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MeSH:(Ether-A-Go-Go Potassium Channels/*genetics)

1.Progress in research on defective protein trafficking and functional restoration in HERG-associated long QT syndrome.

Peiliang FANG ; Jiangfang LIAN

Chinese Journal of Medical Genetics 2016;33(1):101-104

2.Effect of matrine on human ether à go-go related gene (HERG) channels expressed in Chinese hamster ovary cells.

Hong-jin WU ; An-ruo ZOU ; Fang XIE ; Yi-mei DU ; Yu CAO ; Yu-na LIU ; Ji-yuan YANG ; Xin-min LI

Chinese journal of integrative medicine 2010;16(5):430-434

3.The persistent expression of HERG channel in Xenopus oocyte and alteration of current.

Xian-Pei WANG ; Lu LI ; An-Ruo ZOU ; Dan-Na TU ; Yu-Hua LIAO

Chinese Journal of Applied Physiology 2008;24(3):329-333

4.Construction of pcDNA3-HERG-G572R expression vector and establishment of a cell line stably expressing HKE-HERG-G572R.

Yang YANG ; Na HUANG ; Ling GAO ; Su'e CHANG ; Bo GUO ; Lili HU ; Tusheng SONG ; Chen HUANG

Journal of Southern Medical University 2014;34(3):308-311

5.A novel deletion-frameshift mutation in the S1 region of HERG gene in a Chinese family with long QT syndrome.

Ying GAO ; Ping ZHANG ; Xue-bin LI ; Cun-cao WU ; Ji-hong GUO

Chinese Medical Journal 2013;126(16):3093-3096

6.Electrophysiological characterization of long QT syndrome associated mutations V630A and N633S.

Hai-ru SHE ; Si-yong TENG ; Jie-lin PU ; Zheng-lu SHANG ; Ru-tai HUI

Chinese Journal of Cardiology 2006;34(6):523-527

7.Functional expression of congenital long QT syndrome related HERG mutation A561V in vitro.

Yu LI ; Chang-cong CUI ; Yong-hui ZHAO ; Xiao-lin XUE ; Ai-feng ZHANG ; Jiang-fang LIAN ; Chen HUANG

Chinese Journal of Cardiology 2007;35(2):143-146

8.Analysis and analyzing mechanisms of HERG channel kinetics.

Xianpei WANG ; Lu LI ; Anruo ZOU ; Danna TU ; Yuhua LIAO

Journal of Biomedical Engineering 2008;25(5):1068-1073

9.Long QT syndrome gene diagnosis by haplotype analysis.

Jiang-fang LIAN ; Chang-cong CUI ; Xiao-lin XUE ; Chen HUANG ; Han-bing CUI ; Hai-zhu ZHANG

Chinese Journal of Medical Genetics 2004;21(3):272-273

10.KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome.

Qian-hao ZHAO ; Chao LIU ; Long-wu LU ; Guo-li LÜ ; Hong LIU ; Shuang-bo TANG ; Li QUAN ; Jian-ding CHENG

Journal of Forensic Medicine 2012;28(5):337-346

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