about
Centrosome dysfunction contributes to chromosome instability, chromoanagenesis, and genome reprograming in cancerPrimary ciliogenesis requires the distal appendage component Cep123.The cytosolic carboxypeptidases CCP2 and CCP3 catalyze posttranslational removal of acidic amino acidsThe kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesDirect recording and molecular identification of the calcium channel of primary cilia.Stress-induced localization of HSPA6 (HSP70B') and HSPA1A (HSP70-1) proteins to centrioles in human neuronal cellsRab11 endosomes contribute to mitotic spindle organization and orientationProduction of Basal Bodies in bulk for dense multicilia formationLong range physical cell-to-cell signalling via mitochondria inside membrane nanotubes: a hypothesis.Human basal body basicsCellular Mechanisms of Ciliary Length ControlConnections between cadherin-catenin proteins, spindle misorientation, and cancerHuman Nek7-interactor RGS2 is required for mitotic spindle organization.Centrosomal nucleolin is required for microtubule network organization.Cep169, a Novel Microtubule Plus-End-Tracking Centrosomal Protein, Binds to CDK5RAP2 and Regulates Microtubule StabilityDiacylglycerol kinase α establishes T cell polarity by shaping diacylglycerol accumulation at the immunological synapseSequence evidence for common ancestry of eukaryotic endomembrane coatomers.Computational support for a scaffolding mechanism of centriole assembly.The Structure of the Plk4 Cryptic Polo Box Reveals Two Tandem Polo Boxes Required for Centriole DuplicationThe Mechanism of Dynein Light Chain LC8-mediated Oligomerization of the Ana2 Centriole Duplication FactorSAS-6 engineering reveals interdependence between cartwheel and microtubules in determining centriole architectureA deep proteomics perspective on CRM1-mediated nuclear export and nucleocytoplasmic partitioning.The roles of evolutionarily conserved functional modules in cilia-related trafficking.C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals.The PLK4-STIL-SAS-6 module at the core of centriole duplicationNephrocystin proteins NPHP5 and Cep290 regulate BBSome integrity, ciliary trafficking and cargo deliveryThe conserved Wdr8-hMsd1/SSX2IP complex localises to the centrosome and ensures proper spindle length and orientationBioanalysis of eukaryotic organellesSDCCAG8 regulates pericentriolar material recruitment and neuronal migration in the developing cortexThe ubiquitin receptor S5a/Rpn10 links centrosomal proteasomes with dendrite development in the mammalian brainExploring the evolutionary history of centrosomesNucleoporin Nup62 maintains centrosome homeostasisDiacylglycerol promotes centrosome polarization in T cells via reciprocal localization of dynein and myosin IISite-specific basal body duplication in Chlamydomonas.Excess centrosomes disrupt endothelial cell migration via centrosome scattering.C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle.Asterless is required for centriole length control and sperm developmentNovel role for the midbody in primary ciliogenesis by polarized epithelial cells.Cell-free reconstitution reveals centriole cartwheel assembly mechanisms.Lesion complexity drives age related cancer susceptibility in human mammary epithelial cells.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The centrosome in cells and organisms.
@en
The centrosome in cells and organisms.
@nl
type
label
The centrosome in cells and organisms.
@en
The centrosome in cells and organisms.
@nl
prefLabel
The centrosome in cells and organisms.
@en
The centrosome in cells and organisms.
@nl
P2860
P356
P1433
P1476
The centrosome in cells and organisms.
@en
P2093
Michel Bornens
P2860
P304
P356
10.1126/SCIENCE.1209037
P407
P577
2012-01-01T00:00:00Z