Distinct mutants of retrograde intraflagellar transport (IFT) share similar morphological and molecular defects
about
TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary ciliaDisruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and miceA novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cellsSubunit interactions and organization of the Chlamydomonas reinhardtii intraflagellar transport complex A proteinsIntraflagellar transport motors in cilia: moving along the cell's antennaIn-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 mouseIntraflagellar transport: the eyes have itChlamydomonas fla mutants reveal a link between deflagellation and intraflagellar transportCellular Mechanisms of Ciliary Length ControlCilia/Ift protein and motor -related bone diseases and mouse modelsA NIMA-related kinase, CNK4, regulates ciliary stability and length.Crystal structure of the intraflagellar transport complex 25/27Crystal structure of a Chlamydomonas reinhardtii flagellar RabGAP TBC-domain at 1.8 Å resolutionProtein particles in Chlamydomonas flagella undergo a transport cycle consisting of four phasesThe intraflagellar transport machinery of Chlamydomonas reinhardtii.Characterization of the intraflagellar transport complex B core: direct interaction of the IFT81 and IFT74/72 subunits.Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles.Retrograde intraflagellar transport mutants identify complex A proteins with multiple genetic interactions in Chlamydomonas reinhardtii.Electron-tomographic analysis of intraflagellar transport particle trains in situ.Direct interactions of intraflagellar transport complex B proteins IFT88, IFT52, and IFT46.Architecture and function of IFT complex proteins in ciliogenesisThe BBSome controls IFT assembly and turnaround in cilia.Transition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexesIFT20 links kinesin II with a mammalian intraflagellar transport complex that is conserved in motile flagella and sensory ciliaCiliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19Cilia and developmental signalingIntraflagellar transport (IFT) protein IFT25 is a phosphoprotein component of IFT complex B and physically interacts with IFT27 in ChlamydomonasCaenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory ciliaIntraflagellar transport protein 122 antagonizes Sonic Hedgehog signaling and controls ciliary localization of pathway componentsTHM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in ciliaComplex interactions between genes controlling trafficking in primary ciliaCauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndromeCartilage abnormalities associated with defects of chondrocytic primary cilia in Bardet-Biedl syndrome mutant mice.Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvementCEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis.Kinesin-II is preferentially targeted to assembling cilia and is required for ciliogenesis and normal cytokinesis in TetrahymenaXBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans.The WD repeat-containing protein IFTA-1 is required for retrograde intraflagellar transport.Distinct IFT mechanisms contribute to the generation of ciliary structural diversity in C. elegans.
P2860
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P2860
Distinct mutants of retrograde intraflagellar transport (IFT) share similar morphological and molecular defects
description
1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1998
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im Dezember 1998 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
@en
vedecký článok (publikovaný 1998/12/14)
@sk
vědecký článek publikovaný v roce 1998
@cs
wetenschappelijk artikel (gepubliceerd op 1998/12/14)
@nl
наукова стаття, опублікована в грудні 1998
@uk
مقالة علمية (نشرت في 14-12-1998)
@ar
name
Distinct mutants of retrograde ...... ological and molecular defects
@ast
Distinct mutants of retrograde ...... ological and molecular defects
@en
Distinct mutants of retrograde ...... ological and molecular defects
@nl
type
label
Distinct mutants of retrograde ...... ological and molecular defects
@ast
Distinct mutants of retrograde ...... ological and molecular defects
@en
Distinct mutants of retrograde ...... ological and molecular defects
@nl
prefLabel
Distinct mutants of retrograde ...... ological and molecular defects
@ast
Distinct mutants of retrograde ...... ological and molecular defects
@en
Distinct mutants of retrograde ...... ological and molecular defects
@nl
P2093
P2860
P3181
P356
P1476
Distinct mutants of retrograde ...... ological and molecular defects
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P2093
P2860
P304
P3181
P356
10.1083/JCB.143.6.1591
P407
P577
1998-12-01T00:00:00Z