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

E Seidman

Showing results (481-490 of 533) with videos related to

Pageof 54
Sort By:
Circulation|January 28, 2020
Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic CardiomyopathyChristopher N Toepfer, Amanda C Garfinkel, Gabriela Venturini, et al.
Circulation. Genomic and Precision Medicine|May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart DiseaseMin Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Elife|October 15, 2020
<i>GATA6</i> mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragmArun Sharma, Lauren K Wasson, Jon Al Willcox, et al.
Scientific Reports|January 17, 2025
Contribution of hypoxia-inducible factor 1alpha to pathogenesis of sarcomeric hypertrophic cardiomyopathySarala Raj Murthi, Andreas Petry, Bachuki Shashikadze, et al.
Circulation|May 28, 2026
Integrative Molecular Analyses of Inflammatory and Autoimmune Signals in Cardiac SarcoidosisMeraj Neyazi, Gabriela Venturini, Kemar J Brown, et al.
Developmental Cell|December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart DiseaseIrfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
Cell|February 19, 2022
Transcription factor protein interactomes reveal genetic determinants in heart diseaseBarbara Gonzalez-Teran, Maureen Pittman, Franco Felix, et al.
Cell Metabolism|December 14, 2011
Heterozygosity for a loss-of-function mutation in GALNT2 improves plasma triglyceride clearance in manAdriaan G Holleboom, Helen Karlsson, Ruei-Shiuan Lin, et al.
Nature Genetics|July 15, 2009
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of FallotSteven C Greenway, Alexandre C Pereira, Jennifer C Lin, et al.
Circulation. Genomic and Precision Medicine|February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Pageof 54

Showing results (481-490 of 533) with videos related to

Sort By:
Pageof 54
Circulation|January 28, 2020
Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic CardiomyopathyChristopher N Toepfer, Amanda C Garfinkel, Gabriela Venturini, et al.
Circulation. Genomic and Precision Medicine|May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart DiseaseMin Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Elife|October 15, 2020
<i>GATA6</i> mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragmArun Sharma, Lauren K Wasson, Jon Al Willcox, et al.
Scientific Reports|January 17, 2025
Contribution of hypoxia-inducible factor 1alpha to pathogenesis of sarcomeric hypertrophic cardiomyopathySarala Raj Murthi, Andreas Petry, Bachuki Shashikadze, et al.
Circulation|May 28, 2026
Integrative Molecular Analyses of Inflammatory and Autoimmune Signals in Cardiac SarcoidosisMeraj Neyazi, Gabriela Venturini, Kemar J Brown, et al.
Developmental Cell|December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart DiseaseIrfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
Cell|February 19, 2022
Transcription factor protein interactomes reveal genetic determinants in heart diseaseBarbara Gonzalez-Teran, Maureen Pittman, Franco Felix, et al.
Cell Metabolism|December 14, 2011
Heterozygosity for a loss-of-function mutation in GALNT2 improves plasma triglyceride clearance in manAdriaan G Holleboom, Helen Karlsson, Ruei-Shiuan Lin, et al.
Nature Genetics|July 15, 2009
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of FallotSteven C Greenway, Alexandre C Pereira, Jennifer C Lin, et al.
Circulation. Genomic and Precision Medicine|February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Pageof 54