Functional dissection of Rab GTPases involved in primary cilium formation - Test2 - elhamkhani - TriplyDB

Functional dissection of Rab GTPases involved in primary cilium formation

Functional dissection of Rab GTPases involved in primary cilium formation

http://www.wikidata.org/entity/Q24321757

about

TBC1D7 is a third subunit of the TSC1-TSC2 complex upstream of mTORC1 Primary ciliogenesis requires the distal appendage component Cep123.Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors Analysis of Rab GTPase-activating proteins indicates that Rab1a/b and Rab43 are important for herpes simplex virus 1 secondary envelopment Functional genomic screen for modulators of ciliogenesis and cilium length CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium Rab13 regulates membrane trafficking between TGN and recycling endosomes in polarized epithelial cells.The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis.The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome RUTBC1 protein, a Rab9A effector that activates GTP hydrolysis by Rab32 and Rab33B proteins Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivo Rab14 and its exchange factor FAM116 link endocytic recycling and adherens junction stability in migrating cells Rab10 associates with primary cilia and the exocyst complex in renal epithelial cells.Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans Intraflagellar transport motors in cilia: moving along the cell's antenna Plk1-dependent and -independent roles of an ODF2 splice variant, hCenexin1, at the centrosome of somatic cells Human basal body basics Molecular complexes that direct rhodopsin transport to primary cilia Rab and Arf proteins in genetic diseases Regulation of mTORC1 by PI3K signaling The Evi5 family in cellular physiology and pathology GTPase networks in membrane traffic A role for the membrane in regulating Chlamydomonas flagellar length.Intermediates in the Guanine Nucleotide Exchange Reaction of Rab8 Protein Catalyzed by Guanine Nucleotide Exchange Factors Rabin8 and GRAB Crystal structure of a Chlamydomonas reinhardtii flagellar RabGAP TBC-domain at 1.8 Å resolution The Msb3/Gyp3 GAP controls the activity of the Rab GTPases Vps21 and Ypt7 at endosomes and vacuoles Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4.The exocyst protein Sec10 is necessary for primary ciliogenesis and cystogenesis in vitro.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?Coordination of Rab8 and Rab11 in primary ciliogenesis Rabs and the exocyst in ciliogenesis, tubulogenesis and beyond.A conserved signal and GTPase complex are required for the ciliary transport of polycystin-1.

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P2860

Functional dissection of Rab GTPases involved in primary cilium formation

http://www.wikidata.org/entity/Q24321757

description

2007 nî lūn-bûn

@nan

2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2007年の論文

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2007年論文

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2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Functional dissection of Rab GTPases involved in primary cilium formation

@ast

Functional dissection of Rab GTPases involved in primary cilium formation

@en

Functional dissection of Rab GTPases involved in primary cilium formation

@en-gb

Functional dissection of Rab GTPases involved in primary cilium formation

@nl

type

label

Functional dissection of Rab GTPases involved in primary cilium formation

@ast

Functional dissection of Rab GTPases involved in primary cilium formation

@en

Functional dissection of Rab GTPases involved in primary cilium formation

@en-gb

Functional dissection of Rab GTPases involved in primary cilium formation

@nl

prefLabel

Functional dissection of Rab GTPases involved in primary cilium formation

@ast

Functional dissection of Rab GTPases involved in primary cilium formation

@en

Functional dissection of Rab GTPases involved in primary cilium formation

@en-gb

Functional dissection of Rab GTPases involved in primary cilium formation

@nl

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P1433

Journal of Cell Biology

P1476

Functional dissection of Rab GTPases involved in primary cilium formation.

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P2093

Alexander K Haas

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

Evelyn Fuchs

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

Francis A Barr

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

Johannes Egerer

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

Shin-Ichiro Yoshimura

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

P2860

The Ciliopathies: An Emerging Class of Human Genetic Disorders

The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly

Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis

Arl2 and Arl3 regulate different microtubule-dependent processes.

Specific Rab GTPase-activating proteins define the Shiga toxin and epidermal growth factor uptake pathways

Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

GRASP55, a second mammalian GRASP protein involved in the stacking of Golgi cisternae in a cell-free system.

Rab17, a novel small GTPase, is specific for epithelial cells and is induced during cell polarization

Rab proteins as membrane organizers

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363-9

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scholarly article

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3085772

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10.1083/JCB.200703047

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P407

P433

3

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P478

178

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2007-07-30T00:00:00Z

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P5875

6193045

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P698

17646400

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P921

regulation of cilium assembly

P932

2064854

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