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Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in DrosophilaExtended conformation of the proline-rich domain of human aryl hydrocarbon receptor-interacting protein-like 1: implications for retina disease.Rab1 small GTP-binding protein regulates cell surface trafficking of the human calcium-sensing receptor.Global Microarray Analysis of Alkaliphilic Halotolerant Bacterium Bacillus sp. N16-5 Salt Stress AdaptationIRE1 directs proteasomal and lysosomal degradation of misfolded rhodopsinA High-Throughput Drug Screening Strategy for Detecting Rhodopsin P23H Mutant Rescue and Degradation.An S-opsin knock-in mouse (F81Y) reveals a role for the native ligand 11-cis-retinal in cone opsin biosynthesisLight Induces Ultrastructural Changes in Rod Outer and Inner Segments, Including Autophagy, in a Transgenic Xenopus laevis P23H Rhodopsin Model of Retinitis Pigmentosa.Denaturation and intermediates study of two sturgeon hemoglobins by n-dodecyl trimethylammonium bromide.Proteasome overload is a common stress factor in multiple forms of inherited retinal degeneration.Interaction of aryl hydrocarbon receptor-interacting protein-like 1 with the farnesyl moietySodium dodecyl sulphate modulates the fibrillation of human serum albumin in a dose-dependent manner and impacts the PC12 cells retraction.The proteostasis boundary in misfolding diseases of membrane traffic.P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis.Proteostasis strategies for restoring alpha1-antitrypsin deficiency.Pharmacological chaperoning of nAChRs: a therapeutic target for Parkinson's disease.Targeting the Proteostasis Network in Rhodopsin Retinitis Pigmentosa.The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.XPORT-dependent transport of TRP and rhodopsin.Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa.Mice deficient in the Vici syndrome gene Epg5 exhibit features of retinitis pigmentosa.Prevention of autosomal dominant retinitis pigmentosa by systemic drug therapy targeting heat shock protein 90 (Hsp90).Calnexin is not essential for mammalian rod opsin biogenesis.AIPL1: A specialized chaperone for the phototransduction effector.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 29 March 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Molecular chaperones and photoreceptor function.
@en
Molecular chaperones and photoreceptor function.
@nl
type
label
Molecular chaperones and photoreceptor function.
@en
Molecular chaperones and photoreceptor function.
@nl
prefLabel
Molecular chaperones and photoreceptor function.
@en
Molecular chaperones and photoreceptor function.
@nl
P2093
P2860
P921
P1476
Molecular chaperones and photoreceptor function
@en
P2093
John S Bett
Maria Kosmaoglou
Nele Schwarz
P2860
P304
P356
10.1016/J.PRETEYERES.2008.03.001
P5008
P577
2008-03-29T00:00:00Z