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 (431-440 of 533) with videos related to

Pageof 54
Sort By:
Mayo Clinic Proceedings|May 26, 2020
Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2-Mediated COVID-19J Martijn Bos, Virginia B Hebl, Ann L Oberg, et al.
Nature Genetics|February 20, 2024
Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart diseaseFeng Xiao, Xiaoran Zhang, Sarah U Morton, et al.
JCI Insight|June 18, 2026
Apelin analog treatment reverses severe pulmonary arterial hypertension and right ventricular heart failureJennie Vu, Pavel Zhabyeyev, Kemar J Brown, et al.
Circulation. Cardiovascular Imaging|September 18, 2014
Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathyGabriella Captur, Luis R Lopes, Timothy J Mohun, et al.
Circulation. Genomic and Precision Medicine|February 7, 2022
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or ObesitySarah U Morton, Alexandre C Pereira, Daniel Quiat, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Plos One|October 8, 2011
Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgeryAmanda A Fox, Mias Pretorius, Kuang-Yu Liu, et al.
Science Translational Medicine|March 8, 2019
Activin type II receptor signaling in cardiac aging and heart failureJason D Roh, Ryan Hobson, Vinita Chaudhari, et al.
JAMA Cardiology|February 28, 2017
The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet StudyCarolyn Y Ho, Sharlene M Day, Steven D Colan, et al.
Pageof 54

Showing results (431-440 of 533) with videos related to

Sort By:
Pageof 54
Mayo Clinic Proceedings|May 26, 2020
Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2-Mediated COVID-19J Martijn Bos, Virginia B Hebl, Ann L Oberg, et al.
Nature Genetics|February 20, 2024
Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart diseaseFeng Xiao, Xiaoran Zhang, Sarah U Morton, et al.
JCI Insight|June 18, 2026
Apelin analog treatment reverses severe pulmonary arterial hypertension and right ventricular heart failureJennie Vu, Pavel Zhabyeyev, Kemar J Brown, et al.
Circulation. Cardiovascular Imaging|September 18, 2014
Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathyGabriella Captur, Luis R Lopes, Timothy J Mohun, et al.
Circulation. Genomic and Precision Medicine|February 7, 2022
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or ObesitySarah U Morton, Alexandre C Pereira, Daniel Quiat, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Plos One|October 8, 2011
Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgeryAmanda A Fox, Mias Pretorius, Kuang-Yu Liu, et al.
Science Translational Medicine|March 8, 2019
Activin type II receptor signaling in cardiac aging and heart failureJason D Roh, Ryan Hobson, Vinita Chaudhari, et al.
JAMA Cardiology|February 28, 2017
The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet StudyCarolyn Y Ho, Sharlene M Day, Steven D Colan, et al.
Pageof 54