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David J Tester

Showing results (11-20 of 212) with videos related to

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Methodist Debakey Cardiovascular Journal|June 17, 2014
Genetics of long QT syndromeDavid J Tester, Michael J Ackerman
Heart Rhythm|October 29, 2005
Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjectsJonathan Sherman, David J Tester, Michael J Ackerman
The American Journal of Cardiology|March 17, 2004
Prenatal molecular genetic diagnosis of congenital long QT syndrome by strategic genotypingDavid J Tester, Jorge McCormack, Michael J Ackerman
Circulation. Genomic and Precision Medicine|May 13, 2018
Response by Kapplinger et al to Letter Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation"Jamie D Kapplinger, David J Tester, Michael J Ackerman
Revista Espanola De Cardiologia (English Ed.)|April 30, 2014
Personalized medicine: genetic diagnosis for inherited cardiomyopathies/channelopathiesMichael J Ackerman, Cherisse A Marcou, David J Tester
Methods in Molecular Medicine|October 31, 2006
Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencingDavid J Tester, Melissa L Will, Michael J Ackerman
Herzschrittmachertherapie & Elektrophysiologie|September 21, 2012
The molecular autopsy: an indispensable step following sudden cardiac death in the young?Nicole J Boczek, David J Tester, Michael J Ackerman
Heart Rhythm|May 3, 2008
Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndromeDavid W Van Norstrand, David J Tester, Michael J Ackerman
International Journal of Cardiology|May 11, 2020
Discovery and characterization of a monogenetic insult, caveolin-3-V37L, that precipitated oligo-proteomic perturbations governing repolarization reserveDan Ye, Wei Zhou, David J Tester, et al.
Heart Rhythm|May 14, 2020
Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcriptDaniel J Clemens, David J Tester, Isabelle Marty, et al.
Pageof 22

Showing results (11-20 of 212) with videos related to

Sort By:
Pageof 22
Methodist Debakey Cardiovascular Journal|June 17, 2014
Genetics of long QT syndromeDavid J Tester, Michael J Ackerman
Heart Rhythm|October 29, 2005
Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjectsJonathan Sherman, David J Tester, Michael J Ackerman
The American Journal of Cardiology|March 17, 2004
Prenatal molecular genetic diagnosis of congenital long QT syndrome by strategic genotypingDavid J Tester, Jorge McCormack, Michael J Ackerman
Circulation. Genomic and Precision Medicine|May 13, 2018
Response by Kapplinger et al to Letter Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation"Jamie D Kapplinger, David J Tester, Michael J Ackerman
Revista Espanola De Cardiologia (English Ed.)|April 30, 2014
Personalized medicine: genetic diagnosis for inherited cardiomyopathies/channelopathiesMichael J Ackerman, Cherisse A Marcou, David J Tester
Methods in Molecular Medicine|October 31, 2006
Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencingDavid J Tester, Melissa L Will, Michael J Ackerman
Herzschrittmachertherapie & Elektrophysiologie|September 21, 2012
The molecular autopsy: an indispensable step following sudden cardiac death in the young?Nicole J Boczek, David J Tester, Michael J Ackerman
Heart Rhythm|May 3, 2008
Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndromeDavid W Van Norstrand, David J Tester, Michael J Ackerman
International Journal of Cardiology|May 11, 2020
Discovery and characterization of a monogenetic insult, caveolin-3-V37L, that precipitated oligo-proteomic perturbations governing repolarization reserveDan Ye, Wei Zhou, David J Tester, et al.
Heart Rhythm|May 14, 2020
Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcriptDaniel J Clemens, David J Tester, Isabelle Marty, et al.
Pageof 22