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Matteo Vatta

Showing results (91-100 of 124) with videos related to

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Circulation|October 25, 2006
Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndromeMatteo Vatta, Michael J Ackerman, Bin Ye, et al.
Human Molecular Genetics|February 2, 2002
Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndromeMatteo Vatta, Robert Dumaine, George Varghese, et al.
Journal of the American College of Cardiology|July 18, 2009
ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy geneMousumi Moulik, Matteo Vatta, Stephanie H Witt, et al.
JAMA Cardiology|August 10, 2022
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic TestingLisa M Dellefave-Castillo, Allison L Cirino, Thomas E Callis, et al.
Cardiovascular Toxicology|October 19, 2007
Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathyEnkhsaikhan Purevjav, David P Nelson, Jacquelin J Varela, et al.
Plos One|January 16, 2016
Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing PanelPatrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, et al.
Plos One|December 5, 2015
Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing PanelPatrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, et al.
HGG Advances|January 14, 2024
Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assayKate L Thomson, Connie Jiang, Ebony Richardson, et al.
Molecular Genetics & Genomic Medicine|August 21, 2020
Novel heterozygous truncating titin variants affecting the A-band are associated with cardiomyopathy and myopathy/muscular dystrophyKelly A Rich, Tia Moscarello, Carly Siskind, et al.
Circulation. Cardiovascular Genetics|February 23, 2010
LAMP2 microdeletions in patients with Danon diseaseZhao Yang, Birgit H Funke, Linda H Cripe, et al.
Pageof 13

Showing results (91-100 of 124) with videos related to

Sort By:
Pageof 13
Circulation|October 25, 2006
Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndromeMatteo Vatta, Michael J Ackerman, Bin Ye, et al.
Human Molecular Genetics|February 2, 2002
Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndromeMatteo Vatta, Robert Dumaine, George Varghese, et al.
Journal of the American College of Cardiology|July 18, 2009
ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy geneMousumi Moulik, Matteo Vatta, Stephanie H Witt, et al.
JAMA Cardiology|August 10, 2022
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic TestingLisa M Dellefave-Castillo, Allison L Cirino, Thomas E Callis, et al.
Cardiovascular Toxicology|October 19, 2007
Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathyEnkhsaikhan Purevjav, David P Nelson, Jacquelin J Varela, et al.
Plos One|January 16, 2016
Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing PanelPatrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, et al.
Plos One|December 5, 2015
Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing PanelPatrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, et al.
HGG Advances|January 14, 2024
Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assayKate L Thomson, Connie Jiang, Ebony Richardson, et al.
Molecular Genetics & Genomic Medicine|August 21, 2020
Novel heterozygous truncating titin variants affecting the A-band are associated with cardiomyopathy and myopathy/muscular dystrophyKelly A Rich, Tia Moscarello, Carly Siskind, et al.
Circulation. Cardiovascular Genetics|February 23, 2010
LAMP2 microdeletions in patients with Danon diseaseZhao Yang, Birgit H Funke, Linda H Cripe, et al.
Pageof 13