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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.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.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|August 22, 2018
Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vectorArtur V Cideciyan, Raghavi Sudharsan, Valérie L Dufour, et al.Human Molecular Genetics|October 5, 2012
Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutantsSamuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, et al.Investigative Ophthalmology & Visual Science|August 30, 2011
Retinal disease course in Usher syndrome 1B due to MYO7A mutationsSamuel G Jacobson, Artur V Cideciyan, Dan Gibbs, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.Human Molecular Genetics|August 11, 2016
Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutationLouise M Downs, Erin M Scott, Artur V Cideciyan, et al.Investigative Ophthalmology & Visual Science|February 28, 2007
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerationsTomas S Aleman, Artur V Cideciyan, Elizabeth A M Windsor, et al.Pageof 11