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Times Cited
Times Co-cited
Similarity
Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis.
Najate Aït-Ali, Ram Fridlich, Géraldine Millet-Puel, Emmanuelle Clérin, François Delalande, Céline Jaillard, Frédéric Blond, Ludivine Perrocheau, Sacha Reichman, Leah C Byrne,[...]. Cell 2015
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Identification and characterization of rod-derived cone viability factor.
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Stimulation of the insulin/mTOR pathway delays cone death in a mouse model of retinitis pigmentosa.
Claudio Punzo, Karl Kornacker, Constance L Cepko. Nat Neurosci 2009
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In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous.
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Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa.
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Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa.
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Activated mTORC1 promotes long-term cone survival in retinitis pigmentosa mice.
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NRF2 promotes neuronal survival in neurodegeneration and acute nerve damage.
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Long-term effect of gene therapy on Leber's congenital amaurosis.
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Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration.
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Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.
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Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.
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Antioxidants reduce cone cell death in a model of retinitis pigmentosa.
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Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration.
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Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors.
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Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosa.
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The Thioredoxin Encoded by the Rod-Derived Cone Viability Factor Gene Protects Cone Photoreceptors Against Oxidative Stress.
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High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors.
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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.
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Thioredoxin rod-derived cone viability factor protects against photooxidative retinal damage.
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Suppression of microglial activation is neuroprotective in a mouse model of human retinitis pigmentosa.
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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement.
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Targeting channelrhodopsin-2 to ON-bipolar cells with vitreally administered AAV Restores ON and OFF visual responses in blind mice.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.