Etsuro Ohta

J-GLOBAL         Last updated: Dec 16, 2018 at 23:53
Etsuro Ohta
Kitasato University
School of Allied Health Sciences

Research Interests


Research Areas


Published Papers

Vulnerability to stress in mouse offspring is ameliorated when pregnant dams are provided a chewing stick during prenatal stress
Kubo KY, Suzuki A, Iinuma M, Sato Y, Nagashio R, Ohta E, Azuma K
Arch Oral Biol   97 150-155   2018   [Refereed]
Establishment of DYT5 patient-specific induced pluripotent stem cells with a GCH1 mutation
Murakami N, Ishikawa T, Kondo T, Keiko Imamura, Tsukita K, Enami T, Funayama M, Shibukawa R, Matsumoto S, Izumi Y, Ohta E, Obata F, Kaji R, Inoue H
Stem Cell Res   24 36-39   2017   [Refereed]
Leucine-rich repeat kinase 2 is a regulator of B cell function, affecting homeostasis, BCR signaling, IgA production, and TI antigen responses
Kubo M, Nagashima R, Ohta E, Maekawa T, Isobe Y, Kurihara M, Eshima K, Iwabuchi K, Sasaoka T, Azuma S, Melrose HL, Farrer MJ, Obata F
J Neuroimmunol   292 1-8   2016   [Refereed]
Ohta E, Nihira T, Uchino A, Imaizumi Y, Okada Y, Akamatsu W, Takahashi K, Hayakawa H, Nagai M, Ohyama M, Ryo M, Ogino M, Murayama S, Takashima A, Nishiyama K, Mizuno Y, Mochizuki H, Obata F, Okano H.
Hum Mol Genet.   24(17) 4879-4900   2015   [Refereed]
Miyajima T, Ohta E, Kawada H, Maekawa T, Obata F
Neurosci Lett   588 142-146   2015   [Refereed]

Research Grants & Projects

Ministry of Education, Culture, Sports, Science and Technology: Grant-in-Aid for Scientific Research (C)
Project Year: Apr 2015       Investigator(s): Etsuro Ohta
Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT): Grant-in-Aid for Scientific Research on Innovative Areas
Project Year: Apr 2015       Investigator(s): Etsuro Ohta
Pathological phenotype of I2020T mutant LRRK2 iPSC-derived neurons in the Sagamihara family
Project Year: 2014       Investigator(s): Etsuro Ohta
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(若手研究(B))
Project Year: 2009 - 2010    Investigator(s): Etsuro OHTA
Mutant LRRK2 is the causal molecule for autosomal dominant familial Parkinson's disease. In the present study, we demonstrated that the protective effect of I2020T LRRK2 against hydrogen peroxide-induced apoptosis was impaired in comparison with t...