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Page 1
Stem cell challenges and opportunities.
Ite K, Toyoda M, Akiyama S, Enosawa S, Yoshioka S, Yukitake T, Yamazaki-Inoue M, Tatsumi K, Akutsu H, Nishina H, Kimura T, Otani N, Nakazawa A, Fukuda A, Kasahara M, Umezawa A. Ite K, et al. Among authors: akutsu h. Prog Mol Biol Transl Sci. 2023;199:379-395. doi: 10.1016/bs.pmbts.2023.03.004. Epub 2023 Jul 26. Prog Mol Biol Transl Sci. 2023. PMID: 37678981
Replication Efficiency of SARS-CoV-2 Omicron Subvariants BA.2.75, BA.5, and XBB.1 in Human Mini-Gut Organoids.
Miyakawa K, Machida M, Kawasaki T, Kakizaki M, Kimura Y, Sugiyama M, Hasegawa H, Umezawa A, Akutsu H, Ryo A. Miyakawa K, et al. Among authors: akutsu h. Cell Mol Gastroenterol Hepatol. 2024;17(6):1066-1068. doi: 10.1016/j.jcmgh.2024.03.003. Epub 2024 Mar 15. Cell Mol Gastroenterol Hepatol. 2024. PMID: 38494057 Free PMC article. No abstract available.
Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1.
Takeuchi I, Tanase-Nakao K, Ogawa A, Sugawara T, Migita O, Kashima M, Yamazaki T, Iguchi A, Naiki Y, Uchiyama T, Tamaoki J, Maeda H, Shimizu H, Kawai T, Taniguchi K, Hirata H, Kobayashi M, Matsumoto K, Naruse K, Hata K, Akutsu H, Kato T, Narumi S, Arai K, Ishiguro A. Takeuchi I, et al. Among authors: akutsu h. J Med Genet. 2024 Feb 21;61(3):239-243. doi: 10.1136/jmg-2023-109444. J Med Genet. 2024. PMID: 37833059 Free article.
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: akutsu h. 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.
558 results