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Page 1
Increased lipid peroxidation in Down's syndrome mouse models.
Ishihara K, Amano K, Takaki E, Ebrahim AS, Shimohata A, Shibazaki N, Inoue I, Takaki M, Ueda Y, Sago H, Epstein CJ, Yamakawa K. Ishihara K, et al. Among authors: inoue i. J Neurochem. 2009 Sep;110(6):1965-76. doi: 10.1111/j.1471-4159.2009.06294.x. Epub 2009 Jul 23. J Neurochem. 2009. PMID: 19645748 Free article.
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: inoue i. 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.
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, Takeuchi T, Itohara S, Yanagawa Y, Obata K, Furuichi T, Hensch TK, Yamakawa K. Ogiwara I, et al. Among authors: inoue i. J Neurosci. 2007 May 30;27(22):5903-14. doi: 10.1523/JNEUROSCI.5270-06.2007. J Neurosci. 2007. PMID: 17537961 Free PMC article.
TDP-43 accelerates age-dependent degeneration of interneurons.
Tsuiji H, Inoue I, Takeuchi M, Furuya A, Yamakage Y, Watanabe S, Koike M, Hattori M, Yamanaka K. Tsuiji H, et al. Among authors: inoue i. Sci Rep. 2017 Nov 2;7(1):14972. doi: 10.1038/s41598-017-14966-w. Sci Rep. 2017. PMID: 29097807 Free PMC article.
SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy.
Morimoto M, Mazaki E, Nishimura A, Chiyonobu T, Sawai Y, Murakami A, Nakamura K, Inoue I, Ogiwara I, Sugimoto T, Yamakawa K. Morimoto M, et al. Among authors: inoue i. Epilepsia. 2006 Oct;47(10):1732-6. doi: 10.1111/j.1528-1167.2006.00645.x. Epilepsia. 2006. PMID: 17054696 Free article.
864 results