H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters

Por Matsumura, Hiroya, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Tomomori, Shunsuke, Motoda, Chikaaki, Amioka, Michitaka, Hironobe, Naoya, Toshishige, Masaaki, Takahashi, Shinya, Imai, Katsuhiko, Sueda, Taijiro, Chayama, Kazuaki, Kihara, Yasuki
Publicado no J Biomed Sci (2017)

A Nonsynonymous Polymorphism in Semaphorin 3A as a Risk Factor for Human Unexplained Cardiac Arrest with Documented Ventricular Fibrillation

Por Nakano, Yukiko, Chayama, Kazuaki, Ochi, Hidenori, Toshishige, Masaaki, Hayashida, Yasufumi, Miki, Daiki, Hayes, C. Nelson, Suzuki, Hidekazu, Tokuyama, Takehito, Oda, Noboru, Suenari, Kazuyoshi, Uchimura-Makita, Yuko, Kajihara, Kenta, Sairaku, Akinori, Motoda, Chikaaki, Fujiwara, Mai, Watanabe, Yoshikazu, Yoshida, Yukihiko, Ohkubo, Kimie, Watanabe, Ichiro, Nogami, Akihiko, Hasegawa, Kanae, Watanabe, Hiroshi, Endo, Naoto, Aiba, Takeshi, Shimizu, Wataru, Ohno, Seiko, Horie, Minoru, Arihiro, Koji, Tashiro, Satoshi, Makita, Naomasa, Kihara, Yasuki
Publicado em 2013