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

Dana Sherill-Rofe

Showing results (11-20 of 13) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 13 results.
Molecular Metabolism|September 28, 2020
Reversal of diet-induced hepatic steatosis by peripheral CB1 receptor blockade in mice is p53/miRNA-22/SIRT1/PPARα dependentShahar Azar, Shiran Udi, Adi Drori, et al.
Plos Genetics|November 14, 2022
Systematic proximal mapping of the classical RAD51 paralogs unravel functionally and clinically relevant interactors for genome stabilityEstelle Simo Cheyou, Jacopo Boni, Jonathan Boulais, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2026
Biallelic SUPT4H1 Variants Cause a Multisystem Neurodevelopmental Disorder Associated with Disrupted TranscriptionChristina Canavati, Mari Oppebøen, Radha Verma, et al.
Pageof 2

Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
Molecular Metabolism|September 28, 2020
Reversal of diet-induced hepatic steatosis by peripheral CB1 receptor blockade in mice is p53/miRNA-22/SIRT1/PPARα dependentShahar Azar, Shiran Udi, Adi Drori, et al.
Plos Genetics|November 14, 2022
Systematic proximal mapping of the classical RAD51 paralogs unravel functionally and clinically relevant interactors for genome stabilityEstelle Simo Cheyou, Jacopo Boni, Jonathan Boulais, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2026
Biallelic SUPT4H1 Variants Cause a Multisystem Neurodevelopmental Disorder Associated with Disrupted TranscriptionChristina Canavati, Mari Oppebøen, Radha Verma, et al.
Pageof 2