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Alfred L George

Showing results (111-120 of 296) with videos related to

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American Journal of Human Genetics|July 31, 2002
KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypesGregor Andelfinger, Andrew R Tapper, Richard C Welch, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 22, 2011
Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channelsHaifa Hallaq, Dao W Wang, Jennifer D Kunic, et al.
Journal of Molecular and Cellular Cardiology|May 13, 2014
Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca(2+) currents and promote proarrhythmic behavior in ventricular myocytesWorawan B Limpitikul, Ivy E Dick, Rosy Joshi-Mukherjee, et al.
Brain Research. Molecular Brain Research|July 11, 2002
Molecular, functional, and genomic characterization of human KCC2, the neuronal K-Cl cotransporterLuyan Song, Adriana Mercado, Norma Vázquez, et al.
Neurobiology of Disease|January 18, 2014
Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome miceAkshitkumar M Mistry, Christopher H Thompson, Alison R Miller, et al.
Heart Rhythm|April 27, 2005
Genetic susceptibility to acquired long QT syndrome: pharmacologic challenge in first-degree relativesPrince J Kannankeril, Dan M Roden, Kris J Norris, et al.
Annals of Clinical and Translational Neurology|January 22, 2025
Genotype-function-phenotype correlations for SCN1A variants identified by clinical genetic testingAndrew T Knox, Christopher H Thompson, Dillon Scott, et al.
BMC Medical Genetics|May 18, 2010
SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103TyrStacy A S Killen, Jennifer Kunic, Lily Wang, et al.
Journal of the American College of Cardiology|January 31, 2015
Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1Alberto Porta, Giulia Girardengo, Vlasta Bari, et al.
Biochemistry|September 26, 2007
Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndromeChanglin Tian, Carlos G Vanoye, Congbao Kang, et al.
Pageof 30

Showing results (111-120 of 296) with videos related to

Sort By:
Pageof 30
American Journal of Human Genetics|July 31, 2002
KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypesGregor Andelfinger, Andrew R Tapper, Richard C Welch, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 22, 2011
Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channelsHaifa Hallaq, Dao W Wang, Jennifer D Kunic, et al.
Journal of Molecular and Cellular Cardiology|May 13, 2014
Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca(2+) currents and promote proarrhythmic behavior in ventricular myocytesWorawan B Limpitikul, Ivy E Dick, Rosy Joshi-Mukherjee, et al.
Brain Research. Molecular Brain Research|July 11, 2002
Molecular, functional, and genomic characterization of human KCC2, the neuronal K-Cl cotransporterLuyan Song, Adriana Mercado, Norma Vázquez, et al.
Neurobiology of Disease|January 18, 2014
Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome miceAkshitkumar M Mistry, Christopher H Thompson, Alison R Miller, et al.
Heart Rhythm|April 27, 2005
Genetic susceptibility to acquired long QT syndrome: pharmacologic challenge in first-degree relativesPrince J Kannankeril, Dan M Roden, Kris J Norris, et al.
Annals of Clinical and Translational Neurology|January 22, 2025
Genotype-function-phenotype correlations for SCN1A variants identified by clinical genetic testingAndrew T Knox, Christopher H Thompson, Dillon Scott, et al.
BMC Medical Genetics|May 18, 2010
SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103TyrStacy A S Killen, Jennifer Kunic, Lily Wang, et al.
Journal of the American College of Cardiology|January 31, 2015
Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1Alberto Porta, Giulia Girardengo, Vlasta Bari, et al.
Biochemistry|September 26, 2007
Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndromeChanglin Tian, Carlos G Vanoye, Congbao Kang, et al.
Pageof 30