Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24564553

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A complex of BBS1 and NPHP7 is required for cilia motility in zebrafish The Chlamydomonas genome reveals the evolution of key animal and plant functions.TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone Bardet-Biedl syndrome proteins 1 and 3 regulate the ciliary trafficking of polycystic kidney disease 1 protein BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling 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 Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins LRRC50, a conserved ciliary protein implicated in polycystic kidney disease 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 Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans 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 Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors.Cellular Mechanisms of Ciliary Length Control Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease Japanese studies on neural circuits and behavior of Caenorhabditis elegans Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain Repression of a potassium channel by nuclear hormone receptor and TGF-β signaling modulates insulin signaling in Caenorhabditis elegans Mutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegans MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome.Characterization of the intraflagellar transport complex B core: direct interaction of the IFT81 and IFT74/72 subunits.Functional coordination of intraflagellar transport motors.Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles.The nonmotile ciliopathies.MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis Architecture and function of IFT complex proteins in ciliogenesis The emerging role of Arf/Arl small GTPases in cilia and ciliopathies.The BBSome controls IFT assembly and turnaround in cilia.Intraflagellar transport complex structure and cargo interactions.

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P2860

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

http://www.wikidata.org/entity/Q24564553

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2004 nî lūn-bûn

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2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի հուլիսին 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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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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type

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... mised intraflagellar transport

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Loss of C. elegans BBS-7 and B ...... ised intraflagellar transport.

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Allan K Mah

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

Chunmei Li

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

David L Baillie

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

Jonathan McCarthy

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

Mark Audeh

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

Michael J Reardon

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

Michel R Leroux

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

Philip L Beales

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

Robert C Johnsen

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

Ronald H A Plasterk

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

P2860

Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome

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

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

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

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

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

Protein particles in Chlamydomonas flagella undergo a transport cycle consisting of four phases

Intraflagellar transport

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

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1630-42

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10.1101/GAD.1194004

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13

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18

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Nicholas Katsanis

Stephen R Wicks

Oliver E Blacque

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2004-07-01T00:00:00Z

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8476495

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15231740

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Caenorhabditis elegans

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443524

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