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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 31, 2023. (Total: 217454Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Torsades de Pointes and KCNE1[original query]
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.
Journal of the American College of Cardiology 2009 Aug 54 (9): 812-9.
Nishio Yukiko, Makiyama Takeru, Itoh Hideki, Sakaguchi Tomoko, Ohno Seiko, Gong Yin-Zhi, Yamamoto Satoshi, Ozawa Tomoya, Ding Wei-Guang, Toyoda Futoshi, Kawamura Mihoko, Akao Masaharu, Matsuura Hiroshi, Kimura Takeshi, Kita Toru, Horie Mino
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Human mutation 2009 Apr 30 (4): 4.
Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M
Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.
The Canadian journal of cardiology 2010 Apr 26 (4): 208-12.
Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.
Circulation. Cardiovascular genetics 2012 Feb 5 (1): 91-9.
Kääb Stefan, Crawford Dana C, Sinner Moritz F, Behr Elijah R, Kannankeril Prince J, Wilde Arthur A M, Bezzina Connie R, Schulze-Bahr Eric, Guicheney Pascale, Bishopric Nanette H, Myerburg Robert J, Schott Jean-Jacques, Pfeufer Arne, Beckmann Britt-Maria, Martens Eimo, Zhang Taifang, Stallmeyer Birgit, Zumhagen Sven, Denjoy Isabelle, Bardai Abdennasser, Van Gelder Isabelle C, Jamshidi Yalda, Dalageorgou Chrysoula, Marshall Vanessa, Jeffery Steve, Shakir Saad, Camm A John, Steinbeck Gerhard, Perz Siegfried, Lichtner Peter, Meitinger Thomas, Peters Annette, Wichmann H-Erich, Ingram Christiana, Bradford Yuki, Carter Shannon, Norris Kris, Ritchie Marylyn D, George Alfred L, Roden Dan
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7.
Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan
Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.
Journal of electrocardiology 2015 Oct .
Yamaguchi Yoshiaki, Mizumaki Koichi, Hata Yukiko, Inoue Hiros
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