Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods. - Wikidata - awgldk - TriplyDB

Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods.

Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods.

http://www.wikidata.org/entity/Q33944067

about

The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice The novel centriolar satellite protein SSX2IP targets Cep290 to the ciliary transition zone Rab10 regulates membrane transport through early endosomes of polarized Madin-Darby canine kidney cells Rab10 associates with primary cilia and the exocyst complex in renal epithelial cells.The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia The role of RPGR in cilia formation and actin stability Pitchfork regulates primary cilia disassembly and left-right asymmetry A Rab8-specific GDP/GTP exchange factor is involved in actin remodeling and polarized membrane transport.How are the cellular functions of myosin VI regulated within the cell?Small GTPase regulation of GPCR anterograde trafficking Molecular complexes that direct rhodopsin transport to primary cilia Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease Regulation of rhodopsin-eGFP distribution in transgenic xenopus rod outer segments by light Structure of Rab11-FIP3-Rabin8 reveals simultaneous binding of FIP3 and Rabin8 effectors to Rab11 Elipsa is an early determinant of ciliogenesis that links the IFT particle to membrane-associated small GTPase Rab8.Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4.Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier?Rabs and the exocyst in ciliogenesis, tubulogenesis and beyond.Architecture and function of IFT complex proteins in ciliogenesis The Arf GAP ASAP1 provides a platform to regulate Arf4- and Rab11-Rab8-mediated ciliary receptor targeting.Trafficking in and to the primary cilium.Crosstalk of Arf and Rab GTPases en route to cilia.Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration Endocytosis genes facilitate protein and membrane transport in C. elegans sensory cilia The Arf and Rab11 effector FIP3 acts synergistically with ASAP1 to direct Rabin8 in ciliary receptor targeting Immunocytochemical evidence of Tulp1-dependent outer segment protein transport pathways in photoreceptor cells Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1 Evolution: Tracing the origins of centrioles, cilia, and flagella Autophagy-based unconventional secretory pathway for extracellular delivery of IL-1β Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy The vertebrate primary cilium in development, homeostasis, and disease Trafficking to the primary cilium membrane.An IFT-A protein is required to delimit functionally distinct zones in mechanosensory cilia.The AP-1 clathrin adaptor facilitates cilium formation and functions with RAB-8 in C. elegans ciliary membrane transport.Transmembrane protein OSTA-1 shapes sensory cilia morphology via regulation of intracellular membrane trafficking in C. elegans.Sept7b is essential for pronephric function and development of left-right asymmetry in zebrafish embryogenesis The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease

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P2860

Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods.

http://www.wikidata.org/entity/Q33944067

description

2001 nî lūn-bûn

@nan

2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի օգոստոսին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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Molecular Biology of the Cell

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Mutant rab8 Impairs docking an ...... th of transgenic Xenopus rods.

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P2093

B M Tam

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

D Deretic

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D S Papermaster

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J Peränen

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L L Hurd

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O L Moritz

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P2860

SNAREs contribute to the specificity of membrane fusion

Isoprenoid modification of rab proteins terminating in CC or CXC motifs

In its active form, the GTP-binding protein rab8 interacts with a stress-activated protein kinase

Rab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membrane

The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis.

Compartmental specificity of cellular membrane fusion encoded in SNARE proteins.

GTP hydrolysis is not important for Ypt1 GTPase function in vesicular transport.

SNAP receptors implicated in vesicle targeting and fusion

SNAREpins: minimal machinery for membrane fusion

Isoprenylation of Rab proteins possessing a C-terminal CaaX motif

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2341-2351

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scholarly article

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10.1091/MBC.12.8.2341

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8

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12

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11830227

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11514620

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58598

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