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Samuel G Jacobson

Showing results (11-20 of 224) with videos related to

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Advances in Experimental Medicine and Biology|October 3, 2015
Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 ProteinsMinghao Jin, Songhua Li, Jane Hu, et al.
JAMA Ophthalmology|July 11, 2014
Late-onset retinal degeneration caused by C1QTNF5 mutation: sub-retinal pigment epithelium deposits and visual consequencesSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|September 18, 2015
Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease FrontArtur V Cideciyan, Malgorzata Swider, Sharon B Schwartz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2013
Reply to Townes-Anderson: RPE65 gene therapy does not alter the natural history of retinal degenerationArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Human Molecular Genetics|July 27, 2006
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal developmentHong Cheng, Tomas S Aleman, Artur V Cideciyan, et al.
Frontiers in Neuroscience|August 28, 2020
Foveal Therapy in Blue Cone Monochromacy: Predictions of Visual Potential From Artificial IntelligenceAlexander Sumaroka, Artur V Cideciyan, Rebecca Sheplock, et al.
Annual Review of Vision Science|July 13, 2021
Measures of Function and Structure to Determine Phenotypic Features, Natural History, and Treatment Outcomes in Inherited Retinal DiseasesArtur V Cideciyan, Arun K Krishnan, Alejandro J Roman, et al.
Journal of Biochemistry|March 11, 2015
Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital AmaurosisSonghua Li, Jane Hu, Robin J Jin, et al.
Journal of Human Genetics|November 3, 2009
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type IIDenise Yan, Xiaomei Ouyang, D Michael Patterson, et al.
The British Journal of Ophthalmology|April 21, 2007
Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Pageof 23

Showing results (11-20 of 224) with videos related to

Sort By:
Pageof 23
Advances in Experimental Medicine and Biology|October 3, 2015
Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 ProteinsMinghao Jin, Songhua Li, Jane Hu, et al.
JAMA Ophthalmology|July 11, 2014
Late-onset retinal degeneration caused by C1QTNF5 mutation: sub-retinal pigment epithelium deposits and visual consequencesSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|September 18, 2015
Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease FrontArtur V Cideciyan, Malgorzata Swider, Sharon B Schwartz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2013
Reply to Townes-Anderson: RPE65 gene therapy does not alter the natural history of retinal degenerationArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Human Molecular Genetics|July 27, 2006
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal developmentHong Cheng, Tomas S Aleman, Artur V Cideciyan, et al.
Frontiers in Neuroscience|August 28, 2020
Foveal Therapy in Blue Cone Monochromacy: Predictions of Visual Potential From Artificial IntelligenceAlexander Sumaroka, Artur V Cideciyan, Rebecca Sheplock, et al.
Annual Review of Vision Science|July 13, 2021
Measures of Function and Structure to Determine Phenotypic Features, Natural History, and Treatment Outcomes in Inherited Retinal DiseasesArtur V Cideciyan, Arun K Krishnan, Alejandro J Roman, et al.
Journal of Biochemistry|March 11, 2015
Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital AmaurosisSonghua Li, Jane Hu, Robin J Jin, et al.
Journal of Human Genetics|November 3, 2009
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type IIDenise Yan, Xiaomei Ouyang, D Michael Patterson, et al.
The British Journal of Ophthalmology|April 21, 2007
Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Pageof 23