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Showing results (111-120 of 172) with videos related to

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Cardiovascular Research|June 28, 2003
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarizationConnie R Bezzina, Arie O Verkerk, Andreas Busjahn, et al.
NPJ Genomic Medicine|June 12, 2021
Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseasesFelix P Chilunga, Peter Henneman, Andrea Venema, et al.
European Journal of Human Genetics : EJHG|June 11, 2009
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cellsJet Bliek, Marielle Alders, Saskia M Maas, et al.
Molecular Human Reproduction|September 13, 2003
Chromosomal region 11p15 is associated with male factor subfertilityJudith Gianotten, Fulco van der Veen, Mariëlle Alders, et al.
Journal of Molecular and Cellular Cardiology|May 25, 2005
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two familiesJeroen P P Smits, Tamara T Koopmann, Ronald Wilders, et al.
Heart Rhythm|June 25, 2011
Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor geneEyal Nof, Bernard Belhassen, Michael Arad, et al.
Atherosclerosis|May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosisA A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Cardiovascular Research|July 27, 2005
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndromeArie O Verkerk, Ronald Wilders, Eric Schulze-Bahr, et al.
Biochimica Et Biophysica Acta|November 14, 2012
A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin bindingJudith B A van de Meerakker, Imke Christiaans, Phil Barnett, et al.
American Journal of Human Genetics|March 17, 2009
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillationMarielle Alders, Tamara T Koopmann, Imke Christiaans, et al.
Pageof 18

Showing results (111-120 of 172) with videos related to

Sort By:
Pageof 18
Cardiovascular Research|June 28, 2003
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarizationConnie R Bezzina, Arie O Verkerk, Andreas Busjahn, et al.
NPJ Genomic Medicine|June 12, 2021
Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseasesFelix P Chilunga, Peter Henneman, Andrea Venema, et al.
European Journal of Human Genetics : EJHG|June 11, 2009
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cellsJet Bliek, Marielle Alders, Saskia M Maas, et al.
Molecular Human Reproduction|September 13, 2003
Chromosomal region 11p15 is associated with male factor subfertilityJudith Gianotten, Fulco van der Veen, Mariëlle Alders, et al.
Journal of Molecular and Cellular Cardiology|May 25, 2005
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two familiesJeroen P P Smits, Tamara T Koopmann, Ronald Wilders, et al.
Heart Rhythm|June 25, 2011
Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor geneEyal Nof, Bernard Belhassen, Michael Arad, et al.
Atherosclerosis|May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosisA A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Cardiovascular Research|July 27, 2005
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndromeArie O Verkerk, Ronald Wilders, Eric Schulze-Bahr, et al.
Biochimica Et Biophysica Acta|November 14, 2012
A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin bindingJudith B A van de Meerakker, Imke Christiaans, Phil Barnett, et al.
American Journal of Human Genetics|March 17, 2009
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillationMarielle Alders, Tamara T Koopmann, Imke Christiaans, et al.
Pageof 18