FullText URL | EpilepsyRes105_1_220.pdf |
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Author | Ohmori, Iori| Hayashi, Keiichiro| Wang, Haijiao| Ouchida, Mamoru| Fujita, Naohiro| Inoue, Takushi| Michiue, Hiroyuki| Nishiki, Teiichi| Matsui, Hideki| |
Published Date | 2013-07 |
Publication Title | Epilepsy Research |
Volume | volume105 |
Issue | issue1-2 |
Publisher | Elsevier Science |
Start Page | 220 |
End Page | 224 |
ISSN | 09201211 |
NCID | AA10726642 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
File Version | author |
PubMed ID | 23375560 |
DOI | 10.1016/j.eplepsyres.2013.01.003 |
Web of Science KeyUT | 000320737500027 |
Related Url | isVersionOf https://doi.org/10.1016/j.eplepsyres.2013.01.003 |
FullText URL | NeurobiolDis_50_209.pdf |
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Author | Ohmori, Iori| Ouchida, Mamoru| Kobayashi, Katsuhiro| Jitsumori, Yoshimi| Mori, Akiko| Michiue, Hiroyuki| Nishiki, Teiichi| Ohtsuka, Yoko| Matsui, Hideki| |
Note | CACNA1A variants contribute to severity of seizures in Dravet syndrome| |
Published Date | 2013-02 |
Publication Title | Neurobiology of disease |
Volume | volume50 |
Publisher | Academic Press |
Start Page | 209 |
End Page | 217 |
ISSN | 09699961 |
NCID | AA11645502 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
File Version | author |
PubMed ID | 23103419 |
DOI | 10.1016/j.nbd.2012.10.016 |
Web of Science KeyUT | 000313758100023 |
Related Url | isVersionOf https://doi.org/10.1016/j.nbd.2012.10.016 |
Author | Hayashi, Keiichiro| Ueshima, Satoshi| Ouchida, Mamoru| Mashimo, Tomoji| Nishiki, Teiichi| Sendo, Toshiaki| Serikawa, Tadao| Matsui, Hideki| Ohmori, Iori| |
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Published Date | 2011-05 |
Publication Title | Epilepsia |
Volume | volume52 |
Issue | issue5 |
Content Type | Journal Article |
Author | Masumoto, Toshio| Suzuki, Koichiro| Ohmori, Iori| Michiue, Hiroyuki| Tomizawa, Kazuhito| Fujimura, Atsushi| Nishiki, Tei-ichi| Matsui, Hideki| |
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Published Date | 2012-01 |
Publication Title | Molecular and Cellular Neuroscience |
Volume | volume49 |
Issue | issue1 |
Content Type | Journal Article |
Author | Fujimura, Atsushi| Michiue, Hiroyuki| Nishiki, Tei-ichi| Ohmori, Iori| Wei, Fanyan| Matsui, Hideki| Tomizawa, Kazuhito| |
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Published Date | 2011-05-14 |
Publication Title | PLoS ONE |
Volume | volume6 |
Issue | issue3 |
Content Type | Journal Article |
Author | Candan, Gerile| Michiue, Hiroyuki| Ishikawa, Sanae| Fujimura, Atsushi| Hayashi, Keiichiro| Uneda, Atsuhito| Mori, Akiko| Ohmori, Iori| Nishiki, Tei-ichi| Matsui, Hideki| Tomizawa, Kazuhito| |
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Published Date | 2012-09 |
Publication Title | Biomaterials |
Volume | volume33 |
Issue | issue27 |
Content Type | Journal Article |
JaLCDOI | 10.18926/AMO/43824 |
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FullText URL | 65_1_1.pdf |
Author | Han, Xiao-Jian| Tomizawa, Kazuhito| Fujimura, Atsushi| Ohmori, Iori| Nishiki, Tei-ichi| Matsushita, Masayuki| Matsui, Hideki| |
Abstract | Mitochondria are important cellular organelles in most metabolic processes and have a highly dynamic nature, undergoing frequent fission and fusion. The dynamic balance between fission and fusion plays critical roles in mitochondrial functions. In recent studies, several large GTPases have been identified as key molecular factors in mitochondrial fission and fusion. Moreover, the posttranslational modifications of these large GTPases, including phosphorylation, ubiquitination and SUMOylation, have been shown to be involved in the regulation of mitochondrial dynamics. Neurons are particularly sensitive and vulnerable to any abnormalities in mitochondrial dynamics, due to their large energy demand and long extended processes. Emerging evidences have thus indicated a strong linkage between mitochondria and neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease and Huntington's disease. In this review, we will describe the regulation of mitochondrial dynamics and its role in neurodegenerative diseases. |
Keywords | mitochondria phosphorylation ubiquitination SUMOylation neurodegeneration |
Amo Type | Review |
Publication Title | Acta Medica Okayama |
Published Date | 2011-02 |
Volume | volume65 |
Issue | issue1 |
Publisher | Okayama University Medical School |
Start Page | 1 |
End Page | 10 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | CopyrightⒸ 2011 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 21339790 |
Web of Science KeyUT | 000287620500001 |
Title Alternative | A CACNB4 mutation showing altered Ca(v)2.1 function in a patient with Dravet syndrome |
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FullText URL | 121_149.pdf |
Author | Ohmori, Iori| Ouchida, Mamoru| Mimaki, Nobuyoshi| Nishiki, Teiichi| Tomizawa, Kazuhito| Matsui, Hideki| |
Keywords | てんかん Dravet 症候群 CACNB4遺伝子 SCN1A 遺伝子 |
Publication Title | 岡山医学会雑誌 |
Published Date | 2009-12-01 |
Volume | volume121 |
Issue | issue3 |
Start Page | 149 |
End Page | 156 |
ISSN | 0030-1558 |
language | Japanese |
Copyright Holders | 岡山医学会 |
File Version | publisher |
DOI | 10.4044/joma.121.149 |
NAID | 120002308814 |