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Engineered kinesin motor proteins amenable to small-molecule inhibitionDYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsNINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in ZebrafishThe Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.Gated entry into the ciliary compartment.A ternary complex comprising transportin1, Rab8 and the ciliary targeting signal directs proteins to ciliary membranes.Ciliary entry of KIF17 is dependent on its binding to the IFT-B complex via IFT46-IFT56 as well as on its nuclear localization signal.Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.Protein Interaction Analysis Provides a Map of the Spatial and Temporal Organization of the Ciliary Gating Zone.Emerging roles of NudC family: from molecular regulation to clinical implications.Ionizing radiation increases primary cilia incidence and induces multiciliation in C2C12 myoblasts.Key roles of Arf small G proteins and biosynthetic trafficking for animal development.The serologically defined colon cancer antigen-3 (SDCCAG3) is involved in the regulation of ciliogenesis.RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly.Proteomic analysis of isolated ciliary transition zones reveals the presence of ESCRT proteins.Practical method for targeted disruption of cilia-related genes by using CRISPR/Cas9-mediated, homology-independent knock-in system.Cilium AssemblyPrimary cilia proteins: ciliary and extraciliary sites and functions.Mechanisms of ciliary targeting: entering importins and Rabs.Kidney-differentiated cells derived from Lowe Syndrome patient's iPSCs show ciliogenesis defects and Six2 retention at the Golgi complex.Morphological and Functional Characterization of the Ciliary Pocket by Electron and Fluorescence Microscopy.Methods for Studying Ciliary Import Mechanisms.BBS1 is involved in retrograde trafficking of ciliary GPCRs in the context of the BBSome complex.A splice site variant in INPP5E causes diffuse cystic renal dysplasia and hepatic fibrosis in dogs
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Ciliopathies: the trafficking connection.
@ast
Ciliopathies: the trafficking connection.
@en
Ciliopathies: the trafficking connection.
@nl
type
label
Ciliopathies: the trafficking connection.
@ast
Ciliopathies: the trafficking connection.
@en
Ciliopathies: the trafficking connection.
@nl
prefLabel
Ciliopathies: the trafficking connection.
@ast
Ciliopathies: the trafficking connection.
@en
Ciliopathies: the trafficking connection.
@nl
P2860
P356
P1433
P1476
Ciliopathies: the trafficking connection.
@en
P2093
Kayalvizhi Madhivanan
Ruben Claudio Aguilar
P2860
P304
P356
10.1111/TRA.12195
P577
2014-08-11T00:00:00Z