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心律失常与单核苷酸多态性

Arrhythmia and single nucleotide polymorphism
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作者 谭琛 浦介麟 王方正
机构地区 中国医学科学院中国协和医科大学心血管病研究所阜外心血管病医病心律失常诊治中心
出处 《中华心律失常学杂志》 2005年第2期155-158,共4页 Chinese Journal of Cardiac Arrhythmias
关键词 心律失常 单核苷酸多态性 基因组计划 人类基因 人类健康 基因研究 全序列 常见病
分类号 R541.7 [医药卫生—心血管疾病] R394 [医药卫生—医学遗传学]
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参考文献20

  • 1杨昭庆,洪坤学.单核苷酸多态性的研究进展[J].国外医学（遗传学分册）,2000,23(1):4-8. 被引量：68
  • 2Keating MT,Atkinson D,Dunn C,et al. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science, 1991,252:704-706.
  • 3Jiang C, Atkinson D, Towbin JA, et al. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity. Nat Genet, 1984,8:141 -147.
  • 4Mohler PJ, Schott J J, Gramolini AO, et al. Ankyrin-B mutation cause type 4 long QT cardiac arrhythmia and sudden cardiac death. Nature ,2003,421,634-638.
  • 5Duggal P, Vesely MR, Wattanasirichaigoon D, et al. Mutation of the gene for Isk associated with both Jervell and LangeNielsen and Roman-Ward forms of long-QT syndrome. Circulation, 1998,97:142-146.
  • 6Splawski I, Tristani-Firouzi M, Lehmann MH. Mutations in the hmink gene cause long QT syndrome and suppress IKs function. Nat Genet, 1997,17:338-340.
  • 7Ai T, Fujiwara Y, Tsuji K, et al. Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia. Circulation,2002,105:2 592-2 594.
  • 8Sanguinetti MN, Jiang C, Curran ME, et al. A mechanistic link between an inherited and an acquired cardiac arrhythmia:HERG encodes the IKr potassium channel. Cell, 1995,81:299-307.
  • 9Weiss R, Barmada MM, Nguyen T,et al. Clinical and molecular heterogeneity in the Brugada syndrome:a novel gene locus on chromosome 3. Circulation,2002,105:707-713.
  • 10Tiso N, Stephan DA, Nava A,et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricnlar cardiomyopathy type 2 (ARVD2). Hum Mol Genet, 2001,10:189-194.

二级参考文献24

  • 1Keating MT, Sanguinetti MC. Molecular and cellular mechanisms of cardiac arrhythmias. Cell, 2001,104: 569-580.
  • 2The Cardiac Arrhythmia Suppression Trial Ⅱ. Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction. N Engl J Med, 1992,327:227-233.
  • 3Zipes DP. Proarrhythmic effects of antiarrhythmic drugs.Am J Cardiol, 1987,59:26E-31E.
  • 4Wang Q, Curran ME, Splawski I, et al. Positional cloning of a novel potassium channel gene: KvLQT1 mutations cause cardiac arrhythmia. Nat Genet, 1995,1:17-23.
  • 5Trudeau MC, Warmke J, Garetzky B, et al. HERG, a human causes inward rectifier in the voltage-gated potassium channel family. Science, 1995,269: 92-95.
  • 6Abbott GW, Sesti T, Splaioski I, et al. MiRP1 forms Iks potassium channels with HERG and is associated with cardiac arrhythmia. Cell, 1999, 97: 175-187.
  • 7Chauhan VS, Tuvia S, Buhusi M, et al. Abnormal cardiac Na+ channel properties and QT heart rate adaptation in neonatal ankyrin B knockout mice. Circ Res, 2000, 86:441-447.
  • 8Splawski I, Shen JX, Timonthy KW, et al. Genomic structure of three Long QT syndrome genes: KvLQT1,HERG, and KCNE1. Genomics, 1998, 51:86-97.
  • 9Keating M, Atkinson D, Dunn C, et al. Linkage of a cardiac arrhythmia, the long QT syndrome and the Harvey ras-1 gene. Science, 1991, 252:704-706.
  • 10Tanaka T, Nakaharo K, Kato N, et al. Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13Japanese families. Hum Genet. 1994, 94:380-384.

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中华心律失常学杂志
2005年 第2期

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