Role of Peripherin/rds in Vertebrate Photoreceptor Architecture and Inherited Retinal Degenerations

Author:

Goldberg Andrew F.X.

Publisher

Elsevier

Reference177 articles.

1. Opsin synthesis and mRNA levels in dystrophic retinas devoid of outer segments in retinal degeneration slow (rds) mice;Agarwal;J. Neurosci.,1990

2. Loss of diurnal arrestin gene expression in rds mutant mouse retinas;Agarwal;Exp. Eye Res.,1994

3. Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy;Ali;Nat. Genet.,2000

4. Mammalian cones: Disc shedding, phagocytosis, and renewal;Anderson;Invest. Ophthalmol. Vis. Sci.,1978

5. Low docosahexaenoic acid levels in rod outer segment membranes of mice with rds/peripherin and P216L peripherin mutations;Anderson;Invest. Ophthalmol. Vis. Sci.,2001

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