about
Casein kinase 1δ functions at the centrosome and Golgi to promote ciliogenesisCopy number variants in obesity-related syndromes: review and perspectives on novel molecular approachesCompartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and diseaseActive transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomainPDE6δ-mediated sorting of INPP5E into the cilium is determined by cargo-carrier affinityTMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndromeBAR Domain-Containing FAM92 Proteins Interact with Chibby1 To Facilitate CiliogenesisGSK3β-Dzip1-Rab8 cascade regulates ciliogenesis after mitosisNINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in ZebrafishAn 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 degenerationEarly 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 functionA bioactive peptide amidating enzyme is required for ciliogenesisRhoGTPase-binding proteins, the exocyst complex and polarized vesicle traffickingActin is required for IFT regulation in Chlamydomonas reinhardtiiAn 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 complexesPrimary 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 ciliaAn intelligent nano-antenna: Primary cilium harnesses TRP channels to decode polymodal stimuliWhole-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 modificationsRegulation of polycystin-1 ciliary trafficking by motifs at its C-terminus and polycystin-2 but not by cleavage at the GPS sitePrimary 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
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.
@nl
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
P2093
P2860
P3181
P356
P1433
P1476
Trafficking in and to the primary cilium.
@en
P2093
Karina Tuz
Russell J Ferland
Yi-Chun Hsiao
P2860
P2888
P3181
P356
10.1186/2046-2530-1-4
P407
P577
2012-04-25T00:00:00Z
P5875
P6179
1015996544