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G Jacobson

Showing results (601-610 of 677) with videos related to

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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
<i>BEST1</i> 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.
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.
Human Mutation|October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone SyndromeAlan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Pageof 68

Showing results (601-610 of 677) with videos related to

Sort By:
Pageof 68
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
<i>BEST1</i> 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.
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.
Human Mutation|October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone SyndromeAlan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Pageof 68