The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization - Test2 - elhamkhani - TriplyDB

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

http://www.wikidata.org/entity/Q26825968

about

Centriole distal appendages promote membrane docking, leading to cilia initiation CCDC41 is required for ciliary vesicle docking to the mother centriole CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base Unique properties of Drosophila spermatocyte primary cilia Novel transglutaminase-like peptidase and C2 domains elucidate the structure, biogenesis and evolution of the ciliary compartment Basal bodies in Xenopus Photoreceptor Sensory Cilium: Traversing the Ciliary Gate Novel Insights into the Development and Function of Cilia Using the Advantages of the Paramecium Cell and Its Many Cilia Autophagy and regulation of cilia function and assembly Ciliary subcompartments: how are they established and what are their functions?Primary cilia in the developing and mature brain Primary cilium and sonic hedgehog signaling during neural tube patterning: role of GPCRs and second messengers Kinesin-2 family motors in the unusual photoreceptor cilium 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 Distinct mechanisms eliminate mother and daughter centrioles in meiosis of starfish oocytes.DLK-1/p38 MAP Kinase Signaling Controls Cilium Length by Regulating RAB-5 Mediated Endocytosis in Caenorhabditis elegans The polarity protein Inturned links NPHP4 to Daam1 to control the subapical actin network in multiciliated cells.Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain 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 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.The Dishevelled Protein Family: Still Rather a Mystery After Over 20 Years of Molecular Studies A Conserved Role for Girdin in Basal Body Positioning and Ciliogenesis TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects Nephrocystin proteins NPHP5 and Cep290 regulate BBSome integrity, ciliary trafficking and cargo delivery A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface BAR Domain-Containing FAM92 Proteins Interact with Chibby1 To Facilitate Ciliogenesis RFX2 Is a Major Transcriptional Regulator of Spermiogenesis Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration Trafficking to the primary cilium membrane.Transmembrane protein OSTA-1 shapes sensory cilia morphology via regulation of intracellular membrane trafficking in C. elegans.An in vitro assay for entry into cilia reveals unique properties of the soluble diffusion barrier Chibby promotes ciliary vesicle formation and basal body docking during airway cell differentiation Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods Lineage specificity of primary cilia in the mouse embryo

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The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

http://www.wikidata.org/entity/Q26825968

description

2012 nî lūn-bûn

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2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2012 թվականի հունիսին 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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The base of the cilium: roles ...... nance and compartmentalization

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The base of the cilium: roles ...... nance and compartmentalization

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The base of the cilium: roles ...... nance and compartmentalization

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Jeremy F Reiter

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Michel R Leroux

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P2860

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

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

Ofd1, a human disease gene, regulates the length and distal structure of centrioles

Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

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

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation

Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome

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608-618

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10.1038/EMBOR.2012.73

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7

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13

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Oliver E Blacque

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2012-06-29T00:00:00Z

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225088129

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22653444

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photoreceptor connecting cilium

ciliary transition fiber

ciliary necklace

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3388784

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