Peripherin/rds and rom-1: Molecular properties and role in photoreceptor cell degeneration
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Cited by (43)
Role of Peripherin/rds in Vertebrate Photoreceptor Architecture and Inherited Retinal Degenerations
2006, International Review of CytologyCitation Excerpt :Recent findings provide an increasingly resolved picture of an oligomeric protein that functions at several stages of photoreceptor outer segment organization and is a key player in a broad spectrum of retinal diseases. Previous overview articles include summaries focused on P/rds protein structure/function (Boesze‐Battaglia and Goldberg, 2002; Molday et al., 2004; Travis and Hepler, 1993; Wright, 2000; Molday, 1994) and human molecular genetics (Keen and Inglehearn, 1996; Kohl et al., 1998). The rds gene is also referred to as Prph2 (in mice).
Photoreceptor renewal: A role for peripherin/rds
2002, International Review of CytologyLipid metabolism in vertebrate retinal rod outer segments
2000, Progress in Lipid ResearchPeripherin/rds influences membrane vesicle morphology. Implications for retinopathies
2000, Journal of Biological Chemistry
Copyright © 1994 Published by Elsevier Ltd.