On the public citation graph
SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells
0 signed · 405 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1526-968x(200001)26:1<26::aid-gene6>3.0.co;2-oopenalex-snapshot
The polo-like kinase PLK-1 is required for nuclear envelope breakdown and the completion of meiosis inCaenorhabditis 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/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/j.cub.2004.06.059openalex-snapshot
Polo-like Kinase-2 Is Required for Centriole Duplication in Mammalian Cells
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/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/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/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/10.1038/10054openalex-snapshot
Centrosome duplication in mammalian somatic cells requires E2F and Cdk2–Cyclin A
inferredcites →https://doi.org/10.1038/nature01959openalex-snapshot
The BTB protein MEL-26 is a substrate-specific adaptor of the CUL-3 ubiquitin-ligase
inferredcites →https://doi.org/10.1038/nature02166openalex-snapshot
Proteomic characterization of the human centrosome by protein correlation profiling
inferredcites →https://doi.org/10.1038/nature03353openalex-snapshot
Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/ncb1146openalex-snapshot
Centriolar SAS-5 is required for centrosome duplication in C. elegans
inferredcites →https://doi.org/10.1073/pnas.042684199openalex-snapshot
Proteome-scale purification of human proteins from bacteria
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.148.3.405openalex-snapshot
A Role for Centrin 3 in Centrosome Reproduction
inferredcites →https://doi.org/10.1091/mbc.9.6.1293openalex-snapshot
The UNI3 Gene Is Required for Assembly of Basal Bodies of Chlamydomonas and Encodes δ-Tubulin, a New Member of the Tubulin Superfamily
inferredcites →https://doi.org/10.1091/mbc.e02-04-0205openalex-snapshot
ε-Tubulin Is an Essential Component of the Centriole
inferredcites →https://doi.org/10.1093/bib/3.3.265openalex-snapshot
PROSITE: A documented database using patterns and profiles as motif descriptors
inferredcites →https://doi.org/10.1093/bioinformatics/btg430openalex-snapshot
The Jalview Java alignment editor
inferredcites →https://doi.org/10.1093/emboj/21.4.483openalex-snapshot
Aurora‐A overexpression reveals tetraploidization as a major route to centrosome amplification in p53−/− cells
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/10.1093/genetics/77.1.71openalex-snapshot
THE GENETICS OF CAENORHABDITIS ELEGANS
inferredcites →https://doi.org/10.1093/nar/gkh479openalex-snapshot
MyHits: a new interactive resource for protein annotation and domain identification
inferredcites →https://doi.org/10.1128/mcb.20.20.7813-7825.2000openalex-snapshot
Protein 4.1 R-135 Interacts with a Novel Centrosomal Protein (CPAP) Which Is Associated with the γ-Tubulin Complex
inferredcites →https://doi.org/10.1186/1471-2121-2-4openalex-snapshot
Role of delta-tubulin and the C-tubule in assembly of Paramecium basal bodies
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/10.1002/9781119312994.apr0375openalex-snapshot
Animal Systems Biology: Towards a Systems View of Development in C . Elegans
inferred← citeshttps://doi.org/10.1002/9781119860914.ch31openalex-snapshot
Centrosome Regulation and Function in the Developing Neocortex
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/ajmg.a.63598openalex-snapshot
Novel biallelic SASS6 variants associated with primary microcephaly and fetal growth restriction
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.20352openalex-snapshot
Centrioles to basal bodies in the spermiogenesis of Mastotermes darwiniensis (Insecta, Isoptera)
inferred← citeshttps://doi.org/10.1002/cm.20384openalex-snapshot
Identification and cell cycle‐dependent localization of nine novel, genuine centrosomal components in Dictyostelium discoideum
inferred← citeshttps://doi.org/10.1002/cm.20433openalex-snapshot
Basal body duplication in Paramecium: The key role of Bld10 in assembly and stability of the cartwheel
inferred← citeshttps://doi.org/10.1002/cm.20536openalex-snapshot
Assessing the localization of centrosomal proteins by PALM/STORM nanoscopy
inferred← citeshttps://doi.org/10.1002/cm.21157openalex-snapshot
The awesome power of dikaryons for studying flagella and basal bodies in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1002/cm.21348openalex-snapshot
Kinetic analysis of de novo centriole assembly in heat‐shocked mammalian cells
inferred← citeshttps://doi.org/10.1002/cm.22031openalex-snapshot
PLK4 : Master Regulator of Centriole Duplication and Its Therapeutic Potential
inferred← citeshttps://doi.org/10.1002/em.20477openalex-snapshot
Centriole separation in DNA damage‐induced centrosome amplification
inferred← citeshttps://doi.org/10.1002/jcp.22222openalex-snapshot
Centrosome biogenesis continues in the absence of microtubules during prolonged S‐phase arrest
inferred← citeshttps://doi.org/10.1002/mrd.21128openalex-snapshot
Vertebrate maternal‐effect genes: Insights into fertilization, early cleavage divisions, and germ cell determinant localization from studies in the zebrafish
inferred← citeshttps://doi.org/10.1007/978-1-0716-0219-5_10openalex-snapshot
Studying Centriole Duplication and Elongation in Human Cells
inferred← citeshttps://doi.org/10.1007/978-1-0716-4224-5_15openalex-snapshot
A Method for Analyzing Acentrosomal Mitotic Spindles in Human Cells
inferred← citeshttps://doi.org/10.1007/978-1-62703-035-9_1openalex-snapshot
Centriole Duplication and Inheritance in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/978-1-62703-035-9_13openalex-snapshot
Centrosomes, DNA Damage and Aneuploidy
inferred← citeshttps://doi.org/10.1007/978-1-62703-035-9_17openalex-snapshot
Mechanisms and Consequences of Centrosome Clustering in Cancer Cells
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/10.1007/978-1-62703-107-3_15openalex-snapshot
Genome-Wide Association Studies
inferred← citeshttps://doi.org/10.1007/978-3-030-58532-7_15openalex-snapshot
Cell Cycle, DNA Replication, Centrosomes, Centrioles and Cell Division
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/10.1007/978-94-007-2004-6_9openalex-snapshot
Primary Cilia are Mechanosensory Organelles with Chemosensory Roles
inferred← citeshttps://doi.org/10.1007/s00018-010-0323-9openalex-snapshot
Centrioles: active players or passengers during mitosis?
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/s00018-026-06080-wopenalex-snapshot
The γ-TuRC: mastermind of multipurpose actions at the centrosome
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/s00709-011-0276-3openalex-snapshot
Extremes in rapid cellular morphogenesis: post-transcriptional regulation of spermatogenesis in Marsilea vestita
inferred← citeshttps://doi.org/10.1007/s10059-009-0017-zopenalex-snapshot
Ab ovo or de novo? Mechanisms of Centriole Duplication
inferred← citeshttps://doi.org/10.1007/s10238-024-01510-0openalex-snapshot
SASS6 promotes tumor proliferation and is associated with TP53 and immune infiltration in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1007/s42764-020-00020-zopenalex-snapshot
Primary microcephaly with an unstable genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.20063-1openalex-snapshot
Centrioles and the Centrosome
inferred← citeshttps://doi.org/10.1016/b978-0-12-396481-6.00013-1openalex-snapshot
The Toxoplasma Cytoskeleton
inferred← citeshttps://doi.org/10.1016/b978-0-12-815041-2.00016-5openalex-snapshot
The Toxoplasma cytoskeleton: structures, proteins, and processes
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.2015.01.017openalex-snapshot
Posttranscriptional control over rapid development and ciliogenesis in Marsilea
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.2015.03.012openalex-snapshot
A yeast two-hybrid approach for probing protein–protein interactions at the centrosome
inferred← citeshttps://doi.org/10.1016/j.bbapap.2007.07.017openalex-snapshot
Mammalian NDR protein kinases: From regulation to a role in centrosome duplication
inferred← citeshttps://doi.org/10.1016/j.canlet.2012.02.006openalex-snapshot
Centrosome amplification in tumorigenesis
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.2013.12.001openalex-snapshot
Mapping molecules to structure: unveiling secrets of centriole and cilia assembly with near-atomic resolution
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.2018.05.030openalex-snapshot
Bimodal Binding of STIL to Plk4 Controls Proper Centriole Copy Number
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.cels.2018.04.011openalex-snapshot
Interrogation of Mammalian Protein Complex Structure, Function, and Membership Using Genome-Scale Fitness Screens
inferred← citeshttps://doi.org/10.1016/j.cub.2005.11.042openalex-snapshot
SAK/PLK4 Is Required for Centriole Duplication and Flagella Development
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.2007.07.025openalex-snapshot
Centrioles: Duplicating Precariously
inferred← citeshttps://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
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.2007.09.031openalex-snapshot
Asterless Is a Centriolar Protein Required for Centrosome Function and Embryo Development in Drosophila
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.cub.2007.12.055openalex-snapshot
The Mammalian SPD-2 Ortholog Cep192 Regulates Centrosome Biogenesis
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.2010.11.055openalex-snapshot
Cnn Dynamics Drive Centrosome Size Asymmetry to Ensure Daughter Centriole Retention in Drosophila Neuroblasts
inferred← citeshttps://doi.org/10.1016/j.cub.2013.06.061openalex-snapshot
Native Architecture of the Centriole Proximal Region Reveals Features Underlying Its 9-Fold Radial Symmetry
inferred← citeshttps://doi.org/10.1016/j.cub.2013.12.054openalex-snapshot
Microcephaly: STIL(l) a Tale of Too Many Centrosomes
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.2015.08.039openalex-snapshot
A Short CEP135 Splice Isoform Controls Centriole Duplication
inferred← citeshttps://doi.org/10.1016/j.cub.2016.03.055openalex-snapshot
CDK1 Prevents Unscheduled PLK4-STIL Complex Assembly in Centriole Biogenesis
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.cub.2020.04.036openalex-snapshot
SAS-6 Association with γ-Tubulin Ring Complex Is Required for Centriole Duplication in Human Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2020.05.078openalex-snapshot
Cep97 Is Required for Centriole Structural Integrity and Cilia Formation in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2025.11.048openalex-snapshot
Cellularization in chytrid fungi uses distinct mechanisms from conventional cytokinesis and cellularization in animals and yeast
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.2007.07.004openalex-snapshot
Regulated HsSAS-6 Levels Ensure Formation of a Single Procentriole per Centriole during the Centrosome Duplication Cycle
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.2014.03.007openalex-snapshot
In Situ Imaging in C. elegans Reveals Developmental Regulation of Microtubule Dynamics
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.2024.12.002openalex-snapshot
Molecular architectures of centrosomes in C. elegans embryos visualized by cryo-electron tomography
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.11.002openalex-snapshot
Primary cilia as architects of the neocortex: Roles in brain development, function, and microcephaly
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.gene.2022.146607openalex-snapshot
Identification, expression and subcellular localization of Orc1 in the microsporidian Nosema bombycis
inferred← citeshttps://doi.org/10.1016/j.ijpara.2011.06.001openalex-snapshot
Mining the Giardia genome and proteome for conserved and unique basal body proteins
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.jbc.2022.102658openalex-snapshot
Cartwheel disassembly regulated by CDK1-cyclin B kinase allows human centriole disengagement and licensing
inferred← citeshttps://doi.org/10.1016/j.meegid.2018.09.016openalex-snapshot
Identification and localization of SAS-6 in the microsporidium Nosema bombycis
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.protis.2016.06.001openalex-snapshot
Ultrastructure of Selenidium pendula, the Type Species of Archigregarines, and Phylogenetic Relations to Other Marine Apicomplexa
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.sbi.2020.08.007openalex-snapshot
The centriolar cartwheel structure: symmetric, stacked, and polarized
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.07.001openalex-snapshot
Centrioles in flies: The exception to the rule?
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.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.str.2020.04.010openalex-snapshot
CCDC61/VFL3 Is a Paralog of SAS6 and Promotes Ciliary Functions
inferred← citeshttps://doi.org/10.1016/j.str.2022.02.005openalex-snapshot
Structures of SAS-6 coiled coil hold implications for the polarity of the centriolar cartwheel
inferred← citeshttps://doi.org/10.1016/j.tcb.2007.03.003openalex-snapshot
Centrosome duplication: of rules and licenses
inferred← citeshttps://doi.org/10.1016/j.tcb.2008.06.004openalex-snapshot
Mechanisms of procentriole formation
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.tice.2010.01.002openalex-snapshot
The insect centriole: A land of discovery
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/10.1016/s0091-679x(08)85009-1openalex-snapshot
Expression and Imaging of Fluorescent Proteins in the C. elegans Gonad and Early Embryo
inferred← citeshttps://doi.org/10.1038/cr.2015.49openalex-snapshot
Paternally contributed centrioles exhibit exceptional persistence in C. elegans embryos
inferred← citeshttps://doi.org/10.1038/emboj.2010.118openalex-snapshot
PLK2 phosphorylation is critical for CPAP function in procentriole formation during the centrosome cycle
inferred← citeshttps://doi.org/10.1038/emboj.2011.378openalex-snapshot
The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation
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/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/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/ncb1320openalex-snapshot
The Polo kinase Plk4 functions in centriole duplication
inferred← citeshttps://doi.org/10.1038/ncb1529openalex-snapshot
Loss of centrosome integrity induces p38—p53—p21-dependent G1—S arrest
inferred← citeshttps://doi.org/10.1038/ncb1889openalex-snapshot
CPAP is a cell-cycle regulated protein that controls centriole length
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/ncb2661openalex-snapshot
SCFFbxw5 mediates transient degradation of actin remodeller Eps8 to allow proper mitotic progression
inferred← citeshttps://doi.org/10.1038/ncb2746openalex-snapshot
Centrosome amplification causes microcephaly
inferred← citeshttps://doi.org/10.1038/ncomms12567openalex-snapshot
Cep295 is a conserved scaffold protein required for generation of a bona fide mother centriole
inferred← citeshttps://doi.org/10.1038/ncomms13508openalex-snapshot
Autophagy controls centrosome number by degrading Cep63
inferred← citeshttps://doi.org/10.1038/ncomms15164openalex-snapshot
DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6
inferred← citeshttps://doi.org/10.1038/ncomms6267openalex-snapshot
Direct interaction of Plk4 with STIL ensures formation of a single procentriole per parental centriole
inferred← citeshttps://doi.org/10.1038/ng.971openalex-snapshot
A primary microcephaly protein complex forms a ring around parental centrioles
inferred← citeshttps://doi.org/10.1038/nrm2180openalex-snapshot
Centrosome biogenesis and function: centrosomics brings new understanding
inferred← citeshttps://doi.org/10.1038/nrm3373openalex-snapshot
Towards a molecular architecture of centriole assembly
inferred← citeshttps://doi.org/10.1038/onc.2012.310openalex-snapshot
DNA damage-induced centrosome amplification occurs via excessive formation of centriolar satellites
inferred← citeshttps://doi.org/10.1038/s41419-018-0632-8openalex-snapshot
Caspase-mediated cleavage of the centrosomal proteins during apoptosis
inferred← citeshttps://doi.org/10.1038/s41467-017-00305-0openalex-snapshot
Human microcephaly protein RTTN interacts with STIL and is required to build full-length centrioles
inferred← citeshttps://doi.org/10.1038/s41467-021-23897-0openalex-snapshot
Tuning SAS-6 architecture with monobodies impairs distinct steps of centriole assembly
inferred← citeshttps://doi.org/10.1038/s41467-024-46454-xopenalex-snapshot
Molecular basis promoting centriole triplet microtubule assembly
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/s41467-025-63002-3openalex-snapshot
The DNA replication machinery transmits dual signals to prevent unscheduled licensing and execution of centrosome duplication
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/s41598-019-40294-2openalex-snapshot
A dynamically interacting flexible loop assists oligomerisation of the Caenorhabditis elegans centriolar protein SAS-6
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/s44319-024-00260-0openalex-snapshot
Amplified centrosomes—more than just a threat
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/10.1038/srep24296openalex-snapshot
Molecular basis of the STIL coiled coil oligomerization explains its requirement for de-novo formation of centrosomes in mammalian cells
inferred← citeshttps://doi.org/10.1038/srep27075openalex-snapshot
Computational support for a scaffolding mechanism of centriole assembly
inferred← citeshttps://doi.org/10.1038/srep28604openalex-snapshot
SAS6-like protein in Plasmodium indicates that conoid-associated apical complex proteins persist in invasive stages within the mosquito vector
inferred← citeshttps://doi.org/10.1042/bc20070162openalex-snapshot
Spindle assembly defects leading to the formation of a monopolar mitotic apparatus
inferred← citeshttps://doi.org/10.1042/bst20160116openalex-snapshot
The PLK4–STIL–SAS-6 module at the core of centriole duplication
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/10.1073/pnas.2612170123openalex-snapshot
The native structure of the Trichonympha centriole cartwheel reveals a zigzag stacking pattern
inferred← citeshttps://doi.org/10.1074/jbc.ac119.012178openalex-snapshot
The ubiquitin ligase FBXW7 targets the centriolar assembly protein HsSAS-6 for degradation and thereby regulates centriole duplication
inferred← citeshttps://doi.org/10.1074/jbc.m109.092627openalex-snapshot
Self-assembling SAS-6 Multimer Is a Core Centriole Building Block
inferred← citeshttps://doi.org/10.1074/jbc.m113.531152openalex-snapshot
Centrobin-Centrosomal Protein 4.1-associated Protein (CPAP) Interaction Promotes CPAP Localization to the Centrioles during Centriole Duplication
inferred← citeshttps://doi.org/10.1074/jbc.m114.576041openalex-snapshot
The Mechanism of Dynein Light Chain LC8-mediated Oligomerization of the Ana2 Centriole Duplication Factor
inferred← citeshttps://doi.org/10.1074/jbc.m114.603423openalex-snapshot
Centrobin-mediated Regulation of the Centrosomal Protein 4.1-associated Protein (CPAP) Level Limits Centriole Length during Elongation Stage
inferred← citeshttps://doi.org/10.1074/jbc.ra120.014780openalex-snapshot
Identification of compounds that bind the centriolar protein SAS-6 and inhibit its oligomerization
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.200703064openalex-snapshot
Molecular characterization of centriole assembly in ciliated epithelial cells
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.200908019openalex-snapshot
Basal body stability and ciliogenesis requires the conserved component Poc1
inferred← citeshttps://doi.org/10.1083/jcb.200910016openalex-snapshot
Drosophila Ana2 is a conserved centriole duplication factor
inferred← citeshttps://doi.org/10.1083/jcb.201003009openalex-snapshot
Cep120 is asymmetrically localized to the daughter centriole and is essential for centriole assembly
inferred← citeshttps://doi.org/10.1083/jcb.201006049openalex-snapshot
Cep152 interacts with Plk4 and is required for centriole duplication
inferred← citeshttps://doi.org/10.1083/jcb.201006135openalex-snapshot
Centrobin–tubulin interaction is required for centriole elongation and stability
inferred← citeshttps://doi.org/10.1083/jcb.201007107openalex-snapshot
Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome
inferred← citeshttps://doi.org/10.1083/jcb.201101005openalex-snapshot
Regulating the transition from centriole to basal body
inferred← citeshttps://doi.org/10.1083/jcb.201101109openalex-snapshot
The conversion of centrioles to centrosomes: essential coupling of duplication with segregation
inferred← citeshttps://doi.org/10.1083/jcb.201307049openalex-snapshot
Mechanisms of HsSAS-6 assembly promoting centriole formation in human cells
inferred← citeshttps://doi.org/10.1083/jcb.201412010openalex-snapshot
KLP-7 acts through the Ndc80 complex to limit pole number in C. elegans oocyte meiotic spindle assembly
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.201604054openalex-snapshot
A USP28–53BP1–p53–p21 signaling axis arrests growth after centrosome loss or prolonged mitosis
inferred← citeshttps://doi.org/10.1083/jcb.201608119openalex-snapshot
The daughter centriole controls ciliogenesis by regulating Neurl-4 localization at the centrosome
inferred← citeshttps://doi.org/10.1083/jcb.201610070openalex-snapshot
Centrioles initiate cilia assembly but are dispensable for maturation and maintenance in C. elegans
inferred← citeshttps://doi.org/10.1083/jcb.201701151openalex-snapshot
Uncoordinated centrosome cycle underlies the instability of non-diploid somatic cells in mammals
inferred← citeshttps://doi.org/10.1083/jcb.201704093openalex-snapshot
Building the right centriole for each cell type
inferred← citeshttps://doi.org/10.1083/jcb.201803041openalex-snapshot
SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STIL
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/10.1089/zeb.2017.1427openalex-snapshot
The Zebrafish curly fry Is Required for Proper Centrosome and Mitotic Spindle Assembly
inferred← citeshttps://doi.org/10.1091/mbc.e07-10-1069openalex-snapshot
A Multicomponent Assembly Pathway Contributes to the Formation of Acentrosomal Microtubule Arrays in Interphase Drosophila Cells
inferred← citeshttps://doi.org/10.1091/mbc.e08-08-0835openalex-snapshot
Basal Body Components Exhibit Differential Protein Dynamics during Nascent Basal Body Assembly
inferred← citeshttps://doi.org/10.1091/mbc.e08-08-0838openalex-snapshot
The Two SAS-6 Homologs inTetrahymena thermophilaHave Distinct Functions in Basal Body Assembly
inferred← citeshttps://doi.org/10.1091/mbc.e08-09-0900openalex-snapshot
TheUNI1andUNI2Genes Function in the Transition of Triplet to Doublet Microtubules between the Centriole and Cilium inChlamydomonas
inferred← citeshttps://doi.org/10.1091/mbc.e09-06-0505openalex-snapshot
Autophosphorylation of Polo-like Kinase 4 and Its Role in Centriole Duplication
inferred← citeshttps://doi.org/10.1091/mbc.e09-12-1049openalex-snapshot
Daughter Centriole Elongation Is Controlled by Proteolysis
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.e10-11-0901openalex-snapshot
Sas-4 proteins are required during basal body duplication inParamecium
inferred← citeshttps://doi.org/10.1091/mbc.e13-03-0149openalex-snapshot
Abnormal centrosomal structure and duplication in Cep135-deficient vertebrate cells
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.e15-10-0713openalex-snapshot
LIN-41 inactivation leads to delayed centrosome elimination and abnormal chromosome behavior during female meiosis in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1091/mbc.e16-09-0643openalex-snapshot
NEK7 is required for G1 progression and procentriole formation
showing the first 200 of 371 · page through all 371
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.