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Science Translational Medicine|April 9, 2010
Safety and efficacy of subretinal readministration of a viral vector in large animals to treat congenital blindnessDefne Amado, Federico Mingozzi, Daniel Hui, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|March 2, 2026
Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis PigmentosaEmmanuelle Clérin, Ying Yang, Delphine Pagan, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy successSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Plos One|May 14, 2013
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized modelsVidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 5, 2004
In utero gene therapy rescues vision in a murine model of congenital blindnessNadine S Dejneka, Enrico M Surace, Tomas S Aleman, et al.
Experimental Eye Research|May 17, 2002
Macular pigment and lutein supplementation in choroideremiaJacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
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