en-aut-sei=Yamada
en-aut-mei=Kiyoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoShigeki
en-aut-sei=Ono
en-aut-mei=Shigeki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
affil-num=1
en-affil=Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Pathology, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Pathology, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Neurological Surgery, General Medical Center, Kawasaki Medical School
kn-affil=
en-keyword=Neurofibromatosis type 1
kn-keyword=Neurofibromatosis type 1
en-keyword=Enucleation
kn-keyword=Enucleation
en-keyword=Eye
kn-keyword=Eye
en-keyword=Pathology
kn-keyword=Pathology
en-keyword=Massive retinal gliosis
kn-keyword=Massive retinal gliosis
en-keyword=Choroidal neurofibroma
kn-keyword=Choroidal neurofibroma
en-keyword=Phthisis
kn-keyword=Phthisis
en-keyword=Buphthalmos
kn-keyword=Buphthalmos
en-keyword=Malignant melanoma
kn-keyword=Malignant melanoma
en-keyword=Cosmetic surgery
kn-keyword=Cosmetic surgery
END
start-ver=1.4
cd-journal=joma
no-vol=51
cd-vols=
no-issue=
article-no=
start-page=15
end-page=26
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240331
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=『三ギニー』における風刺の考察―皮肉的風刺表現―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野和子
kn-aut-sei=小野
kn-aut-mei=和子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院社会文化科学研究科博士前期課程修了生
END
start-ver=1.4
cd-journal=joma
no-vol=9
cd-vols=
no-issue=10
article-no=
start-page=e174618
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240522
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Double-faced CX3CL1 enhances lymphangiogenesis-dependent metastasis in an aggressive subclone of oral squamous cell carcinoma
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Because cancer cells have a genetically unstable nature, they give rise to genetically different variant subclones inside a single tumor. Understanding cancer heterogeneity and subclone characteristics is crucial for developing more efficacious therapies. Oral squamous cell carcinoma (OSCC) is characterized by high heterogeneity and plasticity. On the other hand, CX3C motif ligand 1 (CX3CL1) is a double-faced chemokine with anti- and pro -tumor functions. Our study reported that CX3CL1 functioned differently in tumors with different cancer phenotypes, both in vivo and in vitro. Mouse OSCC 1 (MOC1) and MOC2 cells responded similarly to CX3CL1 in vitro. However, in vivo, CX3CL1 increased keratinization in indolent MOC1 cancer, while CX3CL1 promoted cervical lymphatic metastasis in aggressive MOC2 cancer. These outcomes were due to double-faced CX3CL1 effects on different immune microenvironments indolent and aggressive cancer created. Furthermore, we established that CX3CL1 promoted cancer metastasis via the lymphatic pathway by stimulating lymphangiogenesis and transendothelial migration of lymph -circulating tumor cells. CX3CL1 enrichment in lymphatic metastasis tissues was observed in aggressive murine and human cell lines. OSCC patient samples with CX3CL1 enrichment exhibited a strong correlation with lower overall survival rates and higher recurrence and distant metastasis rates. In conclusion, CX3CL1 is a pivotal factor that stimulates the metastasis of aggressive cancer subclones within the heterogeneous tumors to metastasize, and our study demonstrates the prognostic value of CX3CL1 enrichment in long-term monitoring in OSCC.
en-copyright=
kn-copyright=
en-aut-name=EainHtoo Shwe
en-aut-sei=Eain
en-aut-mei=Htoo Shwe
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=NakayamaMasaaki
en-aut-sei=Nakayama
en-aut-mei=Masaaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OoMay Wathone
en-aut-sei=Oo
en-aut-mei=May Wathone
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=OharaToshiaki
en-aut-sei=Ohara
en-aut-mei=Toshiaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=FukuharaYoko
en-aut-sei=Fukuhara
en-aut-mei=Yoko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=TakabatakeKiyofumi
en-aut-sei=Takabatake
en-aut-mei=Kiyofumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=ShanQuisheng
en-aut-sei=Shan
en-aut-mei=Quisheng
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=SoeYamin
en-aut-sei=Soe
en-aut-mei=Yamin
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=NakanoKeisuke
en-aut-sei=Nakano
en-aut-mei=Keisuke
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=MizukawaNobuyoshi
en-aut-sei=Mizukawa
en-aut-mei=Nobuyoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=IidaSeiji
en-aut-sei=Iida
en-aut-mei=Seiji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
affil-num=1
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Oral Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Pathology and Experimental Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama Universit
kn-affil=
affil-num=6
en-affil=Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=11
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Oral and Maxillofacial Reconstructive Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Oral and Maxillofacial Reconstructive Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=自然と人間の共生観を育むための生活科及び理科教育の基礎的研究
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=ONODERAKaren
en-aut-sei=ONODERA
en-aut-mei=Karen
kn-aut-name=小野寺かれん
kn-aut-sei=小野寺
kn-aut-mei=かれん
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Humanities and Social Sciences, Okayama University
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=西夏軍制史の研究
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=ONOHiroko
en-aut-sei=ONO
en-aut-mei=Hiroko
kn-aut-name=小野裕子
kn-aut-sei=小野
kn-aut-mei=裕子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Humanities and Social Sciences, Okayama University
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=40
cd-vols=
no-issue=15
article-no=
start-page=8074
end-page=8082
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240405
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Engineering Interconnected Open-Porous Particles via Microfluidics Using Bijel Droplets as Structural Templates
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Designing porous structures is key in materials science, particularly for separation, catalysis, and cell culture systems. Bicontinuous interfacially jammed emulsion gels represent a unique class of soft matter formed by kinetically arresting the separation of the spinodal decomposition phase, which is stabilized by colloidal particles with neutral wetting. This study introduces a microfluidic technique to create highly interconnected open-porous particles using bijel droplets stabilized with hexadecyltrimethylammonium bromide (CTAB)-modified silica particles. Monodisperse droplets comprising a hydrophobic monomer, water, ethanol, silica particles, and CTAB were initially formed in the microfluidic device. The diffusion of ethanol from these droplets into the continuous cyclohexane phase triggered spinodal decomposition within the droplets. The phase-separated structure within the droplets was stabilized by the CTAB-modified silica particles, and subsequent photopolymerization yielded microparticles with highly interconnected, open pores. Moreover, the influence of the ratio of the CTAB and silica particles, fluid composition, and microchannel direction on the final structure of the microparticles was explored. Our findings indicated that the phase-separated structure of the particles transitioned from oil-in-water to water-in-oil as the CTAB/silica ratio was increased. At intermediate CTAB/silica ratios, microparticles with bicontinuous structures were formed. Regardless of the fluid composition, the pore size of the particles increased with time after phase separation. However, this coarsening was arrested 15 s after droplet formation in the CTAB-modified silica particles, accompanied by a change in the particle shape from spherical to ellipsoidal. In situ observations of the bijel droplet formation revealed that the particle shape deformation is caused by the rolling of elastic bijel droplets at the bottom of the microchannel. As such, the channel setup was altered from horizontal to vertical to prevent the deformation of bijel droplets, resulting in spherical particles with open pores.
en-copyright=
kn-copyright=
en-aut-name=MasaokaMina
en-aut-sei=Masaoka
en-aut-mei=Mina
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=IshidaHiroaki
en-aut-sei=Ishida
en-aut-mei=Hiroaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=12
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190329
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Newsletter from Course for Prospective Museum Workers, Faculty of Letters, Okayama University
kn-title=学芸員課程 Newsletter 第12号
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=光本順
kn-aut-sei=光本
kn-aut-mei=順
aut-affil-num=1
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=鈴木恒志
kn-aut-sei=鈴木
kn-aut-mei=恒志
aut-affil-num=2
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=木下莉沙
kn-aut-sei=木下
kn-aut-mei=莉沙
aut-affil-num=3
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=黒木恵那
kn-aut-sei=黒木
kn-aut-mei=恵那
aut-affil-num=4
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=多田絢音
kn-aut-sei=多田
kn-aut-mei=絢音
aut-affil-num=5
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野田澪
kn-aut-sei=小野田
kn-aut-mei=澪
aut-affil-num=6
ORCID=
affil-num=1
en-affil=
kn-affil=文学部
affil-num=2
en-affil=
kn-affil=文学部 哲学芸術学専修コース
affil-num=3
en-affil=
kn-affil=文学部 地理学・社会学・文化人類学・社会文化学分野
affil-num=4
en-affil=
kn-affil=文学部 歴史学・考古学分野
affil-num=5
en-affil=
kn-affil=文学部 芸術学・美術史分野
affil-num=6
en-affil=
kn-affil=文学部 歴史学・考古学分野
END
start-ver=1.4
cd-journal=joma
no-vol=43
cd-vols=
no-issue=11
article-no=
start-page=4993
end-page=5001
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2023
dt-pub=202311
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Multimodal Prediction of Cervical Lymph Node Metastasis and Recurrence in Oral Squamous Cell Carcinoma
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Background/Aim: Oral squamous cell carcinoma (OSCC) is the most common malignancy in the head/neck region, and cervical lymph node (CLN) metastasis is a strong poor-prognosis factor. In addition, many patients with OSCC experience recurrence despite multidisciplinary treatment. We sought to identify factors associated with CLN metastasis and recurrence in patients with OSCC. Patients and Methods: We evaluated a total of 45 patients and 233 target CLNs. The longest diameter of the target CLN, the shortest diameter of the target CLN (LS), the area of the target CLN, and the relative computed tomography (CT) values of the target CLNs calculated based on the CT values of the internal jugular vein (LCT) were obtained from preoperative CT images, and the maximum standardized uptake values of the primary tumor (pSUV) and target CLN (nSUV) were obtained from preoperative 18F-fluorodeoxyglucose-positron emission tomography/CT images. We performed immunohistochemical staining for cytokeratin 13 (CK13) and 17 (CK17) on neck dissection tissues. Results: A discrimination equation was used that can predict CLN metastasis with a 92.2% discrimination rate using LS, LCT, pSUV, and nSUV. The CLNs were divided into discrimination and non-discrimination groups based on discriminant equations and CK13 and CK17 were used as the objective variables. A significantly higher recurrence rate was observed in the non-discrimination group (CK13: 5-year recurrence rate 28.6% vs. 64.3%, p<0.01; CK17: 5-year recurrence rate 28.0% vs. 76.0%, p<0.01). Conclusion: CLN metastases in OSCC can be assessed by combining preoperative imaging. The combined use of CK13 and CK17 expression with imaging findings offers an integrated approach to predict OSCC recurrence.
en-copyright=
kn-copyright=
en-aut-name=KANEMOTOHIDEKA
en-aut-sei=KANEMOTO
en-aut-mei=HIDEKA
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OBATAKYOICHI
en-aut-sei=OBATA
en-aut-mei=KYOICHI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=UMEMORIKOKI
en-aut-sei=UMEMORI
en-aut-mei=KOKI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=HASEGAWAKAZUAKI
en-aut-sei=HASEGAWA
en-aut-mei=KAZUAKI
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=ONOSAWAKO
en-aut-sei=ONO
en-aut-mei=SAWAKO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=ONOKISHO
en-aut-sei=ONO
en-aut-mei=KISHO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=YUTORIHIROKAZU
en-aut-sei=YUTORI
en-aut-mei=HIROKAZU
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=IBARAGISOICHIRO
en-aut-sei=IBARAGI
en-aut-mei=SOICHIRO
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Kagawa Prefectural Central Hospital
kn-affil=
affil-num=5
en-affil=Department of Pathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
en-keyword=Oral cancer
kn-keyword=Oral cancer
en-keyword=head and neck squamous cell carcinoma
kn-keyword=head and neck squamous cell carcinoma
en-keyword=neck dissection
kn-keyword=neck dissection
en-keyword=lymph node
kn-keyword=lymph node
en-keyword=discriminant analysis
kn-keyword=discriminant analysis
en-keyword=cytokeratin
kn-keyword=cytokeratin
END
start-ver=1.4
cd-journal=joma
no-vol=20
cd-vols=
no-issue=7
article-no=
start-page=1611
end-page=1619
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240118
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Controlled mechanical properties of poly(ionic liquid)-based hydrophobic ion gels by the introduction of alumina nanoparticles with different shapes
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Ionic–liquid gels, also known as ion gels, have gained considerable attention due to their high ionic conductivity and CO2 absorption capacity. However, their low mechanical strength has hindered their practical applications. A potential solution to this challenge is the incorporation of particles, such as silica nanoparticles, TiO2 nanoparticles, and metal–organic frameworks (MOFs) into ion gels. Comparative studies on the effect of particles with different shapes are still in progress. This study investigated the effect of the shape of particles introduced into ion gels on their mechanical properties. Consequently, alumina/poly(ionic liquid) (PIL) double-network (DN) ion gels consisting of clustered alumina nanoparticles with various shapes (either spherical or rod-shaped) and a chemically crosslinked poly[1-ethyl-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide] (PC2im-TFSI, PIL) network were prepared. The results revealed that the mechanical strengths of the alumina/PIL DN ion gels were superior to those of PIL single-network ion gels without particles. Notably, the fracture energies of the rod-shaped alumina/PIL DN ion gels were approximately 2.6 times higher than those of the spherical alumina/PIL DN ion gels. Cyclic tensile tests were performed, and the results indicate that the loading energy on the ion gel was dissipated through the fracture of the alumina network. TEM observation suggests that the variation in the mechanical strength depending on the shape can be attributed to differences in the aggregation structure of the alumina particles, thus indicating the possibility of tuning the mechanical strength of ion gels by altering not only particle kinds but its shape.
en-copyright=
kn-copyright=
en-aut-name=MizutaniYuna
en-aut-sei=Mizutani
en-aut-mei=Yuna
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=LopezCarlos G.
en-aut-sei=Lopez
en-aut-mei=Carlos G.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Materials Science and Engineering, The Pennsylvania State University
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=113
cd-vols=
no-issue=
article-no=
start-page=1
end-page=6
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2024
dt-pub=20240201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Evaluator of adaptability of S. cerevisiae to grape juice using the oversxpression profiling ADOPT method
kn-title=過剰発現プロファイリングADOPT法を用いたS.cerevisiaeのワイン醸造用ブドウ果汁への適応性評価
en-subtitle=
kn-subtitle=
en-abstract=筆者らは最近,過剰発現プロファイリングADOPT 法を開発した.ADOPT 法では,出芽酵母Saccharomyces cerevisiae ゲノムのほとんどの遺伝子をそれぞれ過剰発現する酵母株を混合・競合培養し,その過程で濃縮されてきた株が過剰発現している遺伝子を体系的に同定する.さらに同定された遺伝子をたよりに,S. cerevisiae の与えられた条件での増殖に必要だが欠落しているボトルネック因子を明らかにできる.これまでの研究では,実験室で人為的に構築したストレス環境でのボトルネックの同定を行ってきたが,本研究では産業上のボトルネックを明らかにできるかをワイン醸造用のブドウ果汁を例として検証した.通常のワイン醸造に用いられる亜硫酸添加ブドウ果汁でのADOPT 実験は,亜硫酸ポンプSSU1とその転写因子FZF1の過剰発現株が強く濃縮された.SSU1機能の強化はワイン用酵母の馴養でも起きることが知られていることから,産業上のボトルネックを探索する際にもADOPT が有効であることが示された.一方,亜硫酸添加のないブドウ果汁ではADOPT で強く濃縮された遺伝子は見られず,ブドウ果汁はS. cerevisiae の増殖にとってボトルネックの少ないバランスのとれた培地であることが示唆された.
kn-abstract=The authors have recently developed the overexpression profiling ADOPT method. In the ADOPT method, yeast strains overexpressing most of the genes in the budding yeast Saccharomyces cerevisiae genome are mixed and competitively cultured, and the genes overexpressed in the enriched strains are systematically identified. Furthermore, the identified genes can be used to identify bottleneck factors that are necessary but lacking for growth of S. cerevisiae under given conditions. In our previous studies, we have identified bottlenecks in artificially created stress environments in the laboratory, but in this study, we used grape juice for winemaking as an example to see if industrial bottlenecks can be identified. ADOPT experiments with sulfite-added grape juice used in conventional winemaking resulted in a strong enrichment of strains overexpressing the sulfite pump SSU1 and its transcription factor FZF1. Since enhancement of SSU1 function is known to occur in wine yeast acclimation, ADOPT was also shown to be useful in the search for industrial bottlenecks. On the other hand, no genes were strongly enriched by ADOPT in grape juice without sulfite addition, suggesting that grape juice is a balanced medium with few bottlenecks for S. cerevisiae growth.
en-copyright=
kn-copyright=
en-aut-name=MoriyaHisao
en-aut-sei=Moriya
en-aut-mei=Hisao
kn-aut-name=守屋央朗
kn-aut-sei=守屋
kn-aut-mei=央朗
aut-affil-num=1
ORCID=
en-aut-name=OnoChiyuki Kohata
en-aut-sei=Ono
en-aut-mei=Chiyuki Kohata
kn-aut-name=小野千由貴
kn-aut-sei=小野
kn-aut-mei=千由貴
aut-affil-num=2
ORCID=
affil-num=1
en-affil=Course of Agrochemical Bioscience
kn-affil=農芸化学コース
affil-num=2
en-affil=Course of Agrochemical Bioscience
kn-affil=農芸化学コース
en-keyword=yeast
kn-keyword=yeast
en-keyword=S. cerevisiae
kn-keyword=S. cerevisiae
en-keyword=overexpression
kn-keyword=overexpression
en-keyword=wine making
kn-keyword=wine making
END
start-ver=1.4
cd-journal=joma
no-vol=142
cd-vols=
no-issue=
article-no=
start-page=106433
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2023
dt-pub=202307
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=EpEX, the soluble extracellular domain of EpCAM, resists cetuximab treatment of EGFR-high head and neck squamous cell carcinoma
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Objectives: Cetuximab (Cmab) is a molecularly targeted monoclonal antibody drug for head and neck squamous cell carcinoma (HNSC), although cetuximab resistance is a serious challenge. Epithelial cell adhesion molecule (EpCAM) is an established marker for many epithelial tumors, while the soluble EpCAM extracellular domain (EpEX) functions as a ligand for epidermal growth factor receptor (EGFR). We investigated the expression of EpCAM in HNSC, its involvement in Cmab action, and the mechanism by which soluble EpEX activated EGFR and played key roles in Cmab resistance.
Materials and methods: We first examined EPCAM expression in HNSCs and its clinical significance by searching gene expression array databases. We then examined the effects of soluble EpEX and Cmab on intracellular signaling and Cmab efficacy in HNSC cell lines (HSC-3 and SAS).
Results: EPCAM expression was found to be enhanced in HNSC tumor tissues compared to normal tissues, and the enhancement was correlated with stage progression and prognosis. Soluble EpEX activated the EGFR-ERK signaling pathway and nuclear translocation of EpCAM intracellular domains (EpICDs) in HNSC cells. EpEX resisted the antitumor effect of Cmab in an EGFR expression-dependent manner.
Conclusion: Soluble EpEX activates EGFR to increase Cmab resistance in HNSC cells. The EpEX-activated Cmab resistance in HNSC is potentially mediated by the EGFR-ERK signaling pathway and the EpCAM cleavage-induced nuclear translocation of EpICD. High expression and cleavage of EpCAM are potential biomarkers for predicting the clinical efficacy and resistance to Cmab.
en-copyright=
kn-copyright=
en-aut-name=UmemoriKoki
en-aut-sei=Umemori
en-aut-mei=Koki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=EguchiTakanori
en-aut-sei=Eguchi
en-aut-mei=Takanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OgawaTatsuo
en-aut-sei=Ogawa
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=YoshidaKunihiro
en-aut-sei=Yoshida
en-aut-mei=Kunihiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=KanemotoHideka
en-aut-sei=Kanemoto
en-aut-mei=Hideka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=SatoKohei
en-aut-sei=Sato
en-aut-mei=Kohei
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=YutoriHirokazu
en-aut-sei=Yutori
en-aut-mei=Hirokazu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=KataseNaoki
en-aut-sei=Katase
en-aut-mei=Naoki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=15
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=16
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Dental Pharmacology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Oral Pathology and Medicine, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=11
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Oral Pathology, Graduate School of Biomedical Sciences, Nagasaki University
kn-affil=
affil-num=14
en-affil=Department of Oral and Maxillofacial Surgery, Shimane University Faculty of Medicine
kn-affil=
affil-num=15
en-affil=Department of Oral Pathology and Medicine, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=16
en-affil=Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
en-keyword=Cetuximab
kn-keyword=Cetuximab
en-keyword=epithelial cell adhesion molecule (EpCAM)
kn-keyword=epithelial cell adhesion molecule (EpCAM)
en-keyword=EpEX
kn-keyword=EpEX
en-keyword=EpICD
kn-keyword=EpICD
en-keyword=epidermal growth factor receptor (EGFR)
kn-keyword=epidermal growth factor receptor (EGFR)
en-keyword=Drug resistance
kn-keyword=Drug resistance
en-keyword=Head and neck squamous cell carcinoma (HNSC)
kn-keyword=Head and neck squamous cell carcinoma (HNSC)
END
start-ver=1.4
cd-journal=joma
no-vol=76
cd-vols=
no-issue=
article-no=
start-page=1
end-page=12
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2023
dt-pub=20231215
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=University Students’ Perceptions towards Teachers
kn-title=大学生が持つ大学教員イメージの検討
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=SumiokaKyoko
en-aut-sei=Sumioka
en-aut-mei=Kyoko
kn-aut-name=住岡恭子
kn-aut-sei=住岡
kn-aut-mei=恭子
aut-affil-num=1
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=山内裕斗
kn-aut-sei=山内
kn-aut-mei=裕斗
aut-affil-num=2
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=瀧北文
kn-aut-sei=瀧北
kn-aut-mei=文
aut-affil-num=3
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=重藤彩伽
kn-aut-sei=重藤
kn-aut-mei=彩伽
aut-affil-num=4
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=河野穂波
kn-aut-sei=河野
kn-aut-mei=穂波
aut-affil-num=5
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野遥香
kn-aut-sei=小野
kn-aut-mei=遥香
aut-affil-num=6
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=島津柊
kn-aut-sei=島津
kn-aut-mei=柊
aut-affil-num=7
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=月輪花菜
kn-aut-sei=月輪
kn-aut-mei=花菜
aut-affil-num=8
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=草野結子
kn-aut-sei=草野
kn-aut-mei=結子
aut-affil-num=9
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=秋田美月
kn-aut-sei=秋田
kn-aut-mei=美月
aut-affil-num=10
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=石村竜大
kn-aut-sei=石村
kn-aut-mei=竜大
aut-affil-num=11
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=井上希美
kn-aut-sei=井上
kn-aut-mei=希美
aut-affil-num=12
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=坂田奈菜子
kn-aut-sei=坂田
kn-aut-mei=奈菜子
aut-affil-num=13
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=森崇人
kn-aut-sei=森
kn-aut-mei=崇人
aut-affil-num=14
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=森脇日菜子
kn-aut-sei=森脇
kn-aut-mei=日菜子
aut-affil-num=15
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=山本美玖
kn-aut-sei=山本
kn-aut-mei=美玖
aut-affil-num=16
ORCID=
affil-num=1
en-affil=
kn-affil=
affil-num=2
en-affil=
kn-affil=
affil-num=3
en-affil=
kn-affil=
affil-num=4
en-affil=
kn-affil=
affil-num=5
en-affil=
kn-affil=
affil-num=6
en-affil=
kn-affil=
affil-num=7
en-affil=
kn-affil=
affil-num=8
en-affil=
kn-affil=
affil-num=9
en-affil=
kn-affil=
affil-num=10
en-affil=
kn-affil=
affil-num=11
en-affil=
kn-affil=
affil-num=12
en-affil=
kn-affil=
affil-num=13
en-affil=
kn-affil=
affil-num=14
en-affil=
kn-affil=
affil-num=15
en-affil=
kn-affil=
affil-num=16
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=11
cd-vols=
no-issue=10
article-no=
start-page=1730
end-page=1740
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20221027
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Lip pleomorphic adenomas: case series and literature review
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Background: Pleomorphic adenoma (PA) is the most frequent benign salivary gland tumor, but a lip PA is rare. Although this tumor may be definitively diagnosed by imaging or a tissue biopsy if it is reasonably large, PAs on the lip are relatively small, and they present findings that are similar to those of other lip lesions, which can make a preoperative diagnosis difficult.
Methods: We analyzed all PAs in the oral region and lesions on the lips treated in our department over the past 20 years, and we discuss them together with the relevant literature.
Results: We found that 11.8% (n=6) of the PAs occurred on a lip (upper lip: 9.8%, lower lip: 2.0%), and ~1% of all mass lesions of the lips were PAs. The average size of the lip PAs was 1.5±0.7 cm (range, 0.7–2.2 cm). For preoperative diagnostic assistance, ultrasonography (US) (n=4), magnetic resonance (MR) (n=3), or no imaging (n=2) was used. An excisional biopsy was performed in all cases, and to date, no recurrence or malignant transformation has been observed.
Conclusions: Lip PA is relatively rare. Because almost all of these lesions are small, a preoperative diagnosis is more difficult compared to palatal lesions. This tumor is also prone to long-term neglect and has the potential for recurrence and malignant transformation. It is thus necessary to perform an excision that includes the capsule and surrounding tissues, and careful postoperative follow-up should be continued.
en-copyright=
kn-copyright=
en-aut-name=UmemoriKoki
en-aut-sei=Umemori
en-aut-mei=Koki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KanemotoHideka
en-aut-sei=Kanemoto
en-aut-mei=Hideka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=NakanoKeisuke
en-aut-sei=Nakano
en-aut-mei=Keisuke
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=5
en-affil=Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=9
en-affil=Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
en-keyword=Pleomorphic adenoma (PA)
kn-keyword=Pleomorphic adenoma (PA)
en-keyword=upper lip
kn-keyword=upper lip
en-keyword=lower lip
kn-keyword=lower lip
en-keyword=minor salivary gland tumor
kn-keyword=minor salivary gland tumor
en-keyword=case series
kn-keyword=case series
END
start-ver=1.4
cd-journal=joma
no-vol=49
cd-vols=
no-issue=
article-no=
start-page=15
end-page=29
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20220331
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=『ダロウェイ夫人』の配色における考察
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野和子
kn-aut-sei=小野
kn-aut-mei=和子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=19
cd-vols=
no-issue=15
article-no=
start-page=2745
end-page=2754
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2023
dt-pub=20230323
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Toughening of poly(ionic liquid)-based ion gels with cellulose nanofibers as a sacrificial network
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Ion gels have the potential to be used in a broad range of applications, such as in carbon dioxide separation membranes and soft electronics. However, their low mechanical strength limits their practical applications. In this study, we developed double-network (DN) ion gels composed of TEMPO-oxidized cellulose nanofibers with hydrophobic groups (TOCNF) and cross-linked poly[1-ethyl-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide] (PC2im-TFSI) networks. The mechanical strength of the gel increased as the amount of TOCNF in the gels increased up to 6 wt%. Moreover, the fracture energy of the DN ion gels with 6 wt% TOCNF was found to be 19 times higher than that of the PC2im-TFSI single network (SN) ion gels. Cyclic stress-strain measurements of the DN gels showed that the loading energy on the gels dissipates owing to the destruction of the physically cross-linked TOCNF network in the gels. The DN ion gels also exhibited a high decomposition temperature of approximately 400 degrees C because of the thermal stability of all components. Additionally, the fracture energy of the TOCNF/poly(ionic liquid) (PIL) DN ion gel was two times higher than that of the silica nanoparticles/PIL DN ion gel developed in our previous study [Watanabe et al., Soft Matter, 2020, 16, 1572-1581]. This suggests that fiber-shaped nanomaterials are more effective than spherical nanomaterials in enhancing the mechanical properties of ion gels. These results show that TOCNF can be used to toughen PIL-based ion gels and hence broaden their applications.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OeEmiho
en-aut-sei=Oe
en-aut-mei=Emiho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=MizutaniYuna
en-aut-sei=Mizutani
en-aut-mei=Yuna
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=55
cd-vols=
no-issue=
article-no=
start-page=119
end-page=139
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2023
dt-pub=20230327
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=“Gja1軍” in the Social-military System of the Tangut Empire―A Critical Analysis of the Tian Sheng Code Vol.4―
kn-title=西夏の「軍gja1」に関する一試論―西夏語文献『天盛禁令』巻4の条文に基づいて―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoHiroko
en-aut-sei=Ono
en-aut-mei=Hiroko
kn-aut-name=小野裕子
kn-aut-sei=小野
kn-aut-mei=裕子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=12
cd-vols=
no-issue=9
article-no=
start-page=2146
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20220903
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Craniomaxillofacial Fibrous Dysplasia Improved Cosmetic and Occlusal Problem by Comprehensive Treatment: A Case Report and Review of Current Treatments
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Fibrous dysplasia (FD) is a fibrous lesion of immature bone, with an incidence of 10-20% in the head and neck region. Most cases are monostotic, but when a lesion occurs on the maxillofacial region and spreads to the surrounding bone, it is classified as polyostotic, despite its localized occurrence. In some cases, surgical intervention is required to improve the cosmetic or functional disturbance of a FD in the maxillofacial region, but it is necessary to confirm symmetry of the maxillofacial region in real time, and a surgical support system is required to compensate. Furthermore, prosthetic intervention is considered when postoperative acquired defects occur or further cosmetic or occlusal function improvement is needed. A comprehensive approach by an oral surgeon and a maxillofacial prosthodontist is necessary for the successful treatment and rehabilitation of such patients. In this article, we describe the case of a craniomaxillofacial FD patient with facial asymmetry and denture incompatibility with improved quality of life measures by integrating surgical treatment using a navigation system and postoperative prosthetic rehabilitation. We also discuss recent diagnostic methods and treatment strategies for craniomaxillofacial FD in the literature.
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=YoshiokaNorie
en-aut-sei=Yoshioka
en-aut-mei=Norie
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=NakamuraYuko
en-aut-sei=Nakamura
en-aut-mei=Yuko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=MinagiShogo
en-aut-sei=Minagi
en-aut-mei=Shogo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Occlusal and Oral Functional Rehabilitation, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
en-keyword=fibrous dysplasia
kn-keyword=fibrous dysplasia
en-keyword=polyostotic
kn-keyword=polyostotic
en-keyword=craniomaxillofacial
kn-keyword=craniomaxillofacial
en-keyword=surgical
kn-keyword=surgical
en-keyword=prosthetic
kn-keyword=prosthetic
en-keyword=comprehensive treatment
kn-keyword=comprehensive treatment
END
start-ver=1.4
cd-journal=joma
no-vol=19
cd-vols=
no-issue=8
article-no=
start-page=1320
end-page=1333
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20220718
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Reproduction of the Antitumor Effect of Cisplatin and Cetuximab Using a Three-dimensional Spheroid Model in Oral Cancer
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Background/Aim: Cancer research has been conducted using cultured cells as part of drug discovery testing, but conventional two-dimensional culture methods are unable to reflect the complex tumor microenvironment. On the other hand, three-dimensional cultures have recently been attracting attention as in vitro models that more closely resemble the in vivo physiological environment. The purpose of this study was to establish a 3D culture method for oral cancer and to verify its practicality.
Materials and Methods: Three-dimensional cultures were performed using several oral cancer cell lines. Western blotting was used for protein expression analysis of the collected cell masses (spheroids), and H-E staining was used for structural observation. The cultures were exposed to cisplatin and cetuximab and the morphological changes of spheroids over time and the expression changes of target proteins were compared.
Results: Each cell line formed spheroidal cell aggregates and showed enhancement of cell adhesion molecules over time. H-E staining showed tumor tissue-like structures specific to each cell line. Cisplatin showed concentration-dependent antitumor effects due to loss of cell adhesion and spheroid disruption in each cell line, while cetuximab exhibited antitumor effects that correlated with EGFR expression in each cell line.
Conclusion: Spheroids made from oral cancer cell lines appeared to have tumor-like characteristics that may reflect their clinical significance. In the future, it may become possible to produce tumor spheroids from tissue samples of oral cancer patients, and then apply them to drug screening and to develop individualized diagnostic and treatment methods.
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=SatoKohei
en-aut-sei=Sato
en-aut-mei=Kohei
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=YoshidaYume
en-aut-sei=Yoshida
en-aut-mei=Yume
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=MurataShogo
en-aut-sei=Murata
en-aut-mei=Shogo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=YoshidaKunihiro
en-aut-sei=Yoshida
en-aut-mei=Kunihiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=KanemotoHideka
en-aut-sei=Kanemoto
en-aut-mei=Hideka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=UmemoriKoki
en-aut-sei=Umemori
en-aut-mei=Koki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=HasegawaKazuaki
en-aut-sei=Hasegawa
en-aut-mei=Kazuaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=15
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=16
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=17
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=11
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Oral and Maxillofacial Surgery, Shimane University Faculty of Medicine
kn-affil=
affil-num=15
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=16
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=17
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
en-keyword=oral cancer
kn-keyword=oral cancer
en-keyword=spheroid
kn-keyword=spheroid
en-keyword=three-dimensional culture
kn-keyword=three-dimensional culture
en-keyword=anticancer drug
kn-keyword=anticancer drug
END
start-ver=1.4
cd-journal=joma
no-vol=2
cd-vols=
no-issue=3
article-no=
start-page=250
end-page=259
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20220126
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Microfluidic Production of Monodisperse Biopolymer Microcapsules for Latent Heat Storage
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Microencapsulation of phase change materials in a polymer shell is a promising technology to prevent them from leakage and to use them as a handleable powder state. However, the microencapsulation process is a time-consuming process because the typical shell-forming step requires polymerization or evaporation of the solvent. In this study, we report a simple and rapid flow process to prepare monodisperse biocompatible cellulose acetate (CA) microcapsules encapsulating n-hexadecane (HD) for latent heat storage applications. The microcapsules were prepared by combining microfluidic droplet formation and subsequent rapid solvent removal from the droplets by solvent diffusion. The diameter and shell thickness of the microcapsules could be controlled by adjusting the flow rate and the HD-to-CA weight ratio in the dispersed phase. We found that 1-hexadecanol added to the microcapsules played the role of a nucleation agent and mitigated the supercooling phenomenon during crystallization. Furthermore, cross-linking of the CA shell with poly(propylene glycol), tolylene 2,4-diisocyanate terminated, resulted in the formation of a thin and dense shell. The microcapsules exhibited a 66 wt % encapsulation efficiency and a 176 J g–1 latent heat storage capacity, with negligible supercooling. We believe that this microflow process can contribute to the preparation of environmentally friendly microcapsules for heat storage applications.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=SakaiYuko
en-aut-sei=Sakai
en-aut-mei=Yuko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=SugimoriNaomi
en-aut-sei=Sugimori
en-aut-mei=Naomi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=IkedaToshinori
en-aut-sei=Ikeda
en-aut-mei=Toshinori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=MonzenMasayuki
en-aut-sei=Monzen
en-aut-mei=Masayuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Chusei Oil Co., Ltd.
kn-affil=
affil-num=4
en-affil=Chusei Oil Co., Ltd.
kn-affil=
affil-num=5
en-affil=Chusei Oil Co., Ltd.
kn-affil=
affil-num=6
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
en-keyword=microfluidics
kn-keyword=microfluidics
en-keyword=phase separation
kn-keyword=phase separation
en-keyword=core−shell
kn-keyword=core−shell
en-keyword=cellulose acetate
kn-keyword=cellulose acetate
en-keyword=latent heat storage
kn-keyword=latent heat storage
END
start-ver=1.4
cd-journal=joma
no-vol=7
cd-vols=
no-issue=1
article-no=
start-page=e148960
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2022
dt-pub=20220111
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Resident stroma-secreted chemokine CCL2 governs myeloid-derived suppressor cells in the tumor microenvironment
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Accumulating evidence has shown that cancer stroma and BM-derived cells (BMDCs) in the tumor microenvironment (TME) play vital roles in tumor progression. However, the mechanism by which oral cancer stroma recruits any particular subset of BMDCs remains largely unknown. Here, we sought to identify the subset of BMDCs that is recruited by cancer stroma. We established a sequential transplantation model in BALB/c nude mice, including (a) BM transplantation of GFP-expressing cells and (b) coxenografting of patient-derived stroma (PDS; 2 cases, designated PDS1 and PDS2) with oral cancer cells (HSC-2). As controls, xenografting was performed with HSC-2 alone or in combination with normal human dermal fibroblasts (HDF). PDS1, PDS2, and HDF all promoted BMDC migration in vitro and recruitment in vivo. Multicolor immunofluorescence revealed that the PDS coxenografts recruited Arginase-1(+)CD11b(+)GR1(+)GFP(+) cells, which are myeloid-derived suppressor cells (MDSCs), to the TME, whereas the HDF coxenograft did not. Screening using microarrays revealed that PDS1 and PDS2 expressed CCL2 mRNA (encoding C-C motif chemokine ligand 2) at higher levels than did HDF. Indeed, PDS xenografts contained significantly higher proportions of CCL2(+) stromal cells and CCR2(+)Arginase-1(+)CD11b(+)GR1(+) MDSCs (as receiver cells) than the HDF coxenograft. Consistently, a CCL2 synthesis inhibitor and a CCR2 antagonist significantly inhibited the PDS-driven migration of BM cells in vitro. Furthermore, i.p. injection of the CCR2 antagonist to the PDS xenograft models significantly reduced the CCR2(+)Arginase-1(+)CD11b(+)GR1(+) MDSC infiltration to the TME. In conclusion, oral cancer stroma-secreted CCL2 is a key signal for recruiting CCR2(+) MDSCs from BM to the TME.
en-copyright=
kn-copyright=
en-aut-name=OoMay Wathone
en-aut-sei=Oo
en-aut-mei=May Wathone
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=TakabatakeKiyofumi
en-aut-sei=Takabatake
en-aut-mei=Kiyofumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=TomidaShuta
en-aut-sei=Tomida
en-aut-mei=Shuta
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=EguchiTakanori
en-aut-sei=Eguchi
en-aut-mei=Takanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=ShanQiusheng
en-aut-sei=Shan
en-aut-mei=Qiusheng
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=OharaToshiaki
en-aut-sei=Ohara
en-aut-mei=Toshiaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=YoshidaSaori
en-aut-sei=Yoshida
en-aut-mei=Saori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=OmoriHaruka
en-aut-sei=Omori
en-aut-mei=Haruka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=SukegawaShintaro
en-aut-sei=Sukegawa
en-aut-mei=Shintaro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=NakanoKeisuke
en-aut-sei=Nakano
en-aut-mei=Keisuke
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=OkamotoKuniaki
en-aut-sei=Okamoto
en-aut-mei=Kuniaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=15
ORCID=
affil-num=1
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Center for Comprehensive Genomic Medicine, Okayama University Hospital
kn-affil=
affil-num=5
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Pathology and Experimental Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=11
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=15
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=4
cd-vols=
no-issue=1
article-no=
start-page=348
end-page=356
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20211222
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Multilayer Poly(ionic liquid) Microcapsules Prepared by Sequential Phase Separation and Subsequent Photopolymerization in Ternary Emulsion Droplets
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We report a simple microfluidic process to prepare multilayer poly(ionic liquid)s (PILs) microcapsules via sequential liquid-liquid phase separation within ternary emulsion droplets followed by the photopolymerization of ionic liquid (IL) monomerrich phases. The emulsion droplets, consisting of a hydrophobic IL monomer, water, and N,N-dimethylformamide (DMF) are first formed in a microfluidic device, and the droplets are then carried by a continuous aqueous phase. Subsequently, DMF diffuses from the droplets into the continuous aqueous phase, resulting in the sequential internal phase separation of the IL-rich and water-rich phases, generating multilayer emulsion droplets comprising alternating IL-rich and water-rich phases. The number of droplet layers was controlled from one to five by varying the initial composition of the dispersed phase. Furthermore, in the conditions where higher-order emulsion droplets were formed, the time scale between the onset of phase separation and the formation of each layer became shorter. Additionally, the IL-rich phases in the multilayer emulsion droplets were easily solidified via photopolymerization, resulting in PILs microcapsules with multilayer structures. Anion exchange of the obtained PILs microcapsules effectuated their transition from a hydrophobic to a hydrophilic nature, resulting in PILs microcapsules with diverse swelling properties and PILs layers permeability across various solvents. We believe that the sequential phase separation system observed in the ternary emulsion droplets can pave the way for the design of PILs-based colloidal materials with thermodynamically non-equilibrium structures, thereby extending their application in functional materials.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=YasuharaYuka
en-aut-sei=Yasuhara
en-aut-mei=Yuka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama 700-8530, Japan
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama 700-8530, Japan
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama 700-8530, Japan
kn-affil=
en-keyword=Microfluidics
kn-keyword=Microfluidics
en-keyword=Multiple emulsion
kn-keyword=Multiple emulsion
en-keyword=Poly(ionic liquid)
kn-keyword=Poly(ionic liquid)
en-keyword=Phase separation
kn-keyword=Phase separation
en-keyword=Non-equilibrium structure
kn-keyword=Non-equilibrium structure
END
start-ver=1.4
cd-journal=joma
no-vol=11
cd-vols=
no-issue=8
article-no=
start-page=1375
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210730
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Comparative Study on Epstein-Barr Virus-Positive Mucocutaneous Ulcer and Methotrexate-Associated Lymphoproliferative Disorders Developed in the Oral Mucosa: A Case Series of 10 Patients and Literature Review
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Methotrexate-associated lymphoproliferative disorder (MTX-LPD) is an iatrogenic immunodeficiency-associated lymphoproliferative disorder that occurs mainly with MTX use. This disorder has been associated with Epstein-Barr virus (EBV) infection. In 2017, the WHO newly defined the disease concept of EBV-positive mucocutaneous ulcer (EBV-MCU) as a good-prognosis EBV-related disease. Here, we report 10 cases of MTX-LPD or EBV-MCU in the oral mucosa. This retrospective, observational study was conducted with MTX-LPD or EBV-MCU in the oral mucosa patients who visited us during the nine year period from 2012 to 2021. We gathered the basic information, underlying disease, histopathological evaluation, treatment and prognosis for the subjects. All were being treated with MTX for rheumatoid arthritis. EBV infection was positive in all cases by immunohistochemistry. A complete or partial response was obtained in all cases with the withdrawal of MTX. Our results suggests that the most common risk factor for developing EBV-MCU is the use of immunosuppressive drugs. The most common site of onset is the oral mucosa, which may be attributed to the mode of EBV infection and the high incidence of chronic irritation of the oral mucosa. A small number of patients had been diagnosed with MTX-LPD, but we consider that these cases were EBV-MCU based on our study.
en-copyright=
kn-copyright=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoSawako
en-aut-sei=Ono
en-aut-mei=Sawako
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=UmemoriKoki
en-aut-sei=Umemori
en-aut-mei=Koki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=YaoMayumi
en-aut-sei=Yao
en-aut-mei=Mayumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=YoshiokaNorie
en-aut-sei=Yoshioka
en-aut-mei=Norie
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Shimane University Faculty of Medicine
kn-affil=
affil-num=3
en-affil=Department of Pathology, Kagawa Prefectural Central Hospital
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Dentistry and Dental Surgery, Tsuyama Chuo Hospital
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
en-keyword=methotrexate
kn-keyword=methotrexate
en-keyword=lymphoproliferative disorders
kn-keyword=lymphoproliferative disorders
en-keyword=Epstein-Barr virus
kn-keyword=Epstein-Barr virus
en-keyword=mucocutaneous ulcer
kn-keyword=mucocutaneous ulcer
en-keyword=rheumatoid arthritis
kn-keyword=rheumatoid arthritis
END
start-ver=1.4
cd-journal=joma
no-vol=9
cd-vols=
no-issue=6
article-no=
start-page=e04321
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210624
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=A case of langerhans cell histiocytosis of the mandible that spontaneously regressed after biopsy in a child
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=In younger patients of LCH, we should consider that the effectiveness of follow-up without aggressive treatment for SS-type LCH in the oral and maxillofacial bone. However, there are very rare case in which an SS-type LCH recurred after showing a healing tendency. Regular follow-up must be performed even after healing.
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=MasuiMasanori
en-aut-sei=Masui
en-aut-mei=Masanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
en-keyword=dentistry
kn-keyword=dentistry
en-keyword=general surgery
kn-keyword=general surgery
en-keyword=oncology
kn-keyword=oncology
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=GPAMゲノム中におけるGPAM抑制のためのRBV応答性シスエレメントの同定
kn-title=Identification of ribavirin-responsive cis-elements for GPAM suppression in the GPAM genome
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnomuraDaichi
en-aut-sei=Onomura
en-aut-mei=Daichi
kn-aut-name=小野村大地
kn-aut-sei=小野村
kn-aut-mei=大地
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=6
cd-vols=
no-issue=15
article-no=
start-page=10030
end-page=10038
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210409
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Design of Clickable Ionic Liquid Monomers to Enhance Ionic Conductivity for Main-Chain 1,2,3-Triazolium-Based Poly(Ionic Liquid)s
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A series of clickable alpha-azide-omega-alkyne ionic liquid (IL) monomers with an ethylene oxide spacer were developed and applied to the synthesis of 1,2,3-triazolium-based poly(ionic liquid)s (TPILs) with high ionic conductivities via one-step thermal azide-alkyne cycloaddition click chemistry. Subsequently, the number of IL moieties in the resultant TPILs was further increased by N-alkylation of the 1,2,3-triazole-based backbones of the TPILs with a quarternizing reagent. This strategy affords the preparation of TPILs having either one or two 1,2,3-triazolium cations with bis(trifluoromethylsulfonyl)imide anions in a monomer unit. Synthesis of the TPILs was confirmed by H-1 and C-13 NMR spectroscopy and gel permeation chromatography. The effects of the length of the ethylene oxide spacer and the number of IL moieties in the IL monomer unit on the physicochemical properties of the TPILs were characterized by differential scanning calorimetry, thermogravimetric analysis, and impedance spectroscopy. The introduction of a longer ethylene oxide spacer or an increase in the number of IL moieties in the monomer unit resulted in TPILs with lower glass-transition temperatures and higher ionic conductivities. The highest ionic conductivity achieved in this study was 2.0 x 10(-5) S cm(-1) at 30 degrees C. These results suggest that the design of the IL monomer provides the resultant polymer with high chain flexibility and a high IL density, and so it is effective for preparing TPILs with high ionic conductivities.
en-copyright=
kn-copyright=
en-aut-name=HiraiRuka
en-aut-sei=Hirai
en-aut-mei=Ruka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=26
cd-vols=
no-issue=
article-no=
start-page=100330
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210228
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=The HMGB1/RAGE axis induces bone pain associated with colonization of 4T1 mouse breast cancer in bone
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Bone pain is a common complication of breast cancer (BC) bone metastasis and is a major cause of increased morbidity and mortality. Although the mechanism of BC-associated bone pain (BCABP) remains poorly understood, involvement of BC products in the pathophysiology of BCABP has been proposed. Aggressive cancers secrete damage-associated molecular patterns (DAMPs) that bind to specific DAMP receptors and modulate cancer microenvironment. A prototypic DAMP, high mobility group box 1 (HMGB1), which acts as a ligand for the receptor for advanced glycation end products (RAGE) and toll-like receptors (TLRs), is increased in its expression in BC patients with poor outcomes. Here we show that 4T1 mouse BC cells colonizing bone up-regulate the expression of molecular pain markers, phosphorylated ERK1/2 (pERK) and pCREB, in the dorsal root ganglia (DRGs) innervating bone and induced BCABP as evaluated by hind-paw mechanical hypersensitivity. Importantly, silencing HMGB1 in 4T1 BC cells by shRNA reduced pERK and pCREB and BCABP with decreased HMGB1 levels in bone. Further, administration of a neutralizing antibody to HMGB1 or an antagonist for RAGE, FPS-ZM1, ameliorated pERK, pCREB and BCABP, while a TLR4 antagonist, TAK242, showed no effects. Consistent with these in vivo results, co-cultures of F11 sensory neuron-like cells with 4T1 BC cells in microfluidic culture platforms increased neurite outgrowth of F11 cells, which was blocked by HMGB1 antibody. Our results show that HMGB1 secreted by BC cells induces BCABP via binding to RAGE of sensory neurons and suggest that the HMGB1/RAGE axis may be a potential novel therapeutic target for BCABP.
en-copyright=
kn-copyright=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=HiasaMasahiro
en-aut-sei=Hiasa
en-aut-mei=Masahiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=RoodmanG. David
en-aut-sei=Roodman
en-aut-mei=G. David
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=WhiteFletcher A.
en-aut-sei=White
en-aut-mei=Fletcher A.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=YonedaToshiyuki
en-aut-sei=Yoneda
en-aut-mei=Toshiyuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=2
en-affil=Department of Biomaterials and Bioengineerings, University of Tokushima Graduate School of Dentistry
kn-affil=
affil-num=3
en-affil=
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=8
en-affil=Department of Medicine, Hematology Oncology, Indiana University School of Medicine
kn-affil=
affil-num=9
en-affil=Department of Anesthesia, Paul and Carole Stark Neurosciences Research Institute
kn-affil=
affil-num=10
en-affil=Department of Cellular and Molecular Biochemistry, Osaka University Graduate School of Dentistry
kn-affil=
en-keyword=Breast cancer
kn-keyword=Breast cancer
en-keyword=Bone pain
kn-keyword=Bone pain
en-keyword=Sensory neurons
kn-keyword=Sensory neurons
en-keyword=HMGB1
kn-keyword=HMGB1
en-keyword=RAGE
kn-keyword=RAGE
END
start-ver=1.4
cd-journal=joma
no-vol=9
cd-vols=
no-issue=1
article-no=
start-page=1769373
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200531
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Triple knockdown of CDC37, HSP90‐alpha and HSP90‐beta diminishes extracellular vesicles‐driven malignancy events and macrophage M2 polarization in oral cancer
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Evidence has been accumulating to indicate that extracellular vesicles (EVs), including exosomes, released by cancer cells can foster tumour progression. The molecular chaperones – CDC37, HSP90α and HSP90β play key roles in cancer progression including epithelial‐mesenchymal transition (EMT), although their contribution to EVs‐mediated cell–cell communication in tumour microenvironment has not been thoroughly examined. Here we show that triple depletion of the chaperone trio attenuates numerous cancer malignancy events exerted through EV release. Metastatic oral cancer‐derived EVs (MEV) were enriched with HSP90α HSP90β and cancer‐initiating cell marker CD326/EpCAM. Depletion of these chaperones individually induced compensatory increases in the other chaperones, whereas triple siRNA targeting of these molecules markedly diminished the levels of the chaperone trio and attenuated EMT. MEV were potent agents in initiating EMT in normal epithelial cells, a process that was attenuated by the triple chaperone depletion. The migration, invasion, and in vitro tumour initiation of oral cancer cells were significantly promoted by MEV, while triple depletion of CDC37/HSP90α/β reversed these MEV‐driven malignancy events. In metastatic oral cancer patient‐derived tumours, HSP90β was significantly accumulated in infiltrating tumour‐associated macrophages (TAM) as compared to lower grade oral cancer cases. HSP90‐enriched MEV‐induced TAM polarization to an M2 phenotype, a transition known to support cancer progression, whereas the triple chaperone depletion attenuated this effect. Mechanistically, the triple chaperone depletion in metastatic oral cancer cells effectively reduced MEV transmission into macrophages. Hence, siRNA‐mediated knockdown of the chaperone trio (CDC37/HSP90α/HSP90β) could potentially be a novel therapeutic strategy to attenuate several EV‐driven malignancy events in the tumour microenvironment.
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=Sogawa Chiharu
en-aut-sei=Sogawa
en-aut-mei= Chiharu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=Manh Tien Tran
en-aut-sei=Manh Tien Tran
en-aut-mei=
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=TahaEman A.
en-aut-sei=Taha
en-aut-mei=Eman A.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=LuYanyin
en-aut-sei=Lu
en-aut-mei=Yanyin
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=May Wathone Oo
en-aut-sei=May Wathone Oo
en-aut-mei=
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=OkushaYuka
en-aut-sei=Okusha
en-aut-mei=Yuka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=OkamuraHirohiko
en-aut-sei=Okamura
en-aut-mei=Hirohiko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=TakigawaMasaharu
en-aut-sei=Takigawa
en-aut-mei=Masaharu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=KozakiKen-Ichi
en-aut-sei=Kozaki
en-aut-mei=Ken-Ichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
en-aut-name=OkamotoKuniaki
en-aut-sei=Okamoto
en-aut-mei=Kuniaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=15
ORCID=
en-aut-name=CalderwoodStuart K.
en-aut-sei=Calderwood
en-aut-mei=Stuart K.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=16
ORCID=
en-aut-name=EguchiTakanori
en-aut-sei=Eguchi
en-aut-mei=Takanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=17
ORCID=
affil-num=1
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=6
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=9
en-affil=Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Hospital
kn-affil=
affil-num=11
en-affil=Advanced Research Center for Oral and Craniofacial Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Hospital
kn-affil=
affil-num=15
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=16
en-affil=Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School
kn-affil=
affil-num=17
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
en-keyword=Extracellular vesicles
kn-keyword=Extracellular vesicles
en-keyword=epithelial‐mesenchymal transition
kn-keyword=epithelial‐mesenchymal transition
en-keyword=tumour‐associated macrophage
kn-keyword=tumour‐associated macrophage
en-keyword=CDC37
kn-keyword=CDC37
en-keyword=HSP90
kn-keyword=HSP90
en-keyword=tetraspanin
kn-keyword=tetraspanin
en-keyword=oral cancer
kn-keyword=oral cancer
END
start-ver=1.4
cd-journal=joma
no-vol=50
cd-vols=
no-issue=
article-no=
start-page=179
end-page=197
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2021
dt-pub=20210127
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Institutional Mechanism of the Borderlands Patrol in the Tangut State: Reinterpretation of Tiansheng Code Vol.4
kn-title=西夏の巡検制度 : 『天盛旧改新定禁令』巻4「辺地巡検門」中の12条を中心に
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoHiroko
en-aut-sei=Ono
en-aut-mei=Hiroko
kn-aut-name=小野裕子
kn-aut-sei=小野
kn-aut-mei=裕子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院社会文化科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=10
cd-vols=
no-issue=62
article-no=
start-page=37743
end-page=37748
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20201013
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=One-pot synthesis of poly(ionic liquid)s with 1,2,3-triazolium-based backbones via clickable ionic liquid monomers
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Clickable α-azide-ω-alkyne ionic liquid monomers were developed and subsequently applied to the one-pot synthesis of ionically conducting poly(ionic liquid)s with 1,2,3-triazolium-based backbones through a click chemistry strategy. This approach does not require the use of solvents, polymerisation mediators, or catalysts. The obtained poly(ionic liquid)s were characterized by NMR, differential scanning calorimetry, thermogravimetric analysis, and impedance spectroscopy analysis. Moreover, these poly(ionic liquid)s were cross-linked via N-alkylation with a dianion quarternizing agent to achieve enhanced ionic conductivity and mechanical strength. The resulting free-standing films showed a Young's modulus up to 4.8 MPa and ionic conductivities up to 4.60 × 10−8 S cm−1 at 30 °C. This facile synthetic strategy has the potential to expand the availability of poly(ionic liquid)s and promote the development of functional materials.
en-copyright=
kn-copyright=
en-aut-name=HiraiRuka
en-aut-sei=Hirai
en-aut-mei=Ruka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=HibinoTatsuki
en-aut-sei=Hibino
en-aut-mei=Tatsuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=44
cd-vols=
no-issue=6
article-no=
start-page=2547
end-page=2558
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20201002
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=High mobility group box 1 induces bone pain associated with bone invasion in a mouse model of advanced head and neck cancer
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Advanced head and neck cancer (HNC) can invade facial bone and cause bone pain, thus posing a significant challenge to the quality of life of patients presenting with advanced HNC. The present study was designed to investigate HNC bone pain (HNC‑BP) in an intratibial mouse xenograft model that utilized an HNC cell line (SAS cells). These mice develop HNC‑BP that is associated with an expression of phosphorylated ERK1/2 (pERK1/2), which is a molecular indicator of neuron excitation in dorsal root ganglia (DRG) sensory neurons. Our experiments demonstrated that the inhibition of high mobility group box 1 (HMGB1) by short hairpin (shRNA) transduction, HMGB1 neutralizing antibody, and HMGB1 receptor antagonist suppressed the HNC‑BP and the pERK1/2 expression in DRG. It was also observed that HNC‑derived HMGB1 increased the expression of the acid‑sensing nociceptor, transient receptor potential vanilloid 1 (TRPV1), which is a major cause of osteoclastic HNC‑BP in DRG. Collectively, our results demonstrated that HMGB1 originating in HNC evokes HNC‑BP via direct HMGB1 signaling and hypersensitization for the acid environment in sensory neurons.
en-copyright=
kn-copyright=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=HasegawaKazuaki
en-aut-sei=Hasegawa
en-aut-mei=Kazuaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=MasuiMasanori
en-aut-sei=Masui
en-aut-mei=Masanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=ShimoTsuyoshi
en-aut-sei=Shimo
en-aut-mei=Tsuyoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science,
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=10
en-affil=Division of Reconstructive Surgery for Oral and Maxillofacial Region, Department of Human Biology and Pathophysiology, School of Dentistry, Health Sciences University of Hokkaido
kn-affil=
affil-num=11
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
en-keyword=head and neck cancer
kn-keyword=head and neck cancer
en-keyword=bone pain
kn-keyword=bone pain
en-keyword=HMGB1
kn-keyword=HMGB1
en-keyword=RAGE
kn-keyword=RAGE
en-keyword=sensory neuron
kn-keyword=sensory neuron
END
start-ver=1.4
cd-journal=joma
no-vol=9
cd-vols=
no-issue=1
article-no=
start-page=180
end-page=184
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20201106
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Surgical resection of a giant peripheral ossifying fibroma in mouth floor managed with fiberscopic intubation
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Tracheal intubation for general anesthesia can sometimes be difficult in patients with a large mass in the mouth floor. Preoperative evaluation of the patient's airway is most important when treating large oral disease.
en-copyright=
kn-copyright=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=HasegawaKazuaki
en-aut-sei=Hasegawa
en-aut-mei=Kazuaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
en-keyword=peripheral ossifying fibroma
kn-keyword=peripheral ossifying fibroma
END
start-ver=1.4
cd-journal=joma
no-vol=531
cd-vols=
no-issue=3
article-no=
start-page=422
end-page=430
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20201020
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=High-mobility group box 1 induces bone destruction associated with advanced oral squamous cancer via RAGE and TLR4
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Bone destruction of maxillary and mandibular bone by invasive oral squamous cell cancer (OSCC) raises various problems in the management of patients, resulting in poor outcomes and survival. However, the mechanism behind bone destruction by OSCC remains unclear. High-mobility group box 1 (HMGB1), a highly conserved ubiquitous nuclear non-histone DNA-binding protein, has been demonstrated to be secreted by aggressive cancers and regulate osteoclastogenesis, a central player during bone destruction. We therefore reasoned that HMGB1 secreted by OSCCs contributes to bone destruction. Our results showed that HMGB1 is produced by human cell lines of OSCC and promotes osteoclastogenesis via up-regulation of the expression of receptor activator of nuclear factor kappa-Β ligand in osteoblasts and osteocytes, and consequently osteoclastic bone destruction in mice. Further, we found that these actions of HMGB1 are mediated via the receptor for advanced glycation end products and toll-like receptors. These findings suggest that HMGB1 of OSCC and its down-stream signal pathways are potential targets for the treatment of bone destruction associated with advanced OSCC.
en-copyright=
kn-copyright=
en-aut-name=SakamotoYumi
en-aut-sei=Sakamoto
en-aut-mei=Yumi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=YonedaToshiyuki
en-aut-sei=Yoneda
en-aut-mei=Toshiyuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=RyumonShoji
en-aut-sei=Ryumon
en-aut-mei=Shoji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=NakamuraTomoya
en-aut-sei=Nakamura
en-aut-mei=Tomoya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=MasuiMasanori
en-aut-sei=Masui
en-aut-mei=Masanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=ShimoTsuyoshi
en-aut-sei=Shimo
en-aut-mei=Tsuyoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=3
en-affil=Department of Cellular and Molecular Biochemistry, Osaka University Graduate School of Dentistry
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=6
en-affil=Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=9
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=11
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
affil-num=12
en-affil=Division of Reconstructive Surgery for Oral and Maxillofacial Region, Department of Human Biology and Pathophysiology, School of Dentistry, Health Sciences University of Hokkaido
kn-affil=
affil-num=13
en-affil=Department of Oral and Maxillofacial Surgery and Biopathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science
kn-affil=
en-keyword=Oral squamous cell cancer
kn-keyword=Oral squamous cell cancer
en-keyword=HMGB1
kn-keyword=HMGB1
en-keyword=Bone destruction
kn-keyword=Bone destruction
en-keyword=Osteoclasts
kn-keyword=Osteoclasts
END
start-ver=1.4
cd-journal=joma
no-vol=9
cd-vols=
no-issue=3
article-no=
start-page=47
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200305
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=A Novel Model of Cancer Drug Resistance: Oncosomal Release of Cytotoxic and Antibody-Based Drugs
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Extracellular vesicles (EVs), such as exosomes or oncosomes, often carry oncogenic molecules derived from tumor cells. In addition, accumulating evidence indicates that tumor cells can eject anti-cancer drugs such as chemotherapeutics and targeted drugs within EVs, a novel mechanism of drug resistance. The EV-releasing drug resistance phenotype is often coupled with cellular dedifferentiation and transformation in cells undergoing epithelial-mesenchymal transition (EMT), and the adoption of a cancer stem cell phenotype. The release of EVs is also involved in immunosuppression. Herein, we address different aspects by which EVs modulate the tumor microenvironment to become resistant to anticancer and antibody-based drugs, as well as the concept of the resistance-associated secretory phenotype (RASP).
en-copyright=
kn-copyright=
en-aut-name=EguchiTakanori
en-aut-sei=Eguchi
en-aut-mei=Takanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=TahaEman Ahmed
en-aut-sei=Taha
en-aut-mei=Eman Ahmed
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=CalderwoodStuart K.
en-aut-sei=Calderwood
en-aut-mei=Stuart K.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=喜章
kn-aut-sei=
kn-aut-mei=喜章
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Hospital
kn-affil=
en-keyword=extracellular vesicle (EV)
kn-keyword=extracellular vesicle (EV)
en-keyword=exosome
kn-keyword=exosome
en-keyword=oncosome
kn-keyword=oncosome
en-keyword=drug resistance
kn-keyword=drug resistance
en-keyword=epithelial-mesenchymal transition (EMT)
kn-keyword=epithelial-mesenchymal transition (EMT)
en-keyword=heat shock protein (HSP)
kn-keyword=heat shock protein (HSP)
en-keyword=cell stress response
kn-keyword=cell stress response
en-keyword=resistance-associated secretory phenotype (RASP)
kn-keyword=resistance-associated secretory phenotype (RASP)
en-keyword=hypoxia
kn-keyword=hypoxia
en-keyword=acidosis
kn-keyword=acidosis
en-keyword=tumor immunology
kn-keyword=tumor immunology
END
start-ver=1.4
cd-journal=joma
no-vol=8
cd-vols=
no-issue=12
article-no=
start-page=2469
end-page=2475
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200730
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=A case of oral cancer with delayed occipital lymph node metastasis: Case report
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Consideration of unexpected metastasis in patients who have undergone neck dissection with advanced tumors must be anticipated with careful follow-up.
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=YoshiokaNorie
en-aut-sei=Yoshioka
en-aut-mei=Norie
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=MasuiMasanori
en-aut-sei=Masui
en-aut-mei=Masanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=ObataKyoichi
en-aut-sei=Obata
en-aut-mei=Kyoichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=KunisadaYuki
en-aut-sei=Kunisada
en-aut-mei=Yuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OkuiTatsuo
en-aut-sei=Okui
en-aut-mei=Tatsuo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=IbaragiSoichiro
en-aut-sei=Ibaragi
en-aut-mei=Soichiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=KawaiHotaka
en-aut-sei=Kawai
en-aut-mei=Hotaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=NagatsukaHitoshi
en-aut-sei=Nagatsuka
en-aut-mei=Hitoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=3
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=5
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=6
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=7
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=8
en-affil=Department of Oral Pathology and Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=9
en-affil=Department of Oral Pathology and Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=10
en-affil=Department of Oral and Maxillofacial Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
en-keyword=delayed metastasis
kn-keyword=delayed metastasis
en-keyword=lymphatic regurgitation
kn-keyword=lymphatic regurgitation
en-keyword=neck dissection
kn-keyword=neck dissection
en-keyword=occipital lymph node
kn-keyword=occipital lymph node
en-keyword=oral cancer
kn-keyword=oral cancer
END
start-ver=1.4
cd-journal=joma
no-vol=220
cd-vols=
no-issue=9
article-no=
start-page=1900021
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190403
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Rapid Synthesis of Poly(methyl methacrylate) Particles with High Molecular Weight by Soap‐Free Emulsion Polymerization Using Water‐in‐Oil Slug Flow
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= flow process for the production of poly(methyl methacrylate) (PMMA) particles is proposed by soap‐free emulsion polymerization using a water‐in‐oil (W/O) slug flow in a microreactor. Thin oil films generated around the dispersed aqueous phase of the W/O slug prevent the prepared particles from adhesion to the microchannel wall, enabling the continuous production of PMMA particles without clogging. The effects of the linear flow rate of the slug flow and the addition of ethanol in the dispersed aqueous phase on the polymerization are evaluated. It is found that increasing the linear flow rate of the slug flow or the addition of ethanol in the dispersed aqueous phase results in PMMA particles with high molecular weight (≈1500 kg mol−1) in 20 min reaction time. It is believed that this process would be a promising way to prepare polymer particles with high molecular weight in a short reaction time.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KaritaKengo
en-aut-sei=Karita
en-aut-mei=Kengo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=TawaraKoki
en-aut-sei=Tawara
en-aut-mei=Koki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=SogaTakuya
en-aut-sei=Soga
en-aut-mei=Takuya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Material and Energy Science, Graduate School of Environmental and Life Science, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
en-keyword=heterogeneous polymerization
kn-keyword=heterogeneous polymerization
en-keyword=internal circulation
kn-keyword=internal circulation
en-keyword=microreactors
kn-keyword=microreactors
en-keyword=microspheres
kn-keyword=microspheres
END
start-ver=1.4
cd-journal=joma
no-vol=520
cd-vols=
no-issue=
article-no=
start-page=764
end-page=770
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2017
dt-pub=20170220
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Indocyanine green-laden poly(ethylene glycol)-block-polylactide (PEG-b-PLA) nanocapsules incorporating reverse micelles: Effects of PEG-b-PLA composition on the nanocapsule diameter and encapsulation efficiency
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Reverse micelles are thermodynamically stable systems, with a capacity to encapsulate hydrophilic molecules in their nanosized core, which is smaller than the core generally obtained with water-in-oil-emulsion droplets. Herein, we present a simple technique for the preparation of poly(ethylene glycol)-block-polylactide (PEG-b-PLA) nanocapsules encapsulating a hydrophilic photosensitizer (indocyanine green, ICG), which exploits reverse micelle formation and subsequent emulsion-solvent diffusion. We establish the effect of the PEG-b-PLA composition and the co-surfactant volume on the diameter and water content of the reverse micelles. We demonstrate that the composition of PEG-b-PLA affects also the diameter and encapsulation efficiency of the resulting nanocapsules. We show that the ICG-laden nanocapsules fabricated under the most optimal conditions have a diameter of approximately 100 nm and an ICG encapsulation efficiency of 58%. We believe that the method proposed here is a promising step towards the preparation of hydrophilic drug-laden polymer nanocapsules with a small diameter and therefore suitable for use in drug delivery applications based on enhanced permeability and retention (EPR) effect-driven passive targeting.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=SakamotoYui
en-aut-sei=Sakamoto
en-aut-mei=Yui
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=InookaTetsuya
en-aut-sei=Inooka
en-aut-mei=Tetsuya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=KimuraYukitaka
en-aut-sei=Kimura
en-aut-mei=Yukitaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Division of Material and Energy Science, Graduate School of Environmental and Life Science, Okayama University
kn-affil=
affil-num=4
en-affil=Division of Material and Energy Science, Graduate School of Environmental and Life Science, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Applied Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=4
cd-vols=
no-issue=10
article-no=
start-page=4872
end-page=4877
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2013
dt-pub=20131210
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Monodisperse polylactide microcapsules with a single aqueous core prepared via spontaneous emulsification and solvent diffusion
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A simple approach to preparing monodisperse poly(D,L-lactide) (PDLLA) microcapsules with a single aqueous core is developed. The method is based on automatic water-in-oil-in-water double emulsion formation from oil-in-water single emulsion via spontaneous emulsification which voluntarily disperses part of continuous aqueous phase into the dispersed oil phase dissolving oil-soluble amphiphilic diblock copolymer, poly(D,L-lactide)-b-poly(2-dimethylaminoethyl methacylate)(PDLLA-b-PDMAEMA), followed by coalescence of tiny water droplets within the polymer droplets, coupled with quick precipitation of polymers by diluting the emulsion with water. In this study, we have investigated the effect of PDLLA to PDLLA-b-PDMAEMA ratios and flow rates of each solution during preparing the emulsion on the final morphology and the size of the microcapsules. It was found that the polymer blend ratio played a crucial role in determining internal structure of the microcapsules. The microcapsules size decreased with the increment of the flow rate ratios of the continuous phase to the dispersed phase and eventually reached 10 μm, while maintaining narrow size distribution. In addition, we have demonstrated that the microcapsules can encapsulate both hydrophilic and hydrophobic compounds during the formation.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KimuraYukitaka
en-aut-sei=Kimura
en-aut-mei=Yukitaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Material and Energy Science, Graduate School of Environmental and Life Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=35
cd-vols=
no-issue=6
article-no=
start-page=2358
end-page=2367
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190110
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Microfluidic Formation of Hydrogel Microcapsules with a Single Aqueous Core by
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We report a simple process to fabricate monodisperse tetra-arm poly(ethylene glycol) (tetra-PEG) hydrogel microcapsules with an aqueous core and a semipermeable hydrogel shell through the formation of aqueous two-phase system (ATPS) droplets consisting of a dextran-rich core and a tetra-PEG macromonomer-rich shell, followed by a spontaneous cross-end coupling reaction of tetra-PEG macromonomers in the shell. Different from conventional techniques, this process enables for the continuous production of hydrogel microcapsules from water-in-oil emulsion droplets under mild conditions in the absence of radical initiators and external stimuli such as heating and ultraviolet light irradiation. We find that rapid cross-end coupling reaction of tetra-PEG macromonomers in ATPS droplets in the range of pH from 7.4 to 7.8 gives hydrogel microcapsules with a kinetically arrested core–shell structure. The diameter and core–shell ratio of the microcapsules can be easily controlled by adjusting flow rates and ATPS compositions. On the other hand, the slow cross-end coupling reaction of tetra-PEG macromonomers in ATPS droplets at pH 7.0 and lower induces structural change from core–shell to Janus during the reaction, which eventually forms hydrogel microparticles with a thermodynamically stable crescent structure. We believe that these hydrogel microparticles with controlled structures can be used in biomedical fields such as cell encapsulation, biosensors, and drug delivery carriers for sensitive biomolecules.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=MotohiroIbuki
en-aut-sei=Motohiro
en-aut-mei=Ibuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Division of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=2
en-affil=Division of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=3
en-affil=Division of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=30
cd-vols=
no-issue=9
article-no=
start-page=2470
end-page=2479
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2014
dt-pub=2014029
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Microfluidic Approach to the Formation of Internally Porous Polymer Particles by Solvent Extraction
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We report the controlled formation of internally porous polyelectrolyte particles with diameters ranging from tens to hundreds of micrometers through selective solvent extraction using microfluidics. Solvent-resistant microdevices, fabricated by frontal photopolymerization, encapsulate binary polymer (P)/solvent (S1) mixtures by a carrier solvent phase (C) to form plugs with well-defined radii and low polydispersity; the suspension is then brought into contact with a selective extraction solvent (S2) that is miscible with C and S1 but not P, leading to the extraction of S1 from the droplets. The ensuing phase inversion yields polymer capsules with a smooth surface but highly porous internal structure. Depending on the liquid extraction time scale, this stage can be carried out in situ, within the chip, or ex situ, in an external S2 bath. Bimodal polymer plugs are achieved using asymmetrically inverted T junctions. For this demonstration, we form sodium poly(styrenesulfonate) (P) particles using water (S1), hexadecane (C), and methyl ethyl ketone (S2). We measure droplet extraction rates as a function of drop size and polymer concentration and propose a simple scaling model to guide particle formation. We find that the extraction time required to form particles from liquid droplets does not depend on the initial polymer concentration but is rather proportional to the initial droplet size. The resulting particle size follows a linear relationship with the initial droplet size for all polymer concentrations, allowing for the precise control of particle size. The internal particle porous structure exhibits a polymer density gradient ranging from a dense surface skin toward an essentially hollow core. Average particle porosities between 10 and 50% are achieved by varying the initial droplet compositions up to 15 wt % polymer. Such particles have potential applications in functional, optical, and coating materials.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=LopezCarlos G.
en-aut-sei=Lopez
en-aut-mei=Carlos G.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=DouglasJack F.
en-aut-sei=Douglas
en-aut-mei=Jack F.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=CabralJoão T.
en-aut-sei=Cabral
en-aut-mei=João T.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil= Department of Chemical Engineering, Imperial College London
kn-affil=
affil-num=3
en-affil= Materials Science and Engineering Division, National Institute of Standards and Technology
kn-affil=
affil-num=4
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Chemical Engineering, Imperial College London
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=29
cd-vols=
no-issue=46
article-no=
start-page=14082
end-page=14088
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2013
dt-pub=20131029
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Microfluidic Fabrication of Monodisperse Polylactide Microcapsules with Tunable Structures through Rapid Precipitation
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We describe a versatile and facile route to the continuous production of monodisperse polylactide (PLA) microcapsules with controllable structures. With the combination of microfluidic emulsification, solvent diffusion, and internal phase separation, uniform PLA microcapsules with a perfluorooctyl bromide (PFOB) core were successfully obtained by simply diluting monodisperse ethyl acetate (EA)-in-water emulsion with pure water. Rapid extraction of EA from the droplets into the aqueous phase enabled the solidification of the polymer droplets in a nonequilibrium state during internal phase separation between a concentrated PLA/EA phase and a PFOB phase. Higher-molecular-weight PLA generated structural complexity of the microcapsules, yielding core–shell microcapsules with covered with small PFOB droplets. Removal of the PFOB via freeze drying gave hollow microcapsules with dimpled surfaces. The core–shell ratios and the diameter of these microcapsules could be finely tuned by just adjusting the concentration of PFOB and flow rates on emulsification, respectively. These biocompatible microcapsules with controllable size and structures are potentially applicable in biomedical fields such as drug delivery carriers of many functional molecules.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KimuraYukitaka
en-aut-sei=Kimura
en-aut-mei=Yukitaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Chemistry and Biotechnology, Graduate School of Natural Science and Technolog
kn-affil=
affil-num=2
en-affil=Department of Material and Energy Science, Graduate School of Environmental and Life Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Chemistry and Biotechnology, Graduate School of Natural Science and Technology
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=16
cd-vols=
no-issue=6
article-no=
start-page=1572
end-page=1581
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20191223
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Preparation of tough, thermally stable, and water-resistant double-network ion gels consisting of silica nanoparticles/poly(ionic liquid)s through photopolymerisation of an ionic monomer and subsequent solvent removal
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We report the preparation of tough, thermally stable, and water-resistant double-network (DN) ion gels, which consist of a partially-clustered silica nanoparticle network and poly(ionic liquid) (PIL) network holding an ionic liquid. Silica nanoparticles/poly([Evim][Tf2N]) DN ion gels are prepared by photo-induced radical polymerisation of [Evim][Tf2N] in a mixture containing silica nanoparticles, [Bmim][Tf2N], ionic liquid based cross-linker [(VIM)2C4][Tf2N]2, and ethyl acetate, followed by subsequent solvent evaporation. Tensile strength measurements show that the mechanical properties of the PIL DN ion gels were higher than those of the PIL single-network (SN) ion gel. A rheological study indicates that an enhancement in mechanical strength of the PIL DN ion gels can be achieved when silica nanoparticles form partial clusters in [Bmim][Tf2N]. The cyclic stress–strain measurement of the PIL DN ion gels shows hysteresis loops, suggesting that the silica nanoparticle clusters rupture and dissipate the loading energy when the PIL DN ion gels undergo a large deformation. The fracture strength and Young's modulus of the PIL DN ion gels increase as the diameter of the silica nanoparticles is decreased. Thermogravimetric analysis measurement shows that the PIL DN ion gel has a high decomposition temperature of approximately 400 °C. Moreover, the swelling test shows that the PIL DN ion gel possesses an excellent water-resistant property because of the hydrophobic nature of the PIL backbone. We believe that such tough, thermally stable, and water-resistant PIL DN ion gels can be used as carbon dioxide separation membranes, sensors, and actuators for soft robotics.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=TakahashiRuri
en-aut-sei=Takahashi
en-aut-mei=Ruri
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Applied Chemistry, Graduate School of Natural Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=7
cd-vols=
no-issue=21
article-no=
start-page=9894
end-page=9897
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110913
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Continuous fabrication of monodisperse polylactide microspheres by droplet-to-particle technology using microfluidic emulsification and emulsion–solvent diffusion
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Monodisperse polylactide (PLA) microspheres were continuously fabricated by microfluidic emulsification and subsequent dilution in water. The diameter was precisely tuned from 6 to 50 μm by changing the flow rate of the fluids in microfluidics or the PLA concentration in the dispersed phase. The use of amphiphilic oil-soluble poly(ethylene glycol)-b-polylactide (o-PEG–PLA) as a matrix resulted in a highly porous microsphere morphology, and the porosity was controlled by blending PLA. Therefore, monodisperse PLA microspheres with the predetermined surface porosity were continuously produced by just enough reagents and energy.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KimuraYukitaka
en-aut-sei=Kimura
en-aut-mei=Yukitaka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Department of Material and Energy Science, Graduate School of Environmental Science, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Material and Energy Science, Graduate School of Environmental Science, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Material and Energy Science, Graduate School of Environmental Science, Okayama University
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=298
cd-vols=
no-issue=
article-no=
start-page=1273
end-page=1281
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200717
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Flow synthesis of monodisperse micron-sized polymer particles by heterogeneous polymerization using a water-in-oil slug flow with a non-ionic surfactant
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Flow synthesis of poly(methyl methacrylate) particles was performed by heterogeneous polymerization of methyl methacrylate using a water-in-oil (W/O) slug flow with or without a non-ionic surfactant in the continuous organic phase. It was found that undesired phenomena in this polymerization system, clogging of the channel and broadening particle size distribution, can occur when growing polymer particles adsorb to the W/O interface during polymerization, and that the addition of non-ionic surfactant to the continuous organic phase prevents the particles from adsorption to the W/O interface and gives monodisperse polymer particles. In addition, it was shown that as the initiator concentration increases, the particle diameter becomes larger, resulting in monodisperse micron-sized polymer particles with 100% monomer conversion at a 120-min reaction time. These results indicated that the heterogeneous polymerization process using a W/O slug flow can be a promising way to continuously prepare monodisperse polymer particles with micron sizes in a short reaction time.
en-copyright=
kn-copyright=
en-aut-name=WatanabeTakaichi
en-aut-sei=Watanabe
en-aut-mei=Takaichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KaritaKengo
en-aut-sei=Karita
en-aut-mei=Kengo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoTsutomu
en-aut-sei=Ono
en-aut-mei=Tsutomu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=3
en-affil=Graduate School of Natural Science and Technology, Okayama University
kn-affil=
en-keyword=Microreactor
kn-keyword=Microreactor
en-keyword=Heterogeneous polymerization
kn-keyword=Heterogeneous polymerization
en-keyword=Slug flow
kn-keyword=Slug flow
en-keyword=Monodisperse
kn-keyword=Monodisperse
en-keyword=Micron-sized particle
kn-keyword=Micron-sized particle
END
start-ver=1.4
cd-journal=joma
no-vol=12
cd-vols=
no-issue=4
article-no=
start-page=881
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200404
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Extracellular Vesicles Enriched with Moonlighting Metalloproteinase Are Highly Transmissive, Pro-Tumorigenic, and Trans-Activates Cellular Communication Network Factor (CCN2/CTGF): CRISPR against Cancer
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Matrix metalloproteinase 3 (MMP3) plays multiple roles in extracellular proteolysis as well as intracellular transcription, prompting a new definition of moonlighting metalloproteinase (MMP), according to a definition of protein moonlighting (or gene sharing), a phenomenon by which a protein can perform more than one function. Indeed, connective tissue growth factor (CTGF, aka cellular communication network factor 2 (CCN2)) is transcriptionally induced as well as cleaved by MMP3. Moreover, several members of the MMP family have been found within tumor-derived extracellular vesicles (EVs). We here investigated the roles of MMP3-rich EVs in tumor progression, molecular transmission, and gene regulation. EVs derived from a rapidly metastatic cancer cell line (LuM1) were enriched in MMP3 and a C-terminal half fragment of CCN2/CTGF. MMP3-rich, LuM1-derived EVs were disseminated to multiple organs through body fluid and were pro-tumorigenic in an allograft mouse model, which prompted us to define LuM1-EVs as oncosomes in the present study. Oncosome-derived MMP3 was transferred into recipient cell nuclei and thereby trans-activated the CCN2/CTGF promoter, and induced CCN2/CTGF production in vitro. TRENDIC and other cis-elements in the CCN2/CTGF promoter were essential for the oncosomal responsivity. The CRISPR/Cas9-mediated knockout of MMP3 showed significant anti-tumor effects such as the inhibition of migration and invasion of tumor cells, and a reduction in CCN2/CTGF promoter activity and fragmentations in vitro. A high expression level of MMP3 or CCN2/CTGF mRNA was prognostic and unfavorable in particular types of cancers including head and neck, lung, pancreatic, cervical, stomach, and urothelial cancers. These data newly demonstrate that oncogenic EVs-derived MMP is a transmissive trans-activator for the cellular communication network gene and promotes tumorigenesis at distant sites.
en-copyright=
kn-copyright=
en-aut-name=OkushaYuka
en-aut-sei=Okusha
en-aut-mei=Yuka
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=EguchiTakanori
en-aut-sei=Eguchi
en-aut-mei=Takanori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=TranManh T.
en-aut-sei=Tran
en-aut-mei=Manh T.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=SogawaChiharu
en-aut-sei=Sogawa
en-aut-mei=Chiharu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=YoshidaKaya
en-aut-sei=Yoshida
en-aut-mei=Kaya
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=ItagakiMami
en-aut-sei=Itagaki
en-aut-mei=Mami
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=TahaEman A.
en-aut-sei=Taha
en-aut-mei=Eman A.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=AoyamaEriko
en-aut-sei=Aoyama
en-aut-mei=Eriko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=OkamuraHirohiko
en-aut-sei=Okamura
en-aut-mei=Hirohiko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=KozakiKen-Ichi
en-aut-sei=Kozaki
en-aut-mei=Ken-Ichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=CalderwoodStuart K.
en-aut-sei=Calderwood
en-aut-mei=Stuart K.
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=TakigawaMasaharu
en-aut-sei=Takigawa
en-aut-mei=Masaharu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=OkamotoKuniaki
en-aut-sei=Okamoto
en-aut-mei=Kuniaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
affil-num=1
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=2
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=3
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=5
en-affil=Department of Oral Healthcare Education, Institute of Biomedical Sciences, Tokushima University Graduate School
kn-affil=
affil-num=6
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=7
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Hospital
kn-affil=
affil-num=9
en-affil=Advanced Research Center for Oral and Craniofacial Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=10
en-affil=Department of Oral Morphology, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
kn-affil=
affil-num=11
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=12
en-affil=Division of Molecular and Cellular Biology, Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School
kn-affil=
affil-num=13
en-affil=Advanced Research Center for Oral and Craniofacial Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=
en-keyword=matrix metalloproteinase
kn-keyword=matrix metalloproteinase
en-keyword=moonlighting metalloproteinase (MMP)
kn-keyword=moonlighting metalloproteinase (MMP)
en-keyword=protein moonlighting
kn-keyword=protein moonlighting
en-keyword=transcription factor
kn-keyword=transcription factor
en-keyword=extracellular vesicles
kn-keyword=extracellular vesicles
en-keyword=oncosome
kn-keyword=oncosome
en-keyword=genome editing
kn-keyword=genome editing
en-keyword=CRISPR
kn-keyword=CRISPR
en-keyword=cellular communication network factor
kn-keyword=cellular communication network factor
en-keyword=CCN2/CTGF
kn-keyword=CCN2/CTGF
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=
dt-pub=
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Aegilops cylindrica Host
kn-title=ヤギムギ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-keyword=イネ科 (Poaceae)
kn-keyword=イネ科 (Poaceae)
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=
dt-pub=
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Descurainia pinnata (Walter) Britton
kn-title=ヒメクジラグサ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-keyword=アブラナ科 (Brassicaceae)
kn-keyword=アブラナ科 (Brassicaceae)
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=小卵胞由来ブタ卵母細胞の成熟能及び初期発生能に関する研究
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoChiyuki
en-aut-sei=Ono
en-aut-mei=Chiyuki
kn-aut-name=小野千由貴
kn-aut-sei=小野
kn-aut-mei=千由貴
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Environmental and Life Science, Okayama University
kn-affil=岡山大学大学院環境生命科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=構造色発色システムを応用した新規コンポジットレジンの色調適合性に関する検討
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoSerina
en-aut-sei=Ono
en-aut-mei=Serina
kn-aut-name=小野瀬里奈
kn-aut-sei=小野
kn-aut-mei=瀬里奈
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2020
dt-pub=20200325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Porphyromonas gingivalisのPGN_0297変異株の作製とその性状解析:PGN_0297がジンジパイン活性に寄与している証拠
kn-title=Construction and characterization of a PGN_0297 mutant of Porphyromonas gingivalis: evidence of the contribution of PGN_0297 to gingipain activity
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoShintaro
en-aut-sei=Ono
en-aut-mei=Shintaro
kn-aut-name=小野晋太郎
kn-aut-sei=小野
kn-aut-mei=晋太郎
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190630
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=上腕動脈の内膜中膜複合体肥厚は糖尿病患者の冠動脈の動脈硬化と関連する
kn-title=Brachial intima-media thickness is associated with coronary artery atherosclerosis in patients with diabetes mellitus
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoTamaki
en-aut-sei=Ono
en-aut-mei=Tamaki
kn-aut-name=小野環
kn-aut-sei=小野
kn-aut-mei=環
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=ポール側面衝突した車両の変形による吸収エネルギー推定を目的とした金属管によるモデル化の提案とその解析
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoTadanori
en-aut-sei=Ono
en-aut-mei=Tadanori
kn-aut-name=小野忠則
kn-aut-sei=小野
kn-aut-mei=忠則
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Natural Science and Technology, Okayama University
kn-affil=岡山大学大学院自然科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2019
dt-pub=20190325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=細胞外小胞のHSPに富む特性は、転移性口腔癌細胞の生存を担う
kn-title=HSP-enriched properties of extracellular vesicles involve survival of metastatic oral cancer cells
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoKisho
en-aut-sei=Ono
en-aut-mei=Kisho
kn-aut-name=小野喜章
kn-aut-sei=小野
kn-aut-mei=喜章
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2018
dt-pub=20180927
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Auslander-Reiten 原理と可換 DG 代数上のlifting の問題
kn-title=An Auslander-Reiten principle and a lifting problem over commutative DG algebras
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoMaiko
en-aut-sei=Ono
en-aut-mei=Maiko
kn-aut-name=小野舞子
kn-aut-sei=小野
kn-aut-mei=舞子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Natural Science and Technology, Okayama University
kn-affil=岡山大学大学院自然科学研究科
END
start-ver=1.4
cd-journal=joma
no-vol=34
cd-vols=
no-issue=
article-no=
start-page=36
end-page=39
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2018
dt-pub=201804
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=The Deodorizing Effect of Weak Acid Hypochlorous Solution against Ammonia
kn-title=弱酸性次亜塩素酸水溶液のアンモニアに対する消臭効果
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=The deodorizing effect of weak acid hypochlorous solution against ammonia was investigated. When atomized particles of weak acid hypochlorous solution contacted ammonia, the ammonia concentration decreased in a concentration-dependent manner. The deodorizing effect was also observed against ammonia generated from the used floor cover for mice. When the floor mat was present, the ammonia concentration gently decreased but then rapidly decreased when the floor mat was removed. In the future, we will examine effective spraying conditions for weak acid hypochlorous solution in laboratory animal facilities, and we will also proceed with the validation of effects other than spraying.
en-copyright=
kn-copyright=
en-aut-name=OnoTomoko
en-aut-sei=Ono
en-aut-mei=Tomoko
kn-aut-name=小野朋子
kn-aut-sei=小野
kn-aut-mei=朋子
aut-affil-num=1
ORCID=
en-aut-name=YamashitaKoji
en-aut-sei=Yamashita
en-aut-mei=Koji
kn-aut-name=山下光治
kn-aut-sei=山下
kn-aut-mei=光治
aut-affil-num=2
ORCID=
affil-num=1
en-affil=Research and Technology Development Division,HSP company
kn-affil=株式会社エイチ・エス・ピー 研究開発部
affil-num=2
en-affil=Research and Technology Development Division,HSP company
kn-affil=株式会社エイチ・エス・ピー 研究開発部
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2018
dt-pub=20180323
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=口腔扁平上皮癌の発生と進展におけるYAPと⊿Np63の役割
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoSawako
en-aut-sei=Ono
en-aut-mei=Sawako
kn-aut-name=小野早和子
kn-aut-sei=小野
kn-aut-mei=早和子
aut-affil-num=1
ORCID=
affil-num=1
en-affil=Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
kn-affil=岡山大学大学院医歯薬学総合研究科
END
start-ver=1.4
cd-journal=joma
no-vol=129
cd-vols=
no-issue=2
article-no=
start-page=93
end-page=99
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2017
dt-pub=20170801
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=The development of a scale to measure stress recognition during the treatment of diabetes patients
kn-title=糖尿病患者の「治療に伴うストレス認知尺度」の開発
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= The purpose of this study was to establish a measurement scale for "stress recognition in receiving treatment" in patients with diabetes. A self-completed questionnaire was distributed to 149 type-2 diabetes outpatients in March-May 2015 after authorization from Okayama Prefectural University and the ethics committee of the hospital.
The "stress recognition in receiving treatment" scale was designed as a second-order factor model consisting of 14 items and the following four factors : the respondent's sense of (1) the burden of being sick, (2) the burden on interpersonal relationships, (3) the burden of treatment, and (4) the burden of medical expenses.
Stress recognition in treatment means recognition of being stressed in the burdens related to the illness, interpersonal relationships, treatment and medical expenses.
The suitability of the questionnaire data was then evaluated with a structural equation model. The suitability of the factor model to the data satisfied the statistically acceptable standards as Comparative Fit Index (CFI) =0.931, Root Mean Square Error of Approximation (RMSEA) =0.096, Tucker-Lewis Index (TLI) =0.946.
As the construct validity was not examined by the scale created in this study or by existing scale, it was verified by using the degrees of mental healthiness and HbA1c that were proved to be associated with the sense of burden.
In addition, the construct validity of the questionnaire was supported by a significant correlation between the Japanese version of the WHO-Five Well-being Index (S-WHO-5-J) and the patients' HbA1c levels. The use of this measure is expected to contribute to the early detection of a decline in a diabetic patient's activities of daily living and to the early confirmation of patients' support status.
en-copyright=
kn-copyright=
en-aut-name=SumiyoshiKazuko
en-aut-sei=Sumiyoshi
en-aut-mei=Kazuko
kn-aut-name=住吉和子
kn-aut-sei=住吉
kn-aut-mei=和子
aut-affil-num=1
ORCID=
en-aut-name=KawataChieko
en-aut-sei=Kawata
en-aut-mei=Chieko
kn-aut-name=川田智恵子
kn-aut-sei=川田
kn-aut-mei=智恵子
aut-affil-num=2
ORCID=
en-aut-name=OkamotoTatsuo
en-aut-sei=Okamoto
en-aut-mei=Tatsuo
kn-aut-name=岡本辰夫
kn-aut-sei=岡本
kn-aut-mei=辰夫
aut-affil-num=3
ORCID=
en-aut-name=OhashiMutsuko
en-aut-sei=Ohashi
en-aut-mei=Mutsuko
kn-aut-name=大橋睦子
kn-aut-sei=大橋
kn-aut-mei=睦子
aut-affil-num=4
ORCID=
en-aut-name=MikaneSakae
en-aut-sei=Mikane
en-aut-mei=Sakae
kn-aut-name=實金栄
kn-aut-sei=實金
kn-aut-mei=栄
aut-affil-num=5
ORCID=
en-aut-name=TakabayashiNoriko
en-aut-sei=Takabayashi
en-aut-mei=Noriko
kn-aut-name=高林範子
kn-aut-sei=高林
kn-aut-mei=範子
aut-affil-num=6
ORCID=
en-aut-name=FutoyuYoshiko
en-aut-sei=Futoyu
en-aut-mei=Yoshiko
kn-aut-name=太湯好子
kn-aut-sei=太湯
kn-aut-mei=好子
aut-affil-num=7
ORCID=
en-aut-name=KimWoesook
en-aut-sei=Kim
en-aut-mei=Woesook
kn-aut-name=金外淑
kn-aut-sei=金
kn-aut-mei=外淑
aut-affil-num=8
ORCID=
en-aut-name=WadaJun
en-aut-sei=Wada
en-aut-mei=Jun
kn-aut-name=和田淳
kn-aut-sei=和田
kn-aut-mei=淳
aut-affil-num=9
ORCID=
en-aut-name=ShikataKenichi
en-aut-sei=Shikata
en-aut-mei=Kenichi
kn-aut-name=四方賢一
kn-aut-sei=四方
kn-aut-mei=賢一
aut-affil-num=10
ORCID=
en-aut-name=NakajimaKazuo
en-aut-sei=Nakajima
en-aut-mei=Kazuo
kn-aut-name=中嶋和夫
kn-aut-sei=中嶋
kn-aut-mei=和夫
aut-affil-num=11
ORCID=
affil-num=1
en-affil=Faculty of Health and Welfare Science, Okayama Prefectural University
kn-affil=岡山県立大学 保健福祉学部
affil-num=2
en-affil=Health and Nursing Sciences Masters Program, Wakayama Medical University
kn-affil=和歌山県立医科大学 大学院保健看護学研究科
affil-num=3
en-affil=Ryobi General Research Institute of Community Care
kn-affil=両備地域ケア総合研究所
affil-num=4
en-affil=Department of Nursing, Okayama University Hospital
kn-affil=岡山大学病院 看護部
affil-num=5
en-affil=Faculty of Health and Welfare Science, Okayama Prefectural University
kn-affil=岡山県立大学 保健福祉学部
affil-num=6
en-affil=Faculty of Health and Welfare Science, Okayama Prefectural University
kn-affil=岡山県立大学 保健福祉学部
affil-num=7
en-affil=School of Health Science and Social Welfare, Kibi International University
kn-affil=吉備国際大学 保健医療福祉学部
affil-num=8
en-affil=College of Nursing Art and Science, University of Hyogo
kn-affil=兵庫県立大学 看護学部
affil-num=9
en-affil=Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 腎・免疫・内分泌代謝内科学
affil-num=10
en-affil=Center for Innovative Clinical Medicine, Okayama University Hospital
kn-affil=岡山大学病院 新医療研究開発センター
affil-num=11
en-affil=Ryobi General Research Institute of Community Care
kn-affil=両備地域ケア総合研究所
en-keyword=糖尿病患者 (diabetes patients)
kn-keyword=糖尿病患者 (diabetes patients)
en-keyword=治療 (treatment)
kn-keyword=治療 (treatment)
en-keyword=ストレス認知 (stress recognition)
kn-keyword=ストレス認知 (stress recognition)
en-keyword=尺度開発 (development of a scale)
kn-keyword=尺度開発 (development of a scale)
END
start-ver=1.4
cd-journal=joma
no-vol=313
cd-vols=
no-issue=1
article-no=
start-page=169
end-page=174
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2017
dt-pub=201707
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=In vitro analysis of radioprotective effect of monoterpenes
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= Monoterpenes are naturally occurring hydrocarbons composed of two units of isoprenes. They exhibit antioxidant activity to scavenge reactive oxygen species, such as hydroxyl radicals. We investigated the potential of monoterpenes such as thymol, linalool, and menthol to act as radioprotectants. The proliferation of EL4 cells, a mouse lymphoma cell line, treated with linalool at a concentration of 500 μM or more was not affected by X-ray irradiation. Plasmid-nicking assay performed using formamidopyrimidine-DNA glycosylase showed that linalool prevented single strand breaks and oxidized purines on pUC19 plasmid DNA. These findings indicate that linalool has the ability to scavenge reactive oxygen species and is a potential radioprotector.
en-copyright=
kn-copyright=
en-aut-name=KudoKen-ichi
en-aut-sei=Kudo
en-aut-mei=Ken-ichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=HanafusaTadashi
en-aut-sei=Hanafusa
en-aut-mei=Tadashi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
affil-num=1
en-affil=
kn-affil=
affil-num=2
en-affil=Department of Radiation Research, Advanced Science Research CenterOkayama University
kn-affil=
affil-num=3
en-affil=Department of Radiation Research, Advanced Science Research CenterOkayama University
kn-affil=
en-keyword=Monoterpenes
kn-keyword=Monoterpenes
en-keyword= Linalool
kn-keyword= Linalool
en-keyword=X-ray irradiation
kn-keyword=X-ray irradiation
en-keyword= Reactive oxygen species
kn-keyword= Reactive oxygen species
en-keyword= SSB
kn-keyword= SSB
END
start-ver=1.4
cd-journal=joma
no-vol=71
cd-vols=
no-issue=3
article-no=
start-page=219
end-page=226
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2017
dt-pub=201706
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=The Immunological Impact of Chemotherapy on the Tumor Microenvironment of Oral Squamous Cell Carcinoma
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= Anticancer drugs induce cell-cycle arrest and apoptosis not only in tumor cells, but also in immune cells. However, many preclinical and clinical findings show that some chemotherapeutic agents can improve the antitumor efficacy of immunotherapy. We immunohistochemically analyzed the degree of immune cell infiltration and the relevance of programmed cell death 1 ligand-1 (PD-L1) expression in surgically resected oral squamous cell carcinoma (OSCC) specimens from patients who had undergone pretreatment with certain chemotherapies and other patients without pretreatment. We divided the patients into the group of neoadjuvant chemotherapy (NAC) patients (n=8) and the nNAC (without NAC) patient group (n=10). We observed that NAC induced infiltrations of CD4, CD8 T cells and CD56 NK cells into the tumor microenvironment. Decreased numbers of Tregs and PD-1-positive cells were observed in the NAC group. No significant difference was observed in the degree of immune-cell infiltration between the patient groups except for CD56 NK cells in the stroma and PD-1 cells in cancer nests. Eighty percent of the nNAC specimens showed intermediate-to-strong PD-L1 protein expression, whereas 75% of the NAC specimens showed down-regulation of the PD-L1 protein, indicating the effectiveness of the chemotherapeutic treatment before surgery.
en-copyright=
kn-copyright=
en-aut-name=TakakuraHiroaki
en-aut-sei=Takakura
en-aut-mei=Hiroaki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=DomaeShohei
en-aut-sei=Domae
en-aut-mei=Shohei
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=SasakiAkira
en-aut-sei=Sasaki
en-aut-mei=Akira
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
affil-num=1
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
kn-affil=
affil-num=4
en-affil=Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
en-keyword=oral squamous cell carcinoma
kn-keyword=oral squamous cell carcinoma
en-keyword=programmed cell death 1 ligand-1
kn-keyword=programmed cell death 1 ligand-1
en-keyword=tumor microenvironment
kn-keyword=tumor microenvironment
en-keyword=neoadjuvant chemotherapy
kn-keyword=neoadjuvant chemotherapy
en-keyword=immunohistochemistry
kn-keyword=immunohistochemistry
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2016
dt-pub=20160930
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=乳がん患者が捉えた乳がんピアサポートプログラムの主観的評価:質的研究
kn-title=Subjective evaluation of a peer support program by women with breast cancer: a qualitative study
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoMiho
en-aut-sei=Ono
en-aut-mei=Miho
kn-aut-name=小野美穂
kn-aut-sei=小野
kn-aut-mei=美穂
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=128
cd-vols=
no-issue=3
article-no=
start-page=201
end-page=205
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2016
dt-pub=20161201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Ectopic sebaceous glands in the esophagus that became evident over a three-year span
kn-title=3 年間の内視鏡所見の変化を観察できた食道異所性皮脂腺の1 例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= A 43-year-old Japanese woman was diagnosed with ectopic sebaceous glands in the esophagus by esophagogastroduodenoscopy and biopsy. At the age of 46, typical ectopic sebaceous glands were recognized in the upper esophagus, whereas yellowish white granules were faintly observed in the lower esophagus. Esophagogastroduodenoscopy examinations were repeated when she was 47 and again at 50 years old, and the lesions in the lower esophagus had become more evident over the ensuing 3 years. Esophageal ectopic sebaceous glands are relatively infrequent, and there have been few case reports describing the progression of the endoscopic features. We also report the clinical and endoscopic features of the five similar cases with pathologically proven ectopic sebaceous glands in the esophagus.
en-copyright=
kn-copyright=
en-aut-name=IwamuroMasaya
en-aut-sei=Iwamuro
en-aut-mei=Masaya
kn-aut-name=岩室雅也
kn-aut-sei=岩室
kn-aut-mei=雅也
aut-affil-num=1
ORCID=
en-aut-name=OkadaHiroyuki
en-aut-sei=Okada
en-aut-mei=Hiroyuki
kn-aut-name=岡田裕之
kn-aut-sei=岡田
kn-aut-mei=裕之
aut-affil-num=2
ORCID=
en-aut-name=HaradaKeita
en-aut-sei=Harada
en-aut-mei=Keita
kn-aut-name=原田馨太
kn-aut-sei=原田
kn-aut-mei=馨太
aut-affil-num=3
ORCID=
en-aut-name=KanzakiHiromitsu
en-aut-sei=Kanzaki
en-aut-mei=Hiromitsu
kn-aut-name=神崎洋光
kn-aut-sei=神崎
kn-aut-mei=洋光
aut-affil-num=4
ORCID=
en-aut-name=HoriKeisuke
en-aut-sei=Hori
en-aut-mei=Keisuke
kn-aut-name=堀圭介
kn-aut-sei=堀
kn-aut-mei=圭介
aut-affil-num=5
ORCID=
en-aut-name=KitaMasahide
en-aut-sei=Kita
en-aut-mei=Masahide
kn-aut-name=喜多雅英
kn-aut-sei=喜多
kn-aut-mei=雅英
aut-affil-num=6
ORCID=
en-aut-name=KawanoSeiji
en-aut-sei=Kawano
en-aut-mei=Seiji
kn-aut-name=川野誠司
kn-aut-sei=川野
kn-aut-mei=誠司
aut-affil-num=7
ORCID=
en-aut-name=KawaharaYoshiro
en-aut-sei=Kawahara
en-aut-mei=Yoshiro
kn-aut-name=河原祥朗
kn-aut-sei=河原
kn-aut-mei=祥朗
aut-affil-num=8
ORCID=
en-aut-name=TanakaTakehiro
en-aut-sei=Tanaka
en-aut-mei=Takehiro
kn-aut-name=田中健大
kn-aut-sei=田中
kn-aut-mei=健大
aut-affil-num=9
ORCID=
en-aut-name=YamamotoKazuhide
en-aut-sei=Yamamoto
en-aut-mei=Kazuhide
kn-aut-name=山本和秀
kn-aut-sei=山本
kn-aut-mei=和秀
aut-affil-num=10
ORCID=
affil-num=1
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
affil-num=2
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
affil-num=3
en-affil=Department of Endoscopy, Okayama University Hospital
kn-affil=岡山大学病院 光学医療診療部
affil-num=4
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
affil-num=5
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
affil-num=6
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
affil-num=7
en-affil=Department of Endoscopy, Okayama University Hospital
kn-affil=岡山大学病院 光学医療診療部
affil-num=8
en-affil=Department of Endoscopy, Okayama University Hospital
kn-affil=岡山大学病院 光学医療診療部
affil-num=9
en-affil=Department of Pathology, Okayama University Hospital
kn-affil=岡山大学病院 病理診断科
affil-num=10
en-affil=Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器・肝臓内科学
en-keyword=食道異所性脂腺(ectopic sebaceous glands in the esophagus)
kn-keyword=食道異所性脂腺(ectopic sebaceous glands in the esophagus)
en-keyword=粘膜下腫瘍(submucosal tumor)
kn-keyword=粘膜下腫瘍(submucosal tumor)
en-keyword=食道黄色腫(esophageal xanthoma)
kn-keyword=食道黄色腫(esophageal xanthoma)
END
start-ver=1.4
cd-journal=joma
no-vol=128
cd-vols=
no-issue=3
article-no=
start-page=191
end-page=196
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2016
dt-pub=20161201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Our experience with the significance of collaborative medical and dental surgeries at the Head and Neck Cancer Center, Okayama University Hospital
kn-title=岡山大学病院頭頸部がんセンターにおける医科歯科合同手術の現状解析とその意義
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= We have been collaborating with head and neck surgeons, plastic surgeons and oral surgeons in surgeries for many patients with head and neck carcinomas( especially oral carcinomas) since 2006( fiscal year 2005). The Head and Neck Cancer Center was established at Okayama University Hospital in 2012.
This Center was the first of its kind at a national university hospital in Japan.
At the Center, 174 operations on head and neck carcinomas and 96 reconstructive operations were performed in 2014( fiscal year).
Medical and dental collaborative operations have been increasing almost every year since the 2005 fiscal year. There were 45 collaborative operations in the 2014 fiscal year, which included 30 cases of bone or metal plate reconstruction or plate reinforcement of the jaws.
There were 76 medical and dental collaborative operations in the 7 years before the establishment of the Center, with a mean of 10.9 operations per year. Since the establishment of the Center, there have been 112 cases over 3 years with a mean of 37.3 operations per year. The number of surgeries has been markedly increased by the establishment of the Head and Neck Cancer Center.
en-copyright=
kn-copyright=
en-aut-name=MizukawaNobuyoshi
en-aut-sei=Mizukawa
en-aut-mei=Nobuyoshi
kn-aut-name=水川展吉
kn-aut-sei=水川
kn-aut-mei=展吉
aut-affil-num=1
ORCID=
en-aut-name=OnodaTomoo
en-aut-sei=Onoda
en-aut-mei=Tomoo
kn-aut-name=小野田友男
kn-aut-sei=小野田
kn-aut-mei=友男
aut-affil-num=2
ORCID=
en-aut-name=MatsumotoHiroshi
en-aut-sei=Matsumoto
en-aut-mei=Hiroshi
kn-aut-name=松本洋
kn-aut-sei=松本
kn-aut-mei=洋
aut-affil-num=3
ORCID=
en-aut-name=TakedaSeiko
en-aut-sei=Takeda
en-aut-mei=Seiko
kn-aut-name=武田斉子
kn-aut-sei=武田
kn-aut-mei=斉子
aut-affil-num=4
ORCID=
en-aut-name=NodaYouhei
en-aut-sei=Noda
en-aut-mei=Youhei
kn-aut-name=野田洋平
kn-aut-sei=野田
kn-aut-mei=洋平
aut-affil-num=5
ORCID=
en-aut-name=OnodaSatoshi
en-aut-sei=Onoda
en-aut-mei=Satoshi
kn-aut-name=小野田聡
kn-aut-sei=小野田
kn-aut-mei=聡
aut-affil-num=6
ORCID=
en-aut-name=FukushimaMai
en-aut-sei=Fukushima
en-aut-mei=Mai
kn-aut-name=福島麻衣
kn-aut-sei=福島
kn-aut-mei=麻衣
aut-affil-num=7
ORCID=
en-aut-name=TsumuraMunechika
en-aut-sei=Tsumura
en-aut-mei=Munechika
kn-aut-name=津村宗近
kn-aut-sei=津村
kn-aut-mei=宗近
aut-affil-num=8
ORCID=
en-aut-name=TakeuchiTetsuo
en-aut-sei=Takeuchi
en-aut-mei=Tetsuo
kn-aut-name=竹内哲男
kn-aut-sei=竹内
kn-aut-mei=哲男
aut-affil-num=9
ORCID=
en-aut-name=SugiyamaNarushi
en-aut-sei=Sugiyama
en-aut-mei=Narushi
kn-aut-name=杉山成史
kn-aut-sei=杉山
kn-aut-mei=成史
aut-affil-num=10
ORCID=
en-aut-name=KimataYoshihiro
en-aut-sei=Kimata
en-aut-mei=Yoshihiro
kn-aut-name=木股敬裕
kn-aut-sei=木股
kn-aut-mei=敬裕
aut-affil-num=11
ORCID=
affil-num=1
en-affil=Departments of Oral and Maxillofacial Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター, 顎口腔再建外科
affil-num=2
en-affil=Departments of Otorhinolaryngology, Head and Neck Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,耳鼻咽喉・頭頸部外科
affil-num=3
en-affil=Departments of Plastic and Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,形成外科
affil-num=4
en-affil=Departments of Oral and Maxillofacial Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,顎口腔再建外科
affil-num=5
en-affil=Departments of Otorhinolaryngology, Head and Neck Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,耳鼻咽喉・頭頸部外科
affil-num=6
en-affil=Departments of Plastic and Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,形成外科
affil-num=7
en-affil=Departments of Oral and Maxillofacial Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,顎口腔再建外科
affil-num=8
en-affil=Departments of Otorhinolaryngology, Head and Neck Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,耳鼻咽喉・頭頸部外科
affil-num=9
en-affil=Departments of Dental Laboratory, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,歯科技工室
affil-num=10
en-affil=Departments of Plastic and Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,形成外科
affil-num=11
en-affil=Departments of Plastic and Reconstructive Surgery, Head and Neck Cancer Center, Okayama University Hospital
kn-affil=岡山大学病院 頭頸部がんセンター,形成外科
en-keyword=頭頸部がん(head and neck carcinoma)
kn-keyword=頭頸部がん(head and neck carcinoma)
en-keyword=口腔がん(oral carcinoma)
kn-keyword=口腔がん(oral carcinoma)
en-keyword=頭頸部がんセンター(Head and Neck Cancer Center)
kn-keyword=頭頸部がんセンター(Head and Neck Cancer Center)
en-keyword=医科歯科合同手術(collaborative medical and dental surgeries)
kn-keyword=医科歯科合同手術(collaborative medical and dental surgeries)
en-keyword=顎骨再建(reconstructive operations of the jaw)
kn-keyword=顎骨再建(reconstructive operations of the jaw)
END
start-ver=1.4
cd-journal=joma
no-vol=70
cd-vols=
no-issue=3
article-no=
start-page=205
end-page=211
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2016
dt-pub=201606
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Structure of a New Palatal Plate and the Artificial Tongue for Articulation Disorder in a Patient with Subtotal Glossectomy
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A palatal augmentation prosthesis (PAP) is used to facilitate improvement in the speech and swallowing functions of patients with tongue resection or tongue movement disorders. However, a PAPʼs effect is limited in cases where articulation disorder is severe due to wide glossectomy and/or segmental mandibulectomy. In this paper, we describe speech outcomes of a patient with an articulation disorder following glossectomy and segmental mandibulectomy. We used a palatal plate (PP) based on a PAP, along with an artificial tongue (KAT). Speech improvement was evaluated by a standardized speech intelligibility test consisting of 100 syllables. The speech intelligibility score was significantly higher when the patient wore both the PP and KAT than when he wore neither (p=0.013). The conversational intelligibility score was significantly improved with the PP and KAT than without PP and KAT (p=0.024). These results suggest that speech function can be improved in patients with hard tissue defects with segmental mandibulectomy using both a PP and a KAT. The nature of the design of the PP and that of the KAT will allow these prostheses to address a wide range of tissue defects.
en-copyright=
kn-copyright=
en-aut-name=KozakiKen-ichi
en-aut-sei=Kozaki
en-aut-mei=Ken-ichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=KawakamiShigehisa
en-aut-sei=Kawakami
en-aut-mei=Shigehisa
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KonishiTakayuki
en-aut-sei=Konishi
en-aut-mei=Takayuki
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OhtaKeiji
en-aut-sei=Ohta
en-aut-mei=Keiji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=YanoJitsuro
en-aut-sei=Yano
en-aut-mei=Jitsuro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnodaTomoo
en-aut-sei=Onoda
en-aut-mei=Tomoo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
en-aut-name=MatsumotoHiroshi
en-aut-sei=Matsumoto
en-aut-mei=Hiroshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=7
ORCID=
en-aut-name=MizukawaNobuyoshi
en-aut-sei=Mizukawa
en-aut-mei=Nobuyoshi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=8
ORCID=
en-aut-name=KimataYoshihiro
en-aut-sei=Kimata
en-aut-mei=Yoshihiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=9
ORCID=
en-aut-name=NishizakiKazunori
en-aut-sei=Nishizaki
en-aut-mei=Kazunori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=10
ORCID=
en-aut-name=IidaSeiji
en-aut-sei=Iida
en-aut-mei=Seiji
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=11
ORCID=
en-aut-name=GofukuAkio
en-aut-sei=Gofuku
en-aut-mei=Akio
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=12
ORCID=
en-aut-name=AbeMasanobu
en-aut-sei=Abe
en-aut-mei=Masanobu
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=13
ORCID=
en-aut-name=MinagiShogo
en-aut-sei=Minagi
en-aut-mei=Shogo
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=14
ORCID=
en-aut-name=Okayama Dream Speech Project
en-aut-sei=Okayama Dream Speech Project
en-aut-mei=
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=15
ORCID=
affil-num=1
en-affil=Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=2
en-affil=Department of Occlusal and Oral Functional Rehabilitation, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=3
en-affil=Division of Physical Medicine and Rehabilitation, Okayama University Hospital
kn-affil=
affil-num=4
en-affil=Dental Laboratory Division, Okayama University Hospital
kn-affil=
affil-num=5
en-affil=Department of Occlusal and Oral Functional Rehabilitation, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=6
en-affil=Department of Otolaryngology-Head and Neck Surgery Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=7
en-affil=Department of Plastic and Reconstructive Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=8
en-affil=Department of Oral and Maxillofacial Reconstructive Surgery, Okayama University Hospital
kn-affil=
affil-num=9
en-affil=Department of Plastic and Reconstructive Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=10
en-affil=Department of Otolaryngology-Head and Neck Surgery Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=11
en-affil=Department of Oral and Maxillofacial Reconstructive Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=12
en-affil=Graduate School of Natural Science and Technology, Okayama University
kn-affil=
affil-num=13
en-affil=Department of Computer Science, Okayama University
kn-affil=
affil-num=14
en-affil=Department of Occlusal and Oral Functional Rehabilitation, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
kn-affil=
affil-num=15
en-affil=
kn-affil=
en-keyword=palatal augmentation prosthesis
kn-keyword=palatal augmentation prosthesis
en-keyword=artificial tongue
kn-keyword=artificial tongue
en-keyword=articulation disorder
kn-keyword=articulation disorder
en-keyword=glossectomy
kn-keyword=glossectomy
en-keyword=mandibulectomy
kn-keyword=mandibulectomy
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2016
dt-pub=20160325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=ラット実験モデルを用いたリンパ管静脈吻合術後の組織学的検討:開存例と閉塞例の比較
kn-title=Histological Evaluation of Lymphaticovenular Anastomosis Outcomes in the Rat Experimental Model: Comparison of Cases with Patency and Obstruction
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnodaSatoshi
en-aut-sei=Onoda
en-aut-mei=Satoshi
kn-aut-name=小野田聡
kn-aut-sei=小野田
kn-aut-mei=聡
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=127
cd-vols=
no-issue=3
article-no=
start-page=219
end-page=222
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2015
dt-pub=20151201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Drug-induced liver injury due to the long-term oral administration of rosuvastatin
kn-title=長期のロスバスタチンカルシウム服用にて発症したと考えられる薬物性肝障害の一例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A 67-year-old man was admitted to our hospital presenting with a liver injury. He had used several types of oral medication for the prior 2 years, including rosuvastatin calcium for hypertension, hyperlipidemia, and prostatic hypertrophy. His liver dysfunction was noted for the first time in February 2013, and at re-examination in March 2013 he showed exacerbation of the liver dysfunction, he was admitted to our hospital at that time. We stopped all of his oral medications, and his liver function improved steadily. We conducted a drug-induced lymphocyte transformation test (DLST), and the rosuvastatin calcium result was positive. He was diagnosed as having a drug-induced (by rosvastatin calcium) liver injury. He resumed oral medications other than rosuvastatin calcium from the time of discharge, with no exacerbation of liver dysfunction since then. Reports of drug-induced liver injury due to drugs with a long-term oral administration are extremely rare. We discuss the relevant literature herein.
en-copyright=
kn-copyright=
en-aut-name=OonishiAyano
en-aut-sei=Oonishi
en-aut-mei=Ayano
kn-aut-name=大西理乃
kn-aut-sei=大西
kn-aut-mei=理乃
aut-affil-num=1
ORCID=
en-aut-name=KariyamaKazuya
en-aut-sei=Kariyama
en-aut-mei=Kazuya
kn-aut-name=狩山和也
kn-aut-sei=狩山
kn-aut-mei=和也
aut-affil-num=2
ORCID=
en-aut-name=WakutaAkiko
en-aut-sei=Wakuta
en-aut-mei=Akiko
kn-aut-name=湧田暁子
kn-aut-sei=湧田
kn-aut-mei=暁子
aut-affil-num=3
ORCID=
en-aut-name=NishimuraMamoru
en-aut-sei=Nishimura
en-aut-mei=Mamoru
kn-aut-name=西村守
kn-aut-sei=西村
kn-aut-mei=守
aut-affil-num=4
ORCID=
en-aut-name=NousoKazuhiro
en-aut-sei=Nouso
en-aut-mei=Kazuhiro
kn-aut-name=能祖一裕
kn-aut-sei=能祖
kn-aut-mei=一裕
aut-affil-num=5
ORCID=
affil-num=1
en-affil=
kn-affil=岡山市立市民病院
affil-num=2
en-affil=
kn-affil=岡山市立市民病院
affil-num=3
en-affil=
kn-affil=岡山市立市民病院
affil-num=4
en-affil=
kn-affil=岡山市立市民病院
affil-num=5
en-affil=
kn-affil=岡山市立市民病院
en-keyword=薬物性肝障害(drug induced liver injury)
kn-keyword=薬物性肝障害(drug induced liver injury)
en-keyword=ロスバスタチンカルシウム(Rosuvastatin)
kn-keyword=ロスバスタチンカルシウム(Rosuvastatin)
en-keyword=スタチン(statin)
kn-keyword=スタチン(statin)
en-keyword=DLST
kn-keyword=DLST
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2015
dt-pub=20150620
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Adsorption and removal of strontium in aqueous solution by synthetic hydroxyapatite
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Hydroxyapatite (HAP) is a main mineral constituent of bone and tooth and has an outstanding biocompatibility. HAP is a possible sorbent for heavy metals in wastewater due to its high adsorption capacity and low water solubility. We developed a removal system of 90Sr from aqueous solution by HAP column procedure. More than 90 % of 90Sr was adsorbed and removed from the 90Sr containing solution. Divalent cations, Ca2+, had little effect on the removal of 90Sr up to a concentration of 1 mmol L−1. This clearly indicates that the HAP column technique is advantageous with respect to the capacity to adsorb 90Sr from water present in the environment.
en-copyright=
kn-copyright=
en-aut-name=NishiyamaYuichi
en-aut-sei=Nishiyama
en-aut-mei=Yuichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=HanafusaTadashi
en-aut-sei=Hanafusa
en-aut-mei=Tadashi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=YamashitaJun
en-aut-sei=Yamashita
en-aut-mei=Jun
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=YamamotoYoko
en-aut-sei=Yamamoto
en-aut-mei=Yoko
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=
kn-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
affil-num=2
en-affil=
kn-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
affil-num=3
en-affil=
kn-affil=Institute of Plant Science and Resources, Okayama University
affil-num=4
en-affil=
kn-affil=Institute of Plant Science and Resources, Okayama University
affil-num=5
en-affil=
kn-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
en-keyword=Strontium
kn-keyword=Strontium
en-keyword=Hydroxyapatite
kn-keyword=Hydroxyapatite
en-keyword=Adsorption
kn-keyword=Adsorption
en-keyword=Desorption
kn-keyword=Desorption
en-keyword=Divalent cation
kn-keyword=Divalent cation
END
start-ver=1.4
cd-journal=joma
no-vol=31
cd-vols=
no-issue=
article-no=
start-page=33
end-page=36
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2015
dt-pub=201504
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Environmental Disinfection by Hypochlorous Acid Solution
kn-title=次亜塩素酸水溶液による環境消毒について
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Weak Acid Hypochlorous Solution (WAHS) has been used for disinfection of foods (meats, vegetables etc.), and for environmental disinfection in the Retirement homes, Hospitals and Laboratory Animal facilities. We will introduce here some of environmental disinfection tests. 1) To study whether WAHS is available or not for blood
blot inoculated by Acinetobacter baumannii on the plate comparing with Sodium Hypochlorite. 2) Comparison of Ethanol and WAHS on the floor and handrail. 3) To study efficacy of shallowly dipping by WAHS on wagon caster inoculated by Staphylococcus aureus.
The results are: 1) It was observed that WAHS had an efficacy equal to Hypochlorite with lower concentration in the blood test, but in case that the adhesion amount of blood was larger, much higher concentration or adding
physical removal was needed. 2) Ethanol and WAHS had Equivalent efficacy on the test of floor and handrail. 3) It was suggested that shallowly dipping by WAHS was available for disinfection of wagon caster. We hope to proceed to confirm how to use WAHS for environmental disinfection.
en-copyright=
kn-copyright=
en-aut-name=YamashitaKoji
en-aut-sei=Yamashita
en-aut-mei=Koji
kn-aut-name=山下光治
kn-aut-sei=山下
kn-aut-mei=光治
aut-affil-num=1
ORCID=
en-aut-name=HamamotoYuji
en-aut-sei=Hamamoto
en-aut-mei=Yuji
kn-aut-name=濱本裕司
kn-aut-sei=濱本
kn-aut-mei=裕司
aut-affil-num=2
ORCID=
en-aut-name=YasudaYuto
en-aut-sei=Yasuda
en-aut-mei=Yuto
kn-aut-name=安田悠人
kn-aut-sei=安田
kn-aut-mei=悠人
aut-affil-num=3
ORCID=
en-aut-name=OnoTomoko
en-aut-sei=Ono
en-aut-mei=Tomoko
kn-aut-name=小野朋子
kn-aut-sei=小野
kn-aut-mei=朋子
aut-affil-num=4
ORCID=
affil-num=1
en-affil=
kn-affil=株式会社 エイチ・エス・ピー
affil-num=2
en-affil=
kn-affil=株式会社 エイチ・エス・ピー
affil-num=3
en-affil=
kn-affil=株式会社 エイチ・エス・ピー
affil-num=4
en-affil=
kn-affil=株式会社 エイチ・エス・ピー
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2014
dt-pub=20141231
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=トポイソメラーゼ IIβのC末端ドメインへRNAが結合することにより酵素の核内動態と酵素活性が制御されている
kn-title=Nuclear dynamics of topoisomerase IIβ reflects its catalytic activity that is regulated by binding of RNA to the C-terminal domain
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnodaAkihisa
en-aut-sei=Onoda
en-aut-mei=Akihisa
kn-aut-name=小野田彰久
kn-aut-sei=小野田
kn-aut-mei=彰久
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2014
dt-pub=20140630
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=2型糖尿病における微量アルブミン尿の寛解・改善に寄与する因子
kn-title=Factors Associated with Remission and/or Regression of Microalbuminuria in Type 2 Diabetes Mellitus
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoTetsuichiro
en-aut-sei=Ono
en-aut-mei=Tetsuichiro
kn-aut-name=小野哲一郎
kn-aut-sei=小野
kn-aut-mei=哲一郎
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=126
cd-vols=
no-issue=1
article-no=
start-page=59
end-page=63
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2014
dt-pub=20140401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Drug interaction (29. drug interaction of steroids)
kn-title=薬物相互作用(29―ステロイドの薬物相互作用)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=HayashiYouko
en-aut-sei=Hayashi
en-aut-mei=Youko
kn-aut-name=林瑶子
kn-aut-sei=林
kn-aut-mei=瑶子
aut-affil-num=1
ORCID=
en-aut-name=NawaHideki
en-aut-sei=Nawa
en-aut-mei=Hideki
kn-aut-name=名和秀起
kn-aut-sei=名和
kn-aut-mei=秀起
aut-affil-num=2
ORCID=
en-aut-name=KitamuraYoshihisa
en-aut-sei=Kitamura
en-aut-mei=Yoshihisa
kn-aut-name=北村佳久
kn-aut-sei=北村
kn-aut-mei=佳久
aut-affil-num=3
ORCID=
en-aut-name=SendoToshiaki
en-aut-sei=Sendo
en-aut-mei=Toshiaki
kn-aut-name=千堂年昭
kn-aut-sei=千堂
kn-aut-mei=年昭
aut-affil-num=4
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=2
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=3
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=4
en-affil=
kn-affil=岡山大学病院 薬剤部
END
start-ver=1.4
cd-journal=joma
no-vol=126
cd-vols=
no-issue=1
article-no=
start-page=17
end-page=24
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2014
dt-pub=20140401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Concept and management of pancreaticobiliary maljunction
kn-title=膵・胆管合流異常症―その概念と治療―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=NodaTakuo
en-aut-sei=Noda
en-aut-mei=Takuo
kn-aut-name=野田卓男
kn-aut-sei=野田
kn-aut-mei=卓男
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学病院 小児外科
en-keyword=膵・胆管合流異常
kn-keyword=膵・胆管合流異常
en-keyword=先天性胆道拡張症
kn-keyword=先天性胆道拡張症
en-keyword=分流手術胆道癌
kn-keyword=分流手術胆道癌
END
start-ver=1.4
cd-journal=joma
no-vol=6
cd-vols=
no-issue=
article-no=
start-page=27
end-page=34
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1999
dt-pub=19990612
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=「生きる力」を育成する数学の授業改善を目指して 中学校の数学学力診断調査の問題の検討と考察 ―「数と式」を中心に―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=高橋敏雄
kn-aut-sei=高橋
kn-aut-mei=敏雄
aut-affil-num=1
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=黒崎東洋郎
kn-aut-sei=黒崎
kn-aut-mei=東洋郎
aut-affil-num=2
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=洲脇史朗
kn-aut-sei=洲脇
kn-aut-mei=史朗
aut-affil-num=3
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=川上公一
kn-aut-sei=川上
kn-aut-mei=公一
aut-affil-num=4
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=大月一泰
kn-aut-sei=大月
kn-aut-mei=一泰
aut-affil-num=5
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=平野圭一
kn-aut-sei=平野
kn-aut-mei=圭一
aut-affil-num=6
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=秋山真
kn-aut-sei=秋山
kn-aut-mei=真
aut-affil-num=7
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野仁美
kn-aut-sei=小野
kn-aut-mei=仁美
aut-affil-num=8
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=桐野彰子
kn-aut-sei=桐野
kn-aut-mei=彰子
aut-affil-num=9
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=山本真道
kn-aut-sei=山本
kn-aut-mei=真道
aut-affil-num=10
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=景山勝
kn-aut-sei=景山
kn-aut-mei=勝
aut-affil-num=11
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小林武則
kn-aut-sei=小林
kn-aut-mei=武則
aut-affil-num=12
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=高木理行
kn-aut-sei=高木
kn-aut-mei=理行
aut-affil-num=13
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=高杉衣美
kn-aut-sei=高杉
kn-aut-mei=衣美
aut-affil-num=14
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=林俊雄
kn-aut-sei=林
kn-aut-mei=俊雄
aut-affil-num=15
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=村上有希子
kn-aut-sei=村上
kn-aut-mei=有希子
aut-affil-num=16
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=佐官尚宏
kn-aut-sei=佐官
kn-aut-mei=尚宏
aut-affil-num=17
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学教育学部
affil-num=2
en-affil=
kn-affil=岡山大学教育学部
affil-num=3
en-affil=
kn-affil=岡山理科大学
affil-num=4
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=5
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=6
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=7
en-affil=
kn-affil=岡山市立中山中学校
affil-num=8
en-affil=
kn-affil=岡山市立吉備中学校
affil-num=9
en-affil=
kn-affil=岡山市立富山中学校
affil-num=10
en-affil=
kn-affil=岡山市立桑田中学校
affil-num=11
en-affil=
kn-affil=倉敷市立東陽中学校
affil-num=12
en-affil=
kn-affil=倉敷市立多津美中学校
affil-num=13
en-affil=
kn-affil=倉敷市立琴浦中学校
affil-num=14
en-affil=
kn-affil=倉敷市立庄中学校
affil-num=15
en-affil=
kn-affil=玉野市立宇野中学校
affil-num=16
en-affil=
kn-affil=灘崎町立灘崎中学校
affil-num=17
en-affil=
kn-affil=御津町立御津中学校
END
start-ver=1.4
cd-journal=joma
no-vol=7
cd-vols=
no-issue=
article-no=
start-page=13
end-page=21
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2000
dt-pub=20000610
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=「生きる力」を育成する中学校数学「数量関係」に関する学力診断調査問題の考察
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=高橋敏雄
kn-aut-sei=高橋
kn-aut-mei=敏雄
aut-affil-num=1
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=黒崎東洋郎
kn-aut-sei=黒崎
kn-aut-mei=東洋郎
aut-affil-num=2
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=洲脇史郎
kn-aut-sei=洲脇
kn-aut-mei=史郎
aut-affil-num=3
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=大月一泰
kn-aut-sei=大月
kn-aut-mei=一泰
aut-affil-num=4
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=平野圭一
kn-aut-sei=平野
kn-aut-mei=圭一
aut-affil-num=5
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=川上公一
kn-aut-sei=川上
kn-aut-mei=公一
aut-affil-num=6
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=秋山真
kn-aut-sei=秋山
kn-aut-mei=真
aut-affil-num=7
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野大
kn-aut-sei=小野
kn-aut-mei=大
aut-affil-num=8
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=字津見雅美
kn-aut-sei=字津見
kn-aut-mei=雅美
aut-affil-num=9
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=林俊雄
kn-aut-sei=林
kn-aut-mei=俊雄
aut-affil-num=10
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=桐野彰子
kn-aut-sei=桐野
kn-aut-mei=彰子
aut-affil-num=11
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学教育学部
affil-num=2
en-affil=
kn-affil=岡山大学教育学部
affil-num=3
en-affil=
kn-affil=岡山理科大学
affil-num=4
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=5
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=6
en-affil=
kn-affil=倉敷市立南中学校
affil-num=7
en-affil=
kn-affil=岡山市立中山中学校
affil-num=8
en-affil=
kn-affil=岡山市立上南中学校
affil-num=9
en-affil=
kn-affil=灘崎町立灘崎中学校
affil-num=10
en-affil=
kn-affil=玉野市立宇野中学校
affil-num=11
en-affil=
kn-affil=岡山市立富山中学校
END
start-ver=1.4
cd-journal=joma
no-vol=8
cd-vols=
no-issue=
article-no=
start-page=1
end-page=11
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2001
dt-pub=20010609
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=「生きる力」を育成する中学校数学授業改善を目指して 中学校数学「図形」に関する学力診断調査問題の考察
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=高橋敏雄
kn-aut-sei=高橋
kn-aut-mei=敏雄
aut-affil-num=1
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=黒崎東洋郎
kn-aut-sei=黒崎
kn-aut-mei=東洋郎
aut-affil-num=2
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=洲脇史郎
kn-aut-sei=洲脇
kn-aut-mei=史郎
aut-affil-num=3
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=大月一泰
kn-aut-sei=大月
kn-aut-mei=一泰
aut-affil-num=4
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=平野圭一
kn-aut-sei=平野
kn-aut-mei=圭一
aut-affil-num=5
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=木村善生
kn-aut-sei=木村
kn-aut-mei=善生
aut-affil-num=6
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=秋山真
kn-aut-sei=秋山
kn-aut-mei=真
aut-affil-num=7
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=宇津見雅英
kn-aut-sei=宇津見
kn-aut-mei=雅英
aut-affil-num=8
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=林俊雄
kn-aut-sei=林
kn-aut-mei=俊雄
aut-affil-num=9
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野大
kn-aut-sei=小野
kn-aut-mei=大
aut-affil-num=10
ORCID=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=桐野彰子
kn-aut-sei=桐野
kn-aut-mei=彰子
aut-affil-num=11
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学教育学部
affil-num=2
en-affil=
kn-affil=岡山大学教育学部
affil-num=3
en-affil=
kn-affil=岡山理科大学理学部
affil-num=4
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=5
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=6
en-affil=
kn-affil=岡山大学教育学部附属中学校
affil-num=7
en-affil=
kn-affil=岡山市立中山中学校
affil-num=8
en-affil=
kn-affil=児島郡灘崎町立灘崎中学校
affil-num=9
en-affil=
kn-affil=玉野市立宇野中学校
affil-num=10
en-affil=
kn-affil=岡山市立上南中学校
affil-num=11
en-affil=
kn-affil=岡山市立富山中学校
END
start-ver=1.4
cd-journal=joma
no-vol=125
cd-vols=
no-issue=2
article-no=
start-page=163
end-page=167
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2013
dt-pub=20130801
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Drug interaction (27. anti-emetics during anti-cancer chemotherapy)
kn-title=薬物相互作用(27―がん化学療法における制吐剤の薬物相互作用)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=KurataYasuko
en-aut-sei=Kurata
en-aut-mei=Yasuko
kn-aut-name=蔵田靖子
kn-aut-sei=蔵田
kn-aut-mei=靖子
aut-affil-num=1
ORCID=
en-aut-name=FujiwaraSatoko
en-aut-sei=Fujiwara
en-aut-mei=Satoko
kn-aut-name=藤原聡子
kn-aut-sei=藤原
kn-aut-mei=聡子
aut-affil-num=2
ORCID=
en-aut-name=KajizonoMakoto
en-aut-sei=Kajizono
en-aut-mei=Makoto
kn-aut-name=鍛治園誠
kn-aut-sei=鍛治園
kn-aut-mei=誠
aut-affil-num=3
ORCID=
en-aut-name=AoyagiMegumu
en-aut-sei=Aoyagi
en-aut-mei=Megumu
kn-aut-name=青柳恵
kn-aut-sei=青柳
kn-aut-mei=恵
aut-affil-num=4
ORCID=
en-aut-name=KitamuraYoshihisa
en-aut-sei=Kitamura
en-aut-mei=Yoshihisa
kn-aut-name=北村佳久
kn-aut-sei=北村
kn-aut-mei=佳久
aut-affil-num=5
ORCID=
en-aut-name=SendoToshiaki
en-aut-sei=Sendo
en-aut-mei=Toshiaki
kn-aut-name=千堂年昭
kn-aut-sei=千堂
kn-aut-mei=年昭
aut-affil-num=6
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=2
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=3
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=4
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=5
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=6
en-affil=
kn-affil=岡山大学病院 薬剤部
END
start-ver=1.4
cd-journal=joma
no-vol=14
cd-vols=
no-issue=
article-no=
start-page=207
end-page=207
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1930
dt-pub=19300201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=甜橙の微量砒素及鉛の定量法(要旨)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺伊勢之助
kn-aut-sei=小野寺
kn-aut-mei=伊勢之助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=14
cd-vols=
no-issue=
article-no=
start-page=207
end-page=207
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1930
dt-pub=19300201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=砒酸鉛の砒素定量法に就て(要旨)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺伊勢之助
kn-aut-sei=小野寺
kn-aut-mei=伊勢之助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=125
cd-vols=
no-issue=1
article-no=
start-page=35
end-page=39
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2013
dt-pub=20130401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=An epidemiologically rare case of Vibrio vulnificus infection that occurred in October in an inland city of Japan
kn-title=内陸地津山で発症した季節外れのVibrio vulnificus感染症
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= A 68-year-old man with alcohol addiction, who lived in the suburbs of Tsuyama, an inland city located in northeast Okayama prefecture, was transported to the emergency unit of the Tsuyama Central Hospital in a state of cardiopulmonary arrest (CPA). Despite rigorous systemic investigation and treatment, the patient died 2 hours after arrival. After his death, Vibrio vulnificus was isolated from his blood culture.
Vibrio vulnificus causes fatal infection in humans, usually only in areas located close to the sea where appropriate temperature and suitable salt concentration for its growth are available. Therefore, its occurrence is epidemiologically restricted ; in Japan, the western coastal areas, especially in summers, are reported to be the high-risk regions. This is a rare case because it occurred in a city approximately 50 kilometers from both the Sea of Japan and the Pacific coast of Okayama, and at the end of October in 2011. Economic development and distribution systems have made it possible to transport various food products from coastal areas or abroad to any place in a short time, such that these infections can potentially develop in areas other than expected. We should be aware of the increasing risk of Vibrio vulnificus infection during any season and at any place, especially in patients with abnormal liver function.
en-copyright=
kn-copyright=
en-aut-name=HagiyaHideharu
en-aut-sei=Hagiya
en-aut-mei=Hideharu
kn-aut-name=萩谷英大
kn-aut-sei=萩谷
kn-aut-mei=英大
aut-affil-num=1
ORCID=
en-aut-name=ShiotaSumiko
en-aut-sei=Shiota
en-aut-mei=Sumiko
kn-aut-name=塩田澄子
kn-aut-sei=塩田
kn-aut-mei=澄子
aut-affil-num=2
ORCID=
en-aut-name=MiyoshiShin-ichi
en-aut-sei=Miyoshi
en-aut-mei=Shin-ichi
kn-aut-name=三好伸一
kn-aut-sei=三好
kn-aut-mei=伸一
aut-affil-num=3
ORCID=
en-aut-name=KuroeYasutoshi
en-aut-sei=Kuroe
en-aut-mei=Yasutoshi
kn-aut-name=黒江泰利
kn-aut-sei=黒江
kn-aut-mei=泰利
aut-affil-num=4
ORCID=
en-aut-name=NojimaHiroyoshi
en-aut-sei=Nojima
en-aut-mei=Hiroyoshi
kn-aut-name=野島宏悦
kn-aut-sei=野島
kn-aut-mei=宏悦
aut-affil-num=5
ORCID=
en-aut-name=OtaniShinkichi
en-aut-sei=Otani
en-aut-mei=Shinkichi
kn-aut-name=大谷晋吉
kn-aut-sei=大谷
kn-aut-mei=晋吉
aut-affil-num=6
ORCID=
en-aut-name=SugiyamaJunichi
en-aut-sei=Sugiyama
en-aut-mei=Junichi
kn-aut-name=杉山淳一
kn-aut-sei=杉山
kn-aut-mei=淳一
aut-affil-num=7
ORCID=
en-aut-name=NaitoHiromichi
en-aut-sei=Naito
en-aut-mei=Hiromichi
kn-aut-name=内藤宏道
kn-aut-sei=内藤
kn-aut-mei=宏道
aut-affil-num=8
ORCID=
en-aut-name=KawanishiSusumu
en-aut-sei=Kawanishi
en-aut-mei=Susumu
kn-aut-name=川西進
kn-aut-sei=川西
kn-aut-mei=進
aut-affil-num=9
ORCID=
en-aut-name=HagiokaShingo
en-aut-sei=Hagioka
en-aut-mei=Shingo
kn-aut-name=萩岡信吾
kn-aut-sei=萩岡
kn-aut-mei=信吾
aut-affil-num=10
ORCID=
en-aut-name=MorimotoNaoki
en-aut-sei=Morimoto
en-aut-mei=Naoki
kn-aut-name=森本直樹
kn-aut-sei=森本
kn-aut-mei=直樹
aut-affil-num=11
ORCID=
affil-num=1
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=2
en-affil=
kn-affil=就実大学薬学部 病原微生物学
affil-num=3
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 衛生微生物化学
affil-num=4
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=5
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=6
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=7
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=8
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=9
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=10
en-affil=
kn-affil=津山中央病院 救命救急センター
affil-num=11
en-affil=
kn-affil=津山中央病院 救命救急センター
en-keyword=Vibrio vulnificus
kn-keyword=Vibrio vulnificus
END
start-ver=1.4
cd-journal=joma
no-vol=125
cd-vols=
no-issue=1
article-no=
start-page=5
end-page=7
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2013
dt-pub=20130401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Computational fluid dynamics of carotid arteries after carotid endarterectomy or carotid artery stenting based on postoperative patient-specific medical data
kn-title=頚動脈内膜剥離術あるいは頚動脈ステント留置術施行後の患者固有データに基づく頚動脈血流の流体力学的シミュレーション
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=HayaseHitoshi
en-aut-sei=Hayase
en-aut-mei=Hitoshi
kn-aut-name=早瀬仁志
kn-aut-sei=早瀬
kn-aut-mei=仁志
aut-affil-num=1
ORCID=
en-aut-name=TokunagaKoji
en-aut-sei=Tokunaga
en-aut-mei=Koji
kn-aut-name=徳永浩司
kn-aut-sei=徳永
kn-aut-mei=浩司
aut-affil-num=2
ORCID=
en-aut-name=NakayamaToshio
en-aut-sei=Nakayama
en-aut-mei=Toshio
kn-aut-name=中山敏男
kn-aut-sei=中山
kn-aut-mei=敏男
aut-affil-num=3
ORCID=
en-aut-name=SugiuKenji
en-aut-sei=Sugiu
en-aut-mei=Kenji
kn-aut-name=杉生憲志
kn-aut-sei=杉生
kn-aut-mei=憲志
aut-affil-num=4
ORCID=
en-aut-name=NishidaAyumi
en-aut-sei=Nishida
en-aut-mei=Ayumi
kn-aut-name=西田あゆみ
kn-aut-sei=西田
kn-aut-mei=あゆみ
aut-affil-num=5
ORCID=
en-aut-name=ArimitsuSeiji
en-aut-sei=Arimitsu
en-aut-mei=Seiji
kn-aut-name=有光帥二
kn-aut-sei=有光
kn-aut-mei=帥二
aut-affil-num=6
ORCID=
en-aut-name=HishikawaTomohito
en-aut-sei=Hishikawa
en-aut-mei=Tomohito
kn-aut-name=菱川朋人
kn-aut-sei=菱川
kn-aut-mei=朋人
aut-affil-num=7
ORCID=
en-aut-name=OnoShigeki
en-aut-sei=Ono
en-aut-mei=Shigeki
kn-aut-name=小野成紀
kn-aut-sei=小野
kn-aut-mei=成紀
aut-affil-num=8
ORCID=
en-aut-name=OhtaMakoto
en-aut-sei=Ohta
en-aut-mei=Makoto
kn-aut-name=太田信
kn-aut-sei=太田
kn-aut-mei=信
aut-affil-num=9
ORCID=
en-aut-name=DateIsao
en-aut-sei=Date
en-aut-mei=Isao
kn-aut-name=伊達勲
kn-aut-sei=伊達
kn-aut-mei=勲
aut-affil-num=10
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=2
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=3
en-affil=
kn-affil=東北大学流体科学研究所 知能流システム研究部門生体流動研究分野
affil-num=4
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=5
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=6
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=7
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=8
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
affil-num=9
en-affil=
kn-affil=東北大学流体科学研究所 知能流システム研究部門生体流動研究分野
affil-num=10
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 神経病態外科学
en-keyword=carotid artery stenosis
kn-keyword=carotid artery stenosis
en-keyword=carotid artery stenting
kn-keyword=carotid artery stenting
en-keyword=carotid endarterectomy
kn-keyword=carotid endarterectomy
en-keyword=computational fluid dynamics
kn-keyword=computational fluid dynamics
en-keyword=wall shear stress
kn-keyword=wall shear stress
END
start-ver=1.4
cd-journal=joma
no-vol=13
cd-vols=
no-issue=
article-no=
start-page=58
end-page=67
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1929
dt-pub=19290705
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=甜橙の微量砒素及鉛の定量法
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺伊勢之助
kn-aut-sei=小野寺
kn-aut-mei=伊勢之助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=13
cd-vols=
no-issue=
article-no=
start-page=45
end-page=57
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1929
dt-pub=19290705
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=砒酸鉛の砒素定量法に就て
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺伊勢之助
kn-aut-sei=小野寺
kn-aut-mei=伊勢之助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=2
cd-vols=
no-issue=
article-no=
start-page=78
end-page=110
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1920
dt-pub=19200710
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=紫雲英の稻作に及ぼす影響及其有害作用の原因に就て
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺伊勢之助
kn-aut-sei=小野寺
kn-aut-mei=伊勢之助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=
END
start-ver=1.4
cd-journal=joma
no-vol=124
cd-vols=
no-issue=3
article-no=
start-page=239
end-page=241
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=20121203
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=A case of frontal horn cysts
kn-title=Frontal Horn Cystsの1例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract= We herein report a case of bilateral frontal horn cysts. The infant was delivered with a low birth weight (1,710g) at 31 weeks, 0 days by emergency Cesarean section. She was severely asphyxiated and exhibited respiratory distress syndrome. Surfactant was administered, and mechanical ventilation was required until 21 days of age. Brain computed tomography (CT) at 45 days of age revealed bilateral cysts adjacent to the frontal horns of the lateral ventricles. Her growth and development were normal. At 1 and a half- years of age, she underwent brain CT again and the above-mentioned cystic abnormality had disappeared. No dilatation or irregularity of the lateral ventricles was found. Normal development and transient abnormal cystic findings in brain CT suggested a diagnosis of frontal horn cysts. Frontal horn cysts should be considered as the causes of cystic lesions of the brain.
en-copyright=
kn-copyright=
en-aut-name=MiyakeSusumu
en-aut-sei=Miyake
en-aut-mei=Susumu
kn-aut-name=三宅進
kn-aut-sei=三宅
kn-aut-mei=進
aut-affil-num=1
ORCID=
en-aut-name=MiyamuraTakako
en-aut-sei=Miyamura
en-aut-mei=Takako
kn-aut-name=宮村能子
kn-aut-sei=宮村
kn-aut-mei=能子
aut-affil-num=2
ORCID=
affil-num=1
en-affil=
kn-affil=香川県立中央病院 小児科
affil-num=2
en-affil=
kn-affil=香川県立中央病院 小児科
en-keyword=frontal horn cyst
kn-keyword=frontal horn cyst
en-keyword=頭部CT(Brain CT)
kn-keyword=頭部CT(Brain CT)
en-keyword=新生児(neonate)
kn-keyword=新生児(neonate)
END
start-ver=1.4
cd-journal=joma
no-vol=124
cd-vols=
no-issue=2
article-no=
start-page=167
end-page=173
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=20120801
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Drug interaction (24. drug-drug interactions in intensive care unit)
kn-title=薬物相互作用(24―ICUでの注意すべき薬物相互作用)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=NishimiyaYusuke
en-aut-sei=Nishimiya
en-aut-mei=Yusuke
kn-aut-name=西宮祐輔
kn-aut-sei=西宮
kn-aut-mei=祐輔
aut-affil-num=1
ORCID=
en-aut-name=KonumaToshimitsu
en-aut-sei=Konuma
en-aut-mei=Toshimitsu
kn-aut-name=小沼利光
kn-aut-sei=小沼
kn-aut-mei=利光
aut-affil-num=2
ORCID=
en-aut-name=TasakaKen
en-aut-sei=Tasaka
en-aut-mei=Ken
kn-aut-name=田坂健
kn-aut-sei=田坂
kn-aut-mei=健
aut-affil-num=3
ORCID=
en-aut-name=SendoToshiaki
en-aut-sei=Sendo
en-aut-mei=Toshiaki
kn-aut-name=千堂年昭
kn-aut-sei=千堂
kn-aut-mei=年昭
aut-affil-num=4
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=2
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=3
en-affil=
kn-affil=岡山大学病院 薬剤部
affil-num=4
en-affil=
kn-affil=岡山大学病院 薬剤部
END
start-ver=1.4
cd-journal=joma
no-vol=124
cd-vols=
no-issue=2
article-no=
start-page=149
end-page=153
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=20120801
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=A case of strangulated ileus caused by transomental hernia with reference to previously reported cases
kn-title=術前診断し得た大網裂孔ヘルニアの一例―本邦報告203例の臨床病理学的検討―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Transomental hernia often develops into strangulated ileus. We report on an 81-year-old man with strangulated ileus due to transomental hernia, diagnosed preoperatively by abdominal CT. The patient was referred to our surgical division because of progressive abdominal pain and vomiting. He had no history of laparotomy. An abdominal CT scan showed dilated small intestinal loops with intraluminal air and strangulated small intestinal loops with engorged mesenteric vessels. We diagnosed this as a strangulated internal hernia due to transomental hernia and conducted an emergency laparotomy. The jejunum had herniated through an abnormal hiatus of the greater omentum to the peritoneal cavity. The strangulated intestinal loop, about 15 cm long, was released and the postoperative course was uneventful. In the absence of a previous laparotomy, the differential diagnosis of intestinal obstruction should include internal hernia. An abdominal CT scan is useful for the preoperative and prompt diagnosis of transomental hernia.
en-copyright=
kn-copyright=
en-aut-name=KimuraYuji
en-aut-sei=Kimura
en-aut-mei=Yuji
kn-aut-name=木村裕司
kn-aut-sei=木村
kn-aut-mei=裕司
aut-affil-num=1
ORCID=
en-aut-name=IwakawaKazuhide
en-aut-sei=Iwakawa
en-aut-mei=Kazuhide
kn-aut-name=岩川和秀
kn-aut-sei=岩川
kn-aut-mei=和秀
aut-affil-num=2
ORCID=
en-aut-name=NishieManabu
en-aut-sei=Nishie
en-aut-mei=Manabu
kn-aut-name=西江学
kn-aut-sei=西江
kn-aut-mei=学
aut-affil-num=3
ORCID=
en-aut-name=InagakiMasaru
en-aut-sei=Inagaki
en-aut-mei=Masaru
kn-aut-name=稲垣優
kn-aut-sei=稲垣
kn-aut-mei=優
aut-affil-num=4
ORCID=
en-aut-name=IwagakiHiromi
en-aut-sei=Iwagaki
en-aut-mei=Hiromi
kn-aut-name=岩垣博巳
kn-aut-sei=岩垣
kn-aut-mei=博巳
aut-affil-num=5
ORCID=
affil-num=1
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=2
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=3
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=4
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=5
en-affil=
kn-affil=国立病院機構福山医療センター 外科
en-keyword=大網裂孔ヘルニア(transomental hernia)
kn-keyword=大網裂孔ヘルニア(transomental hernia)
en-keyword=絞扼性イレウス(strangulated ileus)
kn-keyword=絞扼性イレウス(strangulated ileus)
END
start-ver=1.4
cd-journal=joma
no-vol=28
cd-vols=
no-issue=
article-no=
start-page=36
end-page=39
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=201204
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=The Inactivation Effect of Weak Acid Hypochlorous Solution against Cryj1,Cedar Pollen Allergen
kn-title=弱酸性次亜塩素酸水溶液のスギ花粉アレルゲンCryj1に対する不活化効果
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoTomoko
en-aut-sei=Ono
en-aut-mei=Tomoko
kn-aut-name=小野朋子
kn-aut-sei=小野
kn-aut-mei=朋子
aut-affil-num=1
ORCID=
en-aut-name=YamashitaKoji
en-aut-sei=Yamashita
en-aut-mei=Koji
kn-aut-name=山下光治
kn-aut-sei=山下
kn-aut-mei=光治
aut-affil-num=2
ORCID=
affil-num=1
en-affil=
kn-affil=株式会社エイチ・エス・ピー
affil-num=2
en-affil=
kn-affil=株式会社エイチ・エス・ピー
END
start-ver=1.4
cd-journal=joma
no-vol=86
cd-vols=
no-issue=9
article-no=
start-page=1440
end-page=1449
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1995
dt-pub=199509
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=緑膿菌バイオフィルム解析法としてのglycocalyx簡易定量法とATP測定法
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=(背景と目的) 細菌バイオフィルムの各エレメントの解析法として, トルイジンブルーを用いるglycocalyxの簡易定量法, ならびに, bioactivity測定法としてのATP測定法を新たに考案ないし改良して, その有用性に検討を加えた. (結果) 基礎的検討において, 既知量のglycocalyxとしてgellan gumを用いた場合, トルイジンブルー反応量を示す吸光度はgellan gum量4.0×10^<-6>〜1.0×10^<-4>gの範囲で直線性を示した.また, 改良を加えたATP測定法では, ATP量で1×l0^<-4>mol/l, 浮遊菌数で10^3cfuまでの測定が可能であった.また, modified Robbins deviceを使用するin vitro実験系において, 緑膿菌バイオフィルムの経時的形成過程ならびに各種抗菌性物質作用後の変化の解析において, 両測定法によるglycocalyx量とbioactivityに関する成績は, 論理的に矛盾がなく走査型電子顕微鏡所見とも極めてよく一致していた. (結論) したがって, 両測定法は細菌バイオフィルムの新しい解析法として有用であると考えられた.
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野憲昭
kn-aut-sei=小野
kn-aut-mei=憲昭
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=124
cd-vols=
no-issue=1
article-no=
start-page=63
end-page=66
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=20120401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Pathological complete response of advanced gastric cancer with pyloric stenosis to neoadjuvant S-1/CDDP chemotherapy: A case report
kn-title=S-1/CDDP術前化学療法により組織学的CRが得られた幽門狭窄合併進行胃癌の1例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A 59-year-old man with epigastric discomfort and anorexia was referred to our hospital. Endoscopy revealed a type 3 advanced gastric cancer with pyloric stenosis diagnosed as a poorly differentiated adenocarcinoma in the biopsy specimens. A gastrojejunal bypass operation was performed because of direct invasion to the pancreas. The patient was treated by three courses of neoadjuvant chemotherapy with S-1/CDDP. Follow-up abdominal CT scan revealed that the primary tumor had become smaller, suggesting that a partial response had been achieved. Distal gastrectomy with D2 lymphadenectomy was performed. The histopathological examination showed no residual cancer cells in the primary lesion or dissected lymph nodes. Final chemotherapy efficacy was evaluated as Grade 3. The patient was treated with S-1 for one year after the gastrectomy and lymphadenectomy and has been followed up for 18 months without evidence of recurrence.
en-copyright=
kn-copyright=
en-aut-name=NishizakiMasahiko
en-aut-sei=Nishizaki
en-aut-mei=Masahiko
kn-aut-name=西崎正彦
kn-aut-sei=西崎
kn-aut-mei=正彦
aut-affil-num=1
ORCID=
en-aut-name=FujiwaraYasuhiro
en-aut-sei=Fujiwara
en-aut-mei=Yasuhiro
kn-aut-name=藤原康宏
kn-aut-sei=藤原
kn-aut-mei=康宏
aut-affil-num=2
ORCID=
en-aut-name=ChoudaYasuhiro
en-aut-sei=Chouda
en-aut-mei=Yasuhiro
kn-aut-name=丁田泰宏
kn-aut-sei=丁田
kn-aut-mei=泰宏
aut-affil-num=3
ORCID=
en-aut-name=KanazawaTakashi
en-aut-sei=Kanazawa
en-aut-mei=Takashi
kn-aut-name=金澤卓
kn-aut-sei=金澤
kn-aut-mei=卓
aut-affil-num=4
ORCID=
en-aut-name=NinomiyaMotoki
en-aut-sei=Ninomiya
en-aut-mei=Motoki
kn-aut-name=二宮基樹
kn-aut-sei=二宮
kn-aut-mei=基樹
aut-affil-num=5
ORCID=
en-aut-name=FujiwaraToshiyoshi
en-aut-sei=Fujiwara
en-aut-mei=Toshiyoshi
kn-aut-name=藤原俊義
kn-aut-sei=藤原
kn-aut-mei=俊義
aut-affil-num=6
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器外科学
affil-num=2
en-affil=
kn-affil=広島市立広島市民病院 外科
affil-num=3
en-affil=
kn-affil=広島市立広島市民病院 外科
affil-num=4
en-affil=
kn-affil=広島市立広島市民病院 外科
affil-num=5
en-affil=
kn-affil=広島市立広島市民病院 外科
affil-num=6
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 消化器外科学
en-keyword=幽門狭窄 (pyloric stenosis)
kn-keyword=幽門狭窄 (pyloric stenosis)
en-keyword=進行胃癌 (advanced gastric cancer)
kn-keyword=進行胃癌 (advanced gastric cancer)
en-keyword=S-1/CDDP
kn-keyword=S-1/CDDP
en-keyword=術前化学療法 (neoadjuvant chemotherapy)
kn-keyword=術前化学療法 (neoadjuvant chemotherapy)
en-keyword=組織学的CR (pathological CR)
kn-keyword=組織学的CR (pathological CR)
END
start-ver=1.4
cd-journal=joma
no-vol=124
cd-vols=
no-issue=1
article-no=
start-page=53
end-page=57
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2012
dt-pub=20120401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Two cases of lymphoepithelial cyst of the pancreas
kn-title=膵リンパ上皮嚢胞の2例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A 35-year-old man was found to have a cystic mass in the pancreatic body on a routine health examination ; high serum CA19-9 was also detected. The enucleated cyst was diagnosed as a lymphoepithelial cyst (LEC). A 74-year-old man found to have a cystic mass in the pancreatic head by computer tomography as well as high serum CA19-9 was suspected of a cystic neoplasm of the pancreas (IPMN), and pylorus-preserving pancreaticoduodenectomy (PPPD) was performed. Pathologically, the cyst was found to be LEC. It is often difficult to diagnose pancreatic cyst as LEC preoperatively. Care should be taken not to do over-surgery for benign disease LEC.
en-copyright=
kn-copyright=
en-aut-name=HamanoRyosuke
en-aut-sei=Hamano
en-aut-mei=Ryosuke
kn-aut-name=濱野亮輔
kn-aut-sei=濱野
kn-aut-mei=亮輔
aut-affil-num=1
ORCID=
en-aut-name=InagakiMasaru
en-aut-sei=Inagaki
en-aut-mei=Masaru
kn-aut-name=稲垣優
kn-aut-sei=稲垣
kn-aut-mei=優
aut-affil-num=2
ORCID=
en-aut-name=KimuraYuuji
en-aut-sei=Kimura
en-aut-mei=Yuuji
kn-aut-name=木村祐司
kn-aut-sei=木村
kn-aut-mei=祐司
aut-affil-num=3
ORCID=
en-aut-name=IsodaKenta
en-aut-sei=Isoda
en-aut-mei=Kenta
kn-aut-name=磯田健太
kn-aut-sei=磯田
kn-aut-mei=健太
aut-affil-num=4
ORCID=
en-aut-name=KitadaKoji
en-aut-sei=Kitada
en-aut-mei=Koji
kn-aut-name=北田浩二
kn-aut-sei=北田
kn-aut-mei=浩二
aut-affil-num=5
ORCID=
en-aut-name=NishieManabu
en-aut-sei=Nishie
en-aut-mei=Manabu
kn-aut-name=西江学
kn-aut-sei=西江
kn-aut-mei=学
aut-affil-num=6
ORCID=
en-aut-name=NomuraNagahisa
en-aut-sei=Nomura
en-aut-mei=Nagahisa
kn-aut-name=野村長久
kn-aut-sei=野村
kn-aut-mei=長久
aut-affil-num=7
ORCID=
en-aut-name=TokunagaNaoyuki
en-aut-sei=Tokunaga
en-aut-mei=Naoyuki
kn-aut-name=徳永尚之
kn-aut-sei=徳永
kn-aut-mei=尚之
aut-affil-num=8
ORCID=
en-aut-name=TakahashiKenji
en-aut-sei=Takahashi
en-aut-mei=Kenji
kn-aut-name=高橋健司
kn-aut-sei=高橋
kn-aut-mei=健司
aut-affil-num=9
ORCID=
en-aut-name=MiyasouHideaki
en-aut-sei=Miyasou
en-aut-mei=Hideaki
kn-aut-name=宮宗秀明
kn-aut-sei=宮宗
kn-aut-mei=秀明
aut-affil-num=10
ORCID=
en-aut-name=TsunemitsuYosuke
en-aut-sei=Tsunemitsu
en-aut-mei=Yosuke
kn-aut-name=常光洋輔
kn-aut-sei=常光
kn-aut-mei=洋輔
aut-affil-num=11
ORCID=
en-aut-name=OhtsukaShinya
en-aut-sei=Ohtsuka
en-aut-mei=Shinya
kn-aut-name=大塚眞哉
kn-aut-sei=大塚
kn-aut-mei=眞哉
aut-affil-num=12
ORCID=
en-aut-name=MiyoshiKazuya
en-aut-sei=Miyoshi
en-aut-mei=Kazuya
kn-aut-name=三好和也
kn-aut-sei=三好
kn-aut-mei=和也
aut-affil-num=13
ORCID=
en-aut-name=IwakawaKazuhide
en-aut-sei=Iwakawa
en-aut-mei=Kazuhide
kn-aut-name=岩川和秀
kn-aut-sei=岩川
kn-aut-mei=和秀
aut-affil-num=14
ORCID=
en-aut-name=TakahashiMasahiko
en-aut-sei=Takahashi
en-aut-mei=Masahiko
kn-aut-name=高橋正彦
kn-aut-sei=高橋
kn-aut-mei=正彦
aut-affil-num=15
ORCID=
en-aut-name=IwagakiHiromi
en-aut-sei=Iwagaki
en-aut-mei=Hiromi
kn-aut-name=岩垣博巳
kn-aut-sei=岩垣
kn-aut-mei=博巳
aut-affil-num=16
ORCID=
affil-num=1
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=2
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=3
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=4
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=5
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=6
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=7
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=8
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=9
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=10
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=11
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=12
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=13
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=14
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=15
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=16
en-affil=
kn-affil=国立病院機構福山医療センター 外科
en-keyword=リンパ上皮嚢胞 (lymphoepithelial cyst)
kn-keyword=リンパ上皮嚢胞 (lymphoepithelial cyst)
END
start-ver=1.4
cd-journal=joma
no-vol=31
cd-vols=
no-issue=350
article-no=
start-page=281
end-page=290
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1919
dt-pub=19190331
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=「アルカロイド」ノ毒力ト其膠質状態トノ關係
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=小野寺直助
kn-aut-sei=小野寺
kn-aut-mei=直助
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=九州帝國醫科大學
END
start-ver=1.4
cd-journal=joma
no-vol=301
cd-vols=
no-issue=1
article-no=
start-page=57
end-page=62
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Isolation and characterization of human lung cancer antigens by serological screening with autologous antibodies
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Serological analysis of a recombinant cDNA expression library (SEREX) derived from two lung adenocarcinoma cancer cell lines using autologous sera led to the isolation of 41 positive cDNA clones comprising 28 different antigens. They coded for a variety of nuclear and cytoplasmic proteins. Among the antigens, nucleoporin 107 (NUP107) was isolated most frequently (5 of 41 clones). The second most frequently isolated antigen was coded for by C21orf58 (4 of 41 clones). During serological analysis of selected antigens based on their reactivity to sera from normal individuals and lung cancer patients, none of the antigens showed a cancer-restricted recognition pattern. However, five genes including NUP107 showed higher expression when we examined the changes in gene expression in five different adenocarcinoma cell lines, including those used in SEREX, compared with their levels in normal lung tissues by cDNA microarray analysis. On the other hand, the expression levels of five genes including C21orf58 were down regulated in all adenocarcinoma cell lines. This SEREX study combining comprehensive gene expression assays has added to the growing list of lung cancer antigens, which may aid the development of diagnostic and immunotherapeutic reagents for patients with lung cancer.
en-copyright=
kn-copyright=
en-aut-name=HanafusaTadashi
en-aut-sei=Hanafusa
en-aut-mei=Tadashi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=MohamedAli Eldib Ali
en-aut-sei=Mohamed
en-aut-mei=Ali Eldib Ali
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KitaokaKenta
en-aut-sei=Kitaoka
en-aut-mei=Kenta
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OhueYoshihiro
en-aut-sei=Ohue
en-aut-mei=Yoshihiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=NakayamaEiichi
en-aut-sei=Nakayama
en-aut-mei=Eiichi
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=6
ORCID=
affil-num=1
en-affil=
kn-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
affil-num=2
en-affil=
kn-affil=Faculty of Science, Alexandria University
affil-num=3
en-affil=
kn-affil=Hyogo Prefectural Awaji Hospital
affil-num=4
en-affil=
kn-affil=Department of Medicine, Kawasaki Medical University
affil-num=5
en-affil=
kn-affil=Faculty of Health and Welfare, Kawasaki University of Medical Welfare
affil-num=6
en-affil=
kn-affil=Department of Radiation Research, Advanced Science Research Center, Okayama University
en-keyword=Lung adenocarcinoma
kn-keyword=Lung adenocarcinoma
en-keyword=SEREX
kn-keyword=SEREX
en-keyword=Tumor antigen
kn-keyword=Tumor antigen
en-keyword=NUP107
kn-keyword=NUP107
en-keyword=MYL6B
kn-keyword=MYL6B
END
start-ver=1.4
cd-journal=joma
no-vol=123
cd-vols=
no-issue=2
article-no=
start-page=129
end-page=132
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110801
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Laparoscopic surgery for mesenteric Castleman's disease
kn-title=腹腔鏡下に摘出しえた上行結腸間膜発生のCastleman病の1例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=We report herein a case of mesenteric Castleman's disease which was confirmed on pathology. A 60-year-old man was admitted to our hospital complaining of abdominal pain. On the physical examination, there was no palpable mass. Computed tomography findings and magnetic resonance imaging revealed a well circumscribed, lobulated round mass on the right side of the superior mesenteric vein. Laparoscopic surgery for the mesenteric tumor was carried out to obtain a definite diagnosis and treatment. In the operative field, the mass was located on the ascending colic mesentery and measured about 3 cm in size. It was solid and surrounded by a thin fibrous capsule. The histological diagnosis of the mesenteric tumor was hyaline vascular type Castleman's disease. The postoperative course of the patient was uneventful, and he was discharged on the 10th postoperative day.
en-copyright=
kn-copyright=
en-aut-name=NishieManabu
en-aut-sei=Nishie
en-aut-mei=Manabu
kn-aut-name=西江学
kn-aut-sei=西江
kn-aut-mei=学
aut-affil-num=1
ORCID=
en-aut-name=OtsukaShinya
en-aut-sei=Otsuka
en-aut-mei=Shinya
kn-aut-name=大塚真哉
kn-aut-sei=大塚
kn-aut-mei=真哉
aut-affil-num=2
ORCID=
en-aut-name=TomodaJun
en-aut-sei=Tomoda
en-aut-mei=Jun
kn-aut-name=友田純
kn-aut-sei=友田
kn-aut-mei=純
aut-affil-num=3
ORCID=
en-aut-name=FujiwaraKeishi
en-aut-sei=Fujiwara
en-aut-mei=Keishi
kn-aut-name=藤原敬士
kn-aut-sei=藤原
kn-aut-mei=敬士
aut-affil-num=4
ORCID=
affil-num=1
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=2
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=3
en-affil=
kn-affil=国立病院機構福山医療センター 内科
affil-num=4
en-affil=
kn-affil=光生病院 内科
en-keyword=結腸間膜 (mesocolon)
kn-keyword=結腸間膜 (mesocolon)
en-keyword=Castleman病 (Castleman's disease)
kn-keyword=Castleman病 (Castleman's disease)
en-keyword=腹腔鏡手術 (laparoscopic surgery)
kn-keyword=腹腔鏡手術 (laparoscopic surgery)
END
start-ver=1.4
cd-journal=joma
no-vol=
cd-vols=
no-issue=
article-no=
start-page=
end-page=
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110325
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=食に関する教育と新しいスタイルの学校給食-個を尊重する学校教育の視点から-
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OnoHisami
en-aut-sei=Ono
en-aut-mei=Hisami
kn-aut-name=小野尚美
kn-aut-sei=小野
kn-aut-mei=尚美
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学
END
start-ver=1.4
cd-journal=joma
no-vol=46
cd-vols=
no-issue=8
article-no=
start-page=1899
end-page=1922
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1934
dt-pub=19340831
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über die Studien von Spaltung und Ansscheidung des Fettes in der Leber; besonders über den Einfluss der Milz auf diese Mechanismus
kn-title=肝臟ノ脂肪分解及ビ排泄機轉ノ研究竝ニ該機轉ニ及ボス脾臟ノ影響ニ就テ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Der Verfasser studierte experimentelle über das Schicksal der Fett, die hämatogen in die Leber transportiert wurde; und forschte besonders über den Einfluss der Milz darüber. Die Versuchsordnung ist folgende: 1) Zuerst bestätigte quantitativ die Fettsaure im Pfortaderblute, Lebervenenblute, und in der Blasengalle beim normalen Hündchen; gleichzeitig excisierte ein Teil von Leber zur histologischen Untersuchung über die Fettablagerung in der Leber. 2) Bei einer Gruppe von H-ündchen, die ide "Olivenölemulsion" P.K. 10cc. intravenöe injciert wurden, forschte innen 5 Minuten bis 24 Stunden nach der Injektion oben erwähnte Einzellheiten. 3) Bei anderer Gruppe von Hündchen, die splenektomiert wurden, forschte nach 1 Woche oben erwäahnte Einzellheiten. 4) Zuletzt studierte bei splenektomierten Hündchen, die die "Olivenölemulsion" P.K. 10cc. intravenos injciert wurden, oben erwähte Einzellheiten. Die Resultate lauteten: 1) Das Fettwird in der Leber immer zuerst von Sternzellen phagozytiert und dann geht in die Leberzellen über und hier wird es enthalten. 2) Das Fett, das einmal in der Leberzellen enthalten wird, teils gespaltet und ein Teil davon wird zum Lipoid verändert, teils durch Sternzellen wieder in das Blut oder in die Lymphe ausscheiden wird. Ein weniger übniger Teil von Fett wird direkt von Leberzellen als Gallenbestandteil in die Gallenwag ausscheiden. 3) Solche Funktionen von Leberzellen wie Enthaltung oder Spaltung von Fett und Lipoidbildung oder Ausscheidung desselben kommen durch Milzexstirpation deutlich herunter, demgemass vermindert sich stark die Wirkung der Leber zur Enthaltung von Fett.
en-copyright=
kn-copyright=
en-aut-name=OnoTetsuji
en-aut-sei=Ono
en-aut-mei=Tetsuji
kn-aut-name=小野哲二
kn-aut-sei=小野
kn-aut-mei=哲二
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學石山外科教室
END
start-ver=1.4
cd-journal=joma
no-vol=46
cd-vols=
no-issue=8
article-no=
start-page=1749
end-page=1773
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1934
dt-pub=19340831
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über die klinische Bedeutung der Milz auf Fettstoffwechsel der Leber. (II. Mitteilung.)
kn-title=肝臟脂肪新陳代謝機能ニ對スル脾臟ノ意義ニ就テ(第2報)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Als weitere Untersuchungsmethode über die Bedeutung der Milz gegen die Leber, besonders auf Fettstoffwechsel benutzte der Verfasser selbat neu-geschaffte "Olivenölemulsion", die zur Forschung von Fettstoffwechsel ein ideales Mittel ist. Die Versuchstiere teilte der Verfasser folgende 7. Untergruppe ein. 1. Gruppe: Normale Hündchen. 2. Gruppe: Splenektomierte Hündchen. 3-4. Gruppe: Normale und splenektomierte Hündchen, die alle ihre R.E.S. mit Collargollösung brockiert wurden. 5-6. Gruppe: Normale und splenektomierte Hündchen, die alle ihre Leberzellen mit CCl(4) geschädigt wurden. 7. Gruppe: Splenektomierte Hündchen, die alle die Injektion von Milzextrakt
bekaminen. Der Verfasser benutzte diese 7. Gruppe von Hündchen zur Forschung von Fettstoffwechsel
der Leber und dekam folgende Resultate. Die Milzexstirpation gibt keinen Einfluss auf die Funktionsveränderung der Sternzellen über Fettstoffwechsel, sondern mehr Einfluss auf Leberzellen, Die Ursache von dieser Wechselbeziehung zueisehen Milz und Leberzellen sei behufs dem Einfluss von Milzhormon. Der Verfasser studierte weiter die histologische Veränderung von Golgische Apparat von Leberzellen beim normalen und splenektomierten Hündchen und bestätigte deutliche Degeneration beim letzten Tiere.
en-copyright=
kn-copyright=
en-aut-name=OnoTetsuji
en-aut-sei=Ono
en-aut-mei=Tetsuji
kn-aut-name=小野哲二
kn-aut-sei=小野
kn-aut-mei=哲二
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學石山外科教室
END
start-ver=1.4
cd-journal=joma
no-vol=46
cd-vols=
no-issue=7
article-no=
start-page=1627
end-page=1655
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1934
dt-pub=19340731
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über die klinische Bedeutung der Milz auf Fettstoffwechsel der Leber. (I. Mitteilung.)
kn-title=肝臓脂肪新陳代謝機能ニ對スル脾臓ノ意義ニ就テ(第1報)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Der Verfasser studierte experimentelle über die klinische Bedeutung der Milzgegen die Leber in bezug auf Fettstoffwechsel. Als Versuchtier benutzte das Hund und forschte hauptsächlich histologische Veränderung mitsamt biochemische Untersuchung der Leber. Die Ordnung der Untersuchung lautet; 1) Bezüglich der quantitativen Verändernng von Fettablagerung der Leber und Fettgehalt im Blute forschte der Verfasser beim normalen Hunde genau chemisch und noch dazu histologisch. 2) Bei einer Gruppe von Hündchen, die splenektomiert wurden, untersuchte der Verfasser hauptsächlich die Leberveräanderund und der Fettgehalt im Blute. 3) Diese Forschung setzte der Verfasser weiter nach Brockierung von R.E.S. mit 1% Collargollosung beim normale und splenektomierten Hündchen fort. 4) Dann forschte der Verfasser obengenaunte Veränderung der Leber und des Blutes nach Injektion von 1% Collargollösung im Reizdose gegen R.E.S, 5) Nach Schädigung von Funktion der Leberzellen mit CCl4 beim normalen und splenektomierten Hündchen beobachtete der Verfasser 5 W, lang die Veränderung von Leber und Fettgehalt im Blute. 6) Zuletzt injcierte deu Reizdosis von CCl4 zu solchen Händchen und forschte genau oben genaunte Einzellheiten. Schlässsatze; 1) Jede Sternzellen und Leberzellen haben besondere klinische Bedeutung auf Fettstoffwechsel der Leber und zwar stehen Jeder für sich in unterennbarer Beziehung. 2) Es schcint die Abnahme von Fettstoffwechsel der Leber durch Splenektomie hervortreten und infolgedessen wird die Veräuderung von Fettstoffwechsel der Leber herbeiführen. 3) Die Hyperlipämie nach Milzexstirpation soll seine Ursache nicht nur auf die Funktionsstörung von R.E.S. sondern auch auf solche von Leberzellen zurückzuführen.
en-copyright=
kn-copyright=
en-aut-name=OnoTetsuji
en-aut-sei=Ono
en-aut-mei=Tetsuji
kn-aut-name=小野哲二
kn-aut-sei=小野
kn-aut-mei=哲二
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學石山外科教室
END
start-ver=1.4
cd-journal=joma
no-vol=65
cd-vols=
no-issue=2
article-no=
start-page=91
end-page=95
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=201104
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=An Assessment of Radioactivity Levels of 210Pb and 40K in Tobacco and Radiation Exposure from Smoking
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=No research has been conducted on the radiation influence of tobacco on the alimentary system, although there have been some previous works on the respiratory system. In this study, the radioactive concentrations of 210Pb and 40K in a cigarette sample were first measured. The transfer factors of the nuclides from tobacco into smoke and solution (saliva and/or alcohol) were then examined. Moreover, the radiation doses from smoke inhalation were also evaluated. The radioactive concentrations of 210Pb and 40K in the cigarette tobacco were 0.01 and 0.3 Bq/cigarette. Since this 210Pb activity and the 210Po activity previously reported for the same sample were comparable, it can be concluded that there was a radioactive equilibrium between the 2 nuclides. The observed transfer factor of 210Pb (12%) into smoke was almost the same as that of 40K (15%), whereas the reported value for 210Po (60%) was significantly higher. The radiation doses due to inhalation of cigarette smoke varied from organ to organ, depending on the organotropic properties of the nuclide. For example, the kidneys, respiratory tract, and spleen showed relatively high doses from 210Pb and 210Po. The leaching rates indicated an inconsistent tendency related to solution types. This result could suggest that alcohol drinking, which is common in smokers, does not especially enhance the leaching characteristics.
en-copyright=
kn-copyright=
en-aut-name=NagamatsuTomohiro
en-aut-sei=Nagamatsu
en-aut-mei=Tomohiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=1
ORCID=
en-aut-name=SakodaAkihiro
en-aut-sei=Sakoda
en-aut-mei=Akihiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=2
ORCID=
en-aut-name=KataokaTakahiro
en-aut-sei=Kataoka
en-aut-mei=Takahiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=3
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=4
ORCID=
en-aut-name=YamaokaKiyonori
en-aut-sei=Yamaoka
en-aut-mei=Kiyonori
kn-aut-name=
kn-aut-sei=
kn-aut-mei=
aut-affil-num=5
ORCID=
affil-num=1
en-affil=
kn-affil=Graduate School of Health Sciences, Okayama University
affil-num=2
en-affil=
kn-affil=Graduate School of Health Sciences, Okayama University
affil-num=3
en-affil=
kn-affil=Graduate School of Health Sciences, Okayama University
affil-num=4
en-affil=
kn-affil=Department of Radiation Research Shikata Laboratory, Advanced Science Research Center, Okayama University
affil-num=5
en-affil=
kn-affil=Graduate School of Health Sciences, Okayama University
en-keyword=tobacco
kn-keyword=tobacco
en-keyword=radionuclides
kn-keyword=radionuclides
en-keyword=smoking
kn-keyword=smoking
en-keyword=intake
kn-keyword=intake
en-keyword=radiation exposure
kn-keyword=radiation exposure
END
start-ver=1.4
cd-journal=joma
no-vol=51
cd-vols=
no-issue=6
article-no=
start-page=1292
end-page=1307
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1939
dt-pub=19390630
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Serologische Studien über den Hunger. (I. Mitteilung) Über den Einfluss des Hungers auf die Antikörperbildung, Komplementwert und Blutgerinnungszeit.
kn-title=饑餓ノ免疫學的研究(第1報)饑餓ノ免疫體産生ニ及ボス影響(附: 血清補體價竝ニ血液凝固作用ニ及ボス影響)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Der Einfluss des Hungers auf die Antikörperbildung wurde schon von vielen Forschern untersucht, die zu ganz verschiedenen Ergebuissen gelangten. Die einen meinten, dass die Antikörperbilduug bei langdauernder Hungerzeit gehiudert wurde; andere dagegen behaupteten, dass die Antikörperbildung bei Hungerzeit keinen nennensAntikörperbildung viel besser als beim Normalzustand des Versuchtiers beobachtet werden könne. Daher untersuchte ich bei Kaninchen und Meerschweinchen den Einfluss des Hungers auf verschiedene Antikörperarten, besonders unter Anwendung der Ogata'schen Immunkörperverdünnungsmethode bei Präzipitinbestimmung, und bei normalen Tieren den Komplementgehalt und die Blutgerinnungszeit. Die Ergebnisse lassen sich folgendermassen kurz zusammenfassen: 1) Die Präzipitinbildung gegen Ziegenserun bei Versuchstieren lässt beim absoluten Hungerversuch keinen grossen Unterschied gegenüber Kontrolltieren erkennen, bgleich vor dem Tod des Tieres eine etwas raschere Verminderung des Präzipitins als beim Kontrolltier stattfindet. 2) Haemoagglutininbildung gegen Hühnerblutkorperchen wird bei absoluter Hungerzeit etwas vermindert und ist dabei die Dauer des Maximums des Haemoagglutunins beim Versuchtier gegenüber dem Kontrolltier verkürzt. 3) Die Agglutininbildung von Bact. coli bei absolutem Hunger ist ebenso wie beim Haemoagglutinin schwächer als beim Kontrolltiere. 4) Der Einfluss des absoluten Hungers auf den Komplementgehalt ist verschieden, bei den einen wird er vermindert, bei anderen wird keine Verminderung des Komplementgehaltes beobachtet. 5) Im frühen Stadium des Hungerversuchs ist die Blutgerinnungszeit von Kaninchen und Meerschweinchen etwas beschleunigt, beim Spätstadium dagegen verlangsamt.
en-copyright=
kn-copyright=
en-aut-name=OnoHideo
en-aut-sei=Ono
en-aut-mei=Hideo
kn-aut-name=小野英夫
kn-aut-sei=小野
kn-aut-mei=英夫
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學衛生學教室
END
start-ver=1.4
cd-journal=joma
no-vol=123
cd-vols=
no-issue=1
article-no=
start-page=33
end-page=38
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110401
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Investigation of laparoscopic therapy in 56 cases of duodenal ulcer perforation
kn-title=十二指腸潰瘍穿孔に対する治療法の適応についての検討
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Background: Although conservative therapy has been acceptable as the first-line therapy for duodenal ulcer (DU) perforations, surgical therapies are known to have certain advantages. We investigated the indications for laparoscopic (LS) or open surgery (OS) or conservative therapy (CoT) among 56 DU perforation cases over 5 years. Methods: 31 LSs, 22 OSs and 5 CoTs were analyzed for patient's physical and surgical factors and clinical course. Results: Mean age was 51.6. Male/female ratio was 49/9. Survival ratio was 98%. Although the hospital stay (10.9 vs 19.5 days) and analgesic administrations (1.9 vs 4.6 days) were significantly shorter in LS than OS, almost all OS patients were in serious condition as evidenced by longer waiting time before treatment, stronger pain, bigger hole of perforation, more ascites accumulation and higher morbidity of complications. Two cases of multisurgery were experienced in both LS and OS groups due to leakage of seam, abscess formation, relapsed ulcer or idiopathic intestinal perforation. LS is a therapy more widely usable and more beneficial than the other two. Conclusion: LS, a minimally invasive surgery for DU perforation, should be considered as a first-line standard therapy because of significant advantages such as shorter hospital stay. OS or CoT may be selected when appropriate.
en-copyright=
kn-copyright=
en-aut-name=IshidoNobuhiro
en-aut-sei=Ishido
en-aut-mei=Nobuhiro
kn-aut-name=石堂展宏
kn-aut-sei=石堂
kn-aut-mei=展宏
aut-affil-num=1
ORCID=
en-aut-name=TamuraRyuji
en-aut-sei=Tamura
en-aut-mei=Ryuji
kn-aut-name=田村竜二
kn-aut-sei=田村
kn-aut-mei=竜二
aut-affil-num=2
ORCID=
en-aut-name=OkamotoTakahiro
en-aut-sei=Okamoto
en-aut-mei=Takahiro
kn-aut-name=岡本貴大
kn-aut-sei=岡本
kn-aut-mei=貴大
aut-affil-num=3
ORCID=
en-aut-name=KadowakiYoshihiko
en-aut-sei=Kadowaki
en-aut-mei=Yoshihiko
kn-aut-name=門脇嘉彦
kn-aut-sei=門脇
kn-aut-mei=嘉彦
aut-affil-num=4
ORCID=
en-aut-name=MoriTakashi
en-aut-sei=Mori
en-aut-mei=Takashi
kn-aut-name=森隆
kn-aut-sei=森
kn-aut-mei=隆
aut-affil-num=5
ORCID=
affil-num=1
en-affil=
kn-affil=神戸赤十字病院 外科
affil-num=2
en-affil=
kn-affil=神戸赤十字病院 外科
affil-num=3
en-affil=
kn-affil=神戸赤十字病院 外科
affil-num=4
en-affil=
kn-affil=神戸赤十字病院 外科
affil-num=5
en-affil=
kn-affil=神戸赤十字病院 外科
en-keyword=十二指腸潰瘍穿孔 (duodenal ulcer perforation)
kn-keyword=十二指腸潰瘍穿孔 (duodenal ulcer perforation)
en-keyword=腹腔鏡手術 (laparoscopic surgery)
kn-keyword=腹腔鏡手術 (laparoscopic surgery)
en-keyword=保存療法 (conservative therapy)
kn-keyword=保存療法 (conservative therapy)
END
start-ver=1.4
cd-journal=joma
no-vol=52
cd-vols=
no-issue=2
article-no=
start-page=338
end-page=352
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1940
dt-pub=19400229
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über die hemmende Wirkung von Solaesthiu auf die experimentelle Anaphylaxie bei Meerschweinchen
kn-title=「ソレスチン」ノ過敏症豫防機轉ニ就テ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Besredka berichtete, dass Narkotika auf die Anaphylaxie hemmend wirken. Im Jahre 1929 veröffentlichte Sugimoto in unserem Institut eine Arbeit über prophylaktische Wirkung der Äthernarkose auf die Anaphylaxie bei Meerschweinchen; dabei sagte er, dass diese Wirkung im Mechanismus beruht. d.h. auf der Abschwächung der Bindungsabilitat des Präzipitins und seiner lockeren Verbindung mit Präzipitinogen. Verfasser stellte Versuche an über die prophylaktische Wirkung des Solaesthins (Methylenchlorids) auf die Anaphylaxie unter Anwendung der Ogata'schen Präzipitinverdunnungsmethode sowie seinen Einfluss auf den Peptonschock. Die Resultate lassen sich folgendermassen kurz zusammenfassen: 1) Wenn man bei aktiver Anaphylaxie von Meerschweinchen die der Bindungszone 1/2-1/4 mal entsprechende Antigenmenge reinjiziert, so tritt typischer Schocktod ein. Wenn aber das Versuchstier vor und wahrend der Reinjektion mit Solaesthin tief narkotisiert wird, treten die Symptome schwächer als bei der Kontrolle ant und erholt sich das Tier wieder. 2) Das Meerschweinchen wurde mit Antirinderserum von Kaninchen in 1:500 Prazipitineinheiten sensibilisiert und nach 24 stündiger Inkubationszeit das Antigen in einer der Bindungszone entsprechenden Menge reinjiziert. Dabei konnte man typischen Schocktod bei jedem Versuch beohachten. Wenn aber das Versuchstier vor und während der Reinjektion mit Solaesthin narkotisiert wird, treten die Symptome ganz schwach auf und die Abnahme des Präzipitins und des Komplements nach der Reinjektion ist geringer als bei der Kontrolle. Das Präzipitin und das Komplement, die sich nach der Reinjektion stark vermindern, vermehren sich langsame bei jeder Wiederholung des Symptoms. 3) Bei Solaesthinnarkose sieht man keine Abnahme des Präzipitins und des Komplements, sowohl bei aktiv als auch passiv sensibilisierten Tieren, 1 Stunde nach der Narkose zeigt sich eine geringfügige Verminderung und nach 2 Stunden ergibt sich ein gleicher Stand wie vor dem Versuch. 4) Bei den zwei Präzipitinreaktionen, wobei in einem Fall das Präzipitin mit Serum, das von Meerschweinchen während ihrer tiefen Narkose entnommen war, verdünnt wurde, im anderen Fall mit normalem Meerschweinchenserum, sieht man eine leichte Hemmung hinsichtlich der Reaktion, weil bei ersterer die Reaktion etwas langsamer als bei letzterer beobachtet wird. 5) Bei Erschütterung mit Solaesthin direkt im Serum sieht man jedoch keine hemmende Wirkung. 6) Solaesthin zeigt auch eine prophylaktische Wirkung auf den Peptonschock. 7) Aus oben erwähnten Ergebnissen schliesst Verfasser, das die prophylaktische Wirkung des Solaesthins auf die Anaphylaxie auf folgendem Mechanismus beruht: 1. Abschwächung der Bindungsabilität des Präzipitins und seine lockere Bindung mit Präzipitinogen. 2. Lähmung der bronchial glatten Muskeln wie nach den Angaben von Biedle und Kraus.
en-copyright=
kn-copyright=
en-aut-name=OnoHideo
en-aut-sei=Ono
en-aut-mei=Hideo
kn-aut-name=小野英夫
kn-aut-sei=小野
kn-aut-mei=英夫
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學衛生學教室
END
start-ver=1.4
cd-journal=joma
no-vol=52
cd-vols=
no-issue=2
article-no=
start-page=325
end-page=337
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1940
dt-pub=19400229
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über den Einfluss von Morphin auf die experimentelle Anaphylaxie
kn-title=「鹽酸モルヒネ」ノ過敏症ニ及ボス影響ニ就テ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Besredka entdeckte, dass Äther auf die Anaphylaxie hemmend wirkt. Biedle und Kraus prüften diese interessanten Angaben nach und berichteten, das alle Narkotika (z.B. Äther Chloroform, Urethan und Alkohol u.a.) antianaphylaktisch wirken. Farmer, Aoki u.a. dagegen traten obigen Anschauungen entgegen, weil Morphin auf die Anaphylaxie keine hemmende Wirkung zeigt, sondern befördernd wirkt. Motomura, Uno und Oohira stellten fest, dass Morphin auf die Anaphylaxie doch hemmend wirkt. Verfasser untersuchte sowohl bei aktiv oder passiv präparierten Meerschweinchen als auch bei isolierten Darmschlingen die Wirkung von Morphin auf die Anaphylaxie, wobei eine bestimmte Menge von Morphin ca. 1 Stunde vor der Antigenreinjektion subkutan injiziert, den uberlebenden Darmprapäraten aber zugefuhrt wurde, und erzielte folgende Resultate: 1) Bei Vorbehandlung mit Morphin von 0.005-0.02g pro 100g Körpergewicht von Meerschweinchen erzielte man keine schockhemmende Wirkung. Aber bei Vorbehandlung mit einer relativ grossen Menge von Morphin (0.02g pro 100g Körpergewicht) ergab sich beim Versuchstier ein schwächerer Krampf als bei der Kontrolle. 2) Das Meerschweinchen wurde mit 500 Einheiten von Antirinderpräzipitin des Kaninchens vorbehandelt und nach 24 stündiger Inkubationszeit minimal tödliches Antigen (eine der Bindungszone entsprechende Menge) reinjiziert. Dabei sieht man immer typischen Schocktod bei jedem Versuchstier. Durch Vorbehandlung mit Morphin von 0.005-0.02g pro 100g Körpergewicht von Meerschweinchen wurde das Tier vom anaphylaktischen Schocktod nicht gerettet.
Wenn aber die Vorbehandiung mit Morphin relativ gross ist, bemerkt man zuweilen einen etwas schwächeren Krampf. 3) Bei aktiver und passiver Anaphylaxie von isolierten Meerschweinchendärmen sieht man bei Zufuhr von Morphin von 0, 0001-0.25% in dem Nährmedium nicht nur eine die Anaphylaxie hemmende Wirkung, sondern sogar einen etwas beförndernden Einfluss, wenn die Zufuhr von Morphin relativ gering ist. 4) Die Zufuhr von Morphin (von 0.25-0.5%) im Präzipitinverdönnungsmedium zeigt keinen besonderen Einfluss auf die Präzipitinreaktion. Aus oben erwähnten Ergebnissen schliesst Verfasser, dass durch Morphininjektion ein nennenswerter Einfluss auf die experimentelle Anaphylaxie von Meerschweinchen nicht bewirkt werden kann.
en-copyright=
kn-copyright=
en-aut-name=OnoHideo
en-aut-sei=Ono
en-aut-mei=Hideo
kn-aut-name=小野英夫
kn-aut-sei=小野
kn-aut-mei=英夫
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學衛生學教室
END
start-ver=1.4
cd-journal=joma
no-vol=52
cd-vols=
no-issue=1
article-no=
start-page=185
end-page=203
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1940
dt-pub=19400131
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Über die hemmende Wirkung des Antipyrins auf die experimentelle Anaphylasie bei Meerschweinehen
kn-title=「アンチピリン」ノ過敏症豫防機轉ニ就テ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Im Jahre 1928 hat Dr. M. Matsuda berichtet, dass durch Antipyrin die Anaphylaxie stark geschützt wird und danach haben Dr. Matsuoka und Dr. Okubo dies welter nachgeprüft, aber es gibt noch keine genaue Untersuchung über den Mechanismus des Antipyrins bei der Präzipitinreaktion, womit man die Schockerscheinung in vivo nachprüfen kann. Daher studierte Verfasser unter Anwendung der Ogata'schen Methode, welche die Präzipitinmenge durch Überschichtung mit Immunkörperverdünnung bestimmt, die hemmende Wirkung des Antipyrins nach vorliegender Anschauung, ob bei dem antianaphylaktischen Vorgang des Antipyrins irgendeine hemmende Wirkung auf das Präzipitin direkt oder indirekt durch Bindung zwischen Antigen und Präzipitin beobachtet werden kann, und ferner wie sieh das Komplement dabei verhalt. 1) Bei aktiv sensibilisierten Meerschweinchen (rund 250g) wurde der Schocktod nach Antigenreinjektion (1/2-1/4 der Bindungszone entsprechende Antigenmenge) und durch vorliegende Antipyrininjektion, die mit 0.02g pro 100g Körpergewicht intravenös 5-10 Minuten vor der Reinjektion ausgeführt wurde, verhindert, wahrend das Kontrolltier an typischem Schock innerhalb 5 Minuten zugrunde ging und das Präzipitin und Komplement Bich auf fast Null verminderte. Die Abnahme des Präzipitins und des Komplements bei der Antipyrininjektion sind geringer als bei der Kontrolle. 2) Passiv sensibilisierte Meerschweinchen, welchen intravenös 500 Einheiten Immunserum injiziert wurde, wurden durch 1-1/2 der Bindungszone entsprechende Antigenreinjektion nach 24 stündiger Inkubationszeit durch typischen Schocktod abgetötet. Dagegen wurde das Tier durch Antipyrinvorinjektion in gleicher Weise wie bei der aktiven Anaphylaxie gerettet. Die Abnahme des Präzipitins und des Komplements sind dabei auch geringer als bei der Kontrolle. 3) Durch Antipyrininjektion wurde das Präzipitin nach 5 Minuten bei aktiv immunisierten Tieren ungefähr um die Halfte (1:16-1:8) vermindert und bei passiv immunisierten Tieren (1:25-I:12) sieht man eine noch grössere Verminderung. 4) Nach Antigenreinjektion wurde die Bindung zwischen Antigen und Antikörper noch gehemmt, weslialb das Präzipitin zur Kontrolle noch mehr zurückbleibt. 5) Die Präzipitinreaktion, bei der als Verdünnungsmedium Originalmeerschwein- ehenserum angewendet wird, welches 5-10 Minuten nach der Reinjektion des Antipyrins (0.02g pro 100g Körpergewicht) entnommen wird, zeigt einen viel geringeren Titer des Präzipitins und langsamere Geschwindigkeit der Reaktion als bei der Kontrolle das normale Meerschweinchenserum. 6) Bei der Reaktion, wobei Antipyrin direkt dem Medium (1% Gummi arabicum physiologische Kochsalzlüsung) zugefuhrt wird, ist auch der Präzipitintiter geringer und die Geschwindigkeit der Reaktion deutlich geringer als bei der Kontrolle.
Aus oben erwähnten Resultaten kann Verfasser den antianaphylaktischen Mechanismus des Antipyrins aus der Immunreaktion selbst durch folgende 2 Eigenschaften und zwar als einen Teil dieser Wirkung erklären. a) Hemmung der Bindung zwischen Antigen und. Antikörper. b) Langsame Bindung zwischen Antigen und Antikörper durch Veränderung des Kolloidalzustands infolge Zufuhr von Antipyrin.
en-copyright=
kn-copyright=
en-aut-name=OnoHideo
en-aut-sei=Ono
en-aut-mei=Hideo
kn-aut-name=小野英夫
kn-aut-sei=小野
kn-aut-mei=英夫
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學衛生學教室
END
start-ver=1.4
cd-journal=joma
no-vol=52
cd-vols=
no-issue=1
article-no=
start-page=107
end-page=141
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1940
dt-pub=19400131
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Serologische Studien über den Hunger (2. Mitteilung.) Über den Einfluss des Hungers auf die experimentelle Anaphylaxie
kn-title=饑餓ノ免疫學的研究(第2報)實驗的過敏症ニ及ボス饑餓ノ影響ニ就テ
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=In der ersten Mitteilung berichtete Verfasser, dass der Hungerversuch auf die Antikörperbildung bei Tieren einen insgesamt nicht nennenswerten Einflüss ausubt, weil in bezug auf absoluten Hunger die Präzipitinbildung keinen Unterschied zeigt, während die Agglutininbildung ein wenig hemmend wirkt. In dieser Mitteilung beschäftigte er sich weiter mit der Wirkung des Hungers auf die Anaphylaxie und bemerkte einen hemmenden Einfluss des Hungers bei Meerschweinchen und Kaninchen sowohl bei aktiver und passiver Anaphylaxie als auch bei isoliertem Organversuch (Darm und Herzlungenpräparat nach Kusama und Manwaring). Die Präzipitinbestimmung und Antigenmenge zur Reinjektion wurde nach Ogata'scher Verdünnungsmethode angewandt. Die Versuchstiere wurden über 24-48 Stunden lang absolutem Hunger ausgesetzt und oben genannter Versuch angestellt. 1) Das Meerschweinchen wurde mit Antirinderpräzipitin von Kaninchen in 500 Einheiten subkutan sensibilisiert und nach 48 stündiger Inkubationszeit wurde das Antigen in einer Menge, die gemäss der Bindungszone des Präzipitins berechnet wird, intravenös injiziert. Dabei fand Verfasser bei allen Versuchstieren typischen Schocktod innerhalb 5 Minuten nach Antigenreinjektion. Wenn aber das Tier während dieser Inkubationszeit 48 Stunden in absolutem Hunger- zustand gelassen wird, so sieht man viel schwächere Symptome als bei der Kontrolle und das Tier erholt sich vom anaphylaktischen Schocktod wieder. 2) Das Meerschweinchen wurde vorher 24 stündigem absoluten Hunger ausgesetzt und dann 500 Einheiten Antirinderpräzipitin intravenös sensibilisiert. Während der 24 stündigen Inkubationszeit wurde der Hungerversuch noch fortgesetzt. Darauf wurde das Antigen nach 48 stündiger Hungerzeit und nach 24 stundiger Inkubationszeit reinjiziert. Was den Kontrollversuch bei normaler Fütterung des Tieres anbetrifft, ging dieses nach gleicher Sensibilisierung bei der Antigenreinjektion nach unserer Methode gleich an typischen Schock zugrunde. 3) Bei der aktiven Anaphylaxie der Meerschweinchen mit Rinderserum tritt der lypisch anaphylaktische Schocktod durch Reinjektion des Antigens, das 1/4 der Bindungszone entspricht, ein. Wenn aber das Versuchstier etwa 48-72 Stunden vor der Reinjektion absoluten Hunger ausgesetzt wird, zeigten sich schwächere anaphylaktische Symptome und das Versuchstier wurde vom anaphylaktischen Schocktod gerettet. Es ist merkwürdig, dass sowohl bei aktiver als auch bei passiver Anaphylaxie die Verminderung des Präzipitins nach der Antigensreinjektion beim verhungerten Tier und Kontrolltier fast gleich 4) Diese Tatsache gilt auch bei experimenteller Kaninchenanaphylaxie. Wenn man zum Versuch einem Kaninchen, welches mit Rinderserum (pro kilo 1.0cc) intravenos sensibilisiert worden war, diejenige Antigenmenge, die der Bindungszone des Serumpräzipitins entspricht, nach der Inkubation (17-18 Tage) reinjiziert, erscheint, eine dentliche Blutdrucksenkung (10-40mm).
Wenn aber das Versuchstier 5-6 Tage vor der Reiniektion absolutem Hunger ausgesetzt wird, tritt schwächere Blutdrucksenkung (0-10mm) ein, während bei dem Tiere, welches 2-3 Tage lang hungert, eine deutliche Blutdrucksenkung hervorgerufen wird. Die Abnahme des Serumpräzipitins bei diesem Experiment ist gleich wie bei der Kontrolle und wie bei der Anaphylaxie des Meerschweinchens. 5) Wie schon oben angedeutet, entspricht die hemmende Wirkung der Anaphylaxie beim verhungerten Tier nicht der verminderten Bindung zwischen Präzipitin und Antigen und ist daher nur ein kleiner Unterschied zwischen Hungertierserum und Kontrollserum als Verdünnungsmedium zur Präzipitinreaktion festzustellen. 6) Bei Peptonschock des Meerschweinchens sieht man keinen besonderen Unterschied zwischen verhungerten und normalen Tieren. Wittepepton wirkte auf das Hungerkaninchen fast gleich wie auf das normale Kaninchen in bezug auf den Blutdrucksenkungsgrad, doch auf Hungerkaninchen wirkte es langsamer als auf das normale Kaninchen, weil die Blutdrucksenkung und Wiedererhöhung desselben beim Hungertier etwas langsamer als beim normalen Tier verläuft. 7) Bei der passiven und aktiven Anaphylaxie des isolierten Meerschweinchendarmes bemerkte Verfasser beim Hungertierdarm eine gegenüber dem normalen Darm verminderte Kontraktion nach Antigenzuführung. 8) Lunge und Herz des Versuchstieres wurden mit Ringer'scher Lösung durchströmt und während der Strömung wurde die künstliche Atmung angewandt. Nach Antigenmischung mit der strömenden Flüssigkeit sieht man eine Aufblähung der Lunge beim sensibilisierten Tier. Doch ist diese Aufblähung der Lunge beim verhungerten Tier auch viel schwächer als beim normalen Tier. Oben beschriebene Ergebnisse kann man dahin zusammenfassen, dass diese antianaphylaktische Eigenschaft beim Hungertier auf die Verminderung der Reaktionsfähigkeit des Gewebes, die durch den abnormen Stoffwechsel infolge absoluten Hungers verursacht
wird, zurückzuführen ist.
en-copyright=
kn-copyright=
en-aut-name=OnoHideo
en-aut-sei=Ono
en-aut-mei=Hideo
kn-aut-name=小野英夫
kn-aut-sei=小野
kn-aut-mei=英夫
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山醫科大學衛生學教室
END
start-ver=1.4
cd-journal=joma
no-vol=146
cd-vols=
no-issue=
article-no=
start-page=59
end-page=71
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2011
dt-pub=20110225
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Instructional Competence of Teachers in Lessons (Ⅳ): Lessons as Training Process
kn-title=授業における教師の指導性について(Ⅳ)ー「練習」過程としての授業ー
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=学枚での学習活動は少なからぬ時間が「練習」的な学習活動に費やされている。そこにおいて,一方で授業それ自体が全くトレーニング的なものに終始している場合もあれば,他方で「練習」的な学習活動にあまり注意を払わない授業論もある。学習内容には「習熟」を不可欠とするものがあり,そのためには「練習」が欠かせない。しかしその場合も機械的な「練習」ではなく,練習とともに「わかる」「使える」が位置づけられなくてはならない。また考え方や思考方法や学び方を深めていくという点から見れば,授業は「練習」過程である。練習の意味と役割を授業と関連づけて理論・実践的に整理し考察した。
en-copyright=
kn-copyright=
en-aut-name=OnoHiroo
en-aut-sei=Ono
en-aut-mei=Hiroo
kn-aut-name=小野擴男
kn-aut-sei=小野
kn-aut-mei=擴男
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院教育学研究科学校教育学系
en-keyword=練習
kn-keyword=練習
en-keyword=わかる
kn-keyword=わかる
en-keyword=活用
kn-keyword=活用
en-keyword=思考方法
kn-keyword=思考方法
en-keyword=学び方
kn-keyword=学び方
END
start-ver=1.4
cd-journal=joma
no-vol=101
cd-vols=
no-issue=11-12
article-no=
start-page=1009
end-page=1014
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1989
dt-pub=198912
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Ultrastructure of the “open secretion” of beta-cell granules from Langhans' islets in Fe(3+)-NTA-treated diabetic rats
kn-title=Fe(3+)-NTA投与糖尿病ラットのβ細胞開口分泌の電顕的観察
en-subtitle=
kn-subtitle=
en-abstract=The secretion time of endocrine cells is known to be momentary. Therefore, morphologic proof of the secretory mode have relied heavily on various animal models which were treated to accelerate secretion. Ultrastructure, concerning B-cell secretion from Langhans' islets of the pancreas, has been based on immersion-fixation specimens. As an experimental model of prolonged endocrine secretion, we used rat pancreas tissues which were rapidly perfused with a fixative. The fixation process, as reported previously, was 150 ml of 2% glutaraldehyde flushed at 15 ml per minute through the ascending aorta of Fe(3+)-NTA-treated diabetic rats. Afterwards, an ultrastructural study focused on the secreting mode of beta-granules in B-cell of Langhans' islets. This procedure proved an “open secretion” of beta-granules from B-cells; this phenomenon has never been observed in the previous immersion-fixation specimens. Contrary to non-treated normal rats, the varied stages of beta-granule secretion, including immediately before as well as after the secretion, were demonstrated in Fe(3+)-NTA-treated rats. We wish to emphasize the use of rapid perfusion-fixation technique in animal models with a delayed rather than accelerated state of endocrine secretion in order to investigate ultrastractural aspects of “open secretion”.
kn-abstract=内分泌腺細胞の分泌時間は瞬時とされていることから,一般的にその分泌像の形態的観察には,分泌を促進せしめる実験系が用いられている.又膵ラ氏島B細胞分泌の超微形態は,専ら浸漬固定標本で観察されている.今回,我々は分泌が遅延している動物で,高速還流した膵ラ氏島細胞について観察した.即ち,前報と同様のFe(3+)-NTA誘発糖尿病ラットの上行大動脈より2%グルタールアルデヒド150mlを15ml/minの速度で還流固定し,ラ氏島B細胞のβ顆粒分泌像に焦点を絞って観察した.その結果,前報の浸漬固定法では観察されなかった開口分泌像が多数観察され得た.対照の健常動物に比べ, Fe(3+)-NTA投与動物では,分泌直前から分泌後に至るいろいろな段階のβ顆粒の分泌過程が観察された.以上の結果から,開口分泌像の電顕的観察にはむしろ本実験系のように細胞分泌を障害ないし低下せしめ,高速還流固定法を用いることが必要であると結論した.
en-copyright=
kn-copyright=
en-aut-name=HayashiKeiki
en-aut-sei=Hayashi
en-aut-mei=Keiki
kn-aut-name=林肇輝
kn-aut-sei=林
kn-aut-mei=肇輝
aut-affil-num=1
ORCID=
en-aut-name=ShirasugaNaoki
en-aut-sei=Shirasuga
en-aut-mei=Naoki
kn-aut-name=白須賀直樹
kn-aut-sei=白須賀
kn-aut-mei=直樹
aut-affil-num=2
ORCID=
en-aut-name=OnoToshiro
en-aut-sei=Ono
en-aut-mei=Toshiro
kn-aut-name=小野俊郎
kn-aut-sei=小野
kn-aut-mei=俊郎
aut-affil-num=3
ORCID=
en-aut-name=AwaiMichiyasu
en-aut-sei=Awai
en-aut-mei=Michiyasu
kn-aut-name=粟井通泰
kn-aut-sei=粟井
kn-aut-mei=通泰
aut-affil-num=4
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学医学部病理学第一講座
affil-num=2
en-affil=
kn-affil=岡山大学医学部病理学第一講座
affil-num=3
en-affil=
kn-affil=岡山大学医学部病理学第一講座
affil-num=4
en-affil=
kn-affil=岡山大学医学部病理学第一講座
en-keyword=Diabetes mellitus
kn-keyword=Diabetes mellitus
en-keyword=β-cell's granules
kn-keyword=β-cell's granules
en-keyword=open secretion
kn-keyword=open secretion
en-keyword=perfusion fixation
kn-keyword=perfusion fixation
END
start-ver=1.4
cd-journal=joma
no-vol=122
cd-vols=
no-issue=3
article-no=
start-page=265
end-page=267
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2010
dt-pub=20101201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Carotid artery stenosis
kn-title=頸部頸動脈狭窄症
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=OkumaYu
en-aut-sei=Okuma
en-aut-mei=Yu
kn-aut-name=大熊佑
kn-aut-sei=大熊
kn-aut-mei=佑
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院医歯薬学総合研究科 脳神経外科学
END
start-ver=1.4
cd-journal=joma
no-vol=122
cd-vols=
no-issue=3
article-no=
start-page=231
end-page=236
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2010
dt-pub=20101201
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=A case of transverse colon cancer with remarkable extramural invasion to stomach and jejunum
kn-title=壁外性に腫瘤を形成し胃・小腸浸潤を示した横行結腸癌の1例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A 77-year-old woman was admitted to our hospital due to abdominal pain and body weight loss. A palpable mass the size of an infant's head was tender on palpation and identified as an epigastric lesion. Colonoscopic examination revealed stenosis of the transverse colon, although no intraluminal growth of the tumor was found. The histologic findings of the biopsy material were poorly differentiated and/or undifferentiated cells. Abdominal CT scan showed an irregular-shaped tumor with a diameter of 10cm invading the stomach and jejunum. We performed an operation under a diagnosis of extramurally growing cancer or malignant lymphoma of the colon. Partial resection of the transverse colon was done by distal gastrectomy and partial resection of the jejunum. Histologic examination of the operative specimens revealed moderately differentiated adenocarcinoma of the transverse colon, prominently proliferating into the surrounding tissues. The finding of a long stenotic lesion and extramural compression by colonography are characteristic of this tumor, based on a review of 43 literature reports in Japan.
en-copyright=
kn-copyright=
en-aut-name=HamanoRyosuke
en-aut-sei=Hamano
en-aut-mei=Ryosuke
kn-aut-name=濱野亮輔
kn-aut-sei=濱野
kn-aut-mei=亮輔
aut-affil-num=1
ORCID=
en-aut-name=OtsukaShinya
en-aut-sei=Otsuka
en-aut-mei=Shinya
kn-aut-name=大塚眞哉
kn-aut-sei=大塚
kn-aut-mei=眞哉
aut-affil-num=2
ORCID=
en-aut-name=KimuraYuuji
en-aut-sei=Kimura
en-aut-mei=Yuuji
kn-aut-name=木村裕司
kn-aut-sei=木村
kn-aut-mei=裕司
aut-affil-num=3
ORCID=
en-aut-name=NishieManabu
en-aut-sei=Nishie
en-aut-mei=Manabu
kn-aut-name=西江学
kn-aut-sei=西江
kn-aut-mei=学
aut-affil-num=4
ORCID=
en-aut-name=TokunagaNaoyuki
en-aut-sei=Tokunaga
en-aut-mei=Naoyuki
kn-aut-name=徳永尚之
kn-aut-sei=徳永
kn-aut-mei=尚之
aut-affil-num=5
ORCID=
en-aut-name=MiyasouHideaki
en-aut-sei=Miyasou
en-aut-mei=Hideaki
kn-aut-name=宮宗秀明
kn-aut-sei=宮宗
kn-aut-mei=秀明
aut-affil-num=6
ORCID=
en-aut-name=TsunemituYousuke
en-aut-sei=Tsunemitu
en-aut-mei=Yousuke
kn-aut-name=常光洋輔
kn-aut-sei=常光
kn-aut-mei=洋輔
aut-affil-num=7
ORCID=
en-aut-name=InagakiMasaru
en-aut-sei=Inagaki
en-aut-mei=Masaru
kn-aut-name=稲垣優
kn-aut-sei=稲垣
kn-aut-mei=優
aut-affil-num=8
ORCID=
en-aut-name=IwakawaKazuhide
en-aut-sei=Iwakawa
en-aut-mei=Kazuhide
kn-aut-name=岩川和秀
kn-aut-sei=岩川
kn-aut-mei=和秀
aut-affil-num=9
ORCID=
en-aut-name=IwagakiHiromi
en-aut-sei=Iwagaki
en-aut-mei=Hiromi
kn-aut-name=岩垣博巳
kn-aut-sei=岩垣
kn-aut-mei=博巳
aut-affil-num=10
ORCID=
affil-num=1
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=2
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=3
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=4
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=5
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=6
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=7
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=8
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=9
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=10
en-affil=
kn-affil=国立病院機構福山医療センター 外科
en-keyword=大腸癌 (colon cancer)
kn-keyword=大腸癌 (colon cancer)
en-keyword=壁外性発育 (extraluminal growth)
kn-keyword=壁外性発育 (extraluminal growth)
END
start-ver=1.4
cd-journal=joma
no-vol=11
cd-vols=
no-issue=
article-no=
start-page=77
end-page=80
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1953
dt-pub=195306
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=A CASE OF LUNG-CYST
kn-title=嚢胞肺の一例
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=The author reported a patient, aged 32, with many cysts in his left lung. Since he had suffered from fever in suckling age, he caught cold often. bnt was not confined to his bed. A physician diagnosed him as lung tuberculosis on a recent occasion of health examination but intracutaneous tuberculin-reaction and tuberculous bacilli in sputum proved negative. Many cysts of variable sizes with niveau were recognized by means of bronchograph. Wassermann's reaction in serum was positive. By penicillin-therapy his main complaint of thorakalgia and much expectoration was markedly diminished.
en-copyright=
kn-copyright=
en-aut-name=OnodaSusumu
en-aut-sei=Onoda
en-aut-mei=Susumu
kn-aut-name=小野田進
kn-aut-sei=小野田
kn-aut-mei=進
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学溫泉研究所内科
END
start-ver=1.4
cd-journal=joma
no-vol=11
cd-vols=
no-issue=
article-no=
start-page=66
end-page=71
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1953
dt-pub=195306
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=SEASONAL CHANGES IN THE AVERAGE ERYTHROCYTES SEDIMENTATION RATE IN MISASA, TOTTORI-PREFECTURE
kn-title=赤血球沈降速度の季節的動搖
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=Measuring erythrocytes sedimentation rate (E.S.R.) at a constant temperature (37°C) in Misasa, Tottori-Prefecture, the author recognized seasonal fluctuations in the average E.S.R. E.S.R. in Misasa has a tendency to increase in winter than in summer, contrary to the former observations in other districts of Japan. And concerning this contradiction the author calls attention to the effect of the climatological
characteristics in Tottori-Prefecture, e.g. relative high humidity in winter in this district, compared with the relative low humidity in the other (southern eastern part of Japan).
en-copyright=
kn-copyright=
en-aut-name=OnodaSusumu
en-aut-sei=Onoda
en-aut-mei=Susumu
kn-aut-name=小野田進
kn-aut-sei=小野田
kn-aut-mei=進
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学溫泉研究所内科
END
start-ver=1.4
cd-journal=joma
no-vol=10
cd-vols=
no-issue=
article-no=
start-page=17
end-page=27
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1953
dt-pub=195303
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=PROTECTIVE EFFECT OF THERMAL BATHS AGAINST TOTAL BODY-X-IRRADIATION
kn-title=レ線障碍に及ぼす温泉浴の効果
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=The author investigated the effect of a series of thermal baths of Misasa (at 37°C for ten minutes) during ten days on the survival rate and fat index of liver in X-irradiated mice. The radioactive thermal baths prior to or following a lethal dose of total body X-irradiation (800r) were not able to modify the survival or death rate in mice. The radioactive thermal baths prior to LD 50 dose of X-irradiation (450r) improved the survival rate and decreased the liver injury. But the thermal haths following the same dose of
X-irradiation showed no protective effect and seemed to increase the injury of X-irradiation rather. The combination of thermal baths for ten days and daily X-irradiation of 50r for the successive 25 days produced more unfavourable result than control without baths. On the contrary thermal baths prior to the daily X-irradiation of 50r showed a marked protection concerning the lethal effect and fat index of liver in mice. Three kinds of baths were used in this experiment, namely natural strongly radioactive thermal bath of Misasa (50-80m. m. curies Rn per liter). natural weakly radioactive thermal bath (5-10m. m. curie; Rn per liter) and plain water bath. But no significant difference
was proved between the effects of these three kinds of baths.
en-copyright=
kn-copyright=
en-aut-name=OnodaSusumu
en-aut-sei=Onoda
en-aut-mei=Susumu
kn-aut-name=小野田進
kn-aut-sei=小野田
kn-aut-mei=進
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学溫泉研究所内科
END
start-ver=1.4
cd-journal=joma
no-vol=19
cd-vols=
no-issue=
article-no=
start-page=33
end-page=33
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=1957
dt-pub=195709
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=花崗岩に関する諸問題 (7) 花崗岩中の斜長石の組成の一例(要旨)
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
en-copyright=
kn-copyright=
en-aut-name=
en-aut-sei=
en-aut-mei=
kn-aut-name=末野悌六
kn-aut-sei=末野
kn-aut-mei=悌六
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=小野田セメント株式会社
END
start-ver=1.4
cd-journal=joma
no-vol=144
cd-vols=
no-issue=
article-no=
start-page=13
end-page=25
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2010
dt-pub=20100625
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=Instructional Competence of Teachers in Lessons (III) : With Focus on Acquisition of Fundamentals and Basics and Communicative Instruction
kn-title=授業における教師の指導性について(Ⅲ)―「基礎・基本」の習得と「授業展開」―
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=今日,基礎的・基本的な内容についての学習が一方では機械的なトレーニングとして,また他方ではその内容を軽視した話し合い活動のための単なる素材として取り扱われる傾向がある。これは知識や技能の「習得」と「活用」のとらえ方と無関係ではない。前者は「活用」の基礎に練習・記憶による「習得」を位置づけ,後者は豊か思考活動に重きをおいて「習得」や達成についてはあまり配慮を加えない。こうしたあり方に対して,「習得」も「活用」もバランスよく指導することが重要であるともされるが,問題の本質は量的なバランス論にあるのではない。今日の授業の基本的課題として重要なことは,「基礎的・基本的な内容」に込められている意味を確認し,これまでの日本の授業実践の蓄積を読み直すことによって,「基礎的・基本的な内容」の豊かな習得を保障する「授業展開」の仕組みを明らかにすることである。
en-copyright=
kn-copyright=
en-aut-name=OnoHiroo
en-aut-sei=Ono
en-aut-mei=Hiroo
kn-aut-name=小野擴男
kn-aut-sei=小野
kn-aut-mei=擴男
aut-affil-num=1
ORCID=
affil-num=1
en-affil=
kn-affil=岡山大学大学院教育学研究科学校教育学系
en-keyword=基礎
kn-keyword=基礎
en-keyword=基本
kn-keyword=基本
en-keyword=授業展開
kn-keyword=授業展開
en-keyword=発問
kn-keyword=発問
en-keyword=学習形態
kn-keyword=学習形態
END
start-ver=1.4
cd-journal=joma
no-vol=122
cd-vols=
no-issue=2
article-no=
start-page=129
end-page=133
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2010
dt-pub=20100802
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=A case of superior mesenteric artery syndrome after left hemicolectomy for descending colon cancer
kn-title=保存的治療が可能であった左半結腸切除後上腸間膜動脈症候群の1例:本邦報告47例の検討
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=A 58-year-old man was diagnosed as having descending colon cancer and underwent a left colectomy with D3 node dissection and end-to-end anastomosis reconstruction. The accessory middle colic artery was secured as a feeding artery, and the middle colic artery was preserved. Diet was started on postoperative day 5 (POD5), and nausea and vomiting appeared on POD10. An upper gastrointestinal series revealed to-and-fro peristalsis in the third portion of the duodenum and dilatation of the proximal duodenum. Abdominal CT showed that the second portion of the duodenum was markedly dilated and the third portion was compressed by the superior mesenteric artery (SMA). As a result, he was diagnosed with post-operative superior mesenteric artery syndrome (SMAS) and treated with conservative therapy. The symptoms improved with a nasogastric tube, and he started to eat after POD26, followed by a successful outcome.
en-copyright=
kn-copyright=
en-aut-name=HamanoRyousuke
en-aut-sei=Hamano
en-aut-mei=Ryousuke
kn-aut-name=濱野亮輔
kn-aut-sei=濱野
kn-aut-mei=亮輔
aut-affil-num=1
ORCID=
en-aut-name=OtsukaShinya
en-aut-sei=Otsuka
en-aut-mei=Shinya
kn-aut-name=大塚眞哉
kn-aut-sei=大塚
kn-aut-mei=眞哉
aut-affil-num=2
ORCID=
en-aut-name=NishieManabu
en-aut-sei=Nishie
en-aut-mei=Manabu
kn-aut-name=西江学
kn-aut-sei=西江
kn-aut-mei=学
aut-affil-num=3
ORCID=
en-aut-name=NomuraTsunehisa
en-aut-sei=Nomura
en-aut-mei=Tsunehisa
kn-aut-name=野村長久
kn-aut-sei=野村
kn-aut-mei=長久
aut-affil-num=4
ORCID=
en-aut-name=TokunagaNaoyuki
en-aut-sei=Tokunaga
en-aut-mei=Naoyuki
kn-aut-name=徳永尚之
kn-aut-sei=徳永
kn-aut-mei=尚之
aut-affil-num=5
ORCID=
en-aut-name=MiyasouHideaki
en-aut-sei=Miyasou
en-aut-mei=Hideaki
kn-aut-name=宮宗秀明
kn-aut-sei=宮宗
kn-aut-mei=秀明
aut-affil-num=6
ORCID=
en-aut-name=TakahashiKenji
en-aut-sei=Takahashi
en-aut-mei=Kenji
kn-aut-name=高橋健司
kn-aut-sei=高橋
kn-aut-mei=健司
aut-affil-num=7
ORCID=
en-aut-name=TsunemitsuYousuke
en-aut-sei=Tsunemitsu
en-aut-mei=Yousuke
kn-aut-name=常光洋輔
kn-aut-sei=常光
kn-aut-mei=洋輔
aut-affil-num=8
ORCID=
en-aut-name=MiyoshiKazuya
en-aut-sei=Miyoshi
en-aut-mei=Kazuya
kn-aut-name=三好和也
kn-aut-sei=三好
kn-aut-mei=和也
aut-affil-num=9
ORCID=
en-aut-name=InagakiMasaru
en-aut-sei=Inagaki
en-aut-mei=Masaru
kn-aut-name=稲垣優
kn-aut-sei=稲垣
kn-aut-mei=優
aut-affil-num=10
ORCID=
en-aut-name=IwakawaKazuhide
en-aut-sei=Iwakawa
en-aut-mei=Kazuhide
kn-aut-name=岩川和秀
kn-aut-sei=岩川
kn-aut-mei=和秀
aut-affil-num=11
ORCID=
en-aut-name=TakahashiMasahiko
en-aut-sei=Takahashi
en-aut-mei=Masahiko
kn-aut-name=高橋正彦
kn-aut-sei=高橋
kn-aut-mei=正彦
aut-affil-num=12
ORCID=
en-aut-name=IwagakiHiromi
en-aut-sei=Iwagaki
en-aut-mei=Hiromi
kn-aut-name=岩垣博巳
kn-aut-sei=岩垣
kn-aut-mei=博巳
aut-affil-num=13
ORCID=
affil-num=1
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=2
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=3
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=4
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=5
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=6
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=7
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=8
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=9
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=10
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=11
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=12
en-affil=
kn-affil=国立病院機構福山医療センター 外科
affil-num=13
en-affil=
kn-affil=国立病院機構福山医療センター 外科
en-keyword=上腸間膜動脈症候群 (superior mesenteric artery syndrome)
kn-keyword=上腸間膜動脈症候群 (superior mesenteric artery syndrome)
en-keyword=大腸癌 (colon cancer)
kn-keyword=大腸癌 (colon cancer)
END
start-ver=1.4
cd-journal=joma
no-vol=63
cd-vols=
no-issue=1
article-no=
start-page=1
end-page=7
dt-received=
dt-revised=
dt-accepted=
dt-pub-year=2009
dt-pub=200902
dt-online=
en-article=
kn-article=
en-subject=
kn-subject=
en-title=
kn-title=Protein Transduction Method for Cerebrovascular Disorders
en-subtitle=
kn-subtitle=
en-abstract=
kn-abstract=
Many studies have shown that a motif of 11 consecutive arginines (11R) is one of the most effective protein transduction domains (PTD) for introducing proteins into the cell membrane. By conjugating this "11R", all sorts of proteins can effectively and harmlessly be transferred into any kind of cell. We therefore examined the transduction efficiency of 11R in cerebral arteries and obtained results showing that 11R fused enhanced green fluorescent protein (11R-EGFP) immediately and effectively penetrated all layers of the rat basilar artery (BA), especially the tunica media. This method provides a revolutionary approach to cerebral arteries and ours is the first study to demonstrate the successful transductionof a PTD fused protein into the cerebral arteries. In this review, we present an outline of our studies and other key studies related to cerebral vasospasm and 11R, problems to be overcome, and predictions regarding future use of the 11R protein transduction method for cerebral vasospasm (CV).
en-copyright= kn-copyright= en-aut-name=OgawaTomoyuki en-aut-sei=Ogawa en-aut-mei=Tomoyuki kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=1 ORCID= en-aut-name=OnoShigeki en-aut-sei=Ono en-aut-mei=Shigeki kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=2 ORCID= en-aut-name=IchikawaTomotsugu en-aut-sei=Ichikawa en-aut-mei=Tomotsugu kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=3 ORCID= en-aut-name=ArimitsuSeiji en-aut-sei=Arimitsu en-aut-mei=Seiji kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=4 ORCID= en-aut-name=OnodaKeisuke en-aut-sei=Onoda en-aut-mei=Keisuke kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=5 ORCID= en-aut-name=TokunagaKoji en-aut-sei=Tokunaga en-aut-mei=Koji kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=6 ORCID= en-aut-name=SugiuKenji en-aut-sei=Sugiu en-aut-mei=Kenji kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=7 ORCID= en-aut-name=TomizawaKazuhito en-aut-sei=Tomizawa en-aut-mei=Kazuhito kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=8 ORCID= en-aut-name=MatsuiHideki en-aut-sei=Matsui en-aut-mei=Hideki kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=9 ORCID= en-aut-name=DateIsao en-aut-sei=Date en-aut-mei=Isao kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=10 ORCID= affil-num=1 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=2 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=3 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=4 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=5 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=6 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=7 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=8 en-affil= kn-affil=Department of Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=9 en-affil= kn-affil=Department of Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences affil-num=10 en-affil= kn-affil=Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences en-keyword=cerebral vasospasm kn-keyword=cerebral vasospasm en-keyword=11 consecutive arginines (11R) kn-keyword=11 consecutive arginines (11R) en-keyword=enhanced green fluorescent protein (EGFP) kn-keyword=enhanced green fluorescent protein (EGFP) END start-ver=1.4 cd-journal=joma no-vol=48 cd-vols= no-issue=5 article-no= start-page=279 end-page=282 dt-received= dt-revised= dt-accepted= dt-pub-year=1994 dt-pub=199410 dt-online= en-article= kn-article= en-subject= kn-subject= en-title= kn-title=Allergens of the house dust mite, Dermatophagoides pteronyssinus, in patients with mite allergic rhinitis: a clinical investigation by intracutaneous skin tests and nasal provocation tests. en-subtitle= kn-subtitle= en-abstract= kn-abstract=To determine the allergens of mite allergic rhinitis, we studied 31 patients with mite allergic rhinitis by skin tests and nasal provocation tests (15 for skin and 16 for nasal tests) using 6 fractions of Dermatophagoides pteronyssinus (Dp) extract differing in molecular weights (15, 25, 32, 53, 95 and 190 kDMW). In skin testing, patients showed intense positive reactions to the fractions of 15, 25, 32, 95 and 190 kDMW, among which the most patients showed positive reactions to the fractions of 15 and 25 kDMW. Significant differences were found in patients' positive reactivity among each fraction and between low (15 and 25 kD) and high (95 and 190 kD) molecular weight fractions as well. In nasal provocation tests, patients showed intense positive reactions to the fractions of 15, 32, 53 and 95 kDMW, especially to the fractions of 15 and 95 kDMW. Furthermore, the insidence of positive reactions to the 15 kDMW fraction was significantly higher than that to any other fraction in the skin tests (P < 0.05). From these results, the low molecular weight fraction, 15 kDMW, is considered to be the main allergen of this mite and the high molecular weight fractions, 95 and 190 kDMW, may also be considered to be allergens of this mite.
en-copyright= kn-copyright= en-aut-name=NishiokaKeiko en-aut-sei=Nishioka en-aut-mei=Keiko kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=1 ORCID= en-aut-name=SaitoChisato en-aut-sei=Saito en-aut-mei=Chisato kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=2 ORCID= en-aut-name=NaganoToshiaki en-aut-sei=Nagano en-aut-mei=Toshiaki kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=3 ORCID= en-aut-name=OkanoMitsuhiro en-aut-sei=Okano en-aut-mei=Mitsuhiro kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=4 ORCID= en-aut-name=NakagawaFumio en-aut-sei=Nakagawa en-aut-mei=Fumio kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=5 ORCID= en-aut-name=NishiokaSatoko en-aut-sei=Nishioka en-aut-mei=Satoko kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=6 ORCID= en-aut-name=MasudaYu en-aut-sei=Masuda en-aut-mei=Yu kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=7 ORCID= en-aut-name=OnoToshiro en-aut-sei=Ono en-aut-mei=Toshiro kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=8 ORCID= affil-num=1 en-affil= kn-affil=Hiroshima City Hospital affil-num=2 en-affil= kn-affil=Okayama City Hospital affil-num=3 en-affil= kn-affil=Okayama Univeristy affil-num=4 en-affil= kn-affil=Okayama Uniiversity affil-num=5 en-affil= kn-affil=Okayama University affil-num=6 en-affil= kn-affil=Okayama University affil-num=7 en-affil= kn-affil=Okayama University affil-num=8 en-affil= kn-affil=Okayama University en-keyword=mite allergen kn-keyword=mite allergen en-keyword=skin test kn-keyword=skin test en-keyword=nasal provoration test kn-keyword=nasal provoration test en-keyword=allergen rhinitis kn-keyword=allergen rhinitis END start-ver=1.4 cd-journal=joma no-vol=48 cd-vols= no-issue=5 article-no= start-page=279 end-page=282 dt-received= dt-revised= dt-accepted= dt-pub-year=1994 dt-pub=199410 dt-online= en-article= kn-article= en-subject= kn-subject= en-title= kn-title=Allergens of the house dust mite, Dermatophagoides pteronyssinus, in patients with mite allergic rhinitis: a clinical investigation by intracutaneous skin tests and nasal provocation tests. en-subtitle= kn-subtitle= en-abstract= kn-abstract=To determine the allergens of mite allergic rhinitis, we studied 31 patients with mite allergic rhinitis by skin tests and nasal provocation tests (15 for skin and 16 for nasal tests) using 6 fractions of Dermatophagoides pteronyssinus (Dp) extract differing in molecular weights (15, 25, 32, 53, 95 and 190 kDMW). In skin testing, patients showed intense positive reactions to the fractions of 15, 25, 32, 95 and 190 kDMW, among which the most patients showed positive reactions to the fractions of 15 and 25 kDMW. Significant differences were found in patients' positive reactivity among each fraction and between low (15 and 25 kD) and high (95 and 190 kD) molecular weight fractions as well. In nasal provocation tests, patients showed intense positive reactions to the fractions of 15, 32, 53 and 95 kDMW, especially to the fractions of 15 and 95 kDMW. Furthermore, the insidence of positive reactions to the 15 kDMW fraction was significantly higher than that to any other fraction in the skin tests (P < 0.05). From these results, the low molecular weight fraction, 15 kDMW, is considered to be the main allergen of this mite and the high molecular weight fractions, 95 and 190 kDMW, may also be considered to be allergens of this mite.
en-copyright= kn-copyright= en-aut-name=NishiokaKeiko en-aut-sei=Nishioka en-aut-mei=Keiko kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=1 ORCID= en-aut-name=SaitoChisato en-aut-sei=Saito en-aut-mei=Chisato kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=2 ORCID= en-aut-name=NaganoToshiaki en-aut-sei=Nagano en-aut-mei=Toshiaki kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=3 ORCID= en-aut-name=OkanoMitsuhiro en-aut-sei=Okano en-aut-mei=Mitsuhiro kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=4 ORCID= en-aut-name=NakagawaFumio en-aut-sei=Nakagawa en-aut-mei=Fumio kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=5 ORCID= en-aut-name=NishiokaSatoko en-aut-sei=Nishioka en-aut-mei=Satoko kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=6 ORCID= en-aut-name=MasudaYu en-aut-sei=Masuda en-aut-mei=Yu kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=7 ORCID= en-aut-name=OnoToshiro en-aut-sei=Ono en-aut-mei=Toshiro kn-aut-name= kn-aut-sei= kn-aut-mei= aut-affil-num=8 ORCID= affil-num=1 en-affil= kn-affil=Hiroshima City Hospital affil-num=2 en-affil= kn-affil=Okayama City Hospital affil-num=3 en-affil= kn-affil=Okayama Univeristy affil-num=4 en-affil= kn-affil=Okayama University affil-num=5 en-affil= kn-affil=Okayama University affil-num=6 en-affil= kn-affil=Okayama University affil-num=7 en-affil= kn-affil=Okayama University affil-num=8 en-affil= kn-affil=Okayama University en-keyword=mite allergen kn-keyword=mite allergen en-keyword=skin test kn-keyword=skin test en-keyword=nasal provoration test kn-keyword=nasal provoration test en-keyword=allergen rhinitis kn-keyword=allergen rhinitis END start-ver=1.4 cd-journal=joma no-vol=5 cd-vols= no-issue= article-no= start-page= end-page= dt-received= dt-revised= dt-accepted= dt-pub-year=2005 dt-pub=20050120 dt-online= en-article= kn-article= en-subject= kn-subject= en-title= kn-title=Functional promoter upstream p53 regulatory sequence of IGFBP3 that is silenced by tumor specific methylation en-subtitle= kn-subtitle= en-abstract= kn-abstract=Background: Insulin-like growth factor binding protein (IGFBP)-3 functions as a carrier of insulinlike
growth factors (IGFs) in circulation and a mediator of the growth suppression signal in cells. There are two reported p53 regulatory regions in the IGFBP3 gene; one upstream of the promoter and one intronic. We previously reported a hot spot of promoter hypermethylation of IGFBP-3 in
human hepatocellular carcinomas and derivative cell lines. As the hot spot locates at the putative upstream p53 consensus sequences, these p53 consensus sequences are really functional is a question to be answered.
Methods: In this study, we examined the p53 consensus sequences upstream of the IGFBP-3 promoter for the p53 induced expression of IGFBP-3. Deletion, mutagenesis, and methylation
constructs of IGFBP-3 promoter were assessed in the human hepatoblastoma cell line HepG2 for promoter activity.
Results: Deletions and mutations of these sequences completely abolished the expression of IGFBP-3 in the presence of p53 overexpression. In vitro methylation of these p53 consensus
sequences also suppressed IGFBP-3 expression. In contrast, the expression of IGFBP-3 was not affected in the absence of p53 overexpression. Further, we observed by electrophoresis mobility
shift assay that p53 binding to the promoter region was diminished when methylated.
Conclusion: From these observations, we conclude that four out of eleven p53 consensus sequences upstream of the IGFBP-3 promoter are essential for the p53 induced expression of
IGFBP-3, and hypermethylation of these sequences selectively suppresses p53 induced IGFBP-3 expression in HepG2 cells.