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

Samarth

Showing results (921-930 of 927) with videos related to

Pageof 93
Sort By:
You have reached the last page of results.This site can display upto 927 results.
Nature|May 25, 2017
Blocking FSH induces thermogenic adipose tissue and reduces body fatPeng Liu, Yaoting Ji, Tony Yuen, et al.
American Journal of Human Genetics|June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformationsPaweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
American Journal of Human Genetics|July 2, 2019
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe CasesYoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Baratang, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Dendritic cells type 1 control the formation, maintenance, and function of tertiary lymphoid structures in cancerRaphaël Mattiuz, Jesse Boumelha, Pauline Hamon, et al.
Nature Medicine|June 15, 2023
Intratumoral dendritic cell-CD4<sup>+</sup> T helper cell niches enable CD8<sup>+</sup> T cell differentiation following PD-1 blockade in hepatocellular carcinomaAssaf Magen, Pauline Hamon, Nathalie Fiaschi, et al.
NPJ Microgravity|July 3, 2026
Machine learning ensemble reveals distinct molecular pathways of retinal damage in spaceflown miceJames A Casaletto, Ryan T Scott, Aahan Rathod, et al.
Human Mutation|September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeatsPaweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.
Pageof 93

Showing results (921-930 of 927) with videos related to

Sort By:
Pageof 93
You have reached the last page of results.This site can display upto 927 results.
Nature|May 25, 2017
Blocking FSH induces thermogenic adipose tissue and reduces body fatPeng Liu, Yaoting Ji, Tony Yuen, et al.
American Journal of Human Genetics|June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformationsPaweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
American Journal of Human Genetics|July 2, 2019
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe CasesYoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Baratang, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Dendritic cells type 1 control the formation, maintenance, and function of tertiary lymphoid structures in cancerRaphaël Mattiuz, Jesse Boumelha, Pauline Hamon, et al.
Nature Medicine|June 15, 2023
Intratumoral dendritic cell-CD4<sup>+</sup> T helper cell niches enable CD8<sup>+</sup> T cell differentiation following PD-1 blockade in hepatocellular carcinomaAssaf Magen, Pauline Hamon, Nathalie Fiaschi, et al.
NPJ Microgravity|July 3, 2026
Machine learning ensemble reveals distinct molecular pathways of retinal damage in spaceflown miceJames A Casaletto, Ryan T Scott, Aahan Rathod, et al.
Human Mutation|September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeatsPaweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.
Pageof 93