Research theme for competitive and other funds (12):
2022 - 2025 Multilayered Omics for Oxidative Stress Induced Neuronal Cell Death and Epileptogenesis
2020 - 2022 抗腫瘍剤の開発
2016 - 2020 Study of the pathogenesis of west syndrome using a new model rat
2014 - 2017 Development of a animal model of acute encephalopathy and an antibody therapy
2011 - 2012 New approaches of treating developmental disorders in channelopathy
2010 - 2012 Molecular basis of febrile seizure and new treatment
2009 - 2011 Genetic modifiers of an intractable epilepsy with channel gene mutations
2006 - 2008 Molecular mechanism of loss-of-function SCN1A mutations associated with epilepsy
2006 - 2007 脳内ホルモンによる情動行動の調節とその分子機構
2005 - 2006 Oxytocin regulates stress response and anxiety through functional modulation of amygdala
2004 - 2006 Early diagnosis and genetic analysis of severe myoclonic epilepsy in infancy
2003 - 2004 Functional Analysis of the mutated ion-channel gene in severe myoclonic epilepsy in infancy
Show all
Papers (110):
Iori Ohmori, Mamoru Ouchida, Yoshiko Hada, Haruhito A. Uchida, Shinya Toyokuni, Tomoji Mashimo. Txn1mutation is a monogenic cause of chronic kidney disease associated with mitochondrial dysfunction in rats. BioRxiv. 2023
Arata SASAKI, Iori OHMORI, Shawna, M. CARROLL. The Effect of a Film Viewing Intervention Added to Lectures to Improve University Students' Attitudes toward Sexual and Gender Minorities. Kawasaki Journal of Medical Welfare. 2023. 28. 2. 71-85
Iori Ohmori, Mamoru Ouchida, Hirohiko Imai, Saeko Ishida, Shinya Toyokuni, Tomoji Mashimo. Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain. Neurobiology of disease. 2022. 175. 105921-105921
SOCIETY FOR FREE RADICAL RESEARCH JAPAN
, THE JAPAN SOCIETY OF HUMAN GENETICS
, THE PHYSIOLOGICAL SOCIETY OF JAPAN
, THE JAPAN NEUROSCIENCE SOCIETY
, The Japanese Society Of Child Neurology
, JAPAN PEDIATRIC SOCIETY
, JAPAN EPILEPSY SOCIETY