CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content. - Test2 - elhamkhani - TriplyDB

CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.

CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.

http://www.wikidata.org/entity/Q29614822

about

Primary ciliogenesis requires the distal appendage component Cep123.A novel protein LZTFL1 regulates ciliary trafficking of the BBSome and Smoothened Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis The novel centriolar satellite protein SSX2IP targets Cep290 to the ciliary transition zone BBS mutations modify phenotypic expression of CEP290-related ciliopathies The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome The centrosomal kinase Plk1 localizes to the transition zone of primary cilia and induces phosphorylation of nephrocystin-1 CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base Subunit interactions and organization of the Chlamydomonas reinhardtii intraflagellar transport complex A proteins Disruption of CEP290 microtubule/membrane-binding domains causes retinal degeneration The basal bodies of Chlamydomonas reinhardtii Induced Pluripotent Stem Cells and Outer Retinal Disease Photoreceptor Sensory Cilium: Traversing the Ciliary Gate The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization Cilia functions in development The awesome power of dikaryons for studying flagella and basal bodies in Chlamydomonas reinhardtii Molecular complexes that direct rhodopsin transport to primary cilia Ciliary subcompartments: how are they established and what are their functions?Kinesin motors and primary cilia Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease Scrutinizing ciliopathies by unraveling ciliary interaction networks CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies A NIMA-related kinase, CNK4, regulates ciliary stability and length.Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling Assembly of IFT trains at the ciliary base depends on IFT74 Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes The IN/OUT assay: a new tool to study ciliogenesis A role for the membrane in regulating Chlamydomonas flagellar length.KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome MLT1 links cytoskeletal asymmetry to organelle placement in chlamydomonas MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone Crystal structure of the intraflagellar transport complex 25/27 Crystal structure of a Chlamydomonas reinhardtii flagellar RabGAP TBC-domain at 1.8 Å resolution MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.Transition zone proteins and cilia dynamics.

P2860

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P2860

CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.

http://www.wikidata.org/entity/Q29614822

description

2010 nî lūn-bûn

@nan

2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@ast

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@en

type

label

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@ast

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@en

prefLabel

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@ast

CEP290 tethers flagellar trans ...... tes flagellar protein content.

@en

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CEP290 tethers flagellar trans ...... ates flagellar protein content

@en

P2093

Branch Craige

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

Che-Chia Tsao

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

Dennis R Diener

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

George B Witman

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

Joel L Rosenbaum

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

Yuqing Hou

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P2860

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Cep164, a novel centriole appendage protein required for primary cilium formation

Proteomic characterization of the human centrosome by protein correlation profiling

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

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

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

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

CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

Safety and efficacy of gene transfer for Leber's congenital amaurosis

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927-940

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1142443

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10.1083/JCB.201006105

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5

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190

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2010-09-01T00:00:00Z

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46158363

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20819941

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2935561

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