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

John Mitchell

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

Pageof 20
Sort By:
You have reached the last page of results.This site can display upto 200 results.
Human Mutation|May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsySarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Molecular Genetics and Metabolism|August 14, 2012
Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in QuébecJean Larochelle, Fernando Alvarez, Jean-François Bussières, et al.
Aging Cell|May 6, 2024
Clinical validation of C<sub>12</sub>FDG as a marker associated with senescence and osteoarthritic phenotypesWilliam S Hambright, Victoria R Duke, Adam D Goff, et al.
Human Molecular Genetics|December 26, 2006
Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin YMark A Jobling, Iek Chi C Lo, Daniel J Turner, et al.
Pediatric Neurology|June 4, 2018
Health-Related Quality of Life for Patients With Genetically Determined LeukoencephalopathyAmytice Mirchi, Félixe Pelletier, Luan T Tran, et al.
Eclinicalmedicine|March 2, 2026
Minimum combined sleep, physical activity, and nutrition variations associated with lifeSPAN and healthSPAN improvements: a population cohort studyNicholas A Koemel, Raaj K Biswas, Matthew N Ahmadi, et al.
Genome Medicine|March 3, 2025
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severityJasmin J Bennett, Cécile Saint-Martin, Bianca Neumann, et al.
Nature|February 12, 2010
Rfx6 directs islet formation and insulin production in mice and humansStuart B Smith, Hui-Qi Qu, Nadine Taleb, et al.
Frontiers in Plant Science|March 24, 2023
Phylogenomic analyses of Sapindales support new family relationships, rapid Mid-Cretaceous Hothouse diversification, and heterogeneous histories of gene duplicationElizabeth M Joyce, Marc S Appelhans, Sven Buerki, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2017
Amazon plant diversity revealed by a taxonomically verified species listDomingos Cardoso, Tiina Särkinen, Sara Alexander, et al.
Pageof 20

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

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
Human Mutation|May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsySarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Molecular Genetics and Metabolism|August 14, 2012
Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in QuébecJean Larochelle, Fernando Alvarez, Jean-François Bussières, et al.
Aging Cell|May 6, 2024
Clinical validation of C<sub>12</sub>FDG as a marker associated with senescence and osteoarthritic phenotypesWilliam S Hambright, Victoria R Duke, Adam D Goff, et al.
Human Molecular Genetics|December 26, 2006
Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin YMark A Jobling, Iek Chi C Lo, Daniel J Turner, et al.
Pediatric Neurology|June 4, 2018
Health-Related Quality of Life for Patients With Genetically Determined LeukoencephalopathyAmytice Mirchi, Félixe Pelletier, Luan T Tran, et al.
Eclinicalmedicine|March 2, 2026
Minimum combined sleep, physical activity, and nutrition variations associated with lifeSPAN and healthSPAN improvements: a population cohort studyNicholas A Koemel, Raaj K Biswas, Matthew N Ahmadi, et al.
Genome Medicine|March 3, 2025
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severityJasmin J Bennett, Cécile Saint-Martin, Bianca Neumann, et al.
Nature|February 12, 2010
Rfx6 directs islet formation and insulin production in mice and humansStuart B Smith, Hui-Qi Qu, Nadine Taleb, et al.
Frontiers in Plant Science|March 24, 2023
Phylogenomic analyses of Sapindales support new family relationships, rapid Mid-Cretaceous Hothouse diversification, and heterogeneous histories of gene duplicationElizabeth M Joyce, Marc S Appelhans, Sven Buerki, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2017
Amazon plant diversity revealed by a taxonomically verified species listDomingos Cardoso, Tiina Särkinen, Sara Alexander, et al.
Pageof 20