Molecular basis of congenital and acquired long QT syndromes

被引:16
作者
Ackerman, MJ [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Long QT Syndrome Clin & Sudden Death Genom Lab, Dept Med Pediat & Mol Pharmacol, Rochester, MN 55905 USA
关键词
D O I
10.1016/j.jelectrocard.2004.08.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:1 / 6
页数:6
相关论文
共 44 条
[1]   MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia [J].
Abbott, GW ;
Sesti, F ;
Splawski, I ;
Buck, ME ;
Lehmann, WH ;
Timothy, KW ;
Keating, MT ;
Goldstein, SAN .
CELL, 1999, 97 (02) :175-187
[2]   Cardiac channelopathies: it's in the genes [J].
Ackerman, MJ .
NATURE MEDICINE, 2004, 10 (05) :463-464
[3]   Ethnic differences in cardiac potassium channel variants: Implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome [J].
Ackerman, MJ ;
Tester, DJ ;
Jones, GS ;
Will, ML ;
Burrow, CR ;
Curran, ME .
MAYO CLINIC PROCEEDINGS, 2003, 78 (12) :1479-1487
[4]  
Ackerman MJ, 2002, MAYO CLIN PROC, V77, P413
[5]   Mechanisms of disease - Ion channels - Basic science and clinical disease [J].
Ackerman, MJ ;
Clapham, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (22) :1575-1586
[6]   Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome [J].
Ackerman, MJ ;
Siu, BL ;
Sturner, WQ ;
Tester, DJ ;
Valdivia, CR ;
Makielski, JC ;
Towbin, JA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (18) :2264-2269
[7]   Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome [J].
Ackerman, MJ ;
Tester, DJ ;
Porter, CJ .
MAYO CLINIC PROCEEDINGS, 1999, 74 (11) :1088-1094
[8]   Arrhythmogenic mechanisms of QT prolonging drugs: Is QT prolongation really the problem? [J].
Antzelevitch, C .
JOURNAL OF ELECTROCARDIOLOGY, 2004, 37 :15-24
[9]   Mutation in the KCNQ1 gene leading to the short QT-interval syndrome [J].
Bellocq, C ;
van Ginneken, ACG ;
Bezzina, CR ;
Alders, M ;
Escande, D ;
Mannens, MMAM ;
Baró, I ;
Wilde, AAM .
CIRCULATION, 2004, 109 (20) :2394-2397
[10]   Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A) [J].
Benson, DW ;
Wang, DW ;
Dyment, M ;
Knilans, TK ;
Fish, FA ;
Strieper, MJ ;
Rhodes, TH ;
George, AL .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (07) :1019-1028