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Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome.
Kawai T, Kinoshita S, Takayama Y, Ohnishi E, Kamura H, Kojima K, Kikuchi H, Terao M, Sugawara T, Migita O, Kagami M, Isojima T, Yamaguchi Y, Wakui K, Ohashi H, Shimizu K, Mizuno S, Okamoto N, Fukushima Y, Takada F, Kosaki K, Takada S, Akutsu H, Ura K, Nakabayashi K, Hata K. Kawai T, et al. Among authors: terao m. Genet Med Open. 2024 Mar 14;2:101838. doi: 10.1016/j.gimo.2024.101838. eCollection 2024. Genet Med Open. 2024. PMID: 39669601 Free PMC article.
The NIPBL-gene mutation of a Cornelia de Lange Syndrome patient causes deficits in the hepatocyte differentiation of induced Pluripotent Stem Cells via altered chromatin-accessibility.
Foglia M, Guarrera L, Kurosaki M, Cassanmagnago GA, Bolis M, Miduri M, Cereseto A, Umbach A, Craparotta I, Fratelli M, Vallerga A, Paroni G, Zanetti A, Cavallaro AV, Russo L, Garattini E, Terao M. Foglia M, et al. Among authors: terao m. Cell Mol Life Sci. 2024 Oct 25;81(1):439. doi: 10.1007/s00018-024-05481-z. Cell Mol Life Sci. 2024. PMID: 39453535 Free PMC article.
Case report: Intracranial epidermoid cyst in a cat.
Terao M, Uemura T, Hasegawa H, Ashida C, Ehara I, Ozawa T, Kamishina H. Terao M, et al. Front Vet Sci. 2024 Sep 23;11:1426421. doi: 10.3389/fvets.2024.1426421. eCollection 2024. Front Vet Sci. 2024. PMID: 39376918 Free PMC article.
A Case of Cancer of Unknown Primary Presenting with Chylothorax.
Tanaka E, Oda N, Ogawa T, Takata I, Terao M, Ueki T. Tanaka E, et al. Among authors: terao m. Intern Med. 2024 Aug 8. doi: 10.2169/internalmedicine.3988-24. Online ahead of print. Intern Med. 2024. PMID: 39111886 Free article.
362 results