Architecture and function of IFT complex proteins in ciliogenesis - Test2 - elhamkhani - TriplyDB

Architecture and function of IFT complex proteins in ciliogenesis

Architecture and function of IFT complex proteins in ciliogenesis

http://www.wikidata.org/entity/Q28000079

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Novel transglutaminase-like peptidase and C2 domains elucidate the structure, biogenesis and evolution of the ciliary compartment Cilia/Ift protein and motor -related bone diseases and mouse models Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function Assembly of IFT trains at the ciliary base depends on IFT74 Sequence evidence for common ancestry of eukaryotic endomembrane coatomers.MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone Crystal structure of a Chlamydomonas reinhardtii flagellar RabGAP TBC-domain at 1.8 Å resolution Structure of Rab11-FIP3-Rabin8 reveals simultaneous binding of FIP3 and Rabin8 effectors to Rab11 Intraflagellar transport complex structure and cargo interactions.The roles of evolutionarily conserved functional modules in cilia-related trafficking.Nephronophthisis and related syndromes IFT-Cargo Interactions and Protein Transport in Cilia Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization Functional interaction between autophagy and ciliogenesis Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome From Planar Cell Polarity to Ciliogenesis and Back: The Curious Tale of the PPE and CPLANE proteins.Visualization of live primary cilia dynamics using fluorescence microscopy.Direct evidence for BBSome-associated intraflagellar transport reveals distinct properties of native mammalian cilia.IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.IFT trains in different stages of assembly queue at the ciliary base for consecutive release into the cilium.Cytoplasmic carboxypeptidase 5 regulates tubulin glutamylation and zebrafish cilia formation and function Cep164 triggers ciliogenesis by recruiting Tau tubulin kinase 2 to the mother centriole.Ciliopathies: the trafficking connection.Large-scale identification of proteins involved in the development of a sexually dimorphic behavior.A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS LdFlabarin, a new BAR domain membrane protein of Leishmania flagellum.Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome.Function and regulation of primary cilia and intraflagellar transport proteins in the skeleton Cilia and Diseases Dynein and intraflagellar transport.Deletion of IFT20 in early stage T lymphocyte differentiation inhibits the development of collagen-induced arthritis.Components of Intraflagellar Transport Complex A Function Independently of the Cilium to Regulate Canonical Wnt Signaling in Drosophila.IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins.Evolution of modular intraflagellar transport from a coatomer-like progenitor.Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an Essential Component of the IFT-B Peripheral Subcomplex

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Architecture and function of IFT complex proteins in ciliogenesis

http://www.wikidata.org/entity/Q28000079

description

2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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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

Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis.

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis.

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis

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Architecture and function of IFT complex proteins in ciliogenesis.

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J.DIFF.2011.11.001

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Differentiation

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Architecture and function of IFT complex proteins in ciliogenesis

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P2860

The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

Towards a proteome-scale map of the human protein–protein interaction network

MIP-T3, a novel protein linking tumor necrosis factor receptor-associated factor 3 to the microtubule network

Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi

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

C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis

TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia

A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells

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cilium morphogenesis

intraciliary transport particle

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