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Investigative Ophthalmology & Visual Science|December 7, 2007
Intraocular CNTF reduces vision in normal rats in a dose-dependent mannerTrevor J McGill, Glen T Prusky, Robert M Douglas, et al.Human Gene Therapy|July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 yearArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.Current Eye Research|February 29, 2020
Interocular Symmetry of Foveal Cone Topography in Congenital AchromatopsiaKatie M Litts, Michalis Georgiou, Christopher S Langlo, et al.Plos Medicine|June 28, 2007
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutationGeoffrey K Aguirre, András M Komáromy, Artur V Cideciyan, et al.Human Gene Therapy|July 8, 2010
Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in IsraelEyal Banin, Dikla Bandah-Rozenfeld, Alexey Obolensky, et al.Human Gene Therapy|March 12, 2005
Efficient transduction of vascular endothelial cells with recombinant adeno-associated virus serotype 1 and 5 vectorsSifeng Chen, Matthias Kapturczak, Scott A Loiler, et al.Journal of the American Society of Nephrology : JASN|October 28, 2005
IL-10 suppresses chemokines, inflammation, and fibrosis in a model of chronic renal diseaseWei Mu, Xiaosen Ouyang, Anupam Agarwal, et al.Plos One|April 18, 2012
AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsiaJi-jing Pang, Wen-Tao Deng, Xufeng Dai, et al.Plos One|March 28, 2014
Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapyShannon E Boye, Wei-Chieh Huang, Alejandro J Roman, et al.Plos One|May 3, 2013
Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectorsChristine N Kay, Renee C Ryals, George V Aslanidi, et al.Pageof 39