Trafficking in and to the primary cilium. - Wikidata - awgldk - TriplyDB

Trafficking in and to the primary cilium.

Trafficking in and to the primary cilium.

http://www.wikidata.org/entity/Q28000124

about

Casein kinase 1δ functions at the centrosome and Golgi to promote ciliogenesis Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain PDE6δ-mediated sorting of INPP5E into the cilium is determined by cargo-carrier affinity TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome BAR Domain-Containing FAM92 Proteins Interact with Chibby1 To Facilitate Ciliogenesis GSK3β-Dzip1-Rab8 cascade regulates ciliogenesis after mitosis NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations.Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration Early eukaryotic origins for cilia-associated bioactive peptide-amidating activity.PI3K class II α controls spatially restricted endosomal PtdIns3P and Rab11 activation to promote primary cilium function A bioactive peptide amidating enzyme is required for ciliogenesis RhoGTPase-binding proteins, the exocyst complex and polarized vesicle trafficking Actin is required for IFT regulation in Chlamydomonas reinhardtii An assay for clogging the ciliary pore complex distinguishes mechanisms of cytosolic and membrane protein entry.Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole-cilium interface and facilitates proper cilium formation and function.Chlamydomonas axonemal dynein assembly locus ODA8 encodes a conserved flagellar protein needed for cytoplasmic maturation of outer dynein arm complexes Primary cilium suppression by SREBP1c involves distortion of vesicular trafficking by PLA2G3.The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.TOPORS, a Dual E3 Ubiquitin and Sumo1 Ligase, Interacts with 26 S Protease Regulatory Subunit 4, Encoded by the PSMC1 Gene.Dopamine receptors reveal an essential role of IFT-B, KIF17, and Rab23 in delivering specific receptors to primary cilia An intelligent nano-antenna: Primary cilium harnesses TRP channels to decode polymodal stimuli Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.Anoctamin 6 is localized in the primary cilium of renal tubular cells and is involved in apoptosis-dependent cyst lumen formation.Prion protein localizes at the ciliary base during neural and cardiovascular development, and its depletion affects α-tubulin post-translational modifications Regulation of polycystin-1 ciliary trafficking by motifs at its C-terminus and polycystin-2 but not by cleavage at the GPS site Primary cilia and dendritic spines: different but similar signaling compartments.Drosophila sensory cilia lacking MKS proteins exhibit striking defects in development but only subtle defects in adults.A ternary complex comprising transportin1, Rab8 and the ciliary targeting signal directs proteins to ciliary membranes.Functional Genomics Identifies Tis21-Dependent Mechanisms and Putative Cancer Drug Targets Underlying Medulloblastoma Shh-Type Development.Cilia and coordination of signaling networks during heart development.Influences of primary cilia on cortical morphogenesis and neuronal subtype maturation.Evolutionary implications of localization of the signaling scaffold protein parafusin to both cilia and the nucleus.VAMP7 modulates ciliary biogenesis in kidney cells.Primary Cilia in Cystic Kidney Disease.Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis.Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation.

P2860

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P2860

Trafficking in and to the primary cilium.

http://www.wikidata.org/entity/Q28000124

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Trafficking in and to the primary cilium.

@ast

Trafficking in and to the primary cilium.

@en

Trafficking in and to the primary cilium.

@nl

type

label

Trafficking in and to the primary cilium.

@ast

Trafficking in and to the primary cilium.

@en

Trafficking in and to the primary cilium.

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altLabel

Trafficking in and to the primary cilium

@en

prefLabel

Trafficking in and to the primary cilium.

@ast

Trafficking in and to the primary cilium.

@en

Trafficking in and to the primary cilium.

@nl

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Trafficking in and to the primary cilium.

@en

P2093

Karina Tuz

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

Russell J Ferland

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

Yi-Chun Hsiao

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

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

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

The Ciliopathies: An Emerging Class of Human Genetic Disorders

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

BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary cilium

Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling

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

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4

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scholarly article

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3521191

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10.1186/2046-2530-1-4

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1

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1

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2012-04-25T00:00:00Z

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235373952

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1015996544

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23351793

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P921

vesicle targeting, trans-Golgi to periciliary membrane compartment

P932

3541539

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