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Craig T January

Showing results (51-60 of 58) with videos related to

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Circulation. Arrhythmia and Electrophysiology|March 17, 2021
Long QT Syndrome <i>KCNH2</i> Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived CardiomyocytesLi Feng, Jianhua Zhang, ChangHwan Lee, et al.
The Journal of Clinical Investigation|June 14, 2008
Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndromeAhmad S Amin, Lucas J Herfst, Brian P Delisle, et al.
Molecular Pharmacology|April 4, 2020
LUF7244 plus Dofetilide Rescues Aberrant K<sub>v</sub>11.1 Trafficking and Produces Functional I<sub>Kv11.1</sub>Muge Qile, Yuan Ji, Tyona D Golden, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.
Stem Cell Reports|September 26, 2014
Calcium transients closely reflect prolonged action potentials in iPSC models of inherited cardiac arrhythmiaC Ian Spencer, Shiro Baba, Kenta Nakamura, et al.
Circulation|November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel functionStephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Circulation|July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular TachycardiaKevin Ng, Erron W Titus, Krystien V Lieve, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Circulation. Arrhythmia and Electrophysiology|March 17, 2021
Long QT Syndrome <i>KCNH2</i> Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived CardiomyocytesLi Feng, Jianhua Zhang, ChangHwan Lee, et al.
The Journal of Clinical Investigation|June 14, 2008
Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndromeAhmad S Amin, Lucas J Herfst, Brian P Delisle, et al.
Molecular Pharmacology|April 4, 2020
LUF7244 plus Dofetilide Rescues Aberrant K<sub>v</sub>11.1 Trafficking and Produces Functional I<sub>Kv11.1</sub>Muge Qile, Yuan Ji, Tyona D Golden, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.
Stem Cell Reports|September 26, 2014
Calcium transients closely reflect prolonged action potentials in iPSC models of inherited cardiac arrhythmiaC Ian Spencer, Shiro Baba, Kenta Nakamura, et al.
Circulation|November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel functionStephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Circulation|July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular TachycardiaKevin Ng, Erron W Titus, Krystien V Lieve, et al.
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