Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SCN3B[original query] |
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High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts. Journal of medical genetics 2006 Jul 43 (7): 598-608. Park J W, Cai J, McIntosh I, Jabs E W, Fallin M D, Ingersoll R, Hetmanski J B, Vekemans M, Attie-Bitach T, Lovett M, Scott A F, Beaty T |
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort. Heart rhythm : the official journal of the Heart Rhythm Society 2007 Jun 4 (6): 752-5. Koopmann Tamara T, Beekman Leander, Alders Marielle, Meregalli Paola G, Mannens Marcel M A M, Moorman Antoon F M, Wilde Arthur A M, Bezzina Connie |
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population. Biochemical and biophysical research communications 2010 Jul 398 (1): 98-104. Wang Pengyun, Yang Qinbo, Wu Xiaofen, Yang Yanzong, Shi Lisong, Wang Chuchu, Wu Gang, Xia Yunlong, Yang Bo, Zhang Rongfeng, Xu Chengqi, Cheng Xiang, Li Sisi, Zhao Yuanyuan, Fu Fenfen, Liao Yuhua, Fang Fang, Chen Qiuyun, Tu Xin, Wang Qing |
Mutations in sodium channel ß-subunit SCN3B are associated with early-onset lone atrial fibrillation. Cardiovascular research 2011 Mar 89 (4): 786-93. Olesen Morten S, Jespersen Thomas, Nielsen Jonas B, Liang Bo, Møller Daniel V, Hedley Paula, Christiansen Michael, Varró András, Olesen Søren-Peter, Haunsø Stig, Schmitt Nicole, Svendsen Jesper |
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5. Circulation journal : official journal of the Japanese Circulation Society 2012 Dec . Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A |
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder? Forensic science international 2014 Mar 236 38-45. Liu Chao, Tester David J, Hou Yiding, Wang Wen, Lv Guoli, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
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 |
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
An Analysis of the Association between Epilepsy-Related Genes and Vertigo in the Polish Population. Audiology & neuro-otology 2018 Oct 23 (3): 135-144. Pawlak-Osi?ska Katarzyna, Linkowska Katarzyna, Ho?ub Karolina, Winiarska Katarzyna, Stankiewicz Bartosz, Ka?mierczak Henryk, Osi?ski Stanis?aw, Marzec Maria, Grzybowski Toma |
Effects of GRM4, SCN2A and SCN3B polymorphisms on antiepileptic drugs responsiveness and epilepsy susceptibility. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society 2019 Jul 27 (5): 731-737. Al-Eitan Laith N, Al-Dalalah Islam M, Aljamal Hanan |
Significant association of rare variant p.Gly8Ser in cardiac sodium channel ?4-subunit SCN4B with atrial fibrillation. Annals of human genetics 2019 3 83 (4): 239-248. Xiong Hongbo, Yang Qin, Zhang Xiaoping, Wang Pengxia, Chen Feifei, Liu Ying, Wang Pengyun, Zhao Yuanyuan, Li Sisi, Huang Yufeng, Chen Shanshan, Wang Xiaojing, Zhang Hongfu, Yu Dong, Tan Chencheng, Fang Cheng, Huang Yuan, Wu Gang, Wu Yanxia, Cheng Xiang, Liao Yuhua, Zhang Rongfeng, Yang Yanzong, Ke Tie, Ren Xiang, Li Hui, Tu Xin, Xia Yunlong, Xu Chengqi, Chen Qiuyun, Wang Qing |
Prolonged left ventricular contraction duration in apical segments as a marker of arrhythmic risk in patients with long QT syndrome. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2020 6 22 (8): 1279-1286. Borowiec Karolina, Kowalski Miros?aw, Kumor Magdalena, Duliban Joanna, ?migielski Witold, Hoffman Piotr, Biernacka El?bieta Katarzy |
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