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The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries

https://doi.org/10.1038/ncb2345
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/1047-8477(92)90011-xopenalex-snapshot
Centrosome organization and centriole architecture: Their sensitivity to divalent cations
inferredcites →https://doi.org/10.1016/j.ceb.2009.01.008openalex-snapshot
Centriole evolution
inferredcites →https://doi.org/10.1016/j.cell.2006.05.025openalex-snapshot
Flies without Centrioles
inferredcites →https://doi.org/10.1016/j.cell.2007.06.027openalex-snapshot
Cep97 and CP110 Suppress a Cilia Assembly Program
inferredcites →https://doi.org/10.1016/j.cell.2008.05.039openalex-snapshot
Centrosome Amplification Can Initiate Tumorigenesis in Flies
inferredcites →https://doi.org/10.1016/j.cell.2009.10.036openalex-snapshot
Centrioles, Centrosomes, and Cilia in Health and Disease
inferredcites →https://doi.org/10.1016/j.cell.2011.01.008openalex-snapshot
Structural Basis of the 9-Fold Symmetry of Centrioles
inferredcites →https://doi.org/10.1016/j.cellbi.2005.10.001openalex-snapshot
Reappraisal of the Hansemann–Boveri hypothesis on the origin of tumors
inferredcites →https://doi.org/10.1016/j.cub.2005.11.042openalex-snapshot
SAK/PLK4 Is Required for Centriole Duplication and Flagella Development
inferredcites →https://doi.org/10.1016/j.cub.2007.04.036openalex-snapshot
Overexpressing Centriole-Replication Proteins In Vivo Induces Centriole Overduplication and De Novo Formation
inferredcites →https://doi.org/10.1016/j.cub.2007.07.034openalex-snapshot
DSAS-6 Organizes a Tube-like Centriole Precursor, and Its Absence Suggests Modularity in Centriole Assembly
inferredcites →https://doi.org/10.1016/j.cub.2007.11.046openalex-snapshot
SAS-6 is a Cartwheel Protein that Establishes the 9-Fold Symmetry of the Centriole
inferredcites →https://doi.org/10.1016/j.cub.2008.11.037openalex-snapshot
The SCF/Slimb Ubiquitin Ligase Limits Centrosome Amplification through Degradation of SAK/PLK4
inferredcites →https://doi.org/10.1016/j.cub.2009.05.016openalex-snapshot
Control of Centriole Length by CPAP and CP110
inferredcites →https://doi.org/10.1016/j.cub.2009.05.018openalex-snapshot
Overly Long Centrioles and Defective Cell Division upon Excess of the SAS-4-Related Protein CPAP
inferredcites →https://doi.org/10.1016/j.cub.2009.07.034openalex-snapshot
Centriole Age Underlies Asynchronous Primary Cilium Growth in Mammalian Cells
inferredcites →https://doi.org/10.1016/j.cub.2009.09.020openalex-snapshot
The MST1 and hMOB1 Tumor Suppressors Control Human Centrosome Duplication by Regulating NDR Kinase Phosphorylation
inferredcites →https://doi.org/10.1016/j.cub.2010.05.050openalex-snapshot
Centriole Reduplication during Prolonged Interphase Requires Procentriole Maturation Governed by Plk1
inferredcites →https://doi.org/10.1016/j.cub.2010.08.010openalex-snapshot
Building the Centriole
inferredcites →https://doi.org/10.1016/j.cub.2010.11.011openalex-snapshot
Centrioles Regulate Centrosome Size by Controlling the Rate of Cnn Incorporation into the PCM
inferredcites →https://doi.org/10.1016/j.cub.2011.05.047openalex-snapshot
Plk1 Controls the Nek2A-PP1γ Antagonism in Centrosome Disjunction
inferredcites →https://doi.org/10.1016/j.devcel.2004.10.015openalex-snapshot
Centriole Assembly Requires Both Centriolar and Pericentriolar Material Proteins
inferredcites →https://doi.org/10.1016/j.devcel.2007.01.021openalex-snapshot
Functionally Unequal Centrosomes Drive Spindle Orientation in Asymmetrically Dividing Drosophila Neural Stem Cells
inferredcites →https://doi.org/10.1016/j.devcel.2007.07.002openalex-snapshot
Plk4-Induced Centriole Biogenesis in Human Cells
inferredcites →https://doi.org/10.1016/j.devcel.2007.07.004openalex-snapshot
Regulated HsSAS-6 Levels Ensure Formation of a Single Procentriole per Centriole during the Centrosome Duplication Cycle
inferredcites →https://doi.org/10.1016/j.devcel.2008.07.004openalex-snapshot
CP110 Suppresses Primary Cilia Formation through Its Interaction with CEP290, a Protein Deficient in Human Ciliary Disease
inferredcites →https://doi.org/10.1016/j.devcel.2009.07.015openalex-snapshot
Polo Kinase and Separase Regulate the Mitotic Licensing of Centriole Duplication in Human Cells
inferredcites →https://doi.org/10.1016/j.devcel.2009.11.002openalex-snapshot
Phosphorylation of SAS-6 by ZYG-1 Is Critical for Centriole Formation in C. elegans Embryos
inferredcites →https://doi.org/10.1016/j.devcel.2009.12.022openalex-snapshot
Ofd1, a Human Disease Gene, Regulates the Length and Distal Structure of Centrioles
inferredcites →https://doi.org/10.1016/j.devcel.2010.11.010openalex-snapshot
DSas-6 and Ana2 Coassemble into Tubules to Promote Centriole Duplication and Engagement
inferredcites →https://doi.org/10.1016/j.devcel.2011.02.005openalex-snapshot
PP2A Phosphatase Acts upon SAS-5 to Ensure Centriole Formation in C. elegans Embryos
inferredcites →https://doi.org/10.1016/j.devcel.2011.03.007openalex-snapshot
Protein Phosphatase 2A-SUR-6/B55 Regulates Centriole Duplication in C. elegans by Controlling the Levels of Centriole Assembly Factors
inferredcites →https://doi.org/10.1016/j.semcdb.2009.07.002openalex-snapshot
Centriole maturation and transformation to basal body
inferredcites →https://doi.org/10.1016/j.semcdb.2010.01.014openalex-snapshot
The cellular and developmental program connecting the centrosome and cilium duplication cycle
inferredcites →https://doi.org/10.1016/j.tcb.2007.03.003openalex-snapshot
Centrosome duplication: of rules and licenses
inferredcites →https://doi.org/10.1016/j.tcb.2008.06.004openalex-snapshot
Mechanisms of procentriole formation
inferredcites →https://doi.org/10.1016/j.tcb.2010.09.004openalex-snapshot
Common themes in centriole and centrosome movements
inferredcites →https://doi.org/10.1016/j.tig.2011.05.004openalex-snapshot
Centrosomes and cilia in human disease
inferredcites →https://doi.org/10.1016/s0092-8674(00)00130-6openalex-snapshot
Cleavage of Cohesin by the CD Clan Protease Separin Triggers Anaphase in Yeast
inferredcites →https://doi.org/10.1016/s0955-0674(01)00290-3openalex-snapshot
Centrosome composition and microtubule anchoring mechanisms
inferredcites →https://doi.org/10.1038/35000041openalex-snapshot
DNA-replication/DNA-damage-dependent centrosome inactivation in Drosophila embryos
inferredcites →https://doi.org/10.1038/emboj.2011.179openalex-snapshot
Nek9 is a Plk1‐activated kinase that controls early centrosome separation through Nek6/7 and Eg5
inferredcites →https://doi.org/10.1038/emboj.2011.63openalex-snapshot
Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods
inferredcites →https://doi.org/10.1038/nature01241openalex-snapshot
Asymmetric inheritance of centrosomally localized mRNAs during embryonic cleavages
inferredcites →https://doi.org/10.1038/nature02166openalex-snapshot
Proteomic characterization of the human centrosome by protein correlation profiling
inferredcites →https://doi.org/10.1038/nature04985openalex-snapshot
Mechanism limiting centrosome duplication to once per cell cycle
inferredcites →https://doi.org/10.1038/nature05318openalex-snapshot
Centriole assembly in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nature08136openalex-snapshot
A mechanism linking extra centrosomes to chromosomal instability
inferredcites →https://doi.org/10.1038/nature08435openalex-snapshot
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
inferredcites →https://doi.org/10.1038/nature09140openalex-snapshot
SCFCyclin F controls centrosome homeostasis and mitotic fidelity through CP110 degradation
inferredcites →https://doi.org/10.1038/nature09445openalex-snapshot
Asterless is a scaffold for the onset of centriole assembly
inferredcites →https://doi.org/10.1038/ncb1165openalex-snapshot
Centrosome-associated Chk1 prevents premature activation of cyclin-B–Cdk1 kinase
inferredcites →https://doi.org/10.1038/ncb1320openalex-snapshot
The Polo kinase Plk4 functions in centriole duplication
inferredcites →https://doi.org/10.1038/ncb1694openalex-snapshot
Control of daughter centriole formation by the pericentriolar material
inferredcites →https://doi.org/10.1038/ncb1889openalex-snapshot
CPAP is a cell-cycle regulated protein that controls centriole length
inferredcites →https://doi.org/10.1038/ncb2120openalex-snapshot
Components of the Hippo pathway cooperate with Nek2 kinase to regulate centrosome disjunction
inferredcites →https://doi.org/10.1038/ncb2280openalex-snapshot
Cleavage of cohesin rings coordinates the separation of centrioles and chromatids
inferredcites →https://doi.org/10.1038/ncb2282openalex-snapshot
The SCF–FBXW5 E3-ubiquitin ligase is regulated by PLK4 and targets HsSAS-6 to control centrosome duplication
inferredcites →https://doi.org/10.1038/ncomms1245openalex-snapshot
Drosophila neuroblasts retain the daughter centrosome
inferredcites →https://doi.org/10.1038/nrc924openalex-snapshot
Centrosome aberrations: cause or consequence of cancer progression?
inferredcites →https://doi.org/10.1038/nrg2774openalex-snapshot
The primary cilium: a signalling centre during vertebrate development
inferredcites →https://doi.org/10.1038/nrm2100openalex-snapshot
Microtubule-organizing centres: a re-evaluation
inferredcites →https://doi.org/10.1042/0264-6021:3490509openalex-snapshot
NIMA-related kinase 2 (Nek2), a cell-cycle-regulated protein kinase localized to centrosomes, is complexed to protein phosphatase 1
inferredcites →https://doi.org/10.1073/pnas.0803027105openalex-snapshot
Asymmetric mitosis: Unequal segregation of proteins destined for degradation
inferredcites →https://doi.org/10.1074/jbc.m109.092627openalex-snapshot
Self-assembling SAS-6 Multimer Is a Core Centriole Building Block
inferredcites →https://doi.org/10.1083/jcb.130.1.105openalex-snapshot
Dissociation of centrosome replication events from cycles of DNA synthesis and mitotic division in hydroxyurea-arrested Chinese hamster ovary cells.
inferredcites →https://doi.org/10.1083/jcb.141.7.1563openalex-snapshot
C-Nap1, a Novel Centrosomal Coiled-Coil Protein and Candidate Substrate of the Cell Cycle–regulated Protein Kinase Nek2
inferredcites →https://doi.org/10.1083/jcb.149.2.317openalex-snapshot
The Respective Contributions of the Mother and Daughter Centrioles to Centrosome Activity and Behavior in Vertebrate Cells
inferredcites →https://doi.org/10.1083/jcb.151.4.837openalex-snapshot
The Centrosomal Protein C-Nap1 Is Required for Cell Cycle–Regulated Centrosome Cohesion
inferredcites →https://doi.org/10.1083/jcb.200205102openalex-snapshot
De novo formation of centrosomes in vertebrate cells arrested during S phase
inferredcites →https://doi.org/10.1083/jcb.200504107openalex-snapshot
Rootletin forms centriole-associated filaments and functions in centrosome cohesion
inferredcites →https://doi.org/10.1083/jcb.200612140openalex-snapshot
A role for a novel centrosome cycle in asymmetric cell division
inferredcites →https://doi.org/10.1083/jcb.200707181openalex-snapshot
Cep164, a novel centriole appendage protein required for primary cilium formation
inferredcites →https://doi.org/10.1083/jcb.200709102openalex-snapshot
SAS-4 is recruited to a dynamic structure in newly forming centrioles that is stabilized by the γ-tubulin–mediated addition of centriolar microtubules
inferredcites →https://doi.org/10.1083/jcb.200808049openalex-snapshot
The SCFSlimb ubiquitin ligase regulates Plk4/Sak levels to block centriole reduplication
inferredcites →https://doi.org/10.1083/jcb.200808082openalex-snapshot
hPOC5 is a centrin-binding protein required for assembly of full-length centrioles
inferredcites →https://doi.org/10.1083/jcb.200905024openalex-snapshot
The interphase microtubule aster is a determinant of asymmetric division orientation in Drosophila neuroblasts
inferredcites →https://doi.org/10.1083/jcb.200910016openalex-snapshot
Drosophila Ana2 is a conserved centriole duplication factor
inferredcites →https://doi.org/10.1083/jcb.200911102openalex-snapshot
Polo-like kinase 4 kinase activity limits centrosome overduplication by autoregulating its own stability
inferredcites →https://doi.org/10.1083/jcb.201003009openalex-snapshot
Cep120 is asymmetrically localized to the daughter centriole and is essential for centriole assembly
inferredcites →https://doi.org/10.1083/jcb.201006049openalex-snapshot
Cep152 interacts with Plk4 and is required for centriole duplication
inferredcites →https://doi.org/10.1083/jcb.201007107openalex-snapshot
Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome
inferredcites →https://doi.org/10.1083/jcb.201011152openalex-snapshot
Tracing the origins of centrioles, cilia, and flagella
inferredcites →https://doi.org/10.1083/jcb.201101109openalex-snapshot
The conversion of centrioles to centrosomes: essential coupling of duplication with segregation
inferredcites →https://doi.org/10.1091/mbc.e02-08-0510openalex-snapshot
Centrosomes Split in the Presence of Impaired DNA Integrity during Mitosis
inferredcites →https://doi.org/10.1091/mbc.e05-10-0943openalex-snapshot
Rootletin Interacts with C-Nap1 and May Function as a Physical Linker between the Pair of Centrioles/Basal Bodies in Cells
inferredcites →https://doi.org/10.1091/mbc.e09-06-0505openalex-snapshot
Autophosphorylation of Polo-like Kinase 4 and Its Role in Centriole Duplication
inferredcites →https://doi.org/10.1091/mbc.e09-12-1049openalex-snapshot
Daughter Centriole Elongation Is Controlled by Proteolysis
inferredcites →https://doi.org/10.1091/mbc.e10-02-0124openalex-snapshot
A Centrosome-autonomous Signal That Involves Centriole Disengagement Permits Centrosome Duplication in G2 Phase after DNA Damage
inferredcites →https://doi.org/10.1101/gad.1700908openalex-snapshot
Mechanisms to suppress multipolar divisions in cancer cells with extra centrosomes
inferredcites →https://doi.org/10.1126/science.1057330openalex-snapshot
Centrosome-Dependent Exit of Cytokinesis in Animal Cells
inferredcites →https://doi.org/10.1126/science.1087795openalex-snapshot
Orientation of Asymmetric Stem Cell Division by the APC Tumor Suppressor and Centrosome
inferredcites →https://doi.org/10.1126/science.1142950openalex-snapshot
Revisiting the Role of the Mother Centriole in Centriole Biogenesis
inferredcites →https://doi.org/10.1126/science.1199325openalex-snapshot
Structures of SAS-6 Suggest Its Organization in Centrioles
inferredcites →https://doi.org/10.1242/dev.045500openalex-snapshot
Hippo signaling: growth control and beyond
inferredcites →https://doi.org/10.1242/jcs.020248openalex-snapshot
Cep68 and Cep215 (Cdk5rap2) are required for centrosome cohesion
inferredcites →https://doi.org/10.1242/jcs.068502openalex-snapshot
Plk4 trans-autophosphorylation regulates centriole number by controlling βTrCP-mediated degradation
inferredcites →https://doi.org/10.1242/jcs.086488openalex-snapshot
Nuclear Chk1 prevents premature mitotic entry
inferredcites →https://doi.org/10.1371/journal.pbio.0060224openalex-snapshot
A Genome-Wide RNAi Screen to Dissect Centriole Duplication and Centrosome Maturation in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0006564openalex-snapshot
Multipolar Spindle Pole Coalescence Is a Major Source of Kinetochore Mis-Attachment and Chromosome Mis-Segregation in Cancer Cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4692176openalex-extracted
Targeted Localization of the Mother Centrosome in CD8 T Cells Undergoing Asymmetric Cell Division Promotes Memory Formation
inferred← citeshttps://doi.org/10.1002/1873-3468.14204openalex-snapshot
Disruption of desmosome function leads to increased centrosome clustering in 14‐3‐3γ‐knockout cells with supernumerary centrosomes
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001356.pub2openalex-snapshot
Mitosis
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005774.pub2openalex-snapshot
Mitosis: Chromosome Segregation and Stability
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020872openalex-snapshot
Centrosome in Cell Division, Development and Disease
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021863openalex-snapshot
Centrosomes in Asymmetric Cell Division and Neocortical Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022518openalex-snapshot
Mitotic Spindle Assembly: The Roles of Microtubule Nucleation and Assembly
inferred← citeshttps://doi.org/10.1002/9781118647110.ch3openalex-snapshot
Chromosome Instability in Stem Cells
inferred← citeshttps://doi.org/10.1002/9783527698448.ch17openalex-snapshot
Zellzyklus
inferred← citeshttps://doi.org/10.1002/adma.202209529openalex-snapshot
In Response to Precision Medicine: Current Subcellular Targeting Strategies for Cancer Therapy
inferred← citeshttps://doi.org/10.1002/bies.201200082openalex-snapshot
Genome instability: Does genetic diversity amplification drive tumorigenesis?
inferred← citeshttps://doi.org/10.1002/bies.202100114openalex-snapshot
The gamma‐tubulin ring complex: Deciphering the molecular organization and assembly mechanism of a major vertebrate microtubule nucleator
inferred← citeshttps://doi.org/10.1002/cbin.10462openalex-snapshot
Ionizing radiation increases primary cilia incidence and induces multiciliation in C2C12 myoblasts
inferred← citeshttps://doi.org/10.1002/cm.21260openalex-snapshot
Structural characterization of procentrioles in Drosophila spermatids
inferred← citeshttps://doi.org/10.1002/cm.21504openalex-snapshot
Regulating a key mitotic regulator, polo‐like kinase 1 (PLK1)
inferred← citeshttps://doi.org/10.1002/cm.70015openalex-snapshot
Optineurin Localization at the Centrosome, Spindle, and Midbody Implies Its Role in Cell Division
inferred← citeshttps://doi.org/10.1002/cm.70112openalex-snapshot
Domain‐Level Interaction of FAP174 ( MYCBP ‐1) and FAP147 ( MYCBPAP ) Proteins of the C2a Projection of Chlamydomonas Cilia
inferred← citeshttps://doi.org/10.1002/dvg.22937openalex-snapshot
Generation and Characterization of a Tissue‐Specific Centrosome Indicator Mouse Line
inferred← citeshttps://doi.org/10.1002/embr.201337929openalex-snapshot
Msd1/SSX2IP‐dependent microtubule anchorage ensures spindle orientation and primary cilia formation
inferred← citeshttps://doi.org/10.1002/hep.25851openalex-snapshot
The centrosomal protein tax1 binding protein 2 is a novel tumor suppressor in hepatocellular carcinoma regulated by cyclin-dependent kinase 2
inferred← citeshttps://doi.org/10.1002/hep.32461openalex-snapshot
Polo‐like kinase 4 inhibitor CFI‐400945 suppresses liver cancer through cell cycle perturbation and eliciting antitumor immunity
inferred← citeshttps://doi.org/10.1002/jcb.24417openalex-snapshot
Identification of candidate downstream targets of TGFβ signaling during palate development by genome‐wide transcript profiling
inferred← citeshttps://doi.org/10.1002/jcp.24579openalex-snapshot
Link Between DNA Damage and Centriole Disengagement/Reduplication in Untransformed Human Cells
inferred← citeshttps://doi.org/10.1002/med.21926openalex-snapshot
Computational benchmarking of putative KIFC1 inhibitors
inferred← citeshttps://doi.org/10.1002/qub2.71openalex-snapshot
Single‐cell analyses reveal impaired type B spermatogonia differentiation and meiotic entry in C‐Nap1‐null testes
inferred← citeshttps://doi.org/10.1002/wdev.89openalex-snapshot
Genetic causes of microcephaly and lessons for neuronal development
inferred← citeshttps://doi.org/10.1007/112_2013_12openalex-snapshot
The Cardiomyocyte Cell Cycle in Hypertrophy, Tissue Homeostasis, and Regeneration
inferred← citeshttps://doi.org/10.1007/164_2017_31openalex-snapshot
Targeting DNA Repair
inferred← citeshttps://doi.org/10.1007/978-1-0716-3507-0_11openalex-snapshot
Proximity Mapping of Ciliary Proteins by BioID
inferred← citeshttps://doi.org/10.1007/978-1-0716-4418-8_4openalex-snapshot
Integration of RNAi and Small Molecule Library Screens to Identify Targets for Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-1-4939-3542-0_13openalex-snapshot
A Cell-Free System for Real-Time Analyses of Centriole Disengagement and Centriole-to-Centrosome Conversion
inferred← citeshttps://doi.org/10.1007/978-1-4939-9145-7_3openalex-snapshot
Integration of RNAi and Small Molecule Screens to Identify Targets for Drug Development
inferred← citeshttps://doi.org/10.1007/978-1-62703-035-9_9openalex-snapshot
Regulation of the Centrosome Cycle by Protein Degradation
inferred← citeshttps://doi.org/10.1007/978-1-62703-311-4_7openalex-snapshot
Integration of RNAi and Small Molecule Screens to Identify Targets for Drug Development
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_18openalex-snapshot
Centrosome Amplification and Tumorigenesis: Cause or Effect?
inferred← citeshttps://doi.org/10.1007/978-3-031-20848-5_1openalex-snapshot
Cell and Molecular Biology of Centrosome Structure and Function
inferred← citeshttps://doi.org/10.1007/978-3-031-20848-5_2openalex-snapshot
The Centrosome Cycle within the Cell Cycle
inferred← citeshttps://doi.org/10.1007/978-3-032-36189-9_2openalex-snapshot
The Centriole Biogenesis Cycle: Temporal Mechanisms, Autonomy and Coupling to the Cell Cycle and Other Cellular Clocks
inferred← citeshttps://doi.org/10.1007/978-3-319-12136-9_2openalex-snapshot
The Generation, Detection, and Prevention of Genomic Instability During Cancer Progression and Metastasis
inferred← citeshttps://doi.org/10.1007/978-3-319-22816-7_5openalex-snapshot
Quantum-Mechanical Modeling of Mutations, Aging, Evolution, Tumor, and Cancer Development
inferred← citeshttps://doi.org/10.1007/978-3-319-48848-6_68openalex-snapshot
Targeting Genome Instability and DNA Repair
inferred← citeshttps://doi.org/10.1007/978-3-319-57127-0_3openalex-snapshot
Dividing with Extra Centrosomes: A Double Edged Sword for Cancer Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-60855-6_19openalex-snapshot
Parthenogenesis in Insects: The Centriole Renaissance
inferred← citeshttps://doi.org/10.1007/978-3-319-91056-7_3openalex-snapshot
Cellular Organization of the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_1openalex-snapshot
Primary and Motile Cilia: Their Ultrastructure and Ciliogenesis
inferred← citeshttps://doi.org/10.1007/s00018-012-0961-1openalex-snapshot
Such small hands: the roles of centrins/caltractins in the centriole and in genome maintenance
inferred← citeshttps://doi.org/10.1007/s00018-012-1052-zopenalex-snapshot
The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies
inferred← citeshttps://doi.org/10.1007/s00018-016-2171-8openalex-snapshot
Achilles’ heel of pluripotent stem cells: genetic, genomic and epigenetic variations during prolonged culture
inferred← citeshttps://doi.org/10.1007/s00018-016-2236-8openalex-snapshot
HSP70 regulates the function of mitotic centrosomes
inferred← citeshttps://doi.org/10.1007/s00018-016-2315-xopenalex-snapshot
Regulation of centriolar satellite integrity and its physiology
inferred← citeshttps://doi.org/10.1007/s00018-016-2369-9openalex-snapshot
Mechanisms of ciliogenesis suppression in dividing cells
inferred← citeshttps://doi.org/10.1007/s00018-019-03181-7openalex-snapshot
Requirement of NPHP5 in the hierarchical assembly of basal feet associated with basal bodies of primary cilia
inferred← citeshttps://doi.org/10.1007/s00018-022-04570-1openalex-snapshot
Arl13b controls basal cell stemness properties and Hedgehog signaling in the mouse epididymis
inferred← citeshttps://doi.org/10.1007/s00204-020-02782-7openalex-snapshot
Functional genetic variants in centrosome-related genes CEP72 and YWHAG confer susceptibility to gastric cancer
inferred← citeshttps://doi.org/10.1007/s00412-017-0652-7openalex-snapshot
Controlling centriole numbers: Geminin family members as master regulators of centriole amplification and multiciliogenesis
inferred← citeshttps://doi.org/10.1007/s00441-014-1979-5openalex-snapshot
Progenitor genealogy in the developing cerebral cortex
inferred← citeshttps://doi.org/10.1007/s00441-017-2599-7openalex-snapshot
Role of primary cilia in non-dividing and post-mitotic cells
inferred← citeshttps://doi.org/10.1007/s00441-020-03343-1openalex-snapshot
A role for primary cilia in coral calcification?
inferred← citeshttps://doi.org/10.1007/s10577-015-9501-9openalex-snapshot
Mitotic kinase cascades orchestrating timely disjunction and movement of centrosomes maintain chromosomal stability and prevent cancer
inferred← citeshttps://doi.org/10.1007/s10577-015-9502-8openalex-snapshot
The interplay between centrosomes and the Hippo tumor suppressor pathway
inferred← citeshttps://doi.org/10.1007/s10577-015-9506-4openalex-snapshot
Centrosomes are multifunctional regulators of genome stability
inferred← citeshttps://doi.org/10.1007/s10577-015-9508-2openalex-snapshot
Centrosomes in spindle organization and chromosome segregation: a mechanistic view
inferred← citeshttps://doi.org/10.1007/s11033-014-3546-2openalex-snapshot
PLK4 overexpression and its effect on centrosome regulation and chromosome stability in human gastric cancer
inferred← citeshttps://doi.org/10.1007/s11481-017-9743-8openalex-snapshot
Overview on the Current Status of Zika Virus Pathogenesis and Animal Related Research
inferred← citeshttps://doi.org/10.1007/s11914-017-0351-6openalex-snapshot
Functional Diversity of Ciliary Proteins in Bone Development and Disease
inferred← citeshttps://doi.org/10.1007/s12026-014-8582-4openalex-snapshot
Anti-centrosome antibodies in breast cancer are the expression of autoimmunity
inferred← citeshttps://doi.org/10.1007/s12192-013-0459-2openalex-snapshot
Stress-induced localization of HSPA6 (HSP70B′) and HSPA1A (HSP70-1) proteins to centrioles in human neuronal cells
inferred← citeshttps://doi.org/10.1007/s12672-025-02540-0openalex-snapshot
Elevated CEP72 expression facilitates the progression of hepatocellular carcinoma and is associated with unfavorable outcomes
inferred← citeshttps://doi.org/10.1016/b978-0-12-397944-5.00018-3openalex-snapshot
Centrosome Isolation and Analysis by Mass Spectrometry-Based Proteomics
inferred← citeshttps://doi.org/10.1016/b978-0-12-800177-6.00006-2openalex-snapshot
Centrosomes and the Art of Mitotic Spindle Maintenance
inferred← citeshttps://doi.org/10.1016/b978-0-12-822508-0.00014-9openalex-snapshot
Landmark contributions of Chlamydomonas to understanding cilia
inferred← citeshttps://doi.org/10.1016/b978-0-323-35762-3.00017-2openalex-snapshot
Control of Cell Division
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.04.006openalex-snapshot
Germline stem cell homeostasis
inferred← citeshttps://doi.org/10.1016/bs.mcb.2014.12.008openalex-snapshot
Imaging centrosomes and cilia in the mouse kidney
inferred← citeshttps://doi.org/10.1016/bs.mcb.2014.12.012openalex-snapshot
Analysis of primary cilia in the developing mouse brain
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.03.004openalex-snapshot
Purification of centrosomes from mammalian cell lines
inferred← citeshttps://doi.org/10.1016/bs.mcb.2022.10.003openalex-snapshot
Time-lapse imaging of primary cilium behavior with physiological expression of fluorescent ciliary proteins
inferred← citeshttps://doi.org/10.1016/j.ajhg.2013.11.010openalex-snapshot
Mutations in CSPP1, Encoding a Core Centrosomal Protein, Cause a Range of Ciliopathy Phenotypes in Humans
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.735241openalex-snapshot
Telophase of the first cleavage is the key stage for optimally inducing mitotic gynogenesis in rice field eel (Monopterus albus)
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.11.019openalex-snapshot
A role for β-dystroglycan in the organization and structure of the nucleus in myoblasts
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.04.021openalex-snapshot
TEIF associated centrosome activity is regulated by EGF/PI3K/Akt signaling
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2016.03.021openalex-snapshot
Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.01.007openalex-snapshot
Rootletin prevents Cep68 from VHL-mediated proteasomal degradation to maintain centrosome cohesion
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.06.003openalex-snapshot
DRG2 knockdown induces Golgi fragmentation via GSK3β phosphorylation and microtubule stabilization
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.12.108openalex-snapshot
Hedgehog signaling is synergistically enhanced by nutritional deprivation and ligand stimulation in human fibroblasts of Gorlin syndrome
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.01.136openalex-snapshot
The tumor suppressor proteins ASPP1 and ASPP2 interact with C-Nap1 and regulate centrosome linker reassembly
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.10.169openalex-snapshot
The conserved Wdr8-hMsd1/SSX2IP complex localises to the centrosome and ensures proper spindle length and orientation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.05.180openalex-snapshot
Centrosomal MCM7 strengthens the Cep68-VHL interaction and excessive MCM7 leads to centrosome splitting resulting from increase in Cep68 ubiquitination and proteasomal degradation
inferred← citeshttps://doi.org/10.1016/j.biocel.2017.07.001openalex-snapshot
CEP131 indicates poor prognosis and promotes cell proliferation and migration in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112292openalex-snapshot
Centrosomal-associated Proteins: Potential therapeutic targets for solid tumors?
inferred← citeshttps://doi.org/10.1016/j.biosystems.2018.08.007openalex-snapshot
Integration of intracellular signaling: Biological analogues of wires, processors and memories organized by a centrosome 3D reference system
inferred← citeshttps://doi.org/10.1016/j.bpj.2012.05.015openalex-snapshot
STED Microscopy with Optimized Labeling Density Reveals 9-Fold Arrangement of a Centriole Protein
inferred← citeshttps://doi.org/10.1016/j.canlet.2019.12.042openalex-snapshot
TRIM8 interacts with KIF11 and KIFC1 and controls bipolar spindle formation and chromosomal stability
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.05.005openalex-snapshot
Centrosome asymmetry and inheritance during animal development
inferred← citeshttps://doi.org/10.1016/j.ceb.2014.09.005openalex-snapshot
Control of asymmetric cell division
inferred← citeshttps://doi.org/10.1016/j.ceb.2020.01.009openalex-snapshot
Endocytic membrane trafficking in the control of centrosome function
inferred← citeshttps://doi.org/10.1016/j.cell.2013.08.060openalex-snapshot
Asymmetric Inheritance of Centrosome-Associated Primary Cilium Membrane Directs Ciliogenesis after Cell Division
inferred← citeshttps://doi.org/10.1016/j.cell.2013.09.027openalex-snapshot
Remembrance of Cilia Past
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.08.005openalex-snapshot
LRRC45 Is a Centrosome Linker Component Required for Centrosome Cohesion
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.01.003openalex-snapshot
The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.12.097openalex-snapshot
The Microcephaly-Associated Protein Wdr62/CG7337 Is Required to Maintain Centrosome Asymmetry in Drosophila Neuroblasts
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.03.083openalex-snapshot
Fbxo30 Regulates Mammopoiesis by Targeting the Bipolar Mitotic Kinesin Eg5
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.10.028openalex-snapshot
CCDC84 Acetylation Oscillation Regulates Centrosome Duplication by Modulating HsSAS-6 Degradation
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113696openalex-snapshot
Dual roles of CCDC102A in governing centrosome duplication and cohesion
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115127openalex-snapshot
Targeted localization of the mother centrosome in CD8+ T cells undergoing asymmetric cell division promotes memory formation
inferred← citeshttps://doi.org/10.1016/j.chembiol.2014.11.005openalex-snapshot
Pregnenolone Functions in Centriole Cohesion during Mitosis
inferred← citeshttps://doi.org/10.1016/j.conb.2021.06.003openalex-snapshot
Centrosome regulation and function in mammalian cortical neurogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2013.04.032openalex-snapshot
Cell Biology: DUBing CP110 Controls Centrosome Numbers
inferred← citeshttps://doi.org/10.1016/j.cub.2013.06.043openalex-snapshot
Multiple Mechanisms Contribute to Centriole Separation in C. elegans
inferred← citeshttps://doi.org/10.1016/j.cub.2014.08.047openalex-snapshot
Multiciliated Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2014.09.079openalex-snapshot
Centriole Duplication: When PLK4 Meets Ana2/STIL
inferred← citeshttps://doi.org/10.1016/j.cub.2015.02.020openalex-snapshot
Centrosome-Associated Degradation Limits β-Catenin Inheritance by Daughter Cells after Asymmetric Division
inferred← citeshttps://doi.org/10.1016/j.cub.2015.08.039openalex-snapshot
A Short CEP135 Splice Isoform Controls Centriole Duplication
inferred← citeshttps://doi.org/10.1016/j.cub.2015.10.028openalex-snapshot
Mother Centriole Distal Appendages Mediate Centrosome Docking at the Immunological Synapse and Reveal Mechanistic Parallels with Ciliogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2015.11.015openalex-snapshot
Sperm Centrosomes: Kiss Your Asterless Goodbye, for Fertility’s Sake
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.03.011openalex-snapshot
Direct Binding of SAS-6 to ZYG-1 Recruits SAS-6 to the Mother Centriole for Cartwheel Assembly
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.05.016openalex-snapshot
Discovering Regulators of Centriole Biogenesis through siRNA-Based Functional Genomics in Human Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.06.014openalex-snapshot
PHD1 Links Cell-Cycle Progression to Oxygen Sensing through Hydroxylation of the Centrosomal Protein Cep192
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.08.021openalex-snapshot
Deuterosome-Mediated Centriole Biogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.09.029openalex-snapshot
Spindle Formation in the Mouse Embryo Requires Plk4 in the Absence of Centrioles
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.02.013openalex-snapshot
The Centrosome-Specific Phosphorylation of Cnn by Polo/Plk1 Drives Cnn Scaffold Assembly and Centrosome Maturation
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.09.020openalex-snapshot
PLK4 trans-Autoactivation Controls Centriole Biogenesis in Space
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.11.019openalex-snapshot
GAS2L1 Is a Centriole-Associated Protein Required for Centrosome Dynamics and Disjunction
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.10.026openalex-snapshot
Oxidative Stress in Cells with Extra Centrosomes Drives Non-Cell-Autonomous Invasion
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.10.027openalex-snapshot
A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.03.027openalex-snapshot
Spectraplakin Shot Maintains Perinuclear Microtubule Organization in Drosophila Polyploid Cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2014.12.008openalex-snapshot
Spatio-temporal regulation of RAG2 following genotoxic stress
inferred← citeshttps://doi.org/10.1016/j.ejcb.2014.12.001openalex-snapshot
Suppression of centrosome protein TACC3 induces G1 arrest and cell death through activation of p38–p53–p21 stress signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ejmhg.2012.10.006openalex-snapshot
Insight into Nek2A activity regulation and its pharmacological prospects
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.06.030openalex-snapshot
The centrosome duplication cycle in health and disease
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.11.001openalex-snapshot
LRRC45 accelerates bladder cancer development and ferroptosis inhibition via stabilizing NRF2 by competitively KEAP1 interaction
inferred← citeshttps://doi.org/10.1016/j.gde.2013.04.008openalex-snapshot
Hedgehog signaling from the primary cilium to the nucleus: an emerging picture of ciliary localization, trafficking and transduction
inferred← citeshttps://doi.org/10.1016/j.gene.2016.05.002openalex-snapshot
Structure, function and regulation of jade family PHD finger 1 (JADE1)
inferred← citeshttps://doi.org/10.1016/j.isci.2018.10.003openalex-snapshot
Autoamplification and Competition Drive Symmetry Breaking: Initiation of Centriole Duplication by the PLK4-STIL Network
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.04.012openalex-snapshot
Identification of a Structurally Dynamic Domain for Oligomer Formation in Rootletin
inferred← citeshttps://doi.org/10.1016/j.jsb.2018.01.009openalex-snapshot
Cep120 promotes microtubule formation through a unique tubulin binding C2 domain
inferred← citeshttps://doi.org/10.1016/j.molcel.2015.11.006openalex-snapshot
Targeting Mitosis in Cancer: Emerging Strategies
inferred← citeshttps://doi.org/10.1016/j.neuron.2016.09.056openalex-snapshot
Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.05.039openalex-snapshot
Brain Somatic Mutations in MTOR Disrupt Neuronal Ciliogenesis, Leading to Focal Cortical Dyslamination
inferred← citeshttps://doi.org/10.1016/j.pathol.2017.10.007openalex-snapshot
Synchronous tumours of the female reproductive tract
inferred← citeshttps://doi.org/10.1016/j.pep.2021.105856openalex-snapshot
Optimization strategies for expression and purification of soluble N-terminal domain of human centriolar protein SAS-6 in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.phrs.2018.10.002openalex-snapshot
Neuronal and astrocytic primary cilia in the mature brain
inferred← citeshttps://doi.org/10.1016/j.protis.2012.11.003openalex-snapshot
A Centrin3-dependent, Transient, Appendage of the Mother Basal Body Guides the Positioning of the Daughter Basal Body in Paramecium
inferred← citeshttps://doi.org/10.1016/j.prp.2021.153581openalex-snapshot
Coding variants in the PCNT and CEP295 genes contribute to breast cancer risk in Chinese women
inferred← citeshttps://doi.org/10.1016/j.redox.2017.05.007openalex-snapshot
European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS)
inferred← citeshttps://doi.org/10.1016/j.scr.2014.05.001openalex-snapshot
Differential sensitivity of Glioma stem cells to Aurora kinase A inhibitors: Implications for stem cell mitosis and centrosome dynamics
inferred← citeshttps://doi.org/10.1016/j.scr.2014.06.006openalex-snapshot
Primary cilium-associated genes mediate bone marrow stromal cell response to hypoxia
inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.03.005openalex-snapshot
Genomic instability in human cancer: Molecular insights and opportunities for therapeutic attack and prevention through diet and nutrition
inferred← citeshttps://doi.org/10.1016/j.semcdb.2014.02.014openalex-snapshot
Stem cell decisions: A twist of fate or a niche market?
inferred← citeshttps://doi.org/10.1016/j.stemcr.2016.04.004openalex-snapshot
Asymmetric Distribution of Primary Cilia Allocates Satellite Cells for Self-Renewal
inferred← citeshttps://doi.org/10.1016/j.stemcr.2018.08.008openalex-snapshot
Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1016/j.stemcr.2020.08.007openalex-snapshot
Centrosome Reduction Promotes Terminal Differentiation of Human Cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.str.2012.08.025openalex-snapshot
The Structure of the Plk4 Cryptic Polo Box Reveals Two Tandem Polo Boxes Required for Centriole Duplication
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.10.001openalex-snapshot
Amorphous no more: subdiffraction view of the pericentriolar material architecture
inferred← citeshttps://doi.org/10.1016/j.tcb.2014.10.002openalex-snapshot
Centrosome dynamics as a source of chromosomal instability
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.08.002openalex-snapshot
The Cilium: Cellular Antenna and Central Processing Unit
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2015.10.021openalex-snapshot
Polo-like kinase 4 regulates spindle and actin assembly in meiosis and influence of early embryonic development in bovine oocytes
inferred← citeshttps://doi.org/10.1016/j.toxlet.2024.01.001openalex-snapshot
Cadmium promotes the binding and centrosomal translocation of CCDC85C and PLK4 via ROS-GCLM pathway to trigger centrosome amplification in colon cancer cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.05.024openalex-snapshot
Cluap1 localizes preferentially to the base and tip of cilia and is required for ciliogenesis in the mouse embryo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.05.001openalex-snapshot
Cytoskeletal players in single-cell branching morphogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2024.09.006openalex-snapshot
Plk4 regulates centriole duplication in the embryonic development of zebrafish
inferred← citeshttps://doi.org/10.1017/cbo9781139135030.009openalex-snapshot
Structural basis for oocyte–granulosa cell interactions
inferred← citeshttps://doi.org/10.1017/cbo9781139135030.022openalex-snapshot
Parthenogenesis and parthenogenetic stem cells
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b00978openalex-snapshot
Human SAS-6 C-Terminus Nucleates and Promotes Microtubule Assembly in Vitro by Binding to Microtubules
inferred← citeshttps://doi.org/10.1021/acs.jpcb.3c07936openalex-snapshot
Ultraviolet Superradiance from Mega-Networks of Tryptophan in Biological Architectures
inferred← citeshttps://doi.org/10.1021/nn405253dopenalex-snapshot
Carbon Nanotube-Induced Loss of Multicellular Chirality on Micropatterned Substrate Is Mediated by Oxidative Stress
inferred← citeshttps://doi.org/10.1038/bjc.2013.283openalex-snapshot
Gene expression profiling identifies different sub-types of retinoblastoma
inferred← citeshttps://doi.org/10.1038/cdd.2012.61openalex-snapshot
Let's huddle to prevent a muddle: centrosome declustering as an attractive anticancer strategy
inferred← citeshttps://doi.org/10.1038/cddis.2014.370openalex-snapshot
MEIS2 is essential for neuroblastoma cell survival and proliferation by transcriptional control of M-phase progression
inferred← citeshttps://doi.org/10.1038/cr.2016.53openalex-snapshot
Reversing drug resistance of soft tumor-repopulating cells by tumor cell-derived chemotherapeutic microparticles
inferred← citeshttps://doi.org/10.1038/emboj.2013.56openalex-snapshot
Human microcephaly protein CEP135 binds to hSAS‐6 and CPAP, and is required for centriole assembly
inferred← citeshttps://doi.org/10.1038/embor.2012.86openalex-snapshot
Tankyrase 1 regulates centrosome function by controlling CPAP stability
inferred← citeshttps://doi.org/10.1038/modpathol.2016.101openalex-snapshot
CCNE1 amplification and centrosome number abnormality in serous tubal intraepithelial carcinoma: further evidence supporting its role as a precursor of ovarian high-grade serous carcinoma
inferred← citeshttps://doi.org/10.1038/modpathol.2017.159openalex-snapshot
Extrauterine high-grade serous carcinomas with bilateral adnexal involvement as the only two disease sites are clonal based on tp53 sequencing results: implications for biology, classification, and staging
inferred← citeshttps://doi.org/10.1038/ncb2597openalex-snapshot
Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization
inferred← citeshttps://doi.org/10.1038/ncb2880openalex-snapshot
The Cep63 paralogue Deup1 enables massive de novo centriole biogenesis for vertebrate multiciliogenesis
inferred← citeshttps://doi.org/10.1038/ncb3076openalex-snapshot
Degradation of Cep68 and PCNT cleavage mediate Cep215 removal from the PCM to allow centriole separation, disengagement and licensing
inferred← citeshttps://doi.org/10.1038/ncb3370openalex-snapshot
Cilium assembly and disassembly
inferred← citeshttps://doi.org/10.1038/ncomms10072openalex-snapshot
Tank binding kinase 1 is a centrosome-associated kinase necessary for microtubule dynamics and mitosis
inferred← citeshttps://doi.org/10.1038/ncomms11005openalex-snapshot
A CEP215–HSET complex links centrosomes with spindle poles and drives centrosome clustering in cancer
inferred← citeshttps://doi.org/10.1038/ncomms14866openalex-snapshot
USP9X regulates centrosome duplication and promotes breast carcinogenesis
inferred← citeshttps://doi.org/10.1038/ncomms2752openalex-snapshot
SAPK pathways and p53 cooperatively regulate PLK4 activity and centrosome integrity under stress
inferred← citeshttps://doi.org/10.1038/ncomms6081openalex-snapshot
Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
inferred← citeshttps://doi.org/10.1038/ncomms7894openalex-snapshot
C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle
inferred← citeshttps://doi.org/10.1038/ncomms9450openalex-snapshot
Loss of KLF14 triggers centrosome amplification and tumorigenesis
inferred← citeshttps://doi.org/10.1038/nrc3995openalex-snapshot
Centrosomes and cancer: revisiting a long-standing relationship
inferred← citeshttps://doi.org/10.1038/nrm.2017.127openalex-snapshot
Once and only once: mechanisms of centriole duplication and their deregulation in disease
inferred← citeshttps://doi.org/10.1038/nrm3373openalex-snapshot
Towards a molecular architecture of centriole assembly
inferred← citeshttps://doi.org/10.1038/nrm4062openalex-snapshot
Centrosome function and assembly in animal cells
inferred← citeshttps://doi.org/10.1038/nsmb.2846openalex-snapshot
Molecular basis for unidirectional scaffold switching of human Plk4 in centriole biogenesis
inferred← citeshttps://doi.org/10.1038/onc.2013.481openalex-snapshot
The tumor suppressor, TAX1BP2, is a novel substrate of ATM kinase
inferred← citeshttps://doi.org/10.1038/onc.2015.332openalex-snapshot
Structural centrosome aberrations favor proliferation by abrogating microtubule-dependent tissue integrity of breast epithelial mammospheres
inferred← citeshttps://doi.org/10.1038/onc.2016.74openalex-snapshot
Opposing post-translational modifications regulate Cep76 function to suppress centriole amplification
inferred← citeshttps://doi.org/10.1038/onc.2017.92openalex-snapshot
Regulation of spindle integrity and mitotic fidelity by BCCIP
inferred← citeshttps://doi.org/10.1038/s41388-022-02317-7openalex-snapshot
NEDD9 links anaplastic thyroid cancer stemness to chromosomal instability through integrated centrosome asymmetry and DNA sensing regulation
inferred← citeshttps://doi.org/10.1038/s41392-020-00214-7openalex-snapshot
Centrosome dysfunction: a link between senescence and tumor immunity
inferred← citeshttps://doi.org/10.1038/s41418-020-00713-8openalex-snapshot
Genotoxic stress-activated DNA-PK-p53 cascade and autophagy cooperatively induce ciliogenesis to maintain the DNA damage response
inferred← citeshttps://doi.org/10.1038/s41418-022-00937-wopenalex-snapshot
Genetic interaction between PLK1 and downstream MCPH proteins in the control of centrosome asymmetry and cell fate during neural progenitor division
inferred← citeshttps://doi.org/10.1038/s41418-022-01000-4openalex-snapshot
The phosphorylation and dephosphorylation switch of VCP/p97 regulates the architecture of centrosome and spindle
inferred← citeshttps://doi.org/10.1038/s41419-019-1843-3openalex-snapshot
NudC-like protein 2 restrains centriole amplification by stabilizing HERC2
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