The BBSome controls IFT assembly and turnaround in cilia. - Wikidata - wikimedia - TriplyDB

The BBSome controls IFT assembly and turnaround in cilia.

The BBSome controls IFT assembly and turnaround in cilia.

http://www.wikidata.org/entity/Q28000109

about

ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport The intraflagellar transport protein IFT27 promotes BBSome exit from cilia through the GTPase ARL6/BBS3.The role of primary cilia in the development and disease of the retina Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies KymographClear and KymographDirect: two tools for the automated quantitative analysis of molecular and cellular dynamics using kymographs.Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain Crystal structure of the small GTPase Arl6/BBS3 fromTrypanosoma brucei Intraflagellar transport complex structure and cargo interactions.CP110 and its network of partners coordinately regulate cilia assembly.Transition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexes The roles of evolutionarily conserved functional modules in cilia-related trafficking.IFT-Cargo Interactions and Protein Transport in Cilia Nephrocystin proteins NPHP5 and Cep290 regulate BBSome integrity, ciliary trafficking and cargo delivery IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis.Direct evidence for BBSome-associated intraflagellar transport reveals distinct properties of native mammalian cilia.Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia From the cytoplasm into the cilium: bon voyage.A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy.New mutations in flagellar motors identified by whole genome sequencing in Chlamydomonas.Ciliopathies: the trafficking connection.Identification and characterization of a novel allele of Caenorhabditis elegans bbs-7.Function and regulation of primary cilia and intraflagellar transport proteins in the skeleton Alternative Splicing Shapes the Phenotype of a Mutation in BBS8 To Cause Nonsyndromic Retinitis Pigmentosa BBS4 and BBS5 show functional redundancy in the BBSome to regulate the degradative sorting of ciliary sensory receptors.The small GTPase Rab8 interacts with VAMP-3 to regulate the delivery of recycling T-cell receptors to the immune synapse.A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4.Structural Characterization of Bardet-Biedl Syndrome 9 Protein (BBS9).Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish.Functional exploration of the IFT-A complex in intraflagellar transport and ciliogenesis.Structural defects in cilia of the choroid plexus, subfornical organ and ventricular ependyma are associated with ventriculomegaly.Loss of the BBSome perturbs endocytic trafficking and disrupts virulence of Trypanosoma brucei.Cycling of the signaling protein phospholipase D through cilia requires the BBSome only for the export phase.Evolution of modular intraflagellar transport from a coatomer-like progenitor.BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking.Intraflagellar transport drives flagellar surface motility.Depletion of BBS Protein LZTFL1 Affects Growth and Causes Retinal Degeneration in Mice.The hydrolethalus syndrome protein HYLS-1 regulates formation of the ciliary gate

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P2860

The BBSome controls IFT assembly and turnaround in cilia.

http://www.wikidata.org/entity/Q28000109

description

2012 nî lūn-bûn

@nan

2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

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2012年論文

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2012年论文

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name

The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

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type

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

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The BBSome controls IFT assembly and turnaround in cilia.

@nl

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Nature Cell Biology

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The BBSome controls IFT assembly and turnaround in cilia.

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P2093

Jinghua Hu

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

Kun Ling

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

Qing Wei

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

Qing Zhang

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

Yujie Li

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

Yuxia Zhang

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

P2860

Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia

A BBSome subunit links ciliogenesis, microtubule stability, and acetylation

The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia

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

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors.

Chlamydomonas kinesin-II-dependent intraflagellar transport (IFT): IFT particles contain proteins required for ciliary assembly in Caenorhabditis elegans sensory neurons

Rapid single nucleotide polymorphism mapping in C. elegans

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950-7

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scholarly article

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2198218

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10.1038/NCB2560

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9

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14

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2012-09-01T00:00:00Z

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230741659

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1030242090

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22922713

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Bardet-Biedl syndrome 4 (human)

Bardet-Biedl syndrome 7 (human)

Bardet-Biedl syndrome 2 (human)

Bardet-Biedl syndrome 5 (human)

Kinesin family member 17

Bardet-Biedl syndrome 9 (human)

Intraflagellar transport 88

Intraflagellar transport 52

Intraflagellar transport 57

Intraflagellar transport 80

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3434251

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