Literature DB >> 10666657

Molecular biology of arrhythmic syndromes.

M Vatta1, H Li, J A Towbin.   

Abstract

In this review, the up-to-date understanding of the molecular basis of primary ventricular arrhythmias will be outlined. Two disorders have recently been well described at the molecular level, the long QT syndromes and Brugada syndrome, and in this paper we review the current scientific knowledge of each disease.

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Year:  2000        PMID: 10666657     DOI: 10.1097/00001573-200001000-00003

Source DB:  PubMed          Journal:  Curr Opin Cardiol        ISSN: 0268-4705            Impact factor:   2.161


  4 in total

1.  Cytoskeletal basis of ion channel function in cardiac muscle.

Authors:  Matteo Vatta; Georgine Faulkner
Journal:  Future Cardiol       Date:  2006-07

2.  Differentiation in the momentary rating of somatic symptoms covaries with trait emotional awareness in patients at risk for sudden cardiac death.

Authors:  Richard D Lane; Cheryl Carmichael; Harry T Reis
Journal:  Psychosom Med       Date:  2011-01-21       Impact factor: 4.312

3.  Predisposition to arrhythmia and autonomic dysfunction in Nhlh1-deficient mice.

Authors:  Tiziana Cogliati; Deborah J Good; Mark Haigney; Petra Delgado-Romero; Michael A Eckhaus; Walter J Koch; Ilan R Kirsch
Journal:  Mol Cell Biol       Date:  2002-07       Impact factor: 4.272

4.  Hexachlorophene is a potent KCNQ1/KCNE1 potassium channel activator which rescues LQTs mutants.

Authors:  Yueming Zheng; Xuejing Zhu; Pingzheng Zhou; Xi Lan; Haiyan Xu; Min Li; Zhaobing Gao
Journal:  PLoS One       Date:  2012-12-12       Impact factor: 3.240

  4 in total

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