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Plos One|March 7, 2014
Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerationsWilliam A Beltran, Artur V Cideciyan, Karina E Guziewicz, et al.Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.Nature Biotechnology|October 23, 1997
Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosaR M Petters, C A Alexander, K D Wells, et al.Journal of Addiction Medicine|June 6, 2018
Posttraumatic Stress Disorder Symptom Association With Subsequent Risky and Problem Drinking InitiationKara M Bensley, Amber D Seelig, Richard F Armenta, et al.Investigative Ophthalmology & Visual Science|July 19, 2012
RPGR-associated retinal degeneration in human X-linked RP and a murine modelWei Chieh Huang, Alan F Wright, Alejandro J Roman, et al.Iscience|November 14, 2024
Erratum: Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.Ophthalmology|January 25, 2015
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene TherapyLina Zelinger, Artur V Cideciyan, Susanne Kohl, et al.Human Molecular Genetics|August 29, 2003
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degenerationCaroline Hayward, Xinhua Shu, Artur V Cideciyan, et al.American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.Pageof 57