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Samuel G Jacobson

Showing results (61-70 of 224) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Progress in Retinal and Eye Research|January 4, 2020
Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiativesAlexandra V Garafalo, Artur V Cideciyan, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
Investigative Ophthalmology & Visual Science|June 10, 2008
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
The Journal of Biological Chemistry|January 13, 2011
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutationsSanae Sakami, Tadao Maeda, Grzegorz Bereta, et al.
American Journal of Ophthalmology|June 29, 2018
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG MutationGiacomo Calzetti, Richard A Levy, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|September 23, 2015
Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal DegenerationRodrigo Matsui, Artur V Cideciyan, Sharon B Schwartz, et al.
Pageof 23

Showing results (61-70 of 224) with videos related to

Sort By:
Pageof 23
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Progress in Retinal and Eye Research|January 4, 2020
Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiativesAlexandra V Garafalo, Artur V Cideciyan, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
Investigative Ophthalmology & Visual Science|June 10, 2008
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
The Journal of Biological Chemistry|January 13, 2011
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutationsSanae Sakami, Tadao Maeda, Grzegorz Bereta, et al.
American Journal of Ophthalmology|June 29, 2018
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG MutationGiacomo Calzetti, Richard A Levy, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|September 23, 2015
Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal DegenerationRodrigo Matsui, Artur V Cideciyan, Sharon B Schwartz, et al.
Pageof 23