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

A Mackey

Showing results (671-680 of 763) with videos related to

Pageof 77
Sort By:
European Journal of Human Genetics : EJHG|May 18, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
Ophthalmology|April 23, 2021
Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease RegistryLachlan S W Knight, Jonathan B Ruddle, Deepa A Taranath, et al.
American Journal of Human Genetics|October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationKathryn P Burdon, James D McKay, Michèle M Sale, et al.
The Journal of Investigative Dermatology|May 16, 2017
Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin AgingMatthew H Law, Sarah E Medland, Gu Zhu, et al.
Iscience|September 30, 2018
Single-Cell Profiling Identifies Key Pathways Expressed by iPSCs Cultured in Different Commercial MediaMaciej Daniszewski, Quan Nguyen, Hun S Chy, et al.
European Journal of Human Genetics : EJHG|October 13, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
American Journal of Human Genetics|April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucomaManir Ali, Martin McKibbin, Adam Booth, et al.
Investigative Ophthalmology & Visual Science|August 12, 2020
Recurrent Rare Copy Number Variants Increase Risk for EsotropiaMary C Whitman, Silvio Alessandro Di Gioia, Wai-Man Chan, et al.
Nature Communications|November 17, 2024
Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucomaSantiago Diaz-Torres, Weixiong He, Regina Yu, et al.
Nature Genetics|May 3, 2011
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Kathryn P Burdon, Stuart Macgregor, Alex W Hewitt, et al.
Pageof 77

Showing results (671-680 of 763) with videos related to

Sort By:
Pageof 77
European Journal of Human Genetics : EJHG|May 18, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
Ophthalmology|April 23, 2021
Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease RegistryLachlan S W Knight, Jonathan B Ruddle, Deepa A Taranath, et al.
American Journal of Human Genetics|October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationKathryn P Burdon, James D McKay, Michèle M Sale, et al.
The Journal of Investigative Dermatology|May 16, 2017
Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin AgingMatthew H Law, Sarah E Medland, Gu Zhu, et al.
Iscience|September 30, 2018
Single-Cell Profiling Identifies Key Pathways Expressed by iPSCs Cultured in Different Commercial MediaMaciej Daniszewski, Quan Nguyen, Hun S Chy, et al.
European Journal of Human Genetics : EJHG|October 13, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
American Journal of Human Genetics|April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucomaManir Ali, Martin McKibbin, Adam Booth, et al.
Investigative Ophthalmology & Visual Science|August 12, 2020
Recurrent Rare Copy Number Variants Increase Risk for EsotropiaMary C Whitman, Silvio Alessandro Di Gioia, Wai-Man Chan, et al.
Nature Communications|November 17, 2024
Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucomaSantiago Diaz-Torres, Weixiong He, Regina Yu, et al.
Nature Genetics|May 3, 2011
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Kathryn P Burdon, Stuart Macgregor, Alex W Hewitt, et al.
Pageof 77