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D J Zack

Showing results (81-90 of 88) with videos related to

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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.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, 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 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
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.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, 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 9