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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndrome
Belinda Gray, David J Tester, Leonie Ch Wong, et al.
Journal of the American College of Cardiology
|
March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome
David J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology
|
September 10, 2024
A multi-omics atlas of sex-specific differences in obstructive hypertrophic cardiomyopathy
Ramin Garmany, Surendra Dasari, J Martijn Bos, et al.
Circulation Research
|
June 26, 2014
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome
Nicole J Boczek, Dan Ye, Eric K Johnson, et al.
JCI Insight
|
July 15, 2020
Molecular characterization of the calcium release channel deficiency syndrome
David J Tester, C S John Kim, Samantha K Hamrick, et al.
Circulation. Genomic and Precision Medicine
|
February 21, 2023
Multi-Omic Architecture of Obstructive Hypertrophic Cardiomyopathy
Ramin Garmany, J Martijn Bos, David J Tester, et al.
Heart Rhythm
|
December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents
Dan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, 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 Channel
Jennifer L Smith, David J Tester, Allison R Hall, et al.
Circulation. Cardiovascular Genetics
|
March 13, 2016
Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G
Nicole J Boczek, Nieves Gomez-Hurtado, Dan Ye, et al.
Heart Rhythm
|
July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)
Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
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Search research articles
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Showing results (181-190 of 212) with videos related to
Sort By:
Page
of 22
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndrome
Belinda Gray, David J Tester, Leonie Ch Wong, et al.
Journal of the American College of Cardiology
|
March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome
David J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology
|
September 10, 2024
A multi-omics atlas of sex-specific differences in obstructive hypertrophic cardiomyopathy
Ramin Garmany, Surendra Dasari, J Martijn Bos, et al.
Circulation Research
|
June 26, 2014
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome
Nicole J Boczek, Dan Ye, Eric K Johnson, et al.
JCI Insight
|
July 15, 2020
Molecular characterization of the calcium release channel deficiency syndrome
David J Tester, C S John Kim, Samantha K Hamrick, et al.
Circulation. Genomic and Precision Medicine
|
February 21, 2023
Multi-Omic Architecture of Obstructive Hypertrophic Cardiomyopathy
Ramin Garmany, J Martijn Bos, David J Tester, et al.
Heart Rhythm
|
December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents
Dan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, 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 Channel
Jennifer L Smith, David J Tester, Allison R Hall, et al.
Circulation. Cardiovascular Genetics
|
March 13, 2016
Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G
Nicole J Boczek, Nieves Gomez-Hurtado, Dan Ye, et al.
Heart Rhythm
|
July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)
Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
Page
of 22