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Showing results (381-390 of 402) with videos related to

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Cardiology|November 14, 2012
Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutationJasper J van der Smagt, Paul A van der Zwaag, J Peter van Tintelen, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Circulation|January 28, 2020
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT SyndromeArnon Adler, Valeria Novelli, Ahmad S Amin, et al.
European Journal of Immunology|February 4, 2009
DMBT1 functions as pattern-recognition molecule for poly-sulfated and poly-phosphorylated ligandsCaroline End, Floris Bikker, Marcus Renner, et al.
Poultry Science|December 7, 2016
Results of an international phosphorus digestibility ring test with broiler chickensM Rodehutscord, O Adeola, R Angel, et al.
Heart Rhythm|August 5, 2014
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathyJudith A Groeneweg, Amber Ummels, Marcel Mulder, et al.
Clinical Genetics|June 25, 2010
Haplotype sharing test maps genes for familial cardiomyopathiesP A van der Zwaag, J P van Tintelen, F Gerbens, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|February 9, 2011
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasiaP A van der Zwaag, M G P J Cox, C van der Werf, et al.
Circulation. Arrhythmia and Electrophysiology|July 13, 2012
Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relativesChristian van der Werf, Ineke Nederend, Nynke Hofman, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
Pageof 41

Showing results (381-390 of 402) with videos related to

Sort By:
Pageof 41
Cardiology|November 14, 2012
Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutationJasper J van der Smagt, Paul A van der Zwaag, J Peter van Tintelen, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Circulation|January 28, 2020
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT SyndromeArnon Adler, Valeria Novelli, Ahmad S Amin, et al.
European Journal of Immunology|February 4, 2009
DMBT1 functions as pattern-recognition molecule for poly-sulfated and poly-phosphorylated ligandsCaroline End, Floris Bikker, Marcus Renner, et al.
Poultry Science|December 7, 2016
Results of an international phosphorus digestibility ring test with broiler chickensM Rodehutscord, O Adeola, R Angel, et al.
Heart Rhythm|August 5, 2014
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathyJudith A Groeneweg, Amber Ummels, Marcel Mulder, et al.
Clinical Genetics|June 25, 2010
Haplotype sharing test maps genes for familial cardiomyopathiesP A van der Zwaag, J P van Tintelen, F Gerbens, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|February 9, 2011
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasiaP A van der Zwaag, M G P J Cox, C van der Werf, et al.
Circulation. Arrhythmia and Electrophysiology|July 13, 2012
Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relativesChristian van der Werf, Ineke Nederend, Nynke Hofman, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
Pageof 41