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Gene Therapy|January 25, 2013
Retinal gene therapy with a large MYO7A cDNA using adeno-associated virusV S Lopes, S E Boye, C M Louie, et al.
Plos Medicine|October 13, 2006
Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosisAlexis-Pierre Bemelmans, Corinne Kostic, Sylvain V Crippa, et al.
Experimental Eye Research|August 3, 2016
Characterization of intravitreally delivered capsid mutant AAV2-Cre vector to induce tissue-specific mutations in murine retinal ganglion cellsChristophe J Langouet-Astrie, Zhiyong Yang, Sraavya M Polisetti, et al.
Investigative Ophthalmology & Visual Science|July 23, 2011
Long-term preservation of cone photoreceptors and restoration of cone function by gene therapy in the guanylate cyclase-1 knockout (GC1KO) mouseSanford L Boye, Thomas Conlon, Kirsten Erger, et al.
Ophthalmology|June 26, 2017
Gene Therapy for Leber Hereditary Optic Neuropathy: Low- and Medium-Dose Visual ResultsJohn Guy, William J Feuer, Janet L Davis, et al.
The Journal of Biological Chemistry|October 22, 2011
γ-Secretase and presenilin mediate cleavage and phosphorylation of vascular endothelial growth factor receptor-1Jun Cai, Zhijuan Chen, Qing Ruan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2014
STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration modelsKe Jiang, Katherine L Wright, Ping Zhu, et al.
Plos One|July 2, 2010
Functional and behavioral restoration of vision by gene therapy in the guanylate cyclase-1 (GC1) knockout mouseShannon E Boye, Sanford L Boye, Jijing Pang, et al.
Plos One|June 9, 2015
Capsid Mutated Adeno-Associated Virus Delivered to the Anterior Chamber Results in Efficient Transduction of Trabecular Meshwork in Mouse and RatBarbara Bogner, Sanford L Boye, Seok Hong Min, et al.
Gene Therapy|March 14, 2008
Targeting gene expression to cones with human cone opsin promoters in recombinant AAVA M Komáromy, J J Alexander, A E Cooper, et al.
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