2009 Fiscal Year Final Research Report
Understanding the pathology of juvenile myoclonic epilepsy (JME) using Ehhc1-deficient mouse
Project/Area Number |
20790866
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Psychiatric science
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Research Institution | The Institute of Physical and Chemical Research |
Principal Investigator |
SUZUKI Toshimitsu The Institute of Physical and Chemical Research, 神経遺伝研究チーム, 研究員 (20373318)
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Project Period (FY) |
2008 – 2009
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Keywords | てんかん / EFHC1 / 痙攣 / 若年性ミオクローヌスてんかん / 特発性てんかん / マウスモデル |
Research Abstract |
We observed frequent spontaneous myoclonus and increased seizure susceptibility in mice with Efhc1 deficiency. These results suggest that reduction or loss of function of myoclonin1 may be the molecular basis for epilepsies caused by EFHC1 mutations.
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[Journal Article] Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility2009
Author(s)
Toshimitsu Suzuki, Hiroyuki Miyamoto, Takashi Nakahari, Ikuyo Inoue, Takahiro Suemoto, Bin Jiang, Yuki Hirota, Shigeyoshi Itohara, Takaomi C. Saido, Tadaharu Tsumoto, Kazunobu Sawamoto, Takao K. Hensch, Antonio V. Delgado-Escueta, Kazuhiro Yamakawa
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Journal Title
Human Molecular Genetics 18
Pages: 1099-1109
Peer Reviewed
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