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American Journal of Human Genetics|November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patientsM D Weston, P M Kelley, L D Overbeck, 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.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.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.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.Proceedings of the National Academy of Sciences of the United States of America|September 13, 2007
Human cone photoreceptor dependence on RPE65 isomeraseSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.Proceedings of the National Academy of Sciences of the United States of America|March 7, 2018
BEST1 gene therapy corrects a diffuse retina-wide microdetachment modulated by light exposureKarina E Guziewicz, Artur V Cideciyan, William A Beltran, 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.Ophthalmology Science|October 17, 2022
Restoration of Cone Sensitivity to Individuals with Congenital Photoreceptor Blindness within the Phase 1/2 Sepofarsen TrialArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.Investigative Ophthalmology & Visual Science|February 19, 2008
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 geneWaldo Herrera, Tomas S Aleman, Artur V Cideciyan, et al.Pageof 57