Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SCN2B[original query] |
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Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB). Epilepsia 2004 Feb 45 (2): 140-8. Fukuma Goryu, Oguni Hirokazu, Shirasaka Yukiyoshi, Watanabe Kazuyoshi, Miyajima Tasuku, Yasumoto Sawa, Ohfu Masaharu, Inoue Takahito, Watanachai Aruchalean, Kira Ryutaro, Matsuo Muneaki, Muranaka Hideki, Sofue Fumiko, Zhang Bo, Kaneko Sunao, Mitsudome Akihisa, Hirose Shinic |
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 |
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 |
A novel microsatellite polymorphism of sodium channel beta1-subunit gene (SCN1B) may underlie abnormal cardiac excitation manifested by coved-type ST-elevation compatible with Brugada syndrome in Japanese. International journal of clinical pharmacology and therapeutics 2010 Feb 48 (2): 109-19. Ogawa R, Kishi R, Takagi A, Sakaue I, Takahashi H, Matsumoto N, Masuhara K, Nakazawa K, Kobayashi S, Miyake F, Echizen |
Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy. Epilepsy research 2012 Dec 102 (3): 195-200. Wang Ji-wen, Shi Xiu-yu, Kurahashi Hirokazu, Hwang Su-Kyeong, Ishii Atsushi, Higurashi Norimichi, Kaneko Sunao, Hirose Shinichi, |
Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy. Human genetics 2014 May 133 (5): 651-9. Baum Larry, Haerian Batoul Sadat, Ng Ho-Keung, Wong Virginia C N, Ng Ping Wing, Lui Colin H T, Sin Ngai Chuen, Zhang Chunbo, Tomlinson Brian, Wong Gary Wing-Kin, Tan Hui Jan, Raymond Azman Ali, Mohamed Zahurin, Kwan Patri |
Influence of differentially expressed genes from suicide post-mortem study on personality traits as endophenotypes on healthy subjects and suicide attempters. European archives of psychiatry and clinical neuroscience 2014 Aug 264 (5): 423-32. Calati Raffaella, Giegling Ina, Balestri Martina, Antypa Niki, Friedl Marion, Konte Bettina, Hartmann Annette M, Serretti Alessandro, Rujescu D |
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 |
Nine differentially expressed genes from a post mortem study and their association with suicidal status in a sample of suicide completers, attempters and controls. Journal of psychiatric research 2017 Mar 91 98-104. Balestri Martina, Crisafulli Concetta, Donato Luigi, Giegling Ina, Calati Raffaella, Antypa Niki, Schneider Barbara, Marusic Dragan, Tarozzi Maria Eugenia, Marusic Dorjan, Paragi Metka, Hartmann Annette M, Konte Bettina, Marsano Agnese, Serretti Alessandro, Rujescu D |
SCN1B and SCN2B gene variants analysis in dravet syndrome patients: Analysis of 22 cases. Medicine 2019 3 98 (13): e14974. Gong Jiao-E, Liao Hong-Mei, Long Hong-Yu, Li Xiang-Min, Long Li-Li, Zhou Luo, Gu Wen-Ping, Lu Shao-Hua, Qu Qiang, Yang Li-Min, Xiao Bo, Qu Ji |
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 |
Decreased FAM13B Expression Increases Atrial Fibrillation Susceptibility by Regulating Sodium Current and Calcium Handling. JACC. Basic to translational science 2023 12 8 (10): 1357-1378. Gregory Tchou, Daniela Ponce-Balbuena, Nana Liu, Shamone Gore-Panter, Jeffrey Hsu, Fang Liu, Emmanuel Opoku, Gregory Brubaker, Sarah M Schumacher, Christine S Moravec, John Barnard, David R Van Wagoner, Mina K Chung, Jonathan D Smi |
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- Page last updated:Apr 22, 2024
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