Cep164, a novel centriole appendage protein required for primary cilium formation
about
Centrosome dysfunction contributes to chromosome instability, chromoanagenesis, and genome reprograming in cancerDisruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndromeBasal body stability and ciliogenesis requires the conserved component Poc1Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingPrimary ciliogenesis requires the distal appendage component Cep123.Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methodsCandidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathyPoc1A and Poc1B act together in human cells to ensure centriole integrityCentriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophyCEP90 is required for the assembly and centrosomal accumulation of centriolar satellites, which is essential for primary cilia formationThe deubiquitinating enzyme CYLD controls apical docking of basal bodies in ciliated epithelial cellsOfd1, a human disease gene, regulates the length and distal structure of centriolesThe spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesisRBM14 prevents assembly of centriolar protein complexes and maintains mitotic spindle integrityCEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary ciliumCentriole distal appendages promote membrane docking, leading to cilia initiationThe microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis.OCRL localizes to the primary cilium: a new role for cilia in Lowe syndromeEarly steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formationThe CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assemblyCCDC41 is required for ciliary vesicle docking to the mother centriolePitchfork regulates primary cilia disassembly and left-right asymmetryCEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia baseCP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary diseaseCC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290Plk1-dependent and -independent roles of an ODF2 splice variant, hCenexin1, at the centrosome of somatic cellsCep164 is a mediator protein required for the maintenance of genomic stability through modulation of MDC1, RPA, and CHK1A primer on the mouse basal bodyHuman basal body basicsCellular Mechanisms of Ciliary Length ControlCurrent topics of functional links between primary cilia and cell cycleBuilding a ninefold symmetrical barrel: structural dissections of centriole assemblyThe role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologiesThe Seckel syndrome and centrosomal protein Ninein localizes asymmetrically to stem cell centrosomes but is not required for normal development, behavior, or DNA damage response in Drosophilap53 protects against genome instability following centriole duplication failureCentrosomal nucleolin is required for microtubule network organization.Nephronophthisis-associated CEP164 regulates cell cycle progression, apoptosis and epithelial-to-mesenchymal transitionAcute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypesCep57 is a Mis12-interacting kinetochore protein involved in kinetochore targeting of Mad1-Mad2.
P2860
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P2860
Cep164, a novel centriole appendage protein required for primary cilium formation
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Cep164, a novel centriole appendage protein required for primary cilium formation
@ast
Cep164, a novel centriole appendage protein required for primary cilium formation
@en
Cep164, a novel centriole appendage protein required for primary cilium formation
@en-gb
Cep164, a novel centriole appendage protein required for primary cilium formation
@nl
type
label
Cep164, a novel centriole appendage protein required for primary cilium formation
@ast
Cep164, a novel centriole appendage protein required for primary cilium formation
@en
Cep164, a novel centriole appendage protein required for primary cilium formation
@en-gb
Cep164, a novel centriole appendage protein required for primary cilium formation
@nl
prefLabel
Cep164, a novel centriole appendage protein required for primary cilium formation
@ast
Cep164, a novel centriole appendage protein required for primary cilium formation
@en
Cep164, a novel centriole appendage protein required for primary cilium formation
@en-gb
Cep164, a novel centriole appendage protein required for primary cilium formation
@nl
P2093
P2860
P921
P3181
P356
P1476
Cep164, a novel centriole appendage protein required for primary cilium formation
@en
P2093
Mikael Le Clech
Oliver S Gassner
Stefan Lamla
Susanne Graser
Sébastien B Lavoie
York-Dieter Stierhof
P2860
P304
P3181
P356
10.1083/JCB.200707181
P407
P50
P577
2007-10-22T00:00:00Z