Is long QT syndrome entering the era of molecular diagnosis?
作者信息
Priori S G
出版信息
Heart. 1997 Jan;77(1):5-6. doi: 10.1136/hrt.77.1.5.
Abstract
摘要
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Heart. 1997 Jan;77(1):5-6. doi: 10.1136/hrt.77.1.5.
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本文引用的文献
1
Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.遗传性心律失常中HERG钾通道功能障碍的谱系
Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2208-12. doi: 10.1073/pnas.93.5.2208.
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Genomic organization of the human SCN5A gene encoding the cardiac sodium channel.
Genomics. 1996 May 15;34(1):9-16. doi: 10.1006/geno.1996.0236.
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Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome.在一个模拟长QT综合征中存在的SCN5A和HERG缺陷的细胞模型中，对钠通道阻滞、β-肾上腺素能刺激和快速起搏的差异反应。
Circ Res. 1996 Jun;78(6):1009-15. doi: 10.1161/01.res.78.6.1009.
4
Multiple mechanisms of Na+ channel--linked long-QT syndrome.钠通道相关长QT综合征的多种机制
Circ Res. 1996 May;78(5):916-24. doi: 10.1161/01.res.78.5.916.
5
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.长QT综合征（一种遗传性心律失常）患者的心脏钠通道突变。
Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603.
6
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.一个新型钾通道基因的定位克隆：KVLQT1突变导致心律失常。
Nat Genet. 1996 Jan;12(1):17-23. doi: 10.1038/ng0196-17.
7
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.携带SCN5A和HERG基因突变的长QT综合征患者对钠通道阻滞和心率增加有不同反应。对基因特异性治疗的启示。
Circulation. 1995 Dec 15;92(12):3381-6. doi: 10.1161/01.cir.92.12.3381.
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Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.Romano-Ward长QT综合征的遗传异质性证据。对23个家族的分析。
Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635.
9
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.与遗传性心律失常——长QT综合征相关的SCN5A突变。
Cell. 1995 Mar 10;80(5):805-11. doi: 10.1016/0092-8674(95)90359-3.
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.心律失常的分子基础：HERG 突变导致长 QT 综合征。
Cell. 1995 Mar 10;80(5):795-803. doi: 10.1016/0092-8674(95)90358-5.
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