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

Daniel Bernstein

Showing results (191-200 of 218) with videos related to

Pageof 22
Sort By:
Biorxiv : the Preprint Server for Biology|June 19, 2024
YAP dysregulation triggers hypertrophy by CCN2 secretion and TGFβ uptake in human pluripotent stem cell-derived cardiomyocytesOrlando Chirikian, Mohamed A Faynus, Markus Merk, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
Multi-scale models reveal hypertrophic cardiomyopathy MYH7 G256E mutation drives hypercontractility and elevated mitochondrial respirationSoah Lee, Alison S Vander Roest, Cheavar A Blair, et al.
Nature|March 1, 2023
Cardiogenic control of affective behavioural stateBrian Hsueh, Ritchie Chen, YoungJu Jo, et al.
American Journal of Respiratory and Critical Care Medicine|June 2, 2015
RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial HypertensionChristopher J Rhodes, Hogune Im, Aiqin Cao, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 16, 2023
Mutations in latent membrane protein 1 of Epstein-Barr virus are associated with increased risk of posttransplant lymphoproliferative disorder in childrenOlivia M Martinez, Sheri M Krams, Mark A Robien, et al.
Nature|September 17, 2015
Epicardial FSTL1 reconstitution regenerates the adult mammalian heartKe Wei, Vahid Serpooshan, Cecilia Hurtado, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
JAMA Cardiology|October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Communications Medicine|September 27, 2023
Genetic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart diseaseThomas A Miller, Edgar J Hernandez, J William Gaynor, et al.
Plos Genetics|April 9, 2016
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart DefectsJames R Priest, Kazutoyo Osoegawa, Nebil Mohammed, et al.
Pageof 22

Showing results (191-200 of 218) with videos related to

Sort By:
Pageof 22
Biorxiv : the Preprint Server for Biology|June 19, 2024
YAP dysregulation triggers hypertrophy by CCN2 secretion and TGFβ uptake in human pluripotent stem cell-derived cardiomyocytesOrlando Chirikian, Mohamed A Faynus, Markus Merk, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
Multi-scale models reveal hypertrophic cardiomyopathy MYH7 G256E mutation drives hypercontractility and elevated mitochondrial respirationSoah Lee, Alison S Vander Roest, Cheavar A Blair, et al.
Nature|March 1, 2023
Cardiogenic control of affective behavioural stateBrian Hsueh, Ritchie Chen, YoungJu Jo, et al.
American Journal of Respiratory and Critical Care Medicine|June 2, 2015
RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial HypertensionChristopher J Rhodes, Hogune Im, Aiqin Cao, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 16, 2023
Mutations in latent membrane protein 1 of Epstein-Barr virus are associated with increased risk of posttransplant lymphoproliferative disorder in childrenOlivia M Martinez, Sheri M Krams, Mark A Robien, et al.
Nature|September 17, 2015
Epicardial FSTL1 reconstitution regenerates the adult mammalian heartKe Wei, Vahid Serpooshan, Cecilia Hurtado, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
JAMA Cardiology|October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Communications Medicine|September 27, 2023
Genetic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart diseaseThomas A Miller, Edgar J Hernandez, J William Gaynor, et al.
Plos Genetics|April 9, 2016
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart DefectsJames R Priest, Kazutoyo Osoegawa, Nebil Mohammed, et al.
Pageof 22