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2002 1
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2009 1
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Page 1
Cnpy32xHA mice reveal neuronal expression of Cnpy3 in the brain.
Islam MM, Mutoh H, Aoto K, Belal H, Saitsu H. Islam MM, et al. Among authors: aoto k. J Neurosci Methods. 2023 Jan 1;383:109730. doi: 10.1016/j.jneumeth.2022.109730. Epub 2022 Oct 21. J Neurosci Methods. 2023. PMID: 36280087
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathy.
Nakashima M, Kato M, Aoto K, Shiina M, Belal H, Mukaida S, Kumada S, Sato A, Zerem A, Lerman-Sagie T, Lev D, Leong HY, Tsurusaki Y, Mizuguchi T, Miyatake S, Miyake N, Ogata K, Saitsu H, Matsumoto N. Nakashima M, et al. Among authors: aoto k. Ann Neurol. 2018 Apr;83(4):794-806. doi: 10.1002/ana.25208. Ann Neurol. 2018. PMID: 29534297
De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders.
Akita T, Aoto K, Kato M, Shiina M, Mutoh H, Nakashima M, Kuki I, Okazaki S, Magara S, Shiihara T, Yokochi K, Aiba K, Tohyama J, Ohba C, Miyatake S, Miyake N, Ogata K, Fukuda A, Matsumoto N, Saitsu H. Akita T, et al. Among authors: aoto k. Ann Clin Transl Neurol. 2018 Jan 29;5(3):280-296. doi: 10.1002/acn3.528. eCollection 2018 Mar. Ann Clin Transl Neurol. 2018. PMID: 29560374 Free PMC article.
De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy.
Belal H, Nakashima M, Matsumoto H, Yokochi K, Taniguchi-Ikeda M, Aoto K, Amin MB, Maruyama A, Nagase H, Mizuguchi T, Miyatake S, Miyake N, Iijima K, Nonoyama S, Matsumoto N, Saitsu H. Belal H, et al. Among authors: aoto k. Hum Mutat. 2018 Aug;39(8):1070-1075. doi: 10.1002/humu.23550. Epub 2018 May 25. Hum Mutat. 2018. PMID: 29768694
28 results