Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: SCN4B[original query] |
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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 |
Mutations in sodium channel ß1- and ß2-subunits associated with atrial fibrillation. Circulation. Arrhythmia and electrophysiology 2009 Jun 2 (3): 268-75. Watanabe Hiroshi, Darbar Dawood, Kaiser Daniel W, Jiramongkolchai Kim, Chopra Sameer, Donahue Brian S, Kannankeril Prince J, Roden Dan |
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance. Journal of the American College of Cardiology 2010 12 57 (1): 40-7. Barc Julien, Briec François, Schmitt Sébastien, Kyndt Florence, Le Cunff Martine, Baron Estelle, Vieyres Claude, Sacher Frédéric, Redon Richard, Le Caignec Cédric, Le Marec Hervé, Probst Vincent, Schott Jean-Jacqu |
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 |
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 |
Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
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 |
Contribution of Cardiac Sodium Channel ß-Subunit Variants to Brugada Syndrome. Circulation journal : official journal of the Japanese Circulation Society 2015 Jul . Peeters Uschi, Scornik Fabiana, Riuró Helena, Pérez Guillermo, Komurcu-Bayrak Evrim, Van Malderen Sophie, Pappaert Gudrun, Tarradas Anna, Pagans Sara, Daneels Dorien, Breckpot Karine, Brugada Pedro, Bonduelle Maryse, Brugada Ramon, Van Dooren Son |
Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation. PloS one 2017 8 12 (8): e0183690. Husser Daniela, Ueberham Laura, Hindricks Gerhard, Büttner Petra, Ingram Christie, Weeke Peter, Shoemaker M Benjamin, Adams Volker, Arya Arash, Sommer Philipp, Darbar Dawood, Roden Dan M, Bollmann Andre |
Preserved SCN4B expression is an independent indicator of favorable recurrence-free survival in classical papillary thyroid cancer. PloS one 2018 13 (5): e0197007. Gong Yanping, Yang Jing, Wu Wenshuang, Liu Feng, Su Anping, Li Zhihui, Zhu Jingqiang, Wei T |
Copy number variation in a hospital-based cohort of children with epilepsy. Epilepsia open 2017 Jun 2 (2): 244-254. Vlaskamp Danique R M, Callenbach Petra M C, Rump Patrick, Giannini Lucia A A, Dijkhuizen Trijnie, Brouwer Oebele F, van Ravenswaaij-Arts Conny M |
Identification of rare variants in cardiac sodium channel ?4-subunit gene SCN4B associated with ventricular tachycardia. Molecular genetics and genomics : MGG 2019 4 294 (4): 1059-1071. Yang Qin, Xiong Hongbo, Xu Chengqi, Huang Yuan, Tu Xin, Wu Gang, Fu Fenfen, Wang Zhijie, Wang Longfei, Zhao Yuanyuan, Li Sisi, Huang Yufeng, Wang Chuchu, Wang Dan, Yao Yufeng, Wang Fan, Wang Yongbo, Xue Yu, Wang Pengyun, Chen Qiuyun, Pu Jielin, Wang Qing |
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 |
Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome. Frontiers in pharmacology 2022 9 13 984299. Zaklyazminskaya Elena, Shestak Anna, Podolyak Dmitry, Komoliatova Vera, Makarov Leonid, Novitskaya Anna, Revishvili Amir |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
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