HuGE Literature Finder
Records 1-11
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The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study.
The journal of international advanced otology 2019 Apr 15 (1): 130-134. Dai Qingqing, Wang Dan, Zheng Ho |
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Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.
Journal of vestibular research : equilibrium & orientation 2016 Jan 25 (5-6): 211-8. Li Yuan-Jun, Jin Zhan-Guo, Xu Xian-Ro |
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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
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Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.
Biomarkers in medicine 2014 8 (4): 557-70. Nielsen Jonas Bille, Bentzen Bo Hjorth, Olesen Morten Salling, David Jens-Peter, Olesen Søren-Peter, Haunsø Stig, Svendsen Jesper Hastrup, Schmitt Nico |
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A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.
International journal of audiology 2012 Aug . Hietikko E, Kotimäki J, Okuloff A, Sorri M, Männikkö M |
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Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus.
Behavioral and brain functions : BBF 2011 7 (1): 39. Sand Philipp G, Langguth Berthold, Kleinjung Tobi |
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The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
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Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population.
American journal of medical genetics. Part A 2010 Jan 152A (1): 1. Campbell CA, Della Santina CC, Meyer NC, Smith NB, Myrie OA, Stone EM, Fukushima K, Califano J, Carey JP, Hansen MR, Gantz BJ, Minor LB, Smith RJ |
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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 |
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No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.
Clinical endocrinology 2004 Jul 61 (1): 109-12. Tang Nelson L S, Chow C C, Ko Gary T C, Tai Morris H L, Kwok Rachel, Yao X Q, Cockram Clive |
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Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.
Neurology 2003 Sep 61 (6): 857-9. Sternberg D, Tabti N, Fournier E, Hainque B, Fontaine |
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- Page last updated:Feb 24, 2021
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