The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression - Test2 - elhamkhani - TriplyDB

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

http://www.wikidata.org/entity/Q24337908

about

A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence The dynamic cilium in human diseases Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease Primary ciliogenesis requires the distal appendage component Cep123.A novel protein LZTFL1 regulates ciliary trafficking of the BBSome and Smoothened Dissection of epistasis in oligogenic Bardet-Biedl syndrome Cep126 is required for pericentriolar satellite localisation to the centrosome and for primary cilium formation Bardet-Biedl syndrome proteins 1 and 3 regulate the ciliary trafficking of polycystic kidney disease 1 protein Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731 The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation.Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function Proteomic analysis of mammalian sperm cells identifies new components of the centrosome Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling CEP90 is required for the assembly and centrosomal accumulation of centriolar satellites, which is essential for primary cilia formation Direct role of Bardet-Biedl syndrome proteins in transcriptional regulation Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome The novel centriolar satellite protein SSX2IP targets Cep290 to the ciliary transition zone Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)A complex of two centrosomal proteins, CAP350 and FOP, cooperates with EB1 in microtubule anchoring.Nudel contributes to microtubule anchoring at the mother centriole and is involved in both dynein-dependent and -independent centrosomal protein assembly Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)A novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese family Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function Human basal body basics DISC1: a key lead in studying cortical development and associated brain disorders Changes in cGMP levels affect the localization of EGL-4 in AWC in Caenorhabditis elegans Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null mice Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome.The nonmotile ciliopathies.

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P2860

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

http://www.wikidata.org/entity/Q24337908

description

2004 nî lūn-bûn

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2004 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2004 թվականի մայիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

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P1433

Nature Genetics

P1476

The Bardet-Biedl protein BBS4 ...... ing and cell cycle progression

@en

P2093

Alison J Ross

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

Bethan E Hoskins

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Carmen C Leitch

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Josephine Hill

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

Jun Chul Kim

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

Kerrie Venner

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

Michel R Leroux

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

Muneer A Esmail

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Philip L Beales

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Sonja Sibold

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P2860

Cytoplasmic dynein-mediated assembly of pericentrin and gamma tubulin onto centrosomes

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Cytoplasmic dynein binds dynactin through a direct interaction between the intermediate chains and p150Glued

SMART: a web-based tool for the study of genetically mobile domains.

Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.

The p150Glued component of the dynactin complex binds to both microtubules and the actin-related protein centractin (Arp-1)

PCM-1, A 228-kD centrosome autoantigen with a distinct cell cycle distribution

Assembly of centrosomal proteins and microtubule organization depends on PCM-1

Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis

A system for stable expression of short interfering RNAs in mammalian cells

P2888

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462-70

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scholarly article

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1007368

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10.1038/NG1352

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P433

5

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36

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Nicholas Katsanis

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2004-05-01T00:00:00Z

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8597050

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1006244183

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15107855

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P921

protein localization to centrosome

Bardet-Biedl syndrome 4

bardet-biedl syndrome 4 protein

Bardet-Biedl syndrome 4 protein, putative (fragment)

bardet-biedl syndrome 4 protein

TcCLB.510187.130:mRNA

bardet-biedl syndrome 4 protein

bardet-biedl syndrome 4 protein