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Centrobin

https://doi.org/10.1083/jcb.200506185

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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/meth.1998.0681openalex-snapshot

Development of Specific Synaptic Network Functions in Organotypic Central Nervous System (CNS) Cultures: Implications for Transplantation of CNS Neural Cellsin Vivo

inferredcites →https://doi.org/10.1016/0014-4827(80)90282-7openalex-snapshot

The ultrastructure of primary cilia in quiescent 3T3 cells

inferredcites →https://doi.org/10.1016/0955-0674(95)80043-3openalex-snapshot

Centrin, centrosomes, and mitotic spindle poles

inferredcites →https://doi.org/10.1016/s0076-6879(98)98022-3openalex-snapshot

[20] Rapid isolation of centrosomes

inferredcites →https://doi.org/10.1016/s0092-8674(00)00093-3openalex-snapshot

Nucleophosmin/B23 Is a Target of CDK2/Cyclin E in Centrosome Duplication

inferredcites →https://doi.org/10.1016/s0092-8674(01)00411-1openalex-snapshot

The Mouse Mps1p-like Kinase Regulates Centrosome Duplication

inferredcites →https://doi.org/10.1016/s0955-0674(02)00017-0openalex-snapshot

Basal body/centriole assembly and continuity

inferredcites →https://doi.org/10.1016/s0955-0674(99)80015-5openalex-snapshot

Amorphous no longer: the centrosome comes into focus

inferredcites →https://doi.org/10.1016/s0960-9822(01)00412-2openalex-snapshot

Centrosome duplication: Three kinases come up a winner!

inferredcites →https://doi.org/10.1016/s1534-5807(02)00258-7openalex-snapshot

CP110, a Cell Cycle-Dependent CDK Substrate, Regulates Centrosome Duplication in Human Cells

inferredcites →https://doi.org/10.1038/10054openalex-snapshot

Centrosome duplication in mammalian somatic cells requires E2F and Cdk2–Cyclin A

inferredcites →https://doi.org/10.1038/35089575openalex-snapshot

Re-evaluating centrosome function

inferredcites →https://doi.org/10.1038/71350openalex-snapshot

δ-Tubulin and ɛ-tubulin: two new human centrosomal tubulins reveal new aspects of centrosome structure and function

inferredcites →https://doi.org/10.1038/sj.onc.1205772openalex-snapshot

Centrosome amplification and the development of cancer

inferredcites →https://doi.org/10.1073/pnas.032479999openalex-snapshot

Centrosome amplification drives chromosomal instability in breast tumor development

inferredcites →https://doi.org/10.1073/pnas.86.4.1249openalex-snapshot

Distinctive traits of normal and tumor-derived human mammary epithelial cells expressed in a medium that supports long-term growth of both cell types.

inferredcites →https://doi.org/10.1073/pnas.95.6.2950openalex-snapshot

Centrosome hypertrophy in human breast tumors: Implications for genomic stability and cell polarity

inferredcites →https://doi.org/10.1073/pnas.96.6.2817openalex-snapshot

Cyclin-dependent kinase control of centrosome duplication

inferredcites →https://doi.org/10.1074/jbc.275.20.14824openalex-snapshot

PKN Binds and Phosphorylates Human Papillomavirus E6 Oncoprotein

inferredcites →https://doi.org/10.1083/jcb.101.6.2085openalex-snapshot

Monoclonal antibodies specific for an acetylated form of alpha-tubulin recognize the antigen in cilia and flagella from a variety of organisms.

inferredcites →https://doi.org/10.1083/jcb.130.4.919openalex-snapshot

A molecular marker for centriole maturation in the mammalian cell cycle.

inferredcites →https://doi.org/10.1083/jcb.131.5.1261openalex-snapshot

The cell cycle-dependent localization of the CP190 centrosomal protein is determined by the coordinate action of two separable domains.

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.153.1.237openalex-snapshot

Centrosomes Enhance the Fidelity of Cytokinesis in Vertebrates and Are Required for Cell Cycle Progression

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/10.1083/jcb.93.3.938openalex-snapshot

Centrioles in the cell cycle. I. Epithelial cells.

inferredcites →https://doi.org/10.1093/emboj/21.7.1723openalex-snapshot

Human Mps1 kinase is required for the spindle assembly checkpoint but not for centrosome duplication

inferredcites →https://doi.org/10.1126/science.1056866openalex-snapshot

Requirement of a Centrosomal Activity for Cell Cycle Progression Through G 1 into S Phase

inferredcites →https://doi.org/10.1126/science.1057330openalex-snapshot

Centrosome-Dependent Exit of Cytokinesis in Animal Cells

inferredcites →https://doi.org/10.1126/science.283.5403.851openalex-snapshot

Requirement of Cdk2-Cyclin E Activity for Repeated Centrosome Reproduction in Xenopus Egg Extracts

inferredcites →https://doi.org/10.1128/mcb.19.1.733openalex-snapshot

The E6 Oncoproteins of High-Risk Papillomaviruses Bind to a Novel Putative GAP Protein, E6TP1, and Target It for Degradation

inferredcites →https://doi.org/10.1146/annurev.bi.63.070194.003231openalex-snapshot

THE CENTROSOME AND CELLULAR ORGANIZATION

inferredcites →https://doi.org/10.1242/jcs.00341openalex-snapshot

PARP-3 localizes preferentially to the daughter centriole and interferes with the G1/S cell cycle progression

inferredcites →https://doi.org/10.1242/jcs.109.13.3089openalex-snapshot

Most of centrin in animal cells is not centrosome-associated and centrosomal centrin is confined to the distal lumen of centrioles

inferredcites →https://doi.org/10.1242/jcs.113.17.3013openalex-snapshot

Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein

inferredcites →https://doi.org/10.1242/jcs.115.9.1825openalex-snapshot

CEP110 and ninein are located in a specific domain of the centrosome associated with centrosome maturation

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/em.20533openalex-snapshot

Aurora A, centrosome structure, and the centrosome cycle

inferred← citeshttps://doi.org/10.1002/mrd.20990openalex-snapshot

Nip2/centrobin may be a substrate of Nek2 that is required for proper spindle assembly during mitosis in early mouse embryos

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_6openalex-snapshot

Asymmetric Centrosome Behavior in Stem Cell Divisions

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_9openalex-snapshot

Centrosomes and Centrosome Equivalents in Other Systems

inferred← citeshttps://doi.org/10.1007/978-3-7091-1903-7_3openalex-snapshot

Organizational Properties of the Pericentriolar Material

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/s00018-016-2315-xopenalex-snapshot

Regulation of centriolar satellite integrity and its physiology

inferred← citeshttps://doi.org/10.1007/s10059-009-0097-9openalex-snapshot

Centrobin/Nip2 Expression In Vivo Suggests Its Involvement in Cell Proliferation

inferred← citeshttps://doi.org/10.1007/s10549-012-2244-9openalex-snapshot

Genetic polymorphisms in centrobin and Nek2 are associated with breast cancer susceptibility in a Chinese Han population

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/s12038-023-00326-6openalex-snapshot

Appearing and disappearing acts of cilia

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2025.742411openalex-snapshot

Genome sequencing and identification of candidate variants for a red/black color polymorphism in tilapia (Oreochromis spp.)

inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.01.100openalex-snapshot

Interference with BRCA2, which localizes to the centrosome during S and early M phase, leads to abnormal nuclear division

inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.12.106openalex-snapshot

NEK2 phosphorylation antagonizes the microtubule stabilizing activity of centrobin

inferred← citeshttps://doi.org/10.1016/j.cell.2007.06.027openalex-snapshot

Cep97 and CP110 Suppress a Cilia Assembly Program

inferred← citeshttps://doi.org/10.1016/j.cell.2011.11.020openalex-snapshot

The STARD9/Kif16a Kinesin Associates with Mitotic Microtubules and Regulates Spindle Pole Assembly

inferred← citeshttps://doi.org/10.1016/j.cellsig.2010.01.009openalex-snapshot

Inhibition of centriole duplication by centrobin depletion leads to p38–p53 mediated cell-cycle arrest

inferred← citeshttps://doi.org/10.1016/j.celrep.2017.08.005openalex-snapshot

Asymmetric Centriole Numbers at Spindle Poles Cause Chromosome Missegregation in Cancer

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.devcel.2009.12.022openalex-snapshot

Ofd1, a Human Disease Gene, Regulates the Length and Distal Structure of Centrioles

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.ejmech.2025.117287openalex-snapshot

Insights into NEK2 inhibitors as antitumor agents: From mechanisms to potential therapeutics

inferred← citeshttps://doi.org/10.1016/j.genrep.2021.101481openalex-snapshot

Evaluation of the association between centrosome amplification in tumor tissue of breast cancer patients and changes in the expression of CETN1 and CNTROB genes

inferred← citeshttps://doi.org/10.1016/j.jdermsci.2018.03.008openalex-snapshot

Characterization of centriole duplication in human epidermis, Bowen’s disease, and squamous cell carcinoma

inferred← citeshttps://doi.org/10.1016/j.sbi.2020.09.006openalex-snapshot

How the centriole builds its cilium: of mothers, daughters, and the acquisition of appendages

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.semcdb.2020.04.019openalex-snapshot

Centrosome dysfunction in human diseases

inferred← citeshttps://doi.org/10.1016/j.tcb.2008.06.004openalex-snapshot

Mechanisms of procentriole formation

inferred← citeshttps://doi.org/10.1016/j.treopn.2026.04.003openalex-snapshot

Unraveling the molecular details of centriole elongation

inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.01.042openalex-snapshot

Coiled-coil domain containing 42 ( Ccdc 42) is necessary for proper sperm development and male fertility in the mouse

inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.11.019openalex-snapshot

Massive cytoplasmic transport and microtubule organization in fertilized chordate eggs

inferred← citeshttps://doi.org/10.1016/j.ymeth.2026.07.002openalex-snapshot

Cilia SubQ: a modular suite of semi- and fully automated pipelines for analysis of primary cilia and ciliary subdomains

inferred← citeshttps://doi.org/10.1017/s0967199410000183openalex-snapshot

Nek2 and its substrate, centrobin/Nip2, are required for proper meiotic spindle formation of the mouse oocytes

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.2011.63openalex-snapshot

Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods

inferred← citeshttps://doi.org/10.1038/embor.2012.40openalex-snapshot

Neurl4, a novel daughter centriole protein, prevents formation of ectopic microtubule organizing centres

inferred← citeshttps://doi.org/10.1038/ncb1432openalex-snapshot

The retroviral oncoprotein Tax targets the coiled-coil centrosomal protein TAX1BP2 to induce centrosome overduplication

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/ncb2671openalex-snapshot

Centrobin controls mother–daughter centriole asymmetry in Drosophila neuroblasts

inferred← citeshttps://doi.org/10.1038/ncb3576openalex-snapshot

Budding yeast Wee1 distinguishes spindle pole bodies to guide their pattern of age-dependent segregation

inferred← citeshttps://doi.org/10.1038/ncomms1245openalex-snapshot

Drosophila neuroblasts retain the daughter centrosome

inferred← citeshttps://doi.org/10.1038/nrm3373openalex-snapshot

Towards a molecular architecture of centriole assembly

inferred← citeshttps://doi.org/10.1038/onc.2010.37openalex-snapshot

Centrobin regulates the assembly of functional mitotic spindles

inferred← citeshttps://doi.org/10.1038/s41467-018-06286-yopenalex-snapshot

A distal centriolar protein network controls organelle maturation and asymmetry

inferred← citeshttps://doi.org/10.1038/s41467-021-26252-5openalex-snapshot

Sub-centrosomal mapping identifies augmin-γTuRC as part of a centriole-stabilizing scaffold

inferred← citeshttps://doi.org/10.1038/s41598-018-30791-1openalex-snapshot

Multicilin and activated E2f4 induce multiciliated cell differentiation in primary fibroblasts

inferred← citeshttps://doi.org/10.1038/s41598-019-42577-0openalex-snapshot

CEP120 interacts with C2CD3 and Talpid3 and is required for centriole appendage assembly and ciliogenesis

inferred← citeshttps://doi.org/10.1038/s41598-021-91818-8openalex-snapshot

Centrosomal P4.1-associated protein (CPAP) positively regulates endocytic vesicular transport and lysosome targeting of EGFR

inferred← citeshttps://doi.org/10.1038/s41598-022-22036-zopenalex-snapshot

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families

inferred← citeshttps://doi.org/10.1038/s41598-025-94414-2openalex-snapshot

Centrobin serves as a safeguard to guide timely centriole maturation during the cell cycle

inferred← citeshttps://doi.org/10.1038/s42003-025-09249-4openalex-snapshot

A GPER-PKA-Centrin axis regulates centrosome numbers and centriole integrity in colon cancer cells

inferred← citeshttps://doi.org/10.1038/sj.onc.1210685openalex-snapshot

Antizyme, a mediator of ubiquitin-independent proteasomal degradation and its inhibitor localize to centrosomes and modulate centriole amplification

inferred← citeshttps://doi.org/10.1073/pnas.1311520111openalex-snapshot

Spontaneous slow replication fork progression elicits mitosis alterations in homologous recombination-deficient mammalian cells

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.m109.099127openalex-snapshot

Centrobin/NIP2 Is a Microtubule Stabilizer Whose Activity Is Enhanced by PLK1 Phosphorylation during Mitosis

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.m114.603423openalex-snapshot

Centrobin-mediated Regulation of the Centrosomal Protein 4.1-associated Protein (CPAP) Level Limits Centriole Length during Elongation Stage

inferred← citeshttps://doi.org/10.1080/15384101.2014.1000197openalex-snapshot

Centrosomal nucleolin is required for microtubule network organization

inferred← citeshttps://doi.org/10.1080/15384101.2015.1041683openalex-snapshot

The microtubule nucleation activity of centrobin in both the centrosome and cytoplasm

inferred← citeshttps://doi.org/10.1080/15384101.2019.1654796openalex-snapshot

Centrobin plays a role in the cellular response to DNA damage

inferred← citeshttps://doi.org/10.1080/15384101.2021.1988289openalex-snapshot

TRIM37: a critical orchestrator of centrosome function

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.201006135openalex-snapshot

Centrobin–tubulin interaction is required for centriole elongation and stability

inferred← citeshttps://doi.org/10.1083/jcb.201202126openalex-snapshot

Cep164 mediates vesicular docking to the mother centriole during early steps of ciliogenesis

inferred← citeshttps://doi.org/10.1083/jcb.201407087openalex-snapshot

Centriole maturation requires regulated Plk1 activity during two consecutive cell cycles

inferred← citeshttps://doi.org/10.1083/jcb.201510083openalex-snapshot

Distinct mechanisms eliminate mother and daughter centrioles in meiosis of starfish oocytes

inferred← citeshttps://doi.org/10.1083/jcb.201706095openalex-snapshot

Centrobin controls primary ciliogenesis in vertebrates

inferred← citeshttps://doi.org/10.1083/jcb.201801032openalex-snapshot

Centrobin is essential for C-tubule assembly and flagellum development in Drosophila melanogaster spermatogenesis

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.202010180openalex-snapshot

TRIM37 prevents formation of condensate-organized ectopic spindle poles to ensure mitotic fidelity

inferred← citeshttps://doi.org/10.1083/jcb.202203081openalex-snapshot

The central scaffold protein CEP350 coordinates centriole length, stability, and maturation

inferred← citeshttps://doi.org/10.1083/jcb.202311153openalex-snapshot

Centrosome age breaks spindle size symmetry even in cells thought to divide symmetrically

inferred← citeshttps://doi.org/10.1083/jcb.202403022openalex-snapshot

Centriole structural integrity defects are a crucial feature of hydrolethalus syndrome

inferred← citeshttps://doi.org/10.1091/mbc.e06-04-0371openalex-snapshot

CP110 Cooperates with Two Calcium-binding Proteins to Regulate Cytokinesis and Genome Stability

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1091/mbc.e12-08-0577openalex-snapshot

Bld10/Cep135 stabilizes basal bodies to resist cilia-generated forces

inferred← citeshttps://doi.org/10.1091/mbc.e14-11-1561openalex-snapshot

Centriolar satellite– and hMsd1/SSX2IP-dependent microtubule anchoring is critical for centriole assembly

inferred← citeshttps://doi.org/10.1091/mbc.e21-06-0305openalex-snapshot

The SON RNA splicing factor is required for intracellular trafficking structures that promote centriole assembly and ciliogenesis

inferred← citeshttps://doi.org/10.1091/mbc.e26-05-0206openalex-snapshot

Dimerization of the centriolin-like protein Nud1 governs spindle pole body inheritance in budding yeast

inferred← citeshttps://doi.org/10.1095/biolreprod.109.078980openalex-snapshot

RathdMutation Reveals an Essential Role of Centrobin in Spermatid Head Shaping and Assembly of the Head-Tail Coupling Apparatus1

inferred← citeshttps://doi.org/10.1098/rsob.200314openalex-snapshot

Centrosome-centric view of asymmetric stem cell division

inferred← citeshttps://doi.org/10.1098/rsob.230222openalex-snapshot

Towards understanding centriole elimination

inferred← citeshttps://doi.org/10.1098/rstb.2013.0466openalex-snapshot

When fate follows age: unequal centrosomes in asymmetric cell division

inferred← citeshttps://doi.org/10.1101/2023.07.26.549647openalex-snapshot

The maintenance of centriole appendages and motile cilia basal body anchoring relies on TBCCD1

inferred← citeshttps://doi.org/10.1101/2023.09.15.557935openalex-snapshot

Centrosome age breaks spindle size symmetry even in “symmetrically” dividing cells

inferred← citeshttps://doi.org/10.1101/cshperspect.a025049openalex-snapshot

The Centrosome, a Multitalented Renaissance Organelle

inferred← citeshttps://doi.org/10.1101/gad.353426.125openalex-snapshot

CDK1 and CEP97 cooperatively control centriole length to orchestrate ciliogenesis and developmental patterning

inferred← citeshttps://doi.org/10.1111/gtc.12668openalex-snapshot

Cep128 associates with Odf2 to form the subdistal appendage of the centriole

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/10.1128/mcb.02021-07openalex-snapshot

Downregulation of Protein 4.1R, a Mature Centriole Protein, Disrupts Centrosomes, Alters Cell Cycle Progression, and Perturbs Mitotic Spindles and Anaphase

inferred← citeshttps://doi.org/10.1134/s0006297908060023openalex-snapshot

The centrosome is a polyfunctional multiprotein cell complex

inferred← citeshttps://doi.org/10.1134/s0026893311020105openalex-snapshot

Epigenetic status of cell cycle regulation genes in the placenta of human embryos with chromosomal mosaicism

inferred← citeshttps://doi.org/10.11606/t.41.2014.tde-15122014-143541openalex-snapshot

Diferentes abordagens para o entendimento da aneuploidia: interferindo na mitose com o uso de crisotila e vincristina

inferred← citeshttps://doi.org/10.1186/1745-6150-5-7openalex-snapshot

Origin of the cell nucleus, mitosis and sex: roles of intracellular coevolution

inferred← citeshttps://doi.org/10.1186/1747-1028-2-25openalex-snapshot

Mitotic regulation by NIMA-related kinases

inferred← citeshttps://doi.org/10.1186/s13008-022-00077-0openalex-snapshot

An updated view on the centrosome as a cell cycle regulator

inferred← citeshttps://doi.org/10.1242/dev.151407openalex-snapshot

The regulation of cilium assembly and disassembly in development and disease

inferred← citeshttps://doi.org/10.1242/dev.199716openalex-snapshot

Live imaging of the Drosophila ovarian niche shows spectrosome and centrosome dynamics during asymmetric germline stem cell division

inferred← citeshttps://doi.org/10.1242/jcs.005231openalex-snapshot

Structure and duplication of the centrosome

inferred← citeshttps://doi.org/10.1242/jcs.03305openalex-snapshot

Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells

inferred← citeshttps://doi.org/10.1242/jcs.03458openalex-snapshot

Characterization of NIP2/centrobin, a novel substrate of Nek2, and its potential role in microtubule stabilization

inferred← citeshttps://doi.org/10.1242/jcs.078089openalex-snapshot

NEK7 is essential for centriole duplication and centrosomal accumulation of pericentriolar material proteins in interphase cells

inferred← citeshttps://doi.org/10.1242/jcs.111203openalex-snapshot

Poc1A and Poc1B act together in human cells to ensure centriole integrity

inferred← citeshttps://doi.org/10.1242/jcs.114595openalex-snapshot

The RAD51 paralogs ensure cellular protection against mitotic defects and aneuploidy

inferred← citeshttps://doi.org/10.1242/jcs.186338openalex-snapshot

CEP295 interacts with microtubules and is required for centriole elongation

inferred← citeshttps://doi.org/10.1242/jcs.203505openalex-snapshot

Maintaining centrosomes and cilia

inferred← citeshttps://doi.org/10.1242/jcs.259120openalex-snapshot

PLK1 controls centriole distal appendage formation and centrobin removal via independent pathways

inferred← citeshttps://doi.org/10.1242/jcs.259395openalex-snapshot

Centrosome maturation – in tune with the cell cycle

inferred← citeshttps://doi.org/10.1242/jcs.260454openalex-snapshot

The cilium–centrosome axis in coupling cell cycle exit and cell fate

inferred← citeshttps://doi.org/10.13025/16788openalex-snapshot

Centriolar and ciliary responses to DNA damage

inferred← citeshttps://doi.org/10.1371/journal.pbio.3000762openalex-snapshot

Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry

inferred← citeshttps://doi.org/10.1371/journal.pone.0060859openalex-snapshot

Overexpression of Full-Length Centrobin Rescues Limb Malformation but Not Male Fertility of the Hypodactylous (hd) Rats

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/embr.201846735openalex-snapshot

Parental centrioles are dispensable for deuterosome formation and function during basal body amplification

inferred← citeshttps://doi.org/10.1530/rep-14-0370openalex-snapshot

Haplo-deficiency of ODF1/HSPB10 in mouse sperm causes relaxation of head-to-tail linkage

inferred← citeshttps://doi.org/10.18632/oncotarget.27932openalex-snapshot

Loss of CPAP causes sustained EGFR signaling and epithelial-mesenchymal transition in oral cancer

inferred← citeshttps://doi.org/10.2478/s11535-009-0061-xopenalex-snapshot

CLERC and centrosomal leucine-rich repeat proteins

inferred← citeshttps://doi.org/10.3389/fcell.2022.861864openalex-snapshot

Experimental and Natural Induction of de novo Centriole Formation

inferred← citeshttps://doi.org/10.3390/cells10092266openalex-snapshot

The Transformation of the Centrosome into the Basal Body: Similarities and Dissimilarities between Somatic and Male Germ Cells and Their Relevance for Male Fertility

inferred← citeshttps://doi.org/10.3390/cells11030432openalex-snapshot

Estrogens—Origin of Centrosome Defects in Human Cancer?

inferred← citeshttps://doi.org/10.3390/cells12172194openalex-snapshot

ODF2 Negatively Regulates CP110 Levels at the Centrioles/Basal Bodies to Control the Biogenesis of Primary Cilia

inferred← citeshttps://doi.org/10.3390/cells12182219openalex-snapshot

Protein Phosphatase 4 Is Required for Centrobin Function in DNA Damage Repair

inferred← citeshttps://doi.org/10.3390/cells9010115openalex-snapshot

The Singularity of the Drosophila Male Germ Cell Centriole: The Asymmetric Distribution of Sas4 and Sas6

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/ijms18040885openalex-snapshot

A Systems Biology Approach Using Transcriptomic Data Reveals Genes and Pathways in Porcine Skeletal Muscle Affected by Dietary Lysine

inferred← citeshttps://doi.org/10.3390/ijms23136986openalex-snapshot

Molecular Link between DNA Damage Response and Microtubule Dynamics

inferred← citeshttps://doi.org/10.3410/f.735563036.793568843openalex-snapshot

Faculty Opinions recommendation of CEP120 interacts with C2CD3 and Talpid3 and is required for centriole appendage assembly and ciliogenesis.

inferred← citeshttps://doi.org/10.4161/bioa.19766openalex-snapshot

STARD9/Kif16a is a novel mitotic kinesin and antimitotic target

inferred← citeshttps://doi.org/10.4161/cc.21986openalex-snapshot

C-NAP1 and rootletin restrain DNA damage-induced centriole splitting and facilitate ciliogenesis

inferred← citeshttps://doi.org/10.4161/cc.23879openalex-snapshot

Centrobin regulates centrosome function in interphase cells by limiting pericentriolar matrix recruitment

inferred← citeshttps://doi.org/10.4161/cc.24853openalex-snapshot

More isn’t always better: Limiting centrosome size in interphase

inferred← citeshttps://doi.org/10.4161/cib.4.3.14806openalex-snapshot

Gene ontology analysis of the centrosome proteomes of Drosophila and human

inferred← citeshttps://doi.org/10.4252/wjsc.v13.i9.1177openalex-snapshot

Stem cells' centrosomes: How can organelles identified 130 years ago contribute to the future of regenerative medicine?

inferred← citeshttps://doi.org/10.5213/inj.2244284.142openalex-snapshot

Human Endogenous Retroviruses: Friends and Foes in Urology Clinics

inferred← citeshttps://doi.org/10.64898/2026.04.10.717631openalex-snapshot

Cilia SubQ, a modular suite of pipelines for automated analysis of primary cilia and ciliary subdomains

inferred← citeshttps://doi.org/10.64898/2026.05.29.728888openalex-snapshot

CPAP/CENPJ is essential for the stability and function of ESCRT-pathway associated AAA+ ATPase VPS4B

inferred← citeshttps://doi.org/10.7554/elife.05124openalex-snapshot

The equatorial position of the metaphase plate ensures symmetric cell divisions

inferred← citeshttps://doi.org/10.7554/elife.35439openalex-snapshot

A novel Cep120-dependent mechanism inhibits centriole maturation in quiescent cells

inferred← citeshttps://doi.org/10.7554/elife.37846openalex-snapshot

PPP1R35 is a novel centrosomal protein that regulates centriole length in concert with the microcephaly protein RTTN

inferred← citeshttps://doi.org/10.7554/elife.62640openalex-snapshot

TRIM37 prevents formation of centriolar protein assemblies by regulating Centrobin

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