Opsin activation as a cause of congenital night blindness.
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Rod and cone visual pigments and phototransduction through pharmacological, genetic, and physiological approachesConstitutively active rhodopsin and retinal diseaseInsights into congenital stationary night blindness based on the structure of G90D rhodopsinStructural role of the T94I rhodopsin mutation in congenital stationary night blindnessRetinal Attachment Instability Is Diversified among Mammalian Melanopsins.Module structure of interphotoreceptor retinoid-binding protein (IRBP) may provide bases for its complex role in the visual cycle - structure/function study of Xenopus IRBP.Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration.Molecular basis for ultraviolet vision in invertebrates.Modeling activated states of GPCRs: the rhodopsin template.Role of G-proteins in odor-sensing and CO2-sensing neurons in Drosophila.Photoactivation-induced instability of rhodopsin mutants T4K and T17M in rod outer segments underlies retinal degeneration in X. laevis transgenic models of retinitis pigmentosaSubstitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.A naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor.Regulatory dissociation of Tctex-1 light chain from dynein complex is essential for the apical delivery of rhodopsin.A novel form of transducin-dependent retinal degeneration: accelerated retinal degeneration in the absence of rod transducinG protein-coupled receptor rhodopsin.Constitutive activity of a UV cone opsinLight regulates the ciliary protein transport and outer segment disc renewal of mammalian photoreceptors.Molecular mechanisms of disease for mutations at Gly-90 in rhodopsinMembrane receptors and transporters involved in the function and transport of vitamin A and its derivatives.Rhodopsin Forms Nanodomains in Rod Outer Segment Disc Membranes of the Cold-Blooded Xenopus laevis.Structural, energetic, and mechanical perturbations in rhodopsin mutant that causes congenital stationary night blindnessLight and inherited retinal degeneration.11-cis- and all-trans-retinols can activate rod opsin: rational design of the visual cycle.Night blindness and the mechanism of constitutive signaling of mutant G90D rhodopsinConstitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark.Constitutively active rhodopsin mutants causing night blindness are effectively phosphorylated by GRKs but differ in arrestin-1 bindingLight responses in rods of vitamin A-deprived XenopusStructural origins of constitutive activation in rhodopsin: Role of the K296/E113 salt bridgeRetinal Degeneration and Regeneration-Lessons From Fishes and Amphibians.Gene silencing in Xenopus laevis by DNA vector-based RNA interference and transgenesis.Modeling Dominant and Recessive Forms of Retinitis Pigmentosa by Editing Three Rhodopsin-Encoding Genes in Xenopus Laevis Using Crispr/Cas9.Physiological studies of the interaction between opsin and chromophore in rod and cone visual pigments.Activation-dependent hindrance of photoreceptor G protein diffusion by lipid microdomains.The dangers of seeing light in the dark.Teaching resources. G-protein-coupled receptors.
P2860
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P2860
Opsin activation as a cause of congenital night blindness.
description
2003 nî lūn-bûn
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2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
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2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Opsin activation as a cause of congenital night blindness.
@en
Opsin activation as a cause of congenital night blindness.
@nl
type
label
Opsin activation as a cause of congenital night blindness.
@en
Opsin activation as a cause of congenital night blindness.
@nl
prefLabel
Opsin activation as a cause of congenital night blindness.
@en
Opsin activation as a cause of congenital night blindness.
@nl
P2860
P356
P1433
P1476
Opsin activation as a cause of congenital night blindness
@en
P2093
Daniel D Oprian
Shengnan Jin
P2860
P2888
P304
P356
10.1038/NN1070
P407
P50
P577
2003-07-01T00:00:00Z