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 (451-460 of 533) with videos related to

Pageof 54
Sort By:
Molecular Systems Biology|June 24, 2010
Dissecting spatio-temporal protein networks driving human heart development and related disordersKasper Lage, Kjeld Møllgård, Steven Greenway, et al.
Plos Genetics|November 20, 2020
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profilesAlejandro Martin-Trujillo, Nihir Patel, Felix Richter, et al.
Circulation. Genomic and Precision Medicine|December 7, 2020
Associations Between Female Sex, Sarcomere Variants, and Clinical Outcomes in Hypertrophic CardiomyopathyNeal K Lakdawala, Iacopo Olivotto, Sharlene M Day, et al.
Nature Cardiovascular Research|August 28, 2024
An engineered human cardiac tissue model reveals contributions of systemic lupus erythematosus autoantibodies to myocardial injurySharon Fleischer, Trevor R Nash, Manuel A Tamargo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Journal of Crohn'S & Colitis|May 29, 2019
Phenotypic Variation in Paediatric Inflammatory Bowel Disease by Age: A Multicentre Prospective Inception Cohort Study of the Canadian Children IBD NetworkJ Dhaliwal, T D Walters, D R Mack, et al.
Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Molecular & Cellular Proteomics : MCP|December 7, 2007
Comparative proteomics profiling of a phospholamban mutant mouse model of dilated cardiomyopathy reveals progressive intracellular stress responsesAnthony O Gramolini, Thomas Kislinger, Rasoul Alikhani-Koopaei, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2022
An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populationsDaniel Quiat, Seong Won Kim, Qi Zhang, et al.
Pageof 54

Showing results (451-460 of 533) with videos related to

Sort By:
Pageof 54
Molecular Systems Biology|June 24, 2010
Dissecting spatio-temporal protein networks driving human heart development and related disordersKasper Lage, Kjeld Møllgård, Steven Greenway, et al.
Plos Genetics|November 20, 2020
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profilesAlejandro Martin-Trujillo, Nihir Patel, Felix Richter, et al.
Circulation. Genomic and Precision Medicine|December 7, 2020
Associations Between Female Sex, Sarcomere Variants, and Clinical Outcomes in Hypertrophic CardiomyopathyNeal K Lakdawala, Iacopo Olivotto, Sharlene M Day, et al.
Nature Cardiovascular Research|August 28, 2024
An engineered human cardiac tissue model reveals contributions of systemic lupus erythematosus autoantibodies to myocardial injurySharon Fleischer, Trevor R Nash, Manuel A Tamargo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Journal of Crohn'S & Colitis|May 29, 2019
Phenotypic Variation in Paediatric Inflammatory Bowel Disease by Age: A Multicentre Prospective Inception Cohort Study of the Canadian Children IBD NetworkJ Dhaliwal, T D Walters, D R Mack, et al.
Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Molecular & Cellular Proteomics : MCP|December 7, 2007
Comparative proteomics profiling of a phospholamban mutant mouse model of dilated cardiomyopathy reveals progressive intracellular stress responsesAnthony O Gramolini, Thomas Kislinger, Rasoul Alikhani-Koopaei, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2022
An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populationsDaniel Quiat, Seong Won Kim, Qi Zhang, et al.
Pageof 54