Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins.
about
The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalizationCompartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and diseaseThe nephronophthisis-related gene ift-139 is required for ciliogenesis in Caenorhabditis elegansActive transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomainKIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeTransition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexesMeckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndromeProtein arginine methyltransferases interact with intraflagellar transport particles and change location during flagellar growth and resorption.Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory ciliaNPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone.The nphp-2 and arl-13 genetic modules interact to regulate ciliogenesis and ciliary microtubule patterning in C. elegans.Ciliopathy proteins establish a bipartite signaling compartment in a C. elegans thermosensory neuronScoring a backstage pass: mechanisms of ciliogenesis and ciliary access.Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundanceCell- and subunit-specific mechanisms of CNG channel ciliary trafficking and localization in C. elegans.Cilium transition zone proteome reveals compartmentalization and differential dynamics of ciliopathy complexes.Cilia and coordination of signaling networks during heart development.Genetic kidney diseases: Caenorhabditis elegans as model system.GTP-binding of ARL-3 is activated by ARL-13 as a GEF and stabilized by UNC-119.Structural basis of the Inv compartment and ciliary abnormalities in Inv/nphp2 mutant mice.Conserved Ankyrin Repeat Proteins and Their NIMA Kinase Partners Regulate Extracellular Matrix Remodeling and Intracellular Trafficking in Caenorhabditis elegans.Cell type-specific regulation of ciliary transition zone assembly in vertebrates.
P2860
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P2860
Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins.
description
2012 nî lūn-bûn
@nan
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
2012年论文
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2012年论文
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name
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@ast
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@en
type
label
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@ast
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@en
prefLabel
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@ast
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@en
P2093
P2860
P356
P1476
Ciliogenesis in Caenorhabditis ...... tion zone-associated proteins.
@en
P2093
Andrew R Jauregui
Chunmei Li
Maureen M Barr
Michel R Leroux
Simon R F Warburton-Pitt
P2860
P304
P356
10.1242/JCS.095539
P407
P577
2012-03-05T00:00:00Z