Literature DB >> 10690299

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

D M Roden, J R Balser.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1999        PMID： 10690299     DOI： 10.1016/s0008-6363(99)00224-2

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN： 0008-6363            Impact factor:   10.787


× No keyword cloud information.
  11 in total

1.  14-3-3 amplifies and prolongs adrenergic stimulation of HERG K+ channel activity.

Authors:  Anna Kagan; Yonathan F Melman; Andrew Krumerman; Thomas V McDonald
Journal:  EMBO J       Date:  2002-04-15       Impact factor: 11.598

2.  BeKm-1 is a HERG-specific toxin that shares the structure with ChTx but the mechanism of action with ErgTx1.

Authors:  Mei Zhang; Yuliya V Korolkova; Jie Liu; Min Jiang; Eugene V Grishin; Gea-Ny Tseng
Journal:  Biophys J       Date:  2003-05       Impact factor: 4.033

3.  Modelling and imaging cardiac repolarization abnormalities.

Authors:  Y Rudy
Journal:  J Intern Med       Date:  2006-01       Impact factor: 8.989

Review 4.  Computational biology in the study of cardiac ion channels and cell electrophysiology.

Authors:  Yoram Rudy; Jonathan R Silva
Journal:  Q Rev Biophys       Date:  2006-07-19       Impact factor: 5.318

5.  Expression and immunolocalization of ERG1 potassium channels in the rat kidney.

Authors:  Rolando Carrisoza; Carolina Salvador; Norma A Bobadilla; Joyce Trujillo; Laura I Escobar
Journal:  Histochem Cell Biol       Date:  2009-11-17       Impact factor: 4.304

6.  Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.

Authors:  Dagmar I Keller; Julie Grenier; Georges Christé; Frédérique Dubouloz; Stefan Osswald; Marijke Brink; Eckhard Ficker; Mohamed Chahine
Journal:  Can J Cardiol       Date:  2009-08       Impact factor: 5.223

7.  Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.

Authors:  Zahurul A Bhuiyan; Tarek S Momenah; Qiuming Gong; Ahmad S Amin; Saleh Al Ghamdi; Julene S Carvalho; Tessa Homfray; Marcel M A M Mannens; Zhengfeng Zhou; Arthur A M Wilde
Journal:  Heart Rhythm       Date:  2008-01-29       Impact factor: 6.343

8.  Functional interaction between extracellular sodium, potassium and inactivation gating in HERG channels.

Authors:  Franklin M Mullins; Svetlana Z Stepanovic; Niloufar B Gillani; Alfred L George; Jeffrey R Balser
Journal:  J Physiol       Date:  2004-05-28       Impact factor: 5.182

9.  A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.

Authors:  Yanmin Zhang; Nan Zhou; Wenhui Jiang; Jun Peng; Hongmei Wan; Chen Huang; Zenghui Xie; Christopher L-H Huang; Andrew A Grace; Aiqun Ma
Journal:  Eur J Pediatr       Date:  2006-12-14       Impact factor: 3.183

10.  Tracking the motion of the KV 1.2 voltage sensor reveals the molecular perturbations caused by a de novo mutation in a case of epilepsy.

Authors:  Antonios Pantazis; Maki Kaneko; Marina Angelini; Federica Steccanella; Annie M Westerlund; Sarah H Lindström; Michelle Nilsson; Lucie Delemotte; Sulagna C Saitta; Riccardo Olcese
Journal:  J Physiol       Date:  2020-09-21       Impact factor: 5.182
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.