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Samuel G Jacobson

Showing results (101-110 of 224) with videos related to

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Human Molecular Genetics|January 8, 2004
Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequenceArtur V Cideciyan, Tomas S Aleman, Malgorzata Swider, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Human Molecular Genetics|April 16, 2011
The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65Vanda S Lopes, Daniel Gibbs, Richard T Libby, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaJames W Kijas, Artur V Cideciyan, Tomas S Aleman, et al.
Ophthalmology|March 8, 2003
Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosisAnn H Milam, Mark R Barakat, Nisha Gupta, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 23

Showing results (101-110 of 224) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|January 8, 2004
Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequenceArtur V Cideciyan, Tomas S Aleman, Malgorzata Swider, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Human Molecular Genetics|April 16, 2011
The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65Vanda S Lopes, Daniel Gibbs, Richard T Libby, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaJames W Kijas, Artur V Cideciyan, Tomas S Aleman, et al.
Ophthalmology|March 8, 2003
Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosisAnn H Milam, Mark R Barakat, Nisha Gupta, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 23