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G Jacobson

Showing results (541-550 of 677) with videos related to

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Investigative Ophthalmology & Visual Science|March 24, 2004
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosisTomas S Aleman, Samuel G Jacobson, John D Chico, et al.
American Journal of Ophthalmology Case Reports|June 30, 2023
Durable vision improvement after a single intravitreal treatment with antisense oligonucleotide in <i>CEP2</i>90-LCA: Replication in two eyesArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophiesVeronique B D Kitiratschky, Tanja Grau, Antje Bernd, et al.
Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.
Plos One|November 5, 2016
Patterns of Individual Variation in Visual Pathway Structure and Function in the Sighted and BlindGeoffrey K Aguirre, Ritobrato Datta, Noah C Benson, et al.
Pageof 68

Showing results (541-550 of 677) with videos related to

Sort By:
Pageof 68
Investigative Ophthalmology & Visual Science|March 24, 2004
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosisTomas S Aleman, Samuel G Jacobson, John D Chico, et al.
American Journal of Ophthalmology Case Reports|June 30, 2023
Durable vision improvement after a single intravitreal treatment with antisense oligonucleotide in <i>CEP2</i>90-LCA: Replication in two eyesArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophiesVeronique B D Kitiratschky, Tanja Grau, Antje Bernd, et al.
Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.
Plos One|November 5, 2016
Patterns of Individual Variation in Visual Pathway Structure and Function in the Sighted and BlindGeoffrey K Aguirre, Ritobrato Datta, Noah C Benson, et al.
Pageof 68