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Proceedings of the National Academy of Sciences of the United States of America|February 21, 1998
Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in manA V Cideciyan, X Zhao, L Nielsen, et al.Neuroreport|April 17, 2001
Melatonin delays photoreceptor degeneration in the rds/rds mouseF Q Liang, T S Aleman, ZaixinYang, et al.Vision Research|November 1, 1996
The enhanced S cone syndrome: an analysis of receptoral and post-receptoral changesV C Greenstein, Q Zaidi, D C Hood, et al.Investigative Ophthalmology & Visual Science|December 1, 1992
X-linked retinitis pigmentosa: functional phenotype of an RP2 genotypeS G Jacobson, A J Roman, A V Cideciyan, et al.Investigative Ophthalmology & Visual Science|April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosaS G Jacobson, C M Kemp, A V Cideciyan, et al.Investigative Ophthalmology & Visual Science|July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor functionC M Kemp, S G Jacobson, A V Cideciyan, et al.Human Molecular Genetics|July 13, 1999
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locusX Guillonneau, N I Piriev, M Danciger, et al.Nature Genetics|September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin AS G Jacobson, A V Cideciyan, G Regunath, et al.Neuron|August 5, 1999
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway developmentE Banin, A V Cideciyan, T S Alemán, et al.Investigative Ophthalmology & Visual Science|August 1, 1996
Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degenerationC A Kuntz, S G Jacobson, A V Cideciyan, et al.Pageof 13