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David J Tester

Showing results (51-60 of 212) with videos related to

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Biochemical and Biophysical Research Communications|November 23, 2006
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytesSandro L Yong, Ying Ni, Teng Zhang, et al.
The American Journal of Cardiology|October 6, 2010
Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testingDavid J Tester, Amber J Benton, Laura Train, et al.
Heartrhythm Case Reports|June 8, 2018
Even pore-localizing missense variants at highly conserved sites in <i>KCNQ1</i>-encoded K<sub>v</sub>7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretationAshley Paquin, Dan Ye, David J Tester, et al.
The Journal of Thoracic and Cardiovascular Surgery|July 31, 2007
Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysmsStephen H McKellar, David J Tester, Marineh Yagubyan, 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|February 25, 2020
Prevalence and electrophysiological phenotype of rare SCN5A genetic variants identified in unexplained sudden cardiac arrest survivorsJohn R Giudicessi, Dan Ye, Marissa J Stutzman, et al.
Heart Rhythm|January 3, 2022
Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemicSamantha K Hamrick, C S John Kim, David J Tester, et al.
Circulation. Cardiovascular Genetics|August 13, 2011
Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndromeDavid J Tester, Bi-Hua Tan, Argelia Medeiros-Domingo, et al.
Mayo Clinic Proceedings|April 3, 2019
A Novel Truncating Variant in FLNC-Encoded Filamin C May Serve as a Proarrhythmic Genetic Substrate for Arrhythmogenic Bileaflet Mitral Valve Prolapse SyndromeSahej Bains, David J Tester, Samuel J Asirvatham, et al.
Circulation|October 7, 2004
Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromesGrace Choi, Laura J Kopplin, David J Tester, et al.
Heart Rhythm|May 3, 2008
Prevalence of early-onset atrial fibrillation in congenital long QT syndromeJonathan N Johnson, David J Tester, James Perry, et al.
Pageof 22

Showing results (51-60 of 212) with videos related to

Sort By:
Pageof 22
Biochemical and Biophysical Research Communications|November 23, 2006
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytesSandro L Yong, Ying Ni, Teng Zhang, et al.
The American Journal of Cardiology|October 6, 2010
Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testingDavid J Tester, Amber J Benton, Laura Train, et al.
Heartrhythm Case Reports|June 8, 2018
Even pore-localizing missense variants at highly conserved sites in <i>KCNQ1</i>-encoded K<sub>v</sub>7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretationAshley Paquin, Dan Ye, David J Tester, et al.
The Journal of Thoracic and Cardiovascular Surgery|July 31, 2007
Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysmsStephen H McKellar, David J Tester, Marineh Yagubyan, 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|February 25, 2020
Prevalence and electrophysiological phenotype of rare SCN5A genetic variants identified in unexplained sudden cardiac arrest survivorsJohn R Giudicessi, Dan Ye, Marissa J Stutzman, et al.
Heart Rhythm|January 3, 2022
Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemicSamantha K Hamrick, C S John Kim, David J Tester, et al.
Circulation. Cardiovascular Genetics|August 13, 2011
Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndromeDavid J Tester, Bi-Hua Tan, Argelia Medeiros-Domingo, et al.
Mayo Clinic Proceedings|April 3, 2019
A Novel Truncating Variant in FLNC-Encoded Filamin C May Serve as a Proarrhythmic Genetic Substrate for Arrhythmogenic Bileaflet Mitral Valve Prolapse SyndromeSahej Bains, David J Tester, Samuel J Asirvatham, et al.
Circulation|October 7, 2004
Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromesGrace Choi, Laura J Kopplin, David J Tester, et al.
Heart Rhythm|May 3, 2008
Prevalence of early-onset atrial fibrillation in congenital long QT syndromeJonathan N Johnson, David J Tester, James Perry, et al.
Pageof 22