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David J Tester

Showing results (31-40 of 212) with videos related to

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Heart Rhythm|September 2, 2018
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channelDan Ye, David J Tester, Wei Zhou, et al.
Heart Rhythm O2|October 20, 2021
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndromeJohn R Giudicessi, Joseph J Maleszewski, David J Tester, et al.
Pacing and Clinical Electrophysiology : PACE|July 25, 2003
Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndromeJan Nemec, Michael J Ackerman, David J Tester, et al.
Pediatric Cardiology|December 16, 2014
Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case seriesNupoor Narula, David J Tester, Anna Paulmichl, et al.
Heart Rhythm|December 31, 2022
Curcumin, a dietary natural supplement, prolongs the action potential duration of KCNE1-D85N-induced pluripotent stem cell-derived cardiomyocytesKatherine Martinez, Annabel Smith, Dan Ye, et al.
Heartrhythm Case Reports|March 21, 2019
Is variant pathogenicity in the eye of the beholder? A case of unexplained sudden cardiac arrest highlights the potentially dangerous role of historical rare variant compendia in <i>SCN5A</i> rare variant adjudicationMarissa J Stutzman, Dan Ye, David J Tester, et al.
Neurology|February 17, 2017
Congenital myopathy associated with the triadin knockout syndromeAndrew G Engel, Keeley R Redhage, David J Tester, et al.
Archives of Pathology & Laboratory Medicine|December 5, 2013
Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencingChristina G Loporcaro, David J Tester, Joseph J Maleszewski, et al.
Prenatal Diagnosis|August 24, 2017
Whole genome sequencing identifies etiology of recurrent male intrauterine fetal deathOmar Shehab, David J Tester, Nicholas C Ackerman, et al.
Circulation. Cardiovascular Genetics|October 8, 2017
Genomic Triangulation and Coverage Analysis in Whole-Exome Sequencing-Based Molecular AutopsiesGarrett W Shanks, David J Tester, Sneha Nishtala, et al.
Pageof 22

Showing results (31-40 of 212) with videos related to

Sort By:
Pageof 22
Heart Rhythm|September 2, 2018
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channelDan Ye, David J Tester, Wei Zhou, et al.
Heart Rhythm O2|October 20, 2021
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndromeJohn R Giudicessi, Joseph J Maleszewski, David J Tester, et al.
Pacing and Clinical Electrophysiology : PACE|July 25, 2003
Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndromeJan Nemec, Michael J Ackerman, David J Tester, et al.
Pediatric Cardiology|December 16, 2014
Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case seriesNupoor Narula, David J Tester, Anna Paulmichl, et al.
Heart Rhythm|December 31, 2022
Curcumin, a dietary natural supplement, prolongs the action potential duration of KCNE1-D85N-induced pluripotent stem cell-derived cardiomyocytesKatherine Martinez, Annabel Smith, Dan Ye, et al.
Heartrhythm Case Reports|March 21, 2019
Is variant pathogenicity in the eye of the beholder? A case of unexplained sudden cardiac arrest highlights the potentially dangerous role of historical rare variant compendia in <i>SCN5A</i> rare variant adjudicationMarissa J Stutzman, Dan Ye, David J Tester, et al.
Neurology|February 17, 2017
Congenital myopathy associated with the triadin knockout syndromeAndrew G Engel, Keeley R Redhage, David J Tester, et al.
Archives of Pathology & Laboratory Medicine|December 5, 2013
Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencingChristina G Loporcaro, David J Tester, Joseph J Maleszewski, et al.
Prenatal Diagnosis|August 24, 2017
Whole genome sequencing identifies etiology of recurrent male intrauterine fetal deathOmar Shehab, David J Tester, Nicholas C Ackerman, et al.
Circulation. Cardiovascular Genetics|October 8, 2017
Genomic Triangulation and Coverage Analysis in Whole-Exome Sequencing-Based Molecular AutopsiesGarrett W Shanks, David J Tester, Sneha Nishtala, et al.
Pageof 22