KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation
暂无分享,去创建一个
Wei Huang | Shi-Jie Xu | Yi Liu | Jacques Barhanin | Ying Wang | Zhu Chen | S. Bendahhou | J. Barhanin | Wei Huang | Yi-Han Chen | Shi-jie Xu | Xiao-liang Wang | Wenyuan Xu | Hong-wei Jin | Hao Sun | Xiaoyan Su | Q. Zhuang | Yiqing Yang | Yue-bin Li | Yi Liu | Hong-Ju Xu | Xiao-Fei Li | Ning Ma | Chun-Ping Mou | Zhu Chen | Yi-Han Chen | Saı̈d Bendahhou | Xiao-Liang Wang | Ying Wang | Wen-Yuan Xu | Hong-Wei Jin | Hao Sun | Xiao-Yan Su | Qi-Nan Zhuang | Yi-Qing Yang | Yue-Bin Li | Hong-Ju Xu | Xiao-Fei Li | Ning Ma | Chun-Ping Mou
[1] H. Yeh,et al. Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation. , 2002, American heart journal.
[2] G. Landes,et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias , 1996, Nature Genetics.
[3] P. Oldershaw,et al. Relation of human cardiac action potential duration to the interval between beats: implications for the validity of rate corrected QT interval (QTc). , 1987, British heart journal.
[4] S. Nattel. New ideas about atrial fibrillation 50 years on , 2002, Nature.
[5] S. Waldegger,et al. A constitutively open potassium channel formed by KCNQ1 and KCNE3 , 2000, Nature.
[6] A. A. Armoundas,et al. Ectopic expression of KCNE3 accelerates cardiac repolarization and abbreviates the QT interval. , 2002, The Journal of clinical investigation.
[7] J M Rawles,et al. The QT interval in atrial fibrillation. , 1989, British heart journal.
[8] M. Lazdunski,et al. Properties of KvLQT1 K+ channel mutations in Romano–Ward and Jervell and Lange‐Nielsen inherited cardiac arrhythmias , 1997, The EMBO journal.
[9] M. Sanguinetti,et al. Molecular and Cellular Mechanisms of Cardiac Arrhythmias , 2001, Cell.
[10] M. Sanguinetti,et al. Functional Effects of Mutations in KvLQT1 that Cause Long QT Syndrome , 1999, Journal of cardiovascular electrophysiology.
[11] B. Gersh,et al. Epidemiology and natural history of atrial fibrillation: clinical implications. , 2001, Journal of the American College of Cardiology.
[12] A Laupacis,et al. Prevalence, age distribution, and gender of patients with atrial fibrillation. Analysis and implications. , 1995, Archives of internal medicine.
[13] P. C. Viswanathan,et al. A sodium-channel mutation causes isolated cardiac conduction disease , 2001, Nature.
[14] Arthur J Moss,et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome , 1995, Cell.
[15] G. Breithardt,et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation , 1998, Nature.
[16] M. Lazdunski,et al. KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel , 2000, The EMBO journal.
[17] J. Brugada,et al. Identification of a genetic locus for familial atrial fibrillation. , 1997, The New England journal of medicine.
[18] Jacques Barhanin,et al. KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current , 1996, Nature.
[19] D. Cannom. Atrial fibrillation: nonpharmacologic approaches. , 2000, The American journal of cardiology.