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

B Gorin

Showing results (141-150 of 175) with videos related to

Pageof 18
Sort By:
Investigative Ophthalmology & Visual Science|December 21, 2010
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibilityKylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, et al.
Ophthalmology. Glaucoma|April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan AfricaOlusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Journal of Medical Genetics|July 31, 2025
Biallelic loss-of-function variants in <i>C19orf44</i> lead to retinal degenerationHafiz Muhammad Jafar Hussain, Wang Meng, Yumei Li, et al.
American Journal of Human Genetics|November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patientsM D Weston, P M Kelley, L D Overbeck, et al.
Frontiers in Neural Circuits|August 26, 2016
Peripheral Sensory Neurons Expressing Melanopsin Respond to LightAnna Matynia, Eileen Nguyen, Xiaoping Sun, et al.
American Journal of Ophthalmology|April 29, 1998
Long-term tamoxifen citrate use and potential ocular toxicityM B Gorin, R Day, J P Costantino, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
American Journal of Human Genetics|November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.
American Journal of Human Genetics|May 29, 2004
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regionsDaniel E Weeks, Yvette P Conley, Hui-Ju Tsai, et al.
Experimental Eye Research|February 21, 2025
Dissecting the biological complexity of age-related macular degeneration: Is it one disease, multiple separate diseases, or a spectrum?Jason M L Miller, Benjamin R Thompson, James T Handa, et al.
Pageof 18

Showing results (141-150 of 175) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|December 21, 2010
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibilityKylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, et al.
Ophthalmology. Glaucoma|April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan AfricaOlusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Journal of Medical Genetics|July 31, 2025
Biallelic loss-of-function variants in <i>C19orf44</i> lead to retinal degenerationHafiz Muhammad Jafar Hussain, Wang Meng, Yumei Li, et al.
American Journal of Human Genetics|November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patientsM D Weston, P M Kelley, L D Overbeck, et al.
Frontiers in Neural Circuits|August 26, 2016
Peripheral Sensory Neurons Expressing Melanopsin Respond to LightAnna Matynia, Eileen Nguyen, Xiaoping Sun, et al.
American Journal of Ophthalmology|April 29, 1998
Long-term tamoxifen citrate use and potential ocular toxicityM B Gorin, R Day, J P Costantino, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
American Journal of Human Genetics|November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.
American Journal of Human Genetics|May 29, 2004
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regionsDaniel E Weeks, Yvette P Conley, Hui-Ju Tsai, et al.
Experimental Eye Research|February 21, 2025
Dissecting the biological complexity of age-related macular degeneration: Is it one disease, multiple separate diseases, or a spectrum?Jason M L Miller, Benjamin R Thompson, James T Handa, et al.
Pageof 18