...
首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Spectrum of HERG K~+-channel dysfunction in an inherited cardiac arrhythmia
【24h】

Spectrum of HERG K~+-channel dysfunction in an inherited cardiac arrhythmia

机译:遗传性心律不齐中HERG K〜+通道功能障碍的光谱

获取原文
获取原文并翻译 | 示例
           

摘要

Long QT syndrome (LQT) is an autosomal dominant disorder that can cause sudden death from cardiac arrhythmias. We recently discovered that mutations in HERG, a K~+-channel gene, cause chromosome 7-linked LQT. Heter- ologous expression of HERG in Xenopus oocytes revealed that HERG current was similar to a well-characterized cardiac delayed rectifier K+ current, I_Kr, and led to the hypothesis that mutations in HERG reduced I_Kr, causing prolonged myocel- lular action potentials.
机译:长QT综合征(LQT)是常染色体显性遗传疾病,可导致因心律不齐而突然死亡。我们最近发现,HERG(一种K〜+通道基因)中的突变会导致与7号染色体相关的LQT。 HERG在非洲爪蟾卵母细胞中的异源表达表明,HERG电流与特征明确的心脏延迟整流器K +电流I_Kr相似,并得出了这样的假设,即HERG突变会降低I_Kr,从而延长心肌的动作电位。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号