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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: nakabayashi k. 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.
Transwell Culture with Adipose Tissue-Derived Stem Cells and Fertilized Eggs Mimics the In Vivo Development of Fertilized Eggs to Blastocysts in the Fallopian Tube: An Animal Study.
Hirakawa T, Nakabayashi K, Ito N, Hata K, Imi S, Shibata M, Urushiyama D, Miyata K, Yotsumoto F, Yasunaga S, Baba T, Miyamoto S. Hirakawa T, et al. Among authors: nakabayashi k. Antioxidants (Basel). 2024 Jun 8;13(6):704. doi: 10.3390/antiox13060704. Antioxidants (Basel). 2024. PMID: 38929143 Free PMC article.
Delayed diagnosis in a child with strangulated mesenteric hernia.
Tetsuhara K, Nakabayashi K, Muraoka M, Kikuno R, Ueda M, Inoue R, Hayashida M. Tetsuhara K, et al. Among authors: nakabayashi k. Acute Med Surg. 2024 Jun 18;11(1):e977. doi: 10.1002/ams2.977. eCollection 2024 Jan-Dec. Acute Med Surg. 2024. PMID: 38894735 Free PMC article.
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, Shimura K, Abe K, Sugisawa C, Ishii T, Miyako K, Hasegawa Y, Maruo Y, Muroya K, Watanabe N, Nishihara E, Ito Y, Kogai T, Kameyama K, Nakabayashi K, Hata K, Fukami M, Shima H, Kikuchi A, Takayama J, Tamiya G, Hasegawa T. Narumi S, et al. Among authors: nakabayashi k. Nat Genet. 2024 May;56(5):869-876. doi: 10.1038/s41588-024-01735-5. Epub 2024 May 7. Nat Genet. 2024. PMID: 38714868 Free PMC article.
584 results