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

Martin J Barron

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Annals of Neurology|March 30, 2004
Familial myopathy: new insights into the T14709C mitochondrial tRNA mutationRobert McFarland, Andrew M Schaefer, Julie L Gardner, et al.
Journal of Virology|October 17, 2014
Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptorsPhilipp Petermann, Katharina Thier, Elena Rahn, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Journal of the American College of Cardiology|May 28, 2003
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathyRobert W Taylor, Carla Giordano, Mercy M Davidson, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
American Journal of Human Genetics|May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeJames O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2006
Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fissionLaura C Greaves, Sean L Preston, Paul J Tadrous, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Annals of Neurology|March 30, 2004
Familial myopathy: new insights into the T14709C mitochondrial tRNA mutationRobert McFarland, Andrew M Schaefer, Julie L Gardner, et al.
Journal of Virology|October 17, 2014
Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptorsPhilipp Petermann, Katharina Thier, Elena Rahn, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Journal of the American College of Cardiology|May 28, 2003
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathyRobert W Taylor, Carla Giordano, Mercy M Davidson, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
American Journal of Human Genetics|May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeJames O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2006
Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fissionLaura C Greaves, Sean L Preston, Paul J Tadrous, et al.
Pageof 2