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Proceedings of the National Academy of Sciences of the United States of America
|
December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulation
Matthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Plos One
|
September 4, 2014
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesis
Jessica A Hennessey, Nicole J Boczek, Yong-Hui Jiang, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 13, 2016
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks
Nieves Gomez-Hurtado, Nicole J Boczek, Dmytro O Kryshtal, et al.
Circulation Research
|
October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome
Worawan B Limpitikul, Ivy E Dick, David J Tester, et al.
The Journal of Pediatrics
|
October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome
David J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology
|
May 19, 2007
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans
Andrew P Landstrom, Noah Weisleder, Karin B Batalden, et al.
Biorxiv : the Preprint Server for Biology
|
March 11, 2024
A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic Cardiomyopathy
Ramin Garmany, Surendra Dasari, J Martijn Bos, et al.
Heart Rhythm
|
April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Michael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Biochemistry
|
October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation
Don E Burgess, Daniel C Bartos, Allison R Reloj, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5
Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
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Search research articles
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Showing results (171-180 of 212) with videos related to
Sort By:
Page
of 22
Proceedings of the National Academy of Sciences of the United States of America
|
December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulation
Matthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Plos One
|
September 4, 2014
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesis
Jessica A Hennessey, Nicole J Boczek, Yong-Hui Jiang, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 13, 2016
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks
Nieves Gomez-Hurtado, Nicole J Boczek, Dmytro O Kryshtal, et al.
Circulation Research
|
October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome
Worawan B Limpitikul, Ivy E Dick, David J Tester, et al.
The Journal of Pediatrics
|
October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome
David J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology
|
May 19, 2007
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans
Andrew P Landstrom, Noah Weisleder, Karin B Batalden, et al.
Biorxiv : the Preprint Server for Biology
|
March 11, 2024
A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic Cardiomyopathy
Ramin Garmany, Surendra Dasari, J Martijn Bos, et al.
Heart Rhythm
|
April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Michael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Biochemistry
|
October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation
Don E Burgess, Daniel C Bartos, Allison R Reloj, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5
Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Page
of 22