Literature DB >> 18604280

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation.

C A Remme1, A O Verkerk, A A M Wilde, M W Veldkamp, J M T de Bakker, C R Bezzina.   

Abstract

Entities:  

Year:  2007        PMID: 18604280      PMCID: PMC2442896          DOI: 10.1007/bf03085988

Source DB:  PubMed          Journal:  Neth Heart J        ISSN: 1568-5888            Impact factor:   2.380


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  19 in total

Review 1.  The Brugada syndrome: diagnostic criteria and cellular mechanisms.

Authors:  C Antzelevitch
Journal:  Eur Heart J       Date:  2001-03       Impact factor: 29.983

2.  Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism.

Authors:  Colleen E Clancy; Yoram Rudy
Journal:  Circulation       Date:  2002-03-12       Impact factor: 29.690

Review 3.  Genetic control of sodium channel function.

Authors:  Hanno L Tan; Connie R Bezzina; Jeroen P P Smits; Arie O Verkerk; Arthur A M Wilde
Journal:  Cardiovasc Res       Date:  2003-03-15       Impact factor: 10.787

4.  A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Authors:  C Bezzina; M W Veldkamp; M P van Den Berg; A V Postma; M B Rook; J W Viersma; I M van Langen; G Tan-Sindhunata; M T Bink-Boelkens; A H van Der Hout; M M Mannens; A A Wilde
Journal:  Circ Res       Date:  1999 Dec 3-17       Impact factor: 17.367

5.  Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel.

Authors:  M W Veldkamp; P C Viswanathan; C Bezzina; A Baartscheer; A A Wilde; J R Balser
Journal:  Circ Res       Date:  2000-05-12       Impact factor: 17.367

6.  Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome.

Authors:  M P van den Berg; A A Wilde; J Brouwer; J Haaksma; A H van der Hout; I Stolte-Dijkstra; I M Van Langen; G C Beaufort-Krol; J H Cornel; H J Crijns
Journal:  J Cardiovasc Electrophysiol       Date:  2001-06

7.  Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD.

Authors:  Carol Ann Remme; Arie O Verkerk; Dieter Nuyens; Antoni C G van Ginneken; Sandra van Brunschot; Charly N W Belterman; Ronald Wilders; Marian A van Roon; Hanno L Tan; Arthur A M Wilde; Peter Carmeliet; Jacques M T de Bakker; Marieke W Veldkamp; Connie R Bezzina
Journal:  Circulation       Date:  2006-12-04       Impact factor: 29.690

8.  Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Authors:  F Kyndt; V Probst; F Potet; S Demolombe; J C Chevallier; I Baro; J P Moisan; P Boisseau; J J Schott; D Escande; H Le Marec
Journal:  Circulation       Date:  2001-12-18       Impact factor: 29.690

9.  Molecular mechanism for an inherited cardiac arrhythmia.

Authors:  P B Bennett; K Yazawa; N Makita; A L George
Journal:  Nature       Date:  1995-08-24       Impact factor: 49.962

10.  Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.

Authors:  Augustus O Grant; Michael P Carboni; Valentina Neplioueva; C Frank Starmer; Mirella Memmi; Carlo Napolitano; Silvia Priori
Journal:  J Clin Invest       Date:  2002-10       Impact factor: 14.808

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  1 in total

Review 1.  Modeling Inherited Arrhythmia Disorders Using Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Authors:  Vassilios J Bezzerides; Donghui Zhang; William T Pu
Journal:  Circ J       Date:  2016-12-03       Impact factor: 2.993

  1 in total

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