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Mutations of the PRCD gene are associated with rod-cone degeneration in both dogs and humans. Prcd is expressed in the mouse eye… Expand PRCD (progressive rod-cone degeneration) is a small ~6 kDa protein with unknown function that specifically resides in… Expand A mutation of the reln gene gives rise to the Reeler mouse (reln−∕−) displaying an ataxic phenotype and cerebellar hypoplasia. We… Expand Retinitis pigmentosa (RP) is the most common form of hereditary retinal degeneration. Mutations of the PRCD gene are associated… Expand Visual signal transduction takes place on the surface of flat membrane vesicles called photoreceptor discs, which reside inside… Expand Background Retinitis pigmentosa (RP) is the most common form of hereditary retinal degeneration. At least 32 genes and loci have… Expand Progressive rod-cone degeneration (prcd) is a late-onset, autosomal recessive photoreceptor degeneration of dogs and a homolog… Expand Visual cell pathology and rod outer segment renewal were investigated in normal and PRCD-affected miniature poodles using H… Expand Several U.S. Department of Energy (DOE) sites have contact-handled (CH) transuranic (TRU) waste inventories that were packaged in… Expand Visual cell pathology and rod outer segment renewal were investigated in normal and PRCD-affected miniature poodles using 3H… Expand