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Samuel G Jacobson

Showing results (81-90 of 224) with videos related to

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Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 6, 2018
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion MutationsAlexander Sumaroka, Alexandra V Garafalo, Artur V Cideciyan, et al.
Current Eye Research|June 10, 2014
Drusen and photoreceptor abnormalities in African-Americans with intermediate non-neovascular age-related macular degenerationSam Sadigh, Xunda Luo, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trialsArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Plos Medicine|May 17, 2006
Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessMelissa L Williams, Jason E Coleman, Shannon E Haire, et al.
Ophthalmic Genetics|February 9, 2016
SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosaRodrigo Matsui, David B McGuigan Iii, Michaela L Gruzensky, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 11, 2011
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degenerationDebarshi Mustafi, Brian M Kevany, Christel Genoud, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin MutationsSamuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Pageof 23

Showing results (81-90 of 224) with videos related to

Sort By:
Pageof 23
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 6, 2018
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion MutationsAlexander Sumaroka, Alexandra V Garafalo, Artur V Cideciyan, et al.
Current Eye Research|June 10, 2014
Drusen and photoreceptor abnormalities in African-Americans with intermediate non-neovascular age-related macular degenerationSam Sadigh, Xunda Luo, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trialsArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Plos Medicine|May 17, 2006
Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessMelissa L Williams, Jason E Coleman, Shannon E Haire, et al.
Ophthalmic Genetics|February 9, 2016
SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosaRodrigo Matsui, David B McGuigan Iii, Michaela L Gruzensky, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 11, 2011
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degenerationDebarshi Mustafi, Brian M Kevany, Christel Genoud, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin MutationsSamuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Pageof 23