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A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele.
Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H. Yang X, et al. Among authors: kubota t. J Clin Immunol. 2015 Apr;35(3):244-8. doi: 10.1007/s10875-015-0144-6. Epub 2015 Mar 7. J Clin Immunol. 2015. PMID: 25744037
[Epigenetics].
Miyake K, Kubota T. Miyake K, et al. Among authors: kubota t. Nihon Rinsho. 2010 Aug;68 Suppl 8:87-92. Nihon Rinsho. 2010. PMID: 20976890 Review. Japanese. No abstract available.
Role of epigenetics in Rett syndrome.
Kubota T, Miyake K, Hirasawa T. Kubota T, et al. Epigenomics. 2013;5(5):583-92. doi: 10.2217/epi.13.54. Epigenomics. 2013. PMID: 24059803
Clinical and Immunological Characterization of ICF Syndrome in Japan.
Kamae C, Imai K, Kato T, Okano T, Honma K, Nakagawa N, Yeh TW, Noguchi E, Ohara A, Shigemura T, Takahashi H, Takakura S, Hayashi M, Honma A, Watanabe S, Shigemori T, Ohara O, Sasaki H, Kubota T, Morio T, Kanegane H, Nonoyama S. Kamae C, et al. Among authors: kubota t. J Clin Immunol. 2018 Nov;38(8):927-937. doi: 10.1007/s10875-018-0559-y. Epub 2018 Oct 23. J Clin Immunol. 2018. PMID: 30353301
[Molecular mechanism in Rett syndrome].
Miyake K, Kubota T. Miyake K, et al. Among authors: kubota t. Nihon Yakurigaku Zasshi. 2015 Apr;145(4):178-82. doi: 10.1254/fpj.145.178. Nihon Yakurigaku Zasshi. 2015. PMID: 25864827 Review. Japanese. No abstract available.
3,897 results