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Centriolar SAS-5 is required for centrosome duplication in C. elegans

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What this work says

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

inferredcites →https://doi.org/10.1006/jsbi.1997.3928openalex-snapshot
Reconstruction of the Centrosome Cycle from Cryoelectron Micrographs
inferredcites →https://doi.org/10.1007/bf00710603openalex-snapshot
Segregation of holocentric chromosomes at meiosis in the nematode,Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0012-1606(78)90247-6openalex-snapshot
Intersex, a temperature-sensitive mutant of the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0012-1606(80)90445-5openalex-snapshot
Parental effects and phenotypic characterization of mutations that affect early development in Caenorhabditis elegans
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.cub.2004.04.012openalex-snapshot
The Caenorhabditis elegans Centrosomal Protein SPD-2 Is Required for both Pericentriolar Material Recruitment and Centriole Duplication
inferredcites →https://doi.org/10.1016/s0022-5320(78)80071-9openalex-snapshot
Spermatogenesis in males of the free-living nematode, Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0092-8674(01)00338-5openalex-snapshot
The C. elegans zyg-1 Gene Encodes a Regulator of Centrosome Duplication with Distinct Maternal and Paternal Roles in the Embryo
inferredcites →https://doi.org/10.1016/s0092-8674(03)00117-xopenalex-snapshot
SAS-4 Is a C. elegans Centriolar Protein that Controls Centrosome Size
inferredcites →https://doi.org/10.1016/s0169-5347(03)00009-0openalex-snapshot
It takes two to tango
inferredcites →https://doi.org/10.1016/s0378-1119(00)00579-5openalex-snapshot
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0960-9822(00)00869-1openalex-snapshot
RNAi analysis of genes expressed in the ovary of Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0960-9822(02)01019-9openalex-snapshot
Centrin-2 Is Required for Centriole Duplication in Mammalian Cells
inferredcites →https://doi.org/10.1016/s0960-9822(03)00582-7openalex-snapshot
TAC-1 and ZYG-9 Form a Complex that Promotes Microtubule Assembly in C. elegans Embryos
inferredcites →https://doi.org/10.1016/s1097-2765(00)00043-5openalex-snapshot
Asymmetric Segregation of PIE-1 in C. elegans Is Mediated by Two Complementary Mechanisms that Act through Separate PIE-1 Protein Domains
inferredcites →https://doi.org/10.1016/s1534-5807(01)00046-6openalex-snapshot
zyg-8, a Gene Required for Spindle Positioning in C. elegans, Encodes a Doublecortin-Related Kinase that Promotes Microtubule Assembly
inferredcites →https://doi.org/10.1016/s1534-5807(03)00062-5openalex-snapshot
SAS-4 Is Essential for Centrosome Duplication in C. elegans and Is Recruited to Daughter Centrioles Once per Cell Cycle
inferredcites →https://doi.org/10.1016/s1534-5807(04)00066-8openalex-snapshot
Centrosome Maturation and Duplication in C. elegans Require the Coiled-Coil Protein SPD-2
inferredcites →https://doi.org/10.1038/ncb900openalex-snapshot
ɛ-Tubulin is required for centriole duplication and microtubule organization
inferredcites →https://doi.org/10.1083/jcb.123.2.405openalex-snapshot
The calcium-binding protein cell division cycle 31 of Saccharomyces cerevisiae is a component of the half bridge of the spindle pole body.
inferredcites →https://doi.org/10.1083/jcb.141.5.1159openalex-snapshot
ZYG-9, A Caenorhabditis elegans Protein Required for Microtubule Organization and Function, Is a Component of Meiotic and Mitotic Spindle Poles
inferredcites →https://doi.org/10.1083/jcb.144.5.927openalex-snapshot
Dissection of Cell Division Processes in the One Cell Stage Caenorhabditis elegans Embryo by Mutational Analysis
inferredcites →https://doi.org/10.1083/jcb.200202047openalex-snapshot
The kinetically dominant assembly pathway for centrosomal asters in Caenorhabditis elegans is γ-tubulin dependent
inferredcites →https://doi.org/10.1083/jcb.200307064openalex-snapshot
Sfi1p has conserved centrin-binding sites and an essential function in budding yeast spindle pole body duplication
inferredcites →https://doi.org/10.1083/jcb.91.3.814openalex-snapshot
Centriole cycle in Chinese hamster ovary cells as determined by whole-mount electron microscopy.
inferredcites →https://doi.org/10.1091/mbc.e02-04-0205openalex-snapshot
ε-Tubulin Is an Essential Component of the Centriole
inferredcites →https://doi.org/10.1091/mbc.e02-10-0661openalex-snapshot
Fission Yeast cdc31p Is a Component of the Half-bridge and Controls SPB Duplication
inferredcites →https://doi.org/10.1091/mbc.e03-01-0017openalex-snapshot
Mutations in a β-Tubulin Disrupt Spindle Orientation and Microtubule Dynamics in the Early Caenorhabditis elegans Embryo
inferredcites →https://doi.org/10.1093/genetics/157.3.1217openalex-snapshot
Creation of Low-Copy Integrated Transgenic Lines in Caenorhabditis elegans
inferredcites →https://doi.org/10.1101/gad.894001openalex-snapshot
“It Takes Two to Tango”: understanding how centrosome duplication is regulated throughout the cell cycle
inferredcites →https://doi.org/10.1242/dev.00483openalex-snapshot
TheC. elegansHand gene controls embryogenesis and early gonadogenesis

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.3347763openalex-extracted
Centrosomes Control Kinetochore-Fiber Plus-End Dynamics Via HURP to Ensure Symmetric Divisions
inferred← citeshttps://doi.org/10.1002/2211-5463.13771openalex-snapshot
The protein tyrosine phosphatase PPH ‐7 is required for fertility and embryonic development in C. elegans at elevated temperatures
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0375openalex-snapshot
Animal Systems Biology: Towards a Systems View of Development in C . Elegans
inferred← citeshttps://doi.org/10.1002/9781444312249.ch4openalex-snapshot
Animal Systems Biology: Towards a Systems View of Development inC. Elegans
inferred← citeshttps://doi.org/10.1002/bies.201700241openalex-snapshot
The Rise of the Cartwheel: Seeding the Centriole Organelle
inferred← citeshttps://doi.org/10.1002/bies.202100262openalex-snapshot
Nine‐fold symmetry of centriole: The joint efforts of its core proteins
inferred← citeshttps://doi.org/10.1002/bies.20594openalex-snapshot
Finding treasures in frozen cells: new centriole intermediates
inferred← citeshttps://doi.org/10.1002/cm.22031openalex-snapshot
PLK4 : Master Regulator of Centriole Duplication and Its Therapeutic Potential
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/10.1007/978-3-7091-1903-7_5openalex-snapshot
Consequences of Numerical Centrosome Defects in Development and Disease
inferred← citeshttps://doi.org/10.1007/b136685openalex-snapshot
The Centrosome Cycle
inferred← citeshttps://doi.org/10.1007/s00018-010-0324-8openalex-snapshot
The elegans of spindle assembly
inferred← citeshttps://doi.org/10.1007/s00018-012-1102-6openalex-snapshot
Show me your license, please: deregulation of centriole duplication mechanisms that promote amplification
inferred← citeshttps://doi.org/10.1007/s42485-025-00195-7openalex-snapshot
ASH: a new protein domain on the horizon
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.20063-1openalex-snapshot
Centrioles and the Centrosome
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00302-9openalex-snapshot
Further Reading | Centrosome Duplication
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.2015.03.011openalex-snapshot
Genome-wide RNAi screens in S2 cells to identify centrosome components
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.03.012openalex-snapshot
A yeast two-hybrid approach for probing protein–protein interactions at the centrosome
inferred← citeshttps://doi.org/10.1016/j.ceb.2008.09.001openalex-snapshot
Centrioles: some self-assembly required
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.10.016openalex-snapshot
Building a centriole
inferred← citeshttps://doi.org/10.1016/j.cell.2006.05.025openalex-snapshot
Flies without Centrioles
inferred← citeshttps://doi.org/10.1016/j.cell.2009.10.036openalex-snapshot
Centrioles, Centrosomes, and Cilia in Health and Disease
inferred← citeshttps://doi.org/10.1016/j.cell.2011.01.008openalex-snapshot
Structural Basis of the 9-Fold Symmetry of Centrioles
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107630openalex-snapshot
CCDC57 Cooperates with Microtubules and Microcephaly Protein CEP63 and Regulates Centriole Duplication and Mitotic Progression
inferred← citeshttps://doi.org/10.1016/j.cub.2006.07.059openalex-snapshot
Sequential Protein Recruitment in C. elegans Centriole Formation
inferred← citeshttps://doi.org/10.1016/j.cub.2007.04.036openalex-snapshot
Overexpressing Centriole-Replication Proteins In Vivo Induces Centriole Overduplication and De Novo Formation
inferred← citeshttps://doi.org/10.1016/j.cub.2007.08.065openalex-snapshot
Drosophila Spd-2 Recruits PCM to the Sperm Centriole, but Is Dispensable for Centriole Duplication
inferred← citeshttps://doi.org/10.1016/j.cub.2009.04.033openalex-snapshot
HAUS, the 8-Subunit Human Augmin Complex, Regulates Centrosome and Spindle Integrity
inferred← citeshttps://doi.org/10.1016/j.cub.2009.05.016openalex-snapshot
Control of Centriole Length by CPAP and CP110
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.cub.2010.08.010openalex-snapshot
Building the Centriole
inferred← citeshttps://doi.org/10.1016/j.cub.2014.04.023openalex-snapshot
Asterless Licenses Daughter Centrioles to Duplicate for the First Time in Drosophila Embryos
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.2019.03.029openalex-snapshot
PCMD-1 Organizes Centrosome Matrix Assembly in C. elegans
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.061openalex-snapshot
Spindle-Length-Dependent HURP Localization Allows Centrosomes to Control Kinetochore-Fiber Plus-End Dynamics
inferred← citeshttps://doi.org/10.1016/j.devcel.2004.10.015openalex-snapshot
Centriole Assembly Requires Both Centriolar and Pericentriolar Material Proteins
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.08.004openalex-snapshot
Centrosome Duplication and Nematodes: Recent Insights from an Old Relationship
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.07.002openalex-snapshot
Plk4-Induced Centriole Biogenesis in Human Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.09.018openalex-snapshot
The Conserved Protein SZY-20 Opposes the Plk4-Related Kinase ZYG-1 to Limit Centrosome Size
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.11.010openalex-snapshot
DSas-6 and Ana2 Coassemble into Tubules to Promote Centriole Duplication and Engagement
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.02.005openalex-snapshot
PP2A Phosphatase Acts upon SAS-5 to Ensure Centriole Formation in C. elegans Embryos
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.03.021openalex-snapshot
PP2A Targets SAS-5 in Centriole Assembly
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.2019.06.004openalex-snapshot
Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance
inferred← citeshttps://doi.org/10.1016/j.ejcb.2004.10.004openalex-snapshot
Knockdown of the centrosomal component SAS-5 results in defects in nuclear morphology in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108410openalex-snapshot
Site-specific phosphorylation of ZYG-1 regulates ZYG-1 stability and centrosome number
inferred← citeshttps://doi.org/10.1016/j.sbi.2020.08.005openalex-snapshot
Emerging insights into symmetry breaking in centriole duplication: updated view on centriole duplication theory
inferred← citeshttps://doi.org/10.1016/j.str.2013.08.019openalex-snapshot
Structural Analysis of the G-Box Domain of the Microcephaly Protein CPAP Suggests a Role in Centriole Architecture
inferred← citeshttps://doi.org/10.1016/j.tcb.2008.06.004openalex-snapshot
Mechanisms of procentriole formation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.08.054openalex-snapshot
The zebrafish maternal-effect gene cellular atoll encodes the centriolar component sas-6 and defects in its paternal function promote whole genome duplication
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.01.001openalex-snapshot
ZYG-1 promotes limited centriole amplification in the C. elegans seam lineage
inferred← citeshttps://doi.org/10.1038/emboj.2012.280openalex-snapshot
SAS‐6 coiled‐coil structure and interaction with SAS‐5 suggest a regulatory mechanism in C. elegans centriole assembly
inferred← citeshttps://doi.org/10.1038/nature03876openalex-snapshot
Predictive models of molecular machines involved in Caenorhabditis elegans early embryogenesis
inferred← citeshttps://doi.org/10.1038/nature05318openalex-snapshot
Centriole assembly in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1038/ncb1220openalex-snapshot
SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells
inferred← citeshttps://doi.org/10.1038/ncb2282openalex-snapshot
The SCF–FBXW5 E3-ubiquitin ligase is regulated by PLK4 and targets HsSAS-6 to control centrosome duplication
inferred← citeshttps://doi.org/10.1038/nrc3995openalex-snapshot
Centrosomes and cancer: revisiting a long-standing relationship
inferred← citeshttps://doi.org/10.1038/nrm3373openalex-snapshot
Towards a molecular architecture of centriole assembly
inferred← citeshttps://doi.org/10.1038/s41388-019-1115-9openalex-snapshot
Indispensable role of STIL in the regulation of cancer cell motility through the lamellipodial accumulation of ARHGEF7–PAK1 complex
inferred← citeshttps://doi.org/10.1038/s41467-025-59939-0openalex-snapshot
C. elegans SSNA-1 is required for the structural integrity of centrioles and bipolar spindle assembly
inferred← citeshttps://doi.org/10.1038/s41467-025-62696-9openalex-snapshot
Structural insights into SSNA1 self-assembly and its microtubule binding for centriole maintenance
inferred← citeshttps://doi.org/10.1038/s41580-025-00921-5openalex-snapshot
Critical constituents and assembly principles of centriole biogenesis in human cells
inferred← citeshttps://doi.org/10.1038/s41598-025-86548-0openalex-snapshot
Asymmetry in centrosome maturation revealed through AIR-1 dynamics in the early Caenorhabditis elegans embryo
inferred← citeshttps://doi.org/10.1038/s44319-024-00157-yopenalex-snapshot
The kinase ZYG-1 phosphorylates the cartwheel protein SAS-5 to drive centriole assembly in C. elegans
inferred← citeshttps://doi.org/10.1038/s44319-025-00485-7openalex-snapshot
Dynamic SAS-6 phosphorylation aids centrosome duplication and elimination in C. elegans oogenesis
inferred← citeshttps://doi.org/10.1073/pnas.1213888110openalex-snapshot
Meiotic HORMA domain proteins prevent untimely centriole disengagement during Caenorhabditis elegans spermatocyte meiosis
inferred← citeshttps://doi.org/10.1073/pnas.1302721110openalex-snapshot
Caenorhabditis elegans centriolar protein SAS-6 forms a spiral that is consistent with imparting a ninefold symmetry
inferred← citeshttps://doi.org/10.1080/13816810.2024.2430700openalex-snapshot
A novel homozygous missense variant in POC1B causes cone dystrophy in a consanguineous Pakistani family
inferred← citeshttps://doi.org/10.1080/15384101.2022.2078458openalex-snapshot
A combined in silico and in vivo approach to the structure-function annotation of SPD-2 provides mechanistic insight into its functional diversity
inferred← citeshttps://doi.org/10.1083/jcb.200510028openalex-snapshot
NEDD1-dependent recruitment of the γ-tubulin ring complex to the centrosome is necessary for centriole duplication and spindle assembly
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1083/jcb.200905031openalex-snapshot
Ana3 is a conserved protein required for the structural integrity of centrioles and basal bodies
inferred← citeshttps://doi.org/10.1083/jcb.200910016openalex-snapshot
Drosophila Ana2 is a conserved centriole duplication factor
inferred← citeshttps://doi.org/10.1083/jcb.201502088openalex-snapshot
Binding of STIL to Plk4 activates kinase activity to promote centriole assembly
inferred← citeshttps://doi.org/10.1083/jcb.201602053openalex-snapshot
Mother centrioles are kicked out so that starfish zygote can grow
inferred← citeshttps://doi.org/10.1083/jcb.201605106openalex-snapshot
An ordered pattern of Ana2 phosphorylation by Plk4 is required for centriole assembly
inferred← citeshttps://doi.org/10.1083/jcb.201906031openalex-snapshot
Differential turnover of Nup188 controls its levels at centrosomes and role in centriole duplication
inferred← citeshttps://doi.org/10.1083/jcb.201912154openalex-snapshot
Tissue specific requirement of Drosophila Rcd4 for centriole duplication and ciliogenesis
inferred← citeshttps://doi.org/10.1083/jcb.202301092openalex-snapshot
Centrosomal organization of Cep152 provides flexibility in Plk4 and procentriole positioning
inferred← citeshttps://doi.org/10.1089/zeb.2017.1427openalex-snapshot
The Zebrafish curly fry Is Required for Proper Centrosome and Mitotic Spindle Assembly
inferred← citeshttps://doi.org/10.1091/mbc.e10-04-0281openalex-snapshot
Antizyme Restrains Centrosome Amplification by Regulating the Accumulation of Mps1 at Centrosomes
inferred← citeshttps://doi.org/10.1091/mbc.e10-04-0298openalex-snapshot
Mps1 Phosphorylation Sites Regulate the Function of Centrin 2 in Centriole Assembly
inferred← citeshttps://doi.org/10.1091/mbc.e13-09-0514openalex-snapshot
TheCaenorhabditiseleganspericentriolar material components SPD-2 and SPD-5 are monomeric in the cytoplasm before incorporation into the PCM matrix
inferred← citeshttps://doi.org/10.1091/mbc.e16-12-0823openalex-snapshot
Computer simulations reveal mechanisms that organize nuclear dynein forces to separate centrosomes
inferred← citeshttps://doi.org/10.1091/mbc.e17-06-0412openalex-snapshot
Interaction between theCaenorhabditis eleganscentriolar protein SAS-5 and microtubules facilitates organelle assembly
inferred← citeshttps://doi.org/10.1093/g3journal/jkab328openalex-snapshot
Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections
inferred← citeshttps://doi.org/10.1098/rsob.150082openalex-snapshot
Building a ninefold symmetrical barrel: structural dissections of centriole assembly
inferred← citeshttps://doi.org/10.1098/rsob.230222openalex-snapshot
Towards understanding centriole elimination
inferred← citeshttps://doi.org/10.1098/rstb.2013.0452openalex-snapshot
Centrosomes back in the limelight
inferred← citeshttps://doi.org/10.1098/rstb.2013.0458openalex-snapshot
Cartwheel assembly
inferred← citeshttps://doi.org/10.1098/rstb.2013.0460openalex-snapshot
The centriole duplication cycle
inferred← citeshttps://doi.org/10.1101/2023.02.07.527589openalex-snapshot
Separation of function mutations in microcephaly protein CPAP/CENPJ, reveal its role in regulating centriole number and length
inferred← citeshttps://doi.org/10.1101/2023.06.19.545600openalex-snapshot
Centriole elimination during C. elegans oogenesis initiates with loss of the central tube protein SAS-1
inferred← citeshttps://doi.org/10.1101/2024.10.03.616528openalex-snapshot
The C. elegans homolog of Sjögren’s Syndrome Nuclear Antigen 1 is required for the structural integrity of the centriole and bipolar mitotic spindle assembly
inferred← citeshttps://doi.org/10.1101/2025.04.22.650004openalex-snapshot
C. elegans SAS-1 ensures centriole integrity and ciliary function, and operates with SSNA-1
inferred← citeshttps://doi.org/10.1101/449538openalex-snapshot
Impaired chromosome segregation results in sperms with excess centrosomes in emb-27 APC6 mutant C. elegans
inferred← citeshttps://doi.org/10.1101/cshperspect.a015800openalex-snapshot
The Centrosome and Its Duplication Cycle
inferred← citeshttps://doi.org/10.1101/gad.1810409openalex-snapshot
The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation
inferred← citeshttps://doi.org/10.1101/sqb.2010.75.054openalex-snapshot
The Life Cycle of Centrioles
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2009.03929.xopenalex-snapshot
MULTIPOLAR SPINDLE 1 (MPS1), a novel coiled‐coil protein of Arabidopsis thaliana, is required for meiotic spindle organization
inferred← citeshttps://doi.org/10.1111/j.1399-0004.2006.00587.xopenalex-snapshot
New developmental insights from high‐throughput biological analysis in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2009.00905.xopenalex-snapshot
From Zero to Many: Control of Centriole Number in Development and Disease
inferred← citeshttps://doi.org/10.1126/sciadv.adg8682openalex-snapshot
Extensive programmed centriole elimination unveiled in C. elegans embryos
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100616-060454openalex-snapshot
Centriole Biogenesis: From Identifying the Characters to Understanding the Plot
inferred← citeshttps://doi.org/10.1186/s13630-017-0053-9openalex-snapshot
The rise and fall of basal bodies in the nematode Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1242/bio.022418openalex-snapshot
Casein Kinase II is required for proper cell division and acts as a negative regulator of centrosome duplication in C. elegans embryos
inferred← citeshttps://doi.org/10.1242/dev.075440openalex-snapshot
Analysis of centriole elimination during C. elegans oogenesis
inferred← citeshttps://doi.org/10.1242/dev.198416openalex-snapshot
PCMD-1 bridges the centrioles and the pericentriolar material scaffold in C. elegans
inferred← citeshttps://doi.org/10.1242/jcs.050682openalex-snapshot
Control of mitotic and meiotic centriole duplication by the Plk4-related kinase ZYG-1
inferred← citeshttps://doi.org/10.1242/jcs.084715openalex-snapshot
Scaffolding function of theChlamydomonasprocentriole protein CRC70, a member of the conserved Cep70 family
inferred← citeshttps://doi.org/10.1242/jcs.089888openalex-snapshot
Spindle positioning in human cells relies on proper centriole formation and on the microcephaly proteins CPAP and STIL
inferred← citeshttps://doi.org/10.1242/jcs.094797openalex-snapshot
Never tear us apart – the importance of centrosome clustering
inferred← citeshttps://doi.org/10.1242/jcs.097105openalex-snapshot
The C. elegans F-box proteins LIN-23 and SEL-10 antagonize centrosome duplication by regulating ZYG-1 levels
inferred← citeshttps://doi.org/10.1242/jcs.099887openalex-snapshot
Cell-cycle-regulated expression of STIL controls centriole number in human cells
inferred← citeshttps://doi.org/10.1242/jcs.104109openalex-snapshot
STIL is required for centriole duplication in human cells
inferred← citeshttps://doi.org/10.1242/jcs.107326openalex-snapshot
WD40-repeat protein 62 is a JNK-phosphorylated spindle pole protein required for spindle maintenance and timely mitotic progression.
inferred← citeshttps://doi.org/10.1242/jcs.243592openalex-snapshot
Loss of CPAP in developing mouse brain and its functional implication for human primary microcephaly
inferred← citeshttps://doi.org/10.1242/jcs.261297openalex-snapshot
Separation-of-function MCPH-associated mutations in CPAP affect centriole number and length
inferred← citeshttps://doi.org/10.1371/journal.pbio.0060224openalex-snapshot
A Genome-Wide RNAi Screen to Dissect Centriole Duplication and Centrosome Maturation in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001784openalex-snapshot
Molecular architecture of the C. elegans centriole
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004777openalex-snapshot
SAS-1 Is a C2 Domain Protein Critical for Centriole Integrity in C. elegans
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011912openalex-snapshot
C. elegans SAS-1 ensures centriole integrity and ciliary function, and operates with SSNA-1
inferred← citeshttps://doi.org/10.1371/journal.pone.0014600openalex-snapshot
CDK11p58 Is Required for Centriole Duplication and Plk4 Recruitment to Mitotic Centrosomes
inferred← citeshttps://doi.org/10.1371/journal.pone.0110958openalex-snapshot
Centrosome/Cell Cycle Uncoupling and Elimination in the Endoreduplicating Intestinal Cells of C. elegans
inferred← citeshttps://doi.org/10.15252/embj.201488979openalex-snapshot
RBM14 prevents assembly of centriolar protein complexes and maintains mitotic spindle integrity
inferred← citeshttps://doi.org/10.15252/embj.201796883openalex-snapshot
Centriole translocation and degeneration during ciliogenesis in Caenorhabditis elegans neurons
inferred← citeshttps://doi.org/10.15252/embj.2023115076openalex-snapshot
Centriole elimination during Caenorhabditis elegans oogenesis initiates with loss of the central tube protein SAS‐1
inferred← citeshttps://doi.org/10.1534/g3.115.025577openalex-snapshot
The E2F-DP1 Transcription Factor Complex Regulates Centriole Duplication inCaenorhabditis elegans
inferred← citeshttps://doi.org/10.1534/g3.117.300260openalex-snapshot
APC/CFZR-1 Controls SAS-5 Levels To Regulate Centrosome Duplication in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1534/genetics.107.071803openalex-snapshot
Suppressors ofzyg-1Define Regulators of Centrosome Duplication and Nuclear Association inCaenorhabditis elegans
inferred← citeshttps://doi.org/10.1534/genetics.115.182279openalex-snapshot
Manipulation of Karyotype inCaenorhabditis elegansReveals Multiple Inputs Driving Pairwise Chromosome Synapsis During Meiosis
inferred← citeshttps://doi.org/10.1534/genetics.118.301367openalex-snapshot
Mitotic Cell Division in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.17912/micropub.biology.000256openalex-snapshot
Tracking of centriole inheritance in C. elegans
inferred← citeshttps://doi.org/10.1895/wormbook.1.72.1openalex-snapshot
Cell division
inferred← citeshttps://doi.org/10.3389/fonc.2013.00277openalex-snapshot
Centrosome Dysfunction Contributes to Chromosome Instability, Chromoanagenesis, and Genome Reprograming in Cancer
inferred← citeshttps://doi.org/10.3390/cells11050786openalex-snapshot
Role of Polo-like Kinases Plk1 and Plk4 in the Initiation of Centriole Duplication—Impact on Cancer
inferred← citeshttps://doi.org/10.3390/cells11152445openalex-snapshot
Duplication and Segregation of Centrosomes during Cell Division
inferred← citeshttps://doi.org/10.3390/cells7080101openalex-snapshot
Revisiting Centrioles in Nematodes—Historic Findings and Current Topics
inferred← citeshttps://doi.org/10.3390/cells8080841openalex-snapshot
Poc1B and Sas-6 Function Together during the Atypical Centriole Formation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.3390/cells9061429openalex-snapshot
With Age Comes Maturity: Biochemical and Structural Transformation of a Human Centriole in the Making
inferred← citeshttps://doi.org/10.3390/cells9102156openalex-snapshot
Principal Postulates of Centrosomal Biology. Version 2020
inferred← citeshttps://doi.org/10.3390/sym9050074openalex-snapshot
Coupling Form and Function: How the Oligomerisation Symmetry of the SAS-6 Protein Contributes to the Architecture of Centriole Organelles
inferred← citeshttps://doi.org/10.4161/15384101.2014.946830openalex-snapshot
Lack of centrioles and primary cilia inSTIL−/−mouse embryos
inferred← citeshttps://doi.org/10.4161/worm.25214openalex-snapshot
The SAS-5 N-terminal domain is a tetramer, with implications for centriole assembly inC. elegans
inferred← citeshttps://doi.org/10.5075/epfl-thesis-4491openalex-snapshot
Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells
inferred← citeshttps://doi.org/10.70675/9023fab1z003az407bz9b02z2054939e787dopenalex-snapshot
Influence of centrosome amplification on the response to chemotherapy in epithelial ovarian cancer
inferred← citeshttps://doi.org/10.70675/ea490599zc7fcz4bcazb01dz83e591b2fab5openalex-snapshot
Méiose centrosomale de l'ovocyte chez le nématode parthénogénétique rhabditophanes diutinus
inferred← citeshttps://doi.org/10.7554/elife.07236openalex-snapshot
The homo-oligomerisation of both Sas-6 and Ana2 is required for efficient centriole assembly in flies
inferred← citeshttps://doi.org/10.7554/elife.07410openalex-snapshot
The Caenorhabditis elegans protein SAS-5 forms large oligomeric assemblies critical for centriole formation
inferred← citeshttps://doi.org/10.7554/elife.20353openalex-snapshot
Centriolar SAS-7 acts upstream of SPD-2 to regulate centriole assembly and pericentriolar material formation
inferred← citeshttps://doi.org/10.7554/elife.25358openalex-snapshot
How centrioles acquire the ability to reproduce
inferred← citeshttps://doi.org/10.7554/elife.25686openalex-snapshot
Centriolar remodeling underlies basal body maturation during ciliogenesis in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.7554/elife.46054openalex-snapshot
PLK4 promotes centriole duplication by phosphorylating STIL to link the procentriole cartwheel to the microtubule wall
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