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G Jacobson

Showing results (561-570 of 677) with videos related to

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Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Human Molecular Genetics|March 19, 2004
QRX, a novel homeobox gene, modulates photoreceptor gene expressionQing-liang Wang, Shiming Chen, Noriko Esumi, et al.
Experimental Eye Research|January 27, 2005
Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measuresAlejandro J Roman, Sharon B Schwartz, Tomas S Aleman, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 18, 2005
Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindnessGregory M Acland, Gustavo D Aguirre, Jean Bennett, et al.
Elife|March 28, 2023
Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defectsHolly Y Chen, Manju Swaroop, Samantha Papal, et al.
Pageof 68

Showing results (561-570 of 677) with videos related to

Sort By:
Pageof 68
Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Human Molecular Genetics|March 19, 2004
QRX, a novel homeobox gene, modulates photoreceptor gene expressionQing-liang Wang, Shiming Chen, Noriko Esumi, et al.
Experimental Eye Research|January 27, 2005
Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measuresAlejandro J Roman, Sharon B Schwartz, Tomas S Aleman, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 18, 2005
Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindnessGregory M Acland, Gustavo D Aguirre, Jean Bennett, et al.
Elife|March 28, 2023
Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defectsHolly Y Chen, Manju Swaroop, Samantha Papal, et al.
Pageof 68