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David J Tester

Showing results (201-210 of 212) with videos related to

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Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
European Heart Journal|August 8, 2024
KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndromeSahej Bains, Lucilla Giammarino, Saranda Nimani, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 14, 2019
Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding siteGreg J Mellor, Pankaj Panwar, Andrea K Lee, et al.
European Heart Journal|August 30, 2025
AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndromeSaranda Nimani, Sahej Bains, Nicolò Alerni, et al.
Circulation. Arrhythmia and Electrophysiology|August 11, 2017
Loss-of-Function <i>KCNE2</i> Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?Jason D Roberts, Andrew D Krahn, Michael J Ackerman, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel diseaseMichael W T Tanck, Yanushi D Wijeyeratne, Julien Barc, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
Circulation. Genomic and Precision Medicine|November 9, 2020
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> FamiliesYanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Pageof 22

Showing results (201-210 of 212) with videos related to

Sort By:
Pageof 22
Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
European Heart Journal|August 8, 2024
KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndromeSahej Bains, Lucilla Giammarino, Saranda Nimani, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 14, 2019
Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding siteGreg J Mellor, Pankaj Panwar, Andrea K Lee, et al.
European Heart Journal|August 30, 2025
AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndromeSaranda Nimani, Sahej Bains, Nicolò Alerni, et al.
Circulation. Arrhythmia and Electrophysiology|August 11, 2017
Loss-of-Function <i>KCNE2</i> Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?Jason D Roberts, Andrew D Krahn, Michael J Ackerman, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel diseaseMichael W T Tanck, Yanushi D Wijeyeratne, Julien Barc, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
Circulation. Genomic and Precision Medicine|November 9, 2020
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> FamiliesYanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Pageof 22