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Andrew R Webster

Showing results (101-110 of 372) with videos related to

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Journal of Negative Results in Biomedicine|May 24, 2016
Investigation of SLA4A3 as a candidate gene for human retinal diseaseLouise M Downs, Andrew R Webster, Anthony T Moore, et al.
JAMA Ophthalmology|July 28, 2017
Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular DegenerationValentina Cipriani, Ruth E Hogg, Reecha Sofat, et al.
Human Molecular Genetics|October 29, 2004
Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31Naheed A Rana, Neil D Ebenezer, Andrew R Webster, et al.
American Journal of Human Genetics|July 19, 2011
Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosisPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
The Journal of Biological Chemistry|November 1, 2014
Differential light-induced responses in sectorial inherited retinal degenerationEva Ramon, Arnau Cordomí, Mònica Aguilà, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Eye (London, England)|December 5, 2024
Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathySiying Lin, Gavin Arno, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Ophthalmology|October 13, 2009
Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia)Michel Michaelides, Zheng Li, Naheed A Rana, et al.
Pageof 38

Showing results (101-110 of 372) with videos related to

Sort By:
Pageof 38
Journal of Negative Results in Biomedicine|May 24, 2016
Investigation of SLA4A3 as a candidate gene for human retinal diseaseLouise M Downs, Andrew R Webster, Anthony T Moore, et al.
JAMA Ophthalmology|July 28, 2017
Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular DegenerationValentina Cipriani, Ruth E Hogg, Reecha Sofat, et al.
Human Molecular Genetics|October 29, 2004
Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31Naheed A Rana, Neil D Ebenezer, Andrew R Webster, et al.
American Journal of Human Genetics|July 19, 2011
Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosisPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
The Journal of Biological Chemistry|November 1, 2014
Differential light-induced responses in sectorial inherited retinal degenerationEva Ramon, Arnau Cordomí, Mònica Aguilà, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Eye (London, England)|December 5, 2024
Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathySiying Lin, Gavin Arno, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Ophthalmology|October 13, 2009
Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia)Michel Michaelides, Zheng Li, Naheed A Rana, et al.
Pageof 38