Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa.
about
Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration CA dual role for EDEM1 in the processing of rod opsinAutosomal recessive retinitis pigmentosa and E150K mutation in the opsin geneNatural Compounds from Saffron and Bear Bile Prevent Vision Loss and Retinal DegenerationConstitutively active rhodopsin and retinal diseaseChaperone machines for protein folding, unfolding and disaggregationSafranal, a saffron constituent, attenuates retinal degeneration in P23H ratsInactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in DrosophilaFunctional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract.The chaperone environment at the cytoplasmic face of the endoplasmic reticulum can modulate rhodopsin processing and inclusion formationGenomic evidence for rod monochromacy in sloths and armadillos suggests early subterranean history for XenarthraThe effects of IRE1, ATF6, and PERK signaling on adRP-linked rhodopsinsIRE1 signaling affects cell fate during the unfolded protein responseRhodopsin: the functional significance of asn-linked glycosylation and other post-translational modificationsA comparative study of rhodopsin function in the great bowerbird (Ptilonorhynchus nuchalis): Spectral tuning and light-activated kinetics.Automated method for modeling seven-helix transmembrane receptors from experimental data.Restoration of the majority of the visual spectrum by using modified Volvox channelrhodopsin-1.Structure and function in rhodopsin: Mass spectrometric identification of the abnormal intradiscal disulfide bond in misfolded retinitis pigmentosa mutants.N-Glycan structures of squid rhodopsin.Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration.Identification of core amino acids stabilizing rhodopsin.The transmembrane 7-alpha-bundle of rhodopsin: distance geometry calculations with hydrogen bonding constraintsRescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation.Yeast mutants affecting possible quality control of plasma membrane proteins.Endoplasmic reticulum stress and the unfolded protein responses in retinal degeneration.LEDGF(1-326) decreases P23H and wild type rhodopsin aggregates and P23H rhodopsin mediated cell damage in human retinal pigment epithelial cells.Gene augmentation for adRP mutations in RHO.Electrostatic compensation restores trafficking of the autosomal recessive retinitis pigmentosa E150K opsin mutant to the plasma membrane.A naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor.Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosaG protein-coupled receptor rhodopsin: a prospectus.Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.Chemical chaperone 4-phenylbutyrate prevents endoplasmic reticulum stress induced by T17M rhodopsin.Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.Ablation of the proapoptotic genes CHOP or Ask1 does not prevent or delay loss of visual function in a P23H transgenic mouse model of retinitis pigmentosaExclusion of the unfolded protein response in light-induced retinal degeneration in the canine T4R RHO model of autosomal dominant retinitis pigmentosa.Accumulation of the Raf-1 kinase inhibitory protein (Rkip) is associated with Cep290-mediated photoreceptor degeneration in ciliopathies.Molecular Architecture of G Protein-Coupled Receptors.Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsMolecular mechanisms of disease for mutations at Gly-90 in rhodopsin
P2860
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P2860
Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Structure and function in rhod ...... dominant retinitis pigmentosa.
@en
type
label
Structure and function in rhod ...... dominant retinitis pigmentosa.
@en
prefLabel
Structure and function in rhod ...... dominant retinitis pigmentosa.
@en
P356
P1433
P1476
Structure and function in rhod ...... dominant retinitis pigmentosa.
@en
P2093
P304
P356
10.1021/BI00186A011
P407
P577
1994-05-01T00:00:00Z