Structural and functional impairment of endocytic pathways by retinitis pigmentosa mutant rhodopsin-arrestin complexes - Wikidata - awgldk - TriplyDB

Structural and functional impairment of endocytic pathways by retinitis pigmentosa mutant rhodopsin-arrestin complexes

Structural and functional impairment of endocytic pathways by retinitis pigmentosa mutant rhodopsin-arrestin complexes

http://www.wikidata.org/entity/Q24563320

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Accumulation of rhodopsin in late endosomes triggers photoreceptor cell degeneration SARA-regulated vesicular targeting underlies formation of the light-sensing organelle in mammalian rods Negative regulation of the novel norpA(P24) suppressor, diehard4, in the endo-lysosomal trafficking underlies photoreceptor cell degeneration Hsp90 as a Potential Therapeutic Target in Retinal Disease Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods Arrestin can act as a regulator of rhodopsin photochemistry.Light regulates the ciliary protein transport and outer segment disc renewal of mammalian photoreceptors.Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.G protein-coupled receptor kinases: more than just kinases and not only for GPCRs Effect of rapamycin on the fate of P23H opsin associated with retinitis pigmentosa (an American Ophthalmological Society thesis).Alternative pathway of cell death in Drosophila mediated by NF-κB transcription factor Relish Cell-nonautonomous function of ceramidase in photoreceptor homeostasis.The Disease Protein Tulp1 Is Essential for Periactive Zone Endocytosis in Photoreceptor Ribbon Synapses.Structure and activation of rhodopsin.Visual arrestin interaction with clathrin adaptor AP-2 regulates photoreceptor survival in the vertebrate retina.Detection of G protein-selective G protein-coupled receptor (GPCR) conformations in live cells Functional map of arrestin binding to phosphorylated opsin, with and without agonist.Regulation of arrestin binding by rhodopsin phosphorylation level.Hsp90 inhibition protects against inherited retinal degeneration.Aberrant protein trafficking in retinal degenerations: The initial phase of retinal remodeling.Assessing the correlation between mutant rhodopsin stability and the severity of retinitis pigmentosa ROM-1 potentiates photoreceptor specific membrane fusion processes.Arrestins in apoptosis.The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.Targeted disruption of the endogenous zebrafish locus as models of rapid rod photoreceptor degeneration

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Structural and functional impairment of endocytic pathways by retinitis pigmentosa mutant rhodopsin-arrestin complexes

http://www.wikidata.org/entity/Q24563320

description

2004 nî lūn-bûn

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2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2004 թվականի հուլիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Structural and functional impa ...... t rhodopsin-arrestin complexes

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Journal of Clinical Investigation

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Structural and functional impa ...... t rhodopsin-arrestin complexes

@en

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Carrie Vega

http://www.w3.org/2001/XMLSchema#string

Ching-Hwa Sung

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Jen-Zen Chuang

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Wenjin Jun

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P2860

Rhodopsin mutants that bind but fail to activate transducin

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

A beta-arrestin/green fluorescent protein biosensor for detecting G protein-coupled receptor activation

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin

Visualization of TGN to endosome trafficking through fluorescently labeled MPR and AP-1 in living cells

Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE).

Constitutively active mutants of rhodopsin.

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

The endocytic pathway: a mosaic of domains.

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131-40

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scholarly article

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435021

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10.1172/JCI21136

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1

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114

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2004-07-01T00:00:00Z

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15232620

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437971

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