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

Vincent Raymond

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Obesity Research|May 29, 2004
Adipose tissue transcriptome by serial analysis of gene expressionCarl Bolduc, Marianne Larose, Nicolas Lafond, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
Human Molecular Genetics|November 13, 2007
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1AFred B Berry, Jonathan M Skarie, Farideh Mirzayans, et al.
Indian Journal of Ophthalmology|May 13, 2014
Effects of triamcinolone acetonide on human trabecular meshwork cells in vitroAshish Sharma, A Jayaprakash Patil, Navin Gupta, et al.
Molecular Vision|March 7, 2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5qChi Pui Pang, Bao Jian Fan, Oscar Canlas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2006
Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucomaBao Jian Fan, Dexter Y L Leung, Dan Yi Wang, et al.
Human Molecular Genetics|August 22, 2002
Founder TIGR/myocilin mutations for glaucoma in the Québec populationMathieu Faucher, Jean-Louis Anctil, Marc-André Rodrigue, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Obesity Research|May 29, 2004
Adipose tissue transcriptome by serial analysis of gene expressionCarl Bolduc, Marianne Larose, Nicolas Lafond, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
Human Molecular Genetics|November 13, 2007
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1AFred B Berry, Jonathan M Skarie, Farideh Mirzayans, et al.
Indian Journal of Ophthalmology|May 13, 2014
Effects of triamcinolone acetonide on human trabecular meshwork cells in vitroAshish Sharma, A Jayaprakash Patil, Navin Gupta, et al.
Molecular Vision|March 7, 2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5qChi Pui Pang, Bao Jian Fan, Oscar Canlas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2006
Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucomaBao Jian Fan, Dexter Y L Leung, Dan Yi Wang, et al.
Human Molecular Genetics|August 22, 2002
Founder TIGR/myocilin mutations for glaucoma in the Québec populationMathieu Faucher, Jean-Louis Anctil, Marc-André Rodrigue, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Pageof 3