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Epilepsy protein myoclonin1 interacts with inositol 1,4,5-trisphosphate receptor and reduces calcium ions stored in endoplasmic reticulum

Aim: Mutations in the EFHC1 gene have been identified in patients with various epilepsies, including juvenile myoclonic epilepsy (JME). Mice with Efhc1 deficiency also exhibit epileptic phenotypes. The protein myoclonin1, encoded by EFHC1, is not expressed in neurons but in cells with motile cilia,...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Principais autores: Toshimitsu Suzuki, Kripamoy Aguan, Hideaki Mizuno, Ikuyo Inoue, Katsuhiko Mikoshiba, Atsushi Miyawaki, Kazuhiro Yamakawa
פורמט: Artigo
שפה:Inglês
יצא לאור: Open Exploration Publishing Inc. 2025-07-01
סדרה:Exploration of Neuroscience
נושאים:
גישה מקוונת:https://www.explorationpub.com/uploads/Article/A100699/100699.pdf
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