A plethora of mechanisms in the HERG-related long QT syndrome -: Genetics meets electrophysiology

被引：44

作者：

Roden, DM

Balser, JR

机构：

[1] Vanderbilt Univ, Div Clin Pharmacol, Sch Med, Dept Med, Nashville, TN 37232 USA

[2] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37232 USA

[3] Vanderbilt Univ, Sch Med, Dept Anesthesiol, Nashville, TN 37232 USA

来源：

CARDIOVASCULAR RESEARCH | 1999年 / 44卷 / 02期

关键词：

D O I：

10.1016/S0008-6363(99)00224-2

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：242 / 246

页数：5

相关论文

共 43 条

[41] Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature
Zhou, ZF
Gong, QM
Ye, B
Fan, Z
Makielski, JC
Robertson, GA
January, CT
[J]. BIOPHYSICAL JOURNAL, 1998, 74 (01) : 230 - 241
[42] HERG channel dysfunction in human long QT syndrome - Intracellular transport and functional defects
Zhou, ZF
Gong, QM
Epstein, ML
January, CT
[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (33) : 21061 - 21066
[43] A mutation in the pore region of HERG K+ channels expressed in Xenopus oocytes reduces rectification by shifting the voltage dependence of inactivation
Zou, AR
Xu, QP
Sanguinetti, MC
[J]. JOURNAL OF PHYSIOLOGY-LONDON, 1998, 509 (01): : 129 - 137

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