Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Neil E Bowles

Showing results (31-40 of 65) with videos related to

Pageof 7
Sort By:
Human Molecular Genetics|October 21, 2005
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathyKathryn M Meurs, Ximena Sanchez, Ryan M David, et al.
Molecular Genetics and Metabolism|December 7, 2002
Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompactionRui Chen, Tohru Tsuji, Fukiko Ichida, et al.
Molecular Genetics and Metabolism|June 3, 2004
Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12Alexander B Kenton, Ximena Sanchez, Karen J Coveler, et al.
Journal of the American Heart Association|September 1, 2017
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular NoncompactionCe Wang, Yukiko Hata, Keiichi Hirono, et al.
Molecular Genetics and Metabolism|October 23, 2010
Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden deathBo Chang, Tsutomu Nishizawa, Michiko Furutani, 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.
Molecular Genetics and Metabolism|March 28, 2008
SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmiaLishen Shan, Naomasa Makita, Yanlin Xing, 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.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 14, 2017
A Functional Assay for Sick Sinus Syndrome Genetic VariantsChuanchau J Jou, Cammon B Arrington, Spencer Barnett, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 21, 2005
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathyKathryn M Meurs, Ximena Sanchez, Ryan M David, et al.
Molecular Genetics and Metabolism|December 7, 2002
Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompactionRui Chen, Tohru Tsuji, Fukiko Ichida, et al.
Molecular Genetics and Metabolism|June 3, 2004
Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12Alexander B Kenton, Ximena Sanchez, Karen J Coveler, et al.
Journal of the American Heart Association|September 1, 2017
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular NoncompactionCe Wang, Yukiko Hata, Keiichi Hirono, et al.
Molecular Genetics and Metabolism|October 23, 2010
Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden deathBo Chang, Tsutomu Nishizawa, Michiko Furutani, 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.
Molecular Genetics and Metabolism|March 28, 2008
SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmiaLishen Shan, Naomasa Makita, Yanlin Xing, 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.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 14, 2017
A Functional Assay for Sick Sinus Syndrome Genetic VariantsChuanchau J Jou, Cammon B Arrington, Spencer Barnett, et al.
Pageof 7