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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 6, 2023. (Total: 223792Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Torsades de Pointes and KCNH2[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
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.
Circulation. Arrhythmia and electrophysiology 2013 Aug .
Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW
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
hERG potassium channel blockade by the HCN channel inhibitor bradycardic agent ivabradine.
Journal of the American Heart Association 2015 Apr 4 (4): .
Melgari Dario, Brack Kieran E, Zhang Chuan, Zhang Yihong, El Harchi Aziza, Mitcheson John S, Dempsey Christopher E, Ng G André, Hancox Jules
The genetics underlying acquired long QT syndrome: impact for genetic screening.
European heart journal 2015 Dec .
Itoh Hideki, Crotti Lia, Aiba Takeshi, Spazzolini Carla, Denjoy Isabelle, Fressart Véronique, Hayashi Kenshi, Nakajima Tadashi, Ohno Seiko, Makiyama Takeru, Wu Jie, Hasegawa Kanae, Mastantuono Elisa, Dagradi Federica, Pedrazzini Matteo, Yamagishi Masakazu, Berthet Myriam, Murakami Yoshitaka, Shimizu Wataru, Guicheney Pascale, Schwartz Peter J, Horie Mino
Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use.
Scientific reports 2018 May 8 (1): 8443.
Nagasawa Sayaka, Saitoh Hisako, Kasahara Shiori, Chiba Fumiko, Torimitsu Suguru, Abe Hiroko, Yajima Daisuke, Iwase Hirota
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