| Kir2.1与钾通道病 |
| |
| 引用本文： | 李涛,曾晓荣.Kir2.1与钾通道病[J].医学综述,2008,14(19):2884-2886. |
| |
| 作者姓名： | 李涛 曾晓荣 |
| |
| 作者单位： | 泸州医学院心肌电生理学研究室,四川,泸州,646000 |
| |
| 基金项目： | 教育部科学技术研究项目 |
| |
| 摘 要： | Kir2.1是内向整流钾通道(Kir)家族的重要成员之一,其编码基因为KCNJ2。Kir2.1异常可引起钾通道结构的缺陷、离子通道功能异常,病变可累及神经、肌肉、心脏等多器官和系统,通称为钾通道病。本研究综述了Kir2.1及其与钾通道病的研究进展。
|
| 关 键 词： | 内向整流钾通道 Kir2.1 KCNJ2 钾通道病 |
Kir2.1 and Potassium Channelopathies |
| |
| LI Tao,ZENG Xiao-rong.Kir2.1 and Potassium Channelopathies[J].Medical Recapitulate,2008,14(19):2884-2886. |
| |
| Authors: | LI Tao ZENG Xiao-rong |
| |
| Institution: | LI Tao,ZENG Xiao-rong.( Institute of Myocardium Electrophysiology,Luzhou Medical College,Luzhou 646000,China) |
| |
| Abstract: | Kir 2.1 are one of important members of inward rectifying potassium channels,which was encoded by KCNJ2 gene located in chromosome 17.Abnormal kir 2.1 may result in defects of potassium channel structure and the disfunction of potassium channel,the pathological changes of which involve muscle,heart,nerve system and so on.Those pathological changes are named Potassium Channelopathies.This paper reviewed the recent researches in Kir 2.1 and potassium channelopathies. |
| |
| Keywords: | Kir2 1 KCNJ2 |
| 本文献已被 CNKI 维普 万方数据 等数据库收录！ |
|
