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David J Tester

Showing results (151-160 of 212) with videos related to

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Journal of Cardiovascular Translational Research|February 24, 2019
Induced Pluripotent Stem Cell-Derived Cardiomyocytes from a Patient with MYL2-R58Q-Mediated Apical Hypertrophic Cardiomyopathy Show Hypertrophy, Myofibrillar Disarray, and Calcium PerturbationsWei Zhou, J Martijn Bos, Dan Ye, et al.
Journal of Cell Science|March 7, 2018
Localization and functional consequences of a direct interaction between TRIOBP-1 and hERG proteins in the heartDavid K Jones, Ashley C Johnson, Elon C Roti Roti, et al.
Journal of the American College of Cardiology|July 31, 2012
Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testingLia Crotti, Cherisse A Marcou, David J Tester, et al.
Scientific Reports|September 1, 2023
Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathyRamin Garmany, J Martijn Bos, Surendra Dasari, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Elucidation of <i>ALG10B</i> as a Novel Long-QT Syndrome-Susceptibility GeneWei Zhou, Dan Ye, David J Tester, et al.
Heart Rhythm|October 8, 2013
FGF12 is a candidate Brugada syndrome locusJessica A Hennessey, Cherisse A Marcou, Chuan Wang, et al.
Mayo Clinic Proceedings|October 7, 2016
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern ChinaLiyong Zhang, David J Tester, Di Lang, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Circulation. Arrhythmia and Electrophysiology|December 17, 2009
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Circulation|June 27, 2007
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndromeArgelia Medeiros-Domingo, Toshihiko Kaku, David J Tester, et al.
Pageof 22

Showing results (151-160 of 212) with videos related to

Sort By:
Pageof 22
Journal of Cardiovascular Translational Research|February 24, 2019
Induced Pluripotent Stem Cell-Derived Cardiomyocytes from a Patient with MYL2-R58Q-Mediated Apical Hypertrophic Cardiomyopathy Show Hypertrophy, Myofibrillar Disarray, and Calcium PerturbationsWei Zhou, J Martijn Bos, Dan Ye, et al.
Journal of Cell Science|March 7, 2018
Localization and functional consequences of a direct interaction between TRIOBP-1 and hERG proteins in the heartDavid K Jones, Ashley C Johnson, Elon C Roti Roti, et al.
Journal of the American College of Cardiology|July 31, 2012
Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testingLia Crotti, Cherisse A Marcou, David J Tester, et al.
Scientific Reports|September 1, 2023
Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathyRamin Garmany, J Martijn Bos, Surendra Dasari, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Elucidation of <i>ALG10B</i> as a Novel Long-QT Syndrome-Susceptibility GeneWei Zhou, Dan Ye, David J Tester, et al.
Heart Rhythm|October 8, 2013
FGF12 is a candidate Brugada syndrome locusJessica A Hennessey, Cherisse A Marcou, Chuan Wang, et al.
Mayo Clinic Proceedings|October 7, 2016
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern ChinaLiyong Zhang, David J Tester, Di Lang, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Circulation. Arrhythmia and Electrophysiology|December 17, 2009
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Circulation|June 27, 2007
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndromeArgelia Medeiros-Domingo, Toshihiko Kaku, David J Tester, et al.
Pageof 22