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Calnexin is not essential for mammalian rod opsin biogenesis

PURPOSE: Misfolding mutations in rod opsin are a major cause of the inherited blindness retinitis pigmentosa. Therefore, understanding the role of molecular chaperones in facilitating rod opsin biogenesis and the response to mutant rod opsin is important for retinal disease and fundamental retinal c...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Kosmaoglou, Maria, Cheetham, Michael E.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Molecular Vision 2008
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2610292/
https://ncbi.nlm.nih.gov/pubmed/19116670
Tagiau: Ychwanegu Tag
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