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RTTN mutations link primary cilia function to organization of the human cerebral cortexPoc1A and Poc1B act together in human cells to ensure centriole integrityZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyHuman microcephaly protein CEP135 binds to hSAS-6 and CPAP, and is required for centriole assemblyCCDC41 is required for ciliary vesicle docking to the mother centrioleTankyrase 1 regulates centrosome function by controlling CPAP stabilityThe centrosomal kinase Plk1 localizes to the transition zone of primary cilia and induces phosphorylation of nephrocystin-1Unique properties of Drosophila spermatocyte primary ciliaDrosophila melanogaster as a model for basal body researchBuilding a ninefold symmetrical barrel: structural dissections of centriole assemblyOLA1 in centrosome biology alongside the BRCA1/BARD1 complex: looking beyond centrosomesScrutinizing ciliopathies by unraveling ciliary interaction networksCEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathiesCentrosomal nucleolin is required for microtubule network organization.The Structure of the Plk4 Cryptic Polo Box Reveals Two Tandem Polo Boxes Required for Centriole DuplicationSAS-6 coiled-coil structure and interaction with SAS-5 suggest a regulatory mechanism inC. eleganscentriole assemblyCrystal structures of the CPAP/STIL complex reveal its role in centriole assembly and human microcephalyCP110 and its network of partners coordinately regulate cilia assembly.The PLK4-STIL-SAS-6 module at the core of centriole duplicationCentrosome - a promising anti-cancer targetPathogenic NPHP5 mutations impair protein interaction with Cep290, a prerequisite for ciliogenesisNek2 activation of Kif24 ensures cilium disassembly during the cell cycleTranscriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human diseaseMotile cilia harbor serum response factor as a mechanism of environment sensing and injury response in the airwayAcentriolar mitosis activates a p53-dependent apoptosis pathway in the mouse embryoThe coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animalsCPAP is required for cilia formation in neuronal cells.Merlin/ERM proteins establish cortical asymmetry and centrosome position.Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization.A non-canonical mode of microtubule organization operates throughout pre-implantation development in mouseCP110 exhibits novel regulatory activities during centriole assembly in Drosophila.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 developmentStronger net posterior cortical forces and asymmetric microtubule arrays produce simultaneous centration and rotation of the pronuclear complex in the early Caenorhabditis elegans embryoCell-free reconstitution reveals centriole cartwheel assembly mechanisms.USP9X regulates centrosome duplication and promotes breast carcinogenesis.Mutation in PLK4, encoding a master regulator of centriole formation, defines a novel locus for primordial dwarfism.MCPH1: a window into brain development and evolution.The Ca2+-activated Cl- channel ANO1/TMEM16A regulates primary ciliogenesis
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 15 June 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Centrosomes and cilia in human disease.
@en
Centrosomes and cilia in human disease.
@nl
type
label
Centrosomes and cilia in human disease.
@en
Centrosomes and cilia in human disease.
@nl
prefLabel
Centrosomes and cilia in human disease.
@en
Centrosomes and cilia in human disease.
@nl
P2093
P2860
P1433
P1476
Centrosomes and cilia in human disease
@en
P2093
David Pellman
Friedhelm Hildebrandt
Geoff Woods
P2860
P304
P356
10.1016/J.TIG.2011.05.004
P577
2011-06-15T00:00:00Z