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Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.The American Journal of Pathology|September 12, 2000
Photoreceptor-specific expression of platelet-derived growth factor-B results in traction retinal detachmentM S Seo, N Okamoto, M A Vinores, et al.Free Radical Biology & Medicine|January 18, 2015
Thioredoxin rod-derived cone viability factor protects against photooxidative retinal damageG Elachouri, I Lee-Rivera, E Clérin, et al.Journal of Cellular Physiology|June 26, 2001
Pigment epithelium-derived factor inhibits retinal and choroidal neovascularizationK Mori, E Duh, P Gehlbach, 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.American Journal of Human Genetics|August 3, 2001
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophyS E Wilkie, Y Li, E C Deery, et al.Nature Genetics|January 4, 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyK Zhang, M Kniazeva, M Han, et al.Eye (London, England)|March 8, 2014
Vascular tone pathway polymorphisms in relation to primary open-angle glaucomaJ H Kang, S J Loomis, B L Yaspan, et al.Pageof 10