Itohara S - Search Results

1

Limb-clasping, cognitive deficit and increased vulnerability to kainic acid-induced seizures in neuronal glycosylphosphatidylinositol deficiency mouse models.

Kandasamy LC, Tsukamoto M, Banov V, Tsetsegee S, Nagasawa Y, Kato M, Matsumoto N, Takeda J, Itohara S, Ogawa S, Young LJ, Zhang Q. Kandasamy LC, et al. Among authors: itohara s. Hum Mol Genet. 2021 May 28;30(9):758-770. doi: 10.1093/hmg/ddab052. Hum Mol Genet. 2021. PMID: 33607654 Free PMC article.

2

Netrin-G1 regulates fear-like and anxiety-like behaviors in dissociable neural circuits.

Zhang Q, Sano C, Masuda A, Ando R, Tanaka M, Itohara S. Zhang Q, et al. Among authors: itohara s. Sci Rep. 2016 Jun 27;6:28750. doi: 10.1038/srep28750. Sci Rep. 2016. PMID: 27345935 Free PMC article.

3

An Automated T-maze Based Apparatus and Protocol for Analyzing Delay- and Effort-based Decision Making in Free Moving Rodents.

Zhang Q, Kobayashi Y, Goto H, Itohara S. Zhang Q, et al. Among authors: itohara s. J Vis Exp. 2018 Aug 2;(138):57895. doi: 10.3791/57895. J Vis Exp. 2018. PMID: 30124665 Free PMC article.

4

Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.

Suzuki T, Miyamoto H, Nakahari T, Inoue I, Suemoto T, Jiang B, Hirota Y, Itohara S, Saido TC, Tsumoto T, Sawamoto K, Hensch TK, Delgado-Escueta AV, Yamakawa K. Suzuki T, et al. Among authors: itohara s. Hum Mol Genet. 2009 Mar 15;18(6):1099-109. doi: 10.1093/hmg/ddp006. Epub 2009 Jan 15. Hum Mol Genet. 2009. PMID: 19147686 Free PMC article.

5

Diversification of behavior and postsynaptic properties by netrin-G presynaptic adhesion family proteins.

Zhang Q, Goto H, Akiyoshi-Nishimura S, Prosselkov P, Sano C, Matsukawa H, Yaguchi K, Nakashiba T, Itohara S. Zhang Q, et al. Among authors: itohara s. Mol Brain. 2016 Jan 8;9:6. doi: 10.1186/s13041-016-0187-5. Mol Brain. 2016. PMID: 26746425 Free PMC article.

6

Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency.

Miyamoto H, Shimohata A, Abe M, Abe T, Mazaki E, Amano K, Suzuki T, Tatsukawa T, Itohara S, Sakimura K, Yamakawa K. Miyamoto H, et al. Among authors: itohara s. Hum Mol Genet. 2017 Dec 15;26(24):4961-4974. doi: 10.1093/hmg/ddx379. Hum Mol Genet. 2017. PMID: 29040524

7

The hippocampus encodes delay and value information during delay-discounting decision making.

Masuda A, Sano C, Zhang Q, Goto H, McHugh TJ, Fujisawa S, Itohara S. Masuda A, et al. Among authors: itohara s. Elife. 2020 Feb 20;9:e52466. doi: 10.7554/eLife.52466. Elife. 2020. PMID: 32077851 Free PMC article.

8

Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice.

Ganesh S, Delgado-Escueta AV, Sakamoto T, Avila MR, Machado-Salas J, Hoshii Y, Akagi T, Gomi H, Suzuki T, Amano K, Agarwala KL, Hasegawa Y, Bai DS, Ishihara T, Hashikawa T, Itohara S, Cornford EM, Niki H, Yamakawa K. Ganesh S, et al. Among authors: itohara s. Hum Mol Genet. 2002 May 15;11(11):1251-62. doi: 10.1093/hmg/11.11.1251. Hum Mol Genet. 2002. PMID: 12019206

9

Functional and behavioral effects of de novo mutations in calcium-related genes in patients with bipolar disorder.

Nakamura T, Nakajima K, Kobayashi Y, Itohara S, Kasahara T, Tsuboi T, Kato T. Nakamura T, et al. Among authors: itohara s. Hum Mol Genet. 2021 Sep 15;30(19):1851-1862. doi: 10.1093/hmg/ddab152. Hum Mol Genet. 2021. PMID: 34100076 Free PMC article.

10

Calcium-permeable AMPA receptors promote misfolding of mutant SOD1 protein and development of amyotrophic lateral sclerosis in a transgenic mouse model.

Tateno M, Sadakata H, Tanaka M, Itohara S, Shin RM, Miura M, Masuda M, Aosaki T, Urushitani M, Misawa H, Takahashi R. Tateno M, et al. Among authors: itohara s. Hum Mol Genet. 2004 Oct 1;13(19):2183-96. doi: 10.1093/hmg/ddh246. Epub 2004 Aug 4. Hum Mol Genet. 2004. PMID: 15294873

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