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Verkerk

Showing results (711-720 of 778) with videos related to

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Circulation|April 14, 2018
RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium HandlingMaarten M G van den Hoogenhof, Abdelaziz Beqqali, Ahmad S Amin, et al.
Circulation|November 4, 2005
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational studyRuben Coronel, Simona Casini, Tamara T Koopmann, et al.
European Journal of Human Genetics : EJHG|January 28, 2018
CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disabilityAnnemieke J M H Verkerk, Shimriet Zeidler, Guido Breedveld, et al.
Basic Research in Cardiology|March 4, 2009
The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardiumC A Remme, A O Verkerk, W M H Hoogaars, et al.
Nature|April 15, 2026
Prospective evaluation of genomics-guided off-label treatmentK Verkerk, A C Spiekman, S F Haj Mohammad, et al.
Circulation Research|December 14, 2023
The Role of <i>MAPRE2</i> and Microtubules in Maintaining Normal Ventricular ConductionDavid Y Chiang, Arie O Verkerk, Rachelle Victorio, et al.
International Journal of Molecular Sciences|April 12, 2020
Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation IntermediatesSuzan J G Knottnerus, Isabella Mengarelli, Rob C I Wüst, et al.
Cardiovascular Research|March 16, 2012
T-box transcription factor TBX3 reprogrammes mature cardiac myocytes into pacemaker-like cellsMartijn L Bakker, Gerard J J Boink, Bas J Boukens, et al.
Science (New York, N.Y.)|May 18, 2023
Interplay between calcium and sarcomeres directs cardiomyocyte maturation during regenerationPhong D Nguyen, Iris Gooijers, Giulia Campostrini, et al.
Molecular Syndromology|October 30, 2010
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1AR Oegema, A de Klein, A J Verkerk, et al.
Pageof 78

Showing results (711-720 of 778) with videos related to

Sort By:
Pageof 78
Circulation|April 14, 2018
RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium HandlingMaarten M G van den Hoogenhof, Abdelaziz Beqqali, Ahmad S Amin, et al.
Circulation|November 4, 2005
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational studyRuben Coronel, Simona Casini, Tamara T Koopmann, et al.
European Journal of Human Genetics : EJHG|January 28, 2018
CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disabilityAnnemieke J M H Verkerk, Shimriet Zeidler, Guido Breedveld, et al.
Basic Research in Cardiology|March 4, 2009
The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardiumC A Remme, A O Verkerk, W M H Hoogaars, et al.
Nature|April 15, 2026
Prospective evaluation of genomics-guided off-label treatmentK Verkerk, A C Spiekman, S F Haj Mohammad, et al.
Circulation Research|December 14, 2023
The Role of <i>MAPRE2</i> and Microtubules in Maintaining Normal Ventricular ConductionDavid Y Chiang, Arie O Verkerk, Rachelle Victorio, et al.
International Journal of Molecular Sciences|April 12, 2020
Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation IntermediatesSuzan J G Knottnerus, Isabella Mengarelli, Rob C I Wüst, et al.
Cardiovascular Research|March 16, 2012
T-box transcription factor TBX3 reprogrammes mature cardiac myocytes into pacemaker-like cellsMartijn L Bakker, Gerard J J Boink, Bas J Boukens, et al.
Science (New York, N.Y.)|May 18, 2023
Interplay between calcium and sarcomeres directs cardiomyocyte maturation during regenerationPhong D Nguyen, Iris Gooijers, Giulia Campostrini, et al.
Molecular Syndromology|October 30, 2010
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1AR Oegema, A de Klein, A J Verkerk, et al.
Pageof 78