文部科学省科学研究費特定領域研究「性分化機構の解明」 *

研究成果

松本 直通 MATSUMOTO, Naomichi
横浜市立大学 大学院医学研究科
研究項目A03 「性分化異常症の解析」
研究課題 エピゲノム解析から迫るATR-X症候群の性分化異常発症機構の解明

2008年発表論文

Gibbons RJ, Wada T, Fisher CA, Malik N, Mitson MJ, Steensma DP, Fryer A, Goudie DR, Krantz ID, Traeger-Synodinos J. Mutations in the chromatin-associated protein ATRX. Hum Mut 29, 796-802, 2008

Kosho T, Sakazume S, Kawame H, Wakui K, Wada T, Okoshi Y, Mikawa M, Hasegawa T, Matsuura N, Niikawa N, Matsumoto N, Fukushima Y. De novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment. Clin Dysmorphol 17, 31-34, 2008

Yamada-Okabe T, Matsumoto N. Decreased serum dependence in the growth of NIH3T3 cells from the overexpression of human nuclear receptor-binding SET-domain-containing protein (NSD1) or fission yeast su(var)3-9, enhancer-of-zeste, trithorax 2 (SET2). Cell Biochemistry and Function 26, 146-150, 2008

2007年発表論文

Yamasaki-Ishizaki Y, Kayashima T, Christophe M, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T. Role of DNA methylation and histone H3 Lysine 27 methylation in tissue-specific imprinting of mouse Grb10. Mol Cell Biol 27, 732-742, 2007