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The Journal of Biological Chemistry
|
April 15, 2008
A mutation in telethonin alters Nav1.5 function
Amelia Mazzone, Peter R Strege, David J Tester, et al.
Journal of the American College of Cardiology
|
November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis
Argelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
December 6, 2008
Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy
Yuri A Saito, Peter R Strege, David J Tester, et al.
Circulation
|
November 9, 2012
Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: interaction of trafficking and gating
Sadguna Y Balijepalli, Evi Lim, Sarah P Concannon, et al.
Circulation. Genomic and Precision Medicine
|
May 22, 2019
Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance
John R Giudicessi, Krystien V V Lieve, Ram K Rohatgi, et al.
JCI Insight
|
March 15, 2017
Elucidation of <i>MRAS</i>-mediated Noonan syndrome with cardiac hypertrophy
Erin M Higgins, J Martijn Bos, Heather Mason-Suares, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
April 6, 2010
Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytes
Eric C Lin, Katherine M Holzem, Blake D Anson, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics
|
August 6, 2021
Mapping human calreticulin regions important for structural stability
Evaldas Čiplys, Tautvydas Paškevičius, Eimantas Žitkus, et al.
Heart Rhythm
|
November 19, 2021
A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome
Sahej Bains, Steven M Dotzler, Christian Krijger, et al.
Molecular Pharmacology
|
April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndrome
Brian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
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of 22
Search research articles
Search
Showing results (141-150 of 212) with videos related to
Sort By:
Page
of 22
The Journal of Biological Chemistry
|
April 15, 2008
A mutation in telethonin alters Nav1.5 function
Amelia Mazzone, Peter R Strege, David J Tester, et al.
Journal of the American College of Cardiology
|
November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis
Argelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
December 6, 2008
Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy
Yuri A Saito, Peter R Strege, David J Tester, et al.
Circulation
|
November 9, 2012
Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: interaction of trafficking and gating
Sadguna Y Balijepalli, Evi Lim, Sarah P Concannon, et al.
Circulation. Genomic and Precision Medicine
|
May 22, 2019
Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance
John R Giudicessi, Krystien V V Lieve, Ram K Rohatgi, et al.
JCI Insight
|
March 15, 2017
Elucidation of <i>MRAS</i>-mediated Noonan syndrome with cardiac hypertrophy
Erin M Higgins, J Martijn Bos, Heather Mason-Suares, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
April 6, 2010
Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytes
Eric C Lin, Katherine M Holzem, Blake D Anson, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics
|
August 6, 2021
Mapping human calreticulin regions important for structural stability
Evaldas Čiplys, Tautvydas Paškevičius, Eimantas Žitkus, et al.
Heart Rhythm
|
November 19, 2021
A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome
Sahej Bains, Steven M Dotzler, Christian Krijger, et al.
Molecular Pharmacology
|
April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndrome
Brian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
Page
of 22