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Samuel G Jacobson

Showing results (71-80 of 224) with videos related to

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Investigative Ophthalmology & Visual Science|August 13, 2010
Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remainingSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
The Journal of Biological Chemistry|January 10, 2019
A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degenerationIgor V Peshenko, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Mutation|May 28, 2010
Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channelKatja Koeppen, Peggy Reuter, Thomas Ladewig, et al.
American Journal of Ophthalmology|March 22, 2018
Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2DMaria L Stunkel, Scott E Brodie, Artur V Cideciyan, et al.
Translational Vision Science & Technology|September 19, 2018
Translational Retinal Research and TherapiesAlison J Hardcastle, Paul A Sieving, José-Alain Sahel, et al.
Investigative Ophthalmology & Visual Science|December 25, 2014
Pseudo-fovea formation after gene therapy for RPE65-LCAArtur V Cideciyan, Geoffrey K Aguirre, Samuel G Jacobson, et al.
International Journal of Molecular Sciences|January 23, 2024
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an <i>ALG6</i> Modifier VariantElisha Monson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
Molecular Vision|June 9, 2009
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganizationSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Scientific Reports|July 30, 2020
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutationsArtur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, et al.
Pageof 23

Showing results (71-80 of 224) with videos related to

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Pageof 23
Investigative Ophthalmology & Visual Science|August 13, 2010
Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remainingSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
The Journal of Biological Chemistry|January 10, 2019
A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degenerationIgor V Peshenko, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Mutation|May 28, 2010
Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channelKatja Koeppen, Peggy Reuter, Thomas Ladewig, et al.
American Journal of Ophthalmology|March 22, 2018
Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2DMaria L Stunkel, Scott E Brodie, Artur V Cideciyan, et al.
Translational Vision Science & Technology|September 19, 2018
Translational Retinal Research and TherapiesAlison J Hardcastle, Paul A Sieving, José-Alain Sahel, et al.
Investigative Ophthalmology & Visual Science|December 25, 2014
Pseudo-fovea formation after gene therapy for RPE65-LCAArtur V Cideciyan, Geoffrey K Aguirre, Samuel G Jacobson, et al.
International Journal of Molecular Sciences|January 23, 2024
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an <i>ALG6</i> Modifier VariantElisha Monson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
Molecular Vision|June 9, 2009
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganizationSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Scientific Reports|July 30, 2020
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutationsArtur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, et al.
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