Literature DB >> 26958876

Inherited Arrhythmias: Of Channels, Currents, and Swimming.

Maura M Zylla1, Dierk Thomas2.   

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Year:  2016        PMID： 26958876      PMCID： PMC4788755          DOI： 10.1016/j.bpj.2016.02.010

Source DB:  PubMed          Journal:  Biophys J        ISSN： 0006-3495            Impact factor:   4.033


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  22 in total

Review 1.  The cardiac hERG/IKr potassium channel as pharmacological target: structure, function, regulation, and clinical applications.

Authors:  D Thomas; C A Karle; J Kiehn
Journal:  Curr Pharm Des       Date:  2006       Impact factor: 3.116

Review 2.  Molecular aspects of the congenital and acquired Long QT Syndrome: clinical implications.

Authors:  J B Saenen; C J Vrints
Journal:  J Mol Cell Cardiol       Date:  2008-02-09       Impact factor: 5.000

3.  The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel.

Authors:  Patrick A Schweizer; Julian Schröter; Sebastian Greiner; Jan Haas; Pessah Yampolsky; Derliz Mereles; Sebastian J Buss; Claudia Seyler; Claus Bruehl; Andreas Draguhn; Michael Koenen; Benjamin Meder; Hugo A Katus; Dierk Thomas
Journal:  J Am Coll Cardiol       Date:  2014-08-26       Impact factor: 24.094

4.  Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Authors:  P J Schwartz; S G Priori; C Spazzolini; A J Moss; G M Vincent; C Napolitano; I Denjoy; P Guicheney; G Breithardt; M T Keating; J A Towbin; A H Beggs; P Brink; A A Wilde; L Toivonen; W Zareba; J L Robinson; K W Timothy; V Corfield; D Wattanasirichaigoon; C Corbett; W Haverkamp; E Schulze-Bahr; M H Lehmann; K Schwartz; P Coumel; R Bloise
Journal:  Circulation       Date:  2001-01-02       Impact factor: 29.690

5.  Increased left ventricular mass and hypertrophy are associated with increased risk for sudden death.

Authors:  A W Haider; M G Larson; E J Benjamin; D Levy
Journal:  J Am Coll Cardiol       Date:  1998-11       Impact factor: 24.094

6.  Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Authors:  Q Wang; M E Curran; I Splawski; T C Burn; J M Millholland; T J VanRaay; J Shen; K W Timothy; G M Vincent; T de Jager; P J Schwartz; J A Toubin; A J Moss; D L Atkinson; G M Landes; T D Connors; M T Keating
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

Review 7.  Adrenergic regulation of the rapid component of the cardiac delayed rectifier potassium current, I(Kr), and the underlying hERG ion channel.

Authors:  Dierk Thomas; Johann Kiehn; Hugo A Katus; Christoph A Karle
Journal:  Basic Res Cardiol       Date:  2004-04-08       Impact factor: 17.165

Review 8.  Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing.

Authors:  Dierk Thomas; Johann Kiehn; Hugo A Katus; Christoph A Karle
Journal:  Cardiovasc Res       Date:  2003-11-01       Impact factor: 10.787

9.  A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

Authors:  M E Curran; I Splawski; K W Timothy; G M Vincent; E D Green; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

Review 10.  SCN5A and sinoatrial node pacemaker function.

Authors:  Ming Lei; Henggui Zhang; Andrew A Grace; Christopher L-H Huang
Journal:  Cardiovasc Res       Date:  2007-01-19       Impact factor: 10.787
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