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Retinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation

The photoreceptor-specific glycoprotein retinal degeneration slow (RDS, also called PRPH2) is necessary for the formation of rod and cone outer segments. Mutations in RDS cause rod and cone-dominant retinal disease, and it is well established that both cell types have different requirements for RDS....

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Pubblicato in:J Biol Chem
Autori principali: Stuck, Michael W., Conley, Shannon M., Naash, Muna I.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Biochemistry and Molecular Biology 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4646032/
https://ncbi.nlm.nih.gov/pubmed/26420485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M115.683698
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