UScholar Works
 
Filters: Department: "Ophthalmology"
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TitleDateType
1 Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A)2005Text
2 CFH Y402H Confers similar risk of soft Drusen and both forms of advanced AMD2005Text
3 Evaluation of the 17 kda prenyl binding protein as a regulatory protein for phototransduction in retinal photoreceptors2005Text
4 Functional reorganization of primary visual cortex induced by electrical stimulation in the cat.2005Text
5 Loss of ER retention and sequestration of the wild-type ELOVL4 by Stargardt disease dominant negative mutants2005Text
6 Metabolism and transactivation activity of 13,14-dihydroretinoic acid2005Text
7 Novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)2005Text
8 Pharmacological and rAAV gene therapy rescue of visual functions in a blind mouse model of Leber congenital amaurosis2005Text
9 Retinoid absorption and storage is impaired in mice lacking lecithin:retinol acyltransferase (LRAT)2005Text
10 Role of photoreceptor-specific retinol dehyrogenase (prRDH) in the retinoid cycle in vivo2005Text
11 Statistical encoding model for a primary motor cortical brain-computer interface2005Text
12 Cohort study of 27 cases of endophthalmitis at a single institution2005-04Text
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