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Aurora A Protein Kinase: To the Centrosome and Beyond

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What this work says

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

inferredcites →https://doi.org/10.1002/yea.320030306openalex-snapshot

Yeast centromeres

inferredcites →https://doi.org/10.1007/s00412-016-0594-5openalex-snapshot

Late mitotic functions of Aurora kinases

inferredcites →https://doi.org/10.1016/0092-8674(95)90374-7openalex-snapshot

Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles

inferredcites →https://doi.org/10.1016/0168-9525(90)90302-mopenalex-snapshot

Centromeres of mammalian chromosomes

inferredcites →https://doi.org/10.1016/j.ceb.2007.11.007openalex-snapshot

The histone variant CENP-A and centromere specification

inferredcites →https://doi.org/10.1016/j.ceb.2009.09.008openalex-snapshot

Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins

inferredcites →https://doi.org/10.1016/j.cell.2008.07.049openalex-snapshot

Linking Cell Cycle to Asymmetric Division: Aurora-A Phosphorylates the Par Complex to Regulate Numb Localization

inferredcites →https://doi.org/10.1016/j.cell.2009.07.041openalex-snapshot

Identification of an Aurora-A/PinsLINKER/ Dlg Spindle Orientation Pathway using Induced Cell Polarity in S2 Cells

inferredcites →https://doi.org/10.1016/j.cell.2010.06.039openalex-snapshot

Aurora Kinases and Protein Phosphatase 1 Mediate Chromosome Congression through Regulation of CENP-E

inferredcites →https://doi.org/10.1016/j.cell.2012.12.044openalex-snapshot

Branching Microtubule Nucleation in Xenopus Egg Extracts Mediated by Augmin and TPX2

inferredcites →https://doi.org/10.1016/j.cell.2015.08.010openalex-snapshot

Phase Transition of Spindle-Associated Protein Regulate Spindle Apparatus Assembly

inferredcites →https://doi.org/10.1016/j.celrep.2016.02.085openalex-snapshot

Phosphorylation of CPAP by Aurora-A Maintains Spindle Pole Integrity during Mitosis

inferredcites →https://doi.org/10.1016/j.cub.2004.01.055openalex-snapshot

Aurora B Phosphorylates Centromeric MCAK and Regulates Its Localization and Microtubule Depolymerization Activity

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.2006.07.057openalex-snapshot

Aurora B Is Enriched at Merotelic Attachment Sites, Where It Regulates MCAK

inferredcites →https://doi.org/10.1016/j.cub.2007.12.055openalex-snapshot

The Mammalian SPD-2 Ortholog Cep192 Regulates Centrosome Biogenesis

inferredcites →https://doi.org/10.1016/j.cub.2011.05.032openalex-snapshot

Cohesion Fatigue Induces Chromatid Separation in Cells Delayed at Metaphase

inferredcites →https://doi.org/10.1016/j.cub.2011.07.017openalex-snapshot

A Complex of Kif18b and MCAK Promotes Microtubule Depolymerization and Is Negatively Regulated by Aurora Kinases

inferredcites →https://doi.org/10.1016/j.cub.2012.11.046openalex-snapshot

The Role of NEDD1 Phosphorylation by Aurora A in Chromosomal Microtubule Nucleation and Spindle Function

inferredcites →https://doi.org/10.1016/j.cub.2013.07.078openalex-snapshot

Phospho-H2A and Cohesin Specify Distinct Tension-Regulated Sgo1 Pools at Kinetochores and Inner Centromeres

inferredcites →https://doi.org/10.1016/j.cub.2014.10.052openalex-snapshot

Aurora Kinases Phosphorylate Lgl to Induce Mitotic Spindle Orientation in Drosophila Epithelia

inferredcites →https://doi.org/10.1016/j.cub.2014.10.053openalex-snapshot

Aurora A Triggers Lgl Cortical Release during Symmetric Division to Control Planar Spindle Orientation

inferredcites →https://doi.org/10.1016/j.cub.2014.11.052openalex-snapshot

Epithelial Cell Division: Aurora Kicks Lgl to the Cytoplasmic Curb

inferredcites →https://doi.org/10.1016/j.cub.2015.05.013openalex-snapshot

Spatial Regulation of Kinetochore Microtubule Attachments by Destabilization at Spindle Poles in Meiosis I

inferredcites →https://doi.org/10.1016/j.cub.2015.05.061openalex-snapshot

Different Drosophila cell types exhibit differences in mitotic centrosome assembly dynamics

inferredcites →https://doi.org/10.1016/j.cub.2015.06.021openalex-snapshot

Aurora A Kinase Contributes to a Pole-Based Error Correction Pathway

inferredcites →https://doi.org/10.1016/j.cub.2015.12.051openalex-snapshot

NuMA Phosphorylation by Aurora-A Orchestrates Spindle Orientation

inferredcites →https://doi.org/10.1016/j.cub.2017.02.019openalex-snapshot

The N-Terminal Non-Kinase-Domain-Mediated Binding of Haspin to Pds5B Protects Centromeric Cohesion in Mitosis

inferredcites →https://doi.org/10.1016/j.cub.2018.08.052openalex-snapshot

Genetic Interactions between the Aurora Kinases Reveal New Requirements for AURKB and AURKC during Oocyte Meiosis

inferredcites →https://doi.org/10.1016/j.devcel.2013.12.013openalex-snapshot

A Microtubule-Associated Zinc Finger Protein, BuGZ, Regulates Mitotic Chromosome Alignment by Ensuring Bub3 Stability and Kinetochore Targeting

inferredcites →https://doi.org/10.1016/j.devcel.2014.02.013openalex-snapshot

The Centrosome-Specific Phosphorylation of Cnn by Polo/Plk1 Drives Cnn Scaffold Assembly and Centrosome Maturation

inferredcites →https://doi.org/10.1016/j.gde.2005.01.004openalex-snapshot

Centromeric chromatin: what makes it unique?

inferredcites →https://doi.org/10.1016/j.molcel.2013.10.006openalex-snapshot

R Loops Are Linked to Histone H3 S10 Phosphorylation and Chromatin Condensation

inferredcites →https://doi.org/10.1016/j.molcel.2014.06.016openalex-snapshot

The Cep192-Organized Aurora A-Plk1 Cascade Is Essential for Centrosome Cycle and Bipolar Spindle Assembly

inferredcites →https://doi.org/10.1016/j.tcb.2005.03.004openalex-snapshot

Aurora kinases, aneuploidy and cancer, a coincidence or a real link?

inferredcites →https://doi.org/10.1016/j.tcb.2010.10.007openalex-snapshot

Sensing centromere tension: Aurora B and the regulation of kinetochore function

inferredcites →https://doi.org/10.1016/j.tibs.2015.11.002openalex-snapshot

A Centromere-Signaling Network Underlies the Coordination among Mitotic Events

inferredcites →https://doi.org/10.1016/j.yexcr.2009.07.023openalex-snapshot

Epigenetic specification of centromeres by CENP-A

inferredcites →https://doi.org/10.1016/s0092-8674(00)81365-3openalex-snapshot

A Complex of NuMA and Cytoplasmic Dynein Is Essential for Mitotic Spindle Assembly

inferredcites →https://doi.org/10.1016/s0092-8674(03)00115-6openalex-snapshot

Centromeres and Kinetochores

inferredcites →https://doi.org/10.1016/s0960-9822(02)00766-2openalex-snapshot

Drosophila Aurora-A Is Required for Centrosome Maturation and Actin-Dependent Asymmetric Protein Localization during Mitosis

inferredcites →https://doi.org/10.1016/s0960-9822(03)00166-0openalex-snapshot

A Novel Mechanism for Activation of the Protein Kinase Aurora A

inferredcites →https://doi.org/10.1016/s0960-9822(03)00205-7openalex-snapshot

S. pombe Aurora Kinase/Survivin Is Required for Chromosome Condensation and the Spindle Checkpoint Attachment Response

inferredcites →https://doi.org/10.1016/s1097-2765(03)00392-7openalex-snapshot

Structural Basis of Aurora-A Activation by TPX2 at the Mitotic Spindle

inferredcites →https://doi.org/10.1016/s1534-5807(01)00028-4openalex-snapshot

Domain Organization at the Centromere and Neocentromere

inferredcites →https://doi.org/10.1016/s1534-5807(03)00364-2openalex-snapshot

CENP-A Phosphorylation by Aurora-A in Prophase Is Required for Enrichment of Aurora-B at Inner Centromeres and for Kinetochore Function

inferredcites →https://doi.org/10.1016/s1534-5807(04)00025-5openalex-snapshot

Aurora B Regulates MCAK at the Mitotic Centromere

inferredcites →https://doi.org/10.1038/22133openalex-snapshot

Generation of GTP-bound Ran by RCC1 is required for chromatin-induced mitotic spindle formation

inferredcites →https://doi.org/10.1038/343233a0openalex-snapshot

Regulation of microtubule dynamics by cdc2 protein kinase in cell-free extracts of Xenopus eggs

inferredcites →https://doi.org/10.1038/35048096openalex-snapshot

Mitotic kinases as regulators of cell division and its checkpoints

inferredcites →https://doi.org/10.1038/35060009openalex-snapshot

Ran–GTP coordinates regulation of microtubule nucleation and dynamics during mitotic-spindle assembly

inferredcites →https://doi.org/10.1038/35083033openalex-snapshot

Msps/XMAP215 interacts with the centrosomal protein D-TACC to regulate microtubule behaviour

inferredcites →https://doi.org/10.1038/celldisc.2016.49openalex-snapshot

Aurora-A promotes the establishment of spindle assembly checkpoint by priming the Haspin-Aurora-B feedback loop in late G2 phase

inferredcites →https://doi.org/10.1038/emboj.2010.210openalex-snapshot

Proteomic and functional analysis of the mitotic Drosophila centrosome

inferredcites →https://doi.org/10.1038/nature08912openalex-snapshot

Towards building a chromosome segregation machine

inferredcites →https://doi.org/10.1038/ncb0409-365openalex-snapshot

Spindle orientation during asymmetric cell division

inferredcites →https://doi.org/10.1038/ncb1102openalex-snapshot

Correcting improper chromosome–spindle attachments during cell division

inferredcites →https://doi.org/10.1038/ncb1349openalex-snapshot

GCP-WD is a γ-tubulin targeting factor required for centrosomal and chromatin-mediated microtubule nucleation

inferredcites →https://doi.org/10.1038/ncb3060openalex-snapshot

Kinetochore motors drive congression of peripheral polar chromosomes by overcoming random arm-ejection forces

inferredcites →https://doi.org/10.1038/ncb936openalex-snapshot

A Ran signalling pathway mediated by the mitotic kinase Aurora A in spindle assembly

inferredcites →https://doi.org/10.1038/ncomms4885openalex-snapshot

Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size

inferredcites →https://doi.org/10.1038/ncomms9879openalex-snapshot

Spindle assembly checkpoint inactivation fails to suppress neuroblast tumour formation in aurA mutant Drosophila

inferredcites →https://doi.org/10.1038/ng.683openalex-snapshot

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

inferredcites →https://doi.org/10.1038/nrg2103openalex-snapshot

Spindle orientation, asymmetric division and tumour suppression in Drosophila stem cells

inferredcites →https://doi.org/10.1038/nrg2466openalex-snapshot

Epigenetic regulation of centromeric chromatin: old dogs, new tricks?

inferredcites →https://doi.org/10.1038/nrm.2015.5openalex-snapshot

The molecular basis for centromere identity and function

inferredcites →https://doi.org/10.1038/nrm1245openalex-snapshot

The cellular geography of Aurora kinases

inferredcites →https://doi.org/10.1038/nrm3010openalex-snapshot

Asymmetric cell division: recent developments and their implications for tumour biology

inferredcites →https://doi.org/10.1038/nrm3107openalex-snapshot

Centromeres: unique chromatin structures that drive chromosome segregation

inferredcites →https://doi.org/10.1038/nrm3474openalex-snapshot

The chromosomal passenger complex (CPC): from easy rider to the godfather of mitosis

inferredcites →https://doi.org/10.1038/nrm3916openalex-snapshot

Regulation of kinetochore–microtubule attachments through homeostatic control during mitosis

inferredcites →https://doi.org/10.1038/nsmb845openalex-snapshot

Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin

inferredcites →https://doi.org/10.1038/onc.2008.252openalex-snapshot

Aurora-A and ch-TOG act in a common pathway in control of spindle pole integrity

inferredcites →https://doi.org/10.1038/onc.2011.372openalex-snapshot

Regulation of APC/CCdc20 activity by RASSF1A–APC/CCdc20 circuitry

inferredcites →https://doi.org/10.1038/s41467-018-04089-9openalex-snapshot

Aurora A-dependent CENP-A phosphorylation at inner centromeres protects bioriented chromosomes against cohesion fatigue

inferredcites →https://doi.org/10.1038/s41598-017-10935-5openalex-snapshot

Aurora A Phosphorylation of YY1 during Mitosis Inactivates its DNA Binding Activity

inferredcites →https://doi.org/10.1038/sj.onc.1209080openalex-snapshot

Transcription factor YY1: structure, function, and therapeutic implications in cancer biology

inferredcites →https://doi.org/10.1038/sj.onc.1210575openalex-snapshot

Mitotic kinase Aurora-A phosphorylates RASSF1A and modulates RASSF1A-mediated microtubule interaction and M-phase cell cycle regulation

inferredcites →https://doi.org/10.1042/bj20050343openalex-snapshot

Aurora-A site specificity: a study with synthetic peptide substrates

inferredcites →https://doi.org/10.1073/pnas.0901587106openalex-snapshot

The augmin complex plays a critical role in spindle microtubule generation for mitotic progression and cytokinesis in human cells

inferredcites →https://doi.org/10.1073/pnas.1014664107openalex-snapshot

Centrosomal protein of 192 kDa (Cep192) promotes centrosome-driven spindle assembly by engaging in organelle-specific Aurora A activation

inferredcites →https://doi.org/10.1073/pnas.1523157113openalex-snapshot

Aurora kinase-induced phosphorylation excludes transcription factor RUNX from the chromatin to facilitate proper mitotic progression

inferredcites →https://doi.org/10.1074/jbc.m111.266767openalex-snapshot

Aurora-A Phosphorylates Augmin Complex Component Hice1 Protein at an N-terminal Serine/Threonine Cluster to Modulate Its Microtubule Binding Activity during Spindle Assembly

inferredcites →https://doi.org/10.1074/jbc.m115.652453openalex-snapshot

Spatial Compartmentalization Specializes the Function of Aurora A and Aurora B

inferredcites →https://doi.org/10.1074/jbc.m306275200openalex-snapshot

Aurora-A Kinase Maintains the Fidelity of Early and Late Mitotic Events in HeLa Cells

inferredcites →https://doi.org/10.1074/mcp.m116.059394openalex-snapshot

Identification of Candidate Cyclin-dependent kinase 1 (Cdk1) Substrates in Mitosis by Quantitative Phosphoproteomics

inferredcites →https://doi.org/10.1083/jcb.118.5.1097openalex-snapshot

Control of microtubule dynamics and length by cyclin A- and cyclin B-dependent kinases in Xenopus egg extracts.

inferredcites →https://doi.org/10.1083/jcb.128.1.95openalex-snapshot

Identification and partial characterization of mitotic centromere-associated kinesin, a kinesin-related protein that associates with centromeres during mitosis.

inferredcites →https://doi.org/10.1083/jcb.143.3.673openalex-snapshot

Localization of the Kinesin-like Protein Xklp2 to Spindle Poles Requires a Leucine Zipper, a Microtubule-associated Protein, and Dynein

inferredcites →https://doi.org/10.1083/jcb.149.4.851openalex-snapshot

Formation of Spindle Poles by Dynein/Dynactin-Dependent Transport of Numa

inferredcites →https://doi.org/10.1083/jcb.149.7.1405openalex-snapshot

Tpx2, a Novel Xenopus Map Involved in Spindle Pole Organization

inferredcites →https://doi.org/10.1083/jcb.200108051openalex-snapshot

Aurora-A kinase is required for centrosome maturation in Caenorhabditis elegans

inferredcites →https://doi.org/10.1083/jcb.200108135openalex-snapshot

Drosophila Aurora A kinase is required to localize D-TACC to centrosomes and to regulate astral microtubules

inferredcites →https://doi.org/10.1083/jcb.200204155openalex-snapshot

Human TPX2 is required for targeting Aurora-A kinase to the spindle

inferredcites →https://doi.org/10.1083/jcb.200503023openalex-snapshot

Aurora A phosphorylation of TACC3/maskin is required for centrosome-dependent microtubule assembly in mitosis

inferredcites →https://doi.org/10.1083/jcb.200504097openalex-snapshot

Aurora A activates D-TACC–Msps complexes exclusively at centrosomes to stabilize centrosomal microtubules

inferredcites →https://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

inferredcites →https://doi.org/10.1083/jcb.200701163openalex-snapshot

Astrin is required for the maintenance of sister chromatid cohesion and centrosome integrity

inferredcites →https://doi.org/10.1083/jcb.200711053openalex-snapshot

Augmin: a protein complex required for centrosome-independent microtubule generation within the spindle

inferredcites →https://doi.org/10.1083/jcb.201001144openalex-snapshot

Aurora A contributes to p150glued phosphorylation and function during mitosis

inferredcites →https://doi.org/10.1083/jcb.201107134openalex-snapshot

Nucleophosmin/B23 activates Aurora A at the centrosome through phosphorylation of serine 89

inferredcites →https://doi.org/10.1083/jcb.201210060openalex-snapshot

Aurora A is involved in central spindle assembly through phosphorylation of Ser 19 in P150Glued

inferredcites →https://doi.org/10.1083/jcb.201706021openalex-snapshot

TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis

inferredcites →https://doi.org/10.1083/jcb.201706103openalex-snapshot

Aurora A activation in mitosis promoted by BuGZ

inferredcites →https://doi.org/10.1083/jcb.201707160openalex-snapshot

Aurora A kinase phosphorylates Hec1 to regulate metaphase kinetochore–microtubule dynamics

inferredcites →https://doi.org/10.1091/mbc.e07-04-0371openalex-snapshot

CDK5RAP2 Is a Pericentriolar Protein That Functions in Centrosomal Attachment of the γ-Tubulin Ring Complex

inferredcites →https://doi.org/10.1091/mbc.e07-05-0474openalex-snapshot

Proper Recruitment of γ-Tubulin and D-TACC/Msps to EmbryonicDrosophilaCentrosomes Requires Centrosomin Motif 1

inferredcites →https://doi.org/10.1091/mbc.e08-02-0198openalex-snapshot

Aurora A Phosphorylates MCAK to Control Ran-dependent Spindle Bipolarity

inferredcites →https://doi.org/10.1093/hmg/ddm298openalex-snapshot

ASAP is a novel substrate of the oncogenic mitotic kinase Aurora-A: phosphorylation on Ser625 is essential to spindle formation and mitosis

inferredcites →https://doi.org/10.1093/nar/gkl338openalex-snapshot

The tale beyond the tail: histone core domain modifications and the regulation of chromatin structure

inferredcites →https://doi.org/10.1101/cshperspect.a015818openalex-snapshot

The Centromere: Epigenetic Control of Chromosome Segregation during Mitosis

inferredcites →https://doi.org/10.1101/gad.1487506openalex-snapshot

Aurora-A acts as a tumor suppressor and regulates self-renewal of Drosophila neuroblasts

inferredcites →https://doi.org/10.1101/gad.1489406openalex-snapshot

Drosophila Aurora-A kinase inhibits neuroblast self-renewal by regulating aPKC/Numb cortical polarity and spindle orientation

inferredcites →https://doi.org/10.1101/gad.240291.114openalex-snapshot

Tension-dependent removal of pericentromeric shugoshin is an indicator of sister chromosome biorientation

inferredcites →https://doi.org/10.1101/sqb.2010.75.038openalex-snapshot

Centromere Identity, Function, and Epigenetic Propagation across Cell Divisions

inferredcites →https://doi.org/10.1126/science.1101366openalex-snapshot

The Centromeric Protein Sgo1 Is Required to Sense Lack of Tension on Mitotic Chromosomes

inferredcites →https://doi.org/10.1126/science.aaa5175openalex-snapshot

Microtubule detyrosination guides chromosomes during mitosis

inferredcites →https://doi.org/10.1126/science.aan6490openalex-snapshot

A mitosis-specific and R loop–driven ATR pathway promotes faithful chromosome segregation

inferredcites →https://doi.org/10.1126/scisignal.2001497openalex-snapshot

Quantitative Phosphoproteomics Identifies Substrates and Functional Modules of Aurora and Polo-Like Kinase Activities in Mitotic Cells

inferredcites →https://doi.org/10.1128/mcb.00068-15openalex-snapshot

Bimodal Interaction of Mammalian Polo-Like Kinase 1 and a Centrosomal Scaffold, Cep192, in the Regulation of Bipolar Spindle Formation

inferredcites →https://doi.org/10.1128/mcb.01176-14openalex-snapshot

Shugoshins: Tension-Sensitive Pericentromeric Adaptors Safeguarding Chromosome Segregation

inferredcites →https://doi.org/10.1128/mcb.01923-07openalex-snapshot

Hice1, a Novel Microtubule-Associated Protein Required for Maintenance of Spindle Integrity and Chromosomal Stability in Human Cells

inferredcites →https://doi.org/10.1146/annurev-genet-102108-134233openalex-snapshot

Cohesin: Its Roles and Mechanisms

inferredcites →https://doi.org/10.1152/ajpcell.00164.2014openalex-snapshot

The mitosis-regulating and protein-protein interaction activities of Astrin are controlled by Aurora-A-induced phosphorylation

inferredcites →https://doi.org/10.1158/0008-5472.can-09-1554openalex-snapshot

Aurora B–Mediated Phosphorylation of RASSF1A Maintains Proper Cytokinesis by Recruiting Syntaxin16 to the Midzone and Midbody

inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-1405openalex-snapshot

Aurora Kinases: New Targets for Cancer Therapy

inferredcites →https://doi.org/10.1186/s12915-017-0478-zopenalex-snapshot

Two-step interphase microtubule disassembly aids spindle morphogenesis

inferredcites →https://doi.org/10.1242/dev.125.22.4391openalex-snapshot

A highly conserved centrosomal kinase, AIR-1, is required for accurate cell cycle progression and segregation of developmental factors in Caenorhabditis elegans embryos

inferredcites →https://doi.org/10.1242/jcs.013136openalex-snapshot

Aurora-A: the maker and breaker of spindle poles

inferredcites →https://doi.org/10.1242/jcs.02614openalex-snapshot

Silencing Cenp-F weakens centromeric cohesion, prevents chromosome alignment and activates the spindle checkpoint

inferredcites →https://doi.org/10.1242/jcs.076315openalex-snapshot

A single starfish Aurora kinase performs the combined functions of Aurora-A and Aurora-B in human cells

inferredcites →https://doi.org/10.1242/jcs.111.5.557openalex-snapshot

The Xenopus protein kinase pEg2 associates with the centrosome in a cell cycle-dependent manner, binds to the spindle microtubules and is involved in bipolar mitotic spindle assembly

inferredcites →https://doi.org/10.1242/jcs.114.11.2095openalex-snapshot

The non-catalytic domain of the Xenopus laevis auroraA kinase localises the protein to the centrosome

inferredcites →https://doi.org/10.1242/jcs.157537openalex-snapshot

Opposing roles for JNK and Aurora A in regulating WD40-Repeat Protein 62 association with spindle microtubules

inferredcites →https://doi.org/10.1242/jcs.189340openalex-snapshot

Haspin kinase regulates microtubule-organizing center clustering and stability through Aurora kinase C in mouse oocytes

inferredcites →https://doi.org/10.1371/journal.pone.0022969openalex-snapshot

Uncoordinated Loss of Chromatid Cohesion Is a Common Outcome of Extended Metaphase Arrest

inferredcites →https://doi.org/10.15252/embr.201642292openalex-snapshot

Regulation of mitotic spindle orientation: an integrated view

inferredcites →https://doi.org/10.18632/oncotarget.14893openalex-snapshot

Aurora kinases: novel therapy targets in cancers

inferredcites →https://doi.org/10.3389/fonc.2015.00178openalex-snapshot

Possible Role of Aurora-C in Meiosis

inferredcites →https://doi.org/10.3390/cells7090121openalex-snapshot

Centrosomal and Non-Centrosomal Microtubule-Organizing Centers (MTOCs) in Drosophila melanogaster

inferredcites →https://doi.org/10.4161/cc.7.17.6460openalex-snapshot

Aurora kinase-A regulates kinetochore/chromatin associated microtubule assembly in human cells

inferredcites →https://doi.org/10.4161/trns.1.2.12375openalex-snapshot

Yin Yang 1

inferredcites →https://doi.org/10.7554/elife.02667openalex-snapshot

Molecular mechanism of Aurora A kinase autophosphorylation and its allosteric activation by TPX2

inferredcites →https://doi.org/10.7554/elife.11402openalex-snapshot

Aurora-A mediated histone H3 phosphorylation of threonine 118 controls condensin I and cohesin occupancy in mitosis

What points at this work

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

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Triggering mitosis

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Knockout of the BRAP homolog in mice leads to abnormal tracheal cilia

inferred← citeshttps://doi.org/10.1002/bies.202400048openalex-snapshot

Balancing Plk1 activity levels: The secret of synchrony between the cell and the centrosome cycle

inferred← citeshttps://doi.org/10.1002/cm.21710openalex-snapshot

Reconstitution of muscle cell microtubule organization in vitro

inferred← citeshttps://doi.org/10.1002/cm.22034openalex-snapshot

The NLS3 Motif in TPX2 Regulates Spindle Architecture in Xenopus Egg Extracts

inferred← citeshttps://doi.org/10.1002/cm.70015openalex-snapshot

Optineurin Localization at the Centrosome, Spindle, and Midbody Implies Its Role in Cell Division

inferred← citeshttps://doi.org/10.1002/cpt.3584openalex-snapshot

The Role and Mechanisms of Aurora Kinases in Kidney Diseases

inferred← citeshttps://doi.org/10.1002/jcb.70025openalex-snapshot

“Exploration of Novel Anticancerous Agents Targeting Human Aurora Kinase C”

inferred← citeshttps://doi.org/10.1007/s00018-020-03614-8openalex-snapshot

Reciprocal regulation of Aurora kinase A and ATIP3 in the control of metaphase spindle length

inferred← citeshttps://doi.org/10.1007/s00109-020-01895-xopenalex-snapshot

The therapeutic potential of Aurora kinases targeting in glioblastoma: from preclinical research to translational oncology

inferred← citeshttps://doi.org/10.1007/s10577-021-09669-yopenalex-snapshot

Computer simulation of merotelic kinetochore-microtubule attachments: corona size is more important than other cell parameters

inferred← citeshttps://doi.org/10.1007/s10637-020-01012-2openalex-snapshot

Identification and characterization of deschloro-chlorothricin obtained from a large natural product library targeting aurora A kinase in multiple myeloma

inferred← citeshttps://doi.org/10.1016/j.abb.2024.110209openalex-snapshot

AI-assisted generation and in-depth in-silico evaluation of potential inhibitor targeting aurora kinase A (AURKA): An anticancer discovery exploiting synthetic lethality approach

inferred← citeshttps://doi.org/10.1016/j.bbadis.2021.166227openalex-snapshot

Blocking AURKA with MK-5108 attenuates renal fibrosis in chronic kidney disease

inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188777openalex-snapshot

Combination of microtubule targeting agents with other antineoplastics for cancer treatment

inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.154458openalex-snapshot

A nuclear-targeted PROTAC enables subcellular-selective degradation of AURKA

inferred← citeshttps://doi.org/10.1016/j.bcp.2021.114655openalex-snapshot

Future prospects for mitosis-targeted antitumor therapies

inferred← citeshttps://doi.org/10.1016/j.beem.2020.101473openalex-snapshot

Genetics of teratozoospermia: Back to the head

inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110924openalex-snapshot

A look into the link between centrosome amplification and breast cancer

inferred← citeshttps://doi.org/10.1016/j.dci.2022.104424openalex-snapshot

Plasmodium exposure alters midgut epithelial cell dynamics during the immune memory in Anopheles albimanus

inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e11656openalex-snapshot

RETRACTED: PEITC: A resounding molecule averts metastasis in breast cancer cells in vitro by regulating PKCδ/Aurora A interplay

inferred← citeshttps://doi.org/10.1016/j.isci.2024.109785openalex-snapshot

Aurora-A condensation mediated by BuGZ aids its mitotic centrosome functions

inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100676openalex-snapshot

DUSP7 regulates the activity of ERK2 to promote proper chromosome alignment during cell division

inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107761openalex-snapshot

LAT1 supports mitotic progression through Golgi unlinking in an amino acid transport activity-independent manner

inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119148openalex-snapshot

Knockdown of AURKA sensitizes the efficacy of radiation in human colorectal cancer

inferred← citeshttps://doi.org/10.1016/j.mehy.2024.111286openalex-snapshot

Hypothesis: Androgen receptor/Aurora A kinase/NF-κB signaling axis induce inflammatory response during polycystic ovarian syndrome progression

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2020.111716openalex-snapshot

Aurora kinases and DNA damage response

inferred← citeshttps://doi.org/10.1016/j.tiv.2024.105834openalex-snapshot

Triphenyltin chloride exposure inhibits meiotic maturation of mouse oocytes by disrupting cytoskeleton assembly and cell cycle progression

inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.07.008openalex-snapshot

Proteins involved in cell division have broad developmental functions

inferred← citeshttps://doi.org/10.1017/s003118202400101xopenalex-snapshot

Aurora kinase as a putative target to tick control

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01222openalex-snapshot

Identification and Characterization of Natural and Semisynthetic Quinones as Aurora Kinase Inhibitors

inferred← citeshttps://doi.org/10.1038/s41388-021-01766-wopenalex-snapshot

Nuclear localisation of Aurora-A: its regulation and significance for Aurora-A functions in cancer

inferred← citeshttps://doi.org/10.1038/s41392-023-01548-8openalex-snapshot

A new wave of innovations within the DNA damage response

inferred← citeshttps://doi.org/10.1038/s41419-026-08579-3openalex-snapshot

The ATC12 small molecule inhibits the Aurora-A/TPX2 interaction and impairs the proliferation of breast cancer cells

inferred← citeshttps://doi.org/10.1038/s41467-021-21922-wopenalex-snapshot

Bora phosphorylation substitutes in trans for T-loop phosphorylation in Aurora A to promote mitotic entry

inferred← citeshttps://doi.org/10.1038/s41598-021-91468-wopenalex-snapshot

Multiple functions of reversine on the biological characteristics of sheep fibroblasts

inferred← citeshttps://doi.org/10.1038/s42003-025-08104-wopenalex-snapshot

Cellular parameters shaping pathways of targeted protein degradation

inferred← citeshttps://doi.org/10.1038/s44318-025-00564-4openalex-snapshot

Aurora A regulates the material property of spindle poles to orchestrate nuclear organization at mitotic exit

inferred← citeshttps://doi.org/10.1038/s44318-025-00679-8openalex-snapshot

Molecular basis for the activation of Aurora A and Plk1 kinases during mitotic entry

inferred← citeshttps://doi.org/10.1038/s44319-026-00928-9openalex-snapshot

Light-induced spindle assembly through Aurora A clustering

inferred← citeshttps://doi.org/10.1039/d0sc06223eopenalex-snapshot

Total synthesis of biselide A

inferred← citeshttps://doi.org/10.1080/07357907.2025.2559403openalex-snapshot

AURKA Enhances Antitumor Immunity by Activating CD4+ T Cell Proliferation in Colorectal Cancer

inferred← citeshttps://doi.org/10.1080/10428194.2025.2612628openalex-snapshot

Targeting the FOXM1/BUB1B signaling network in multiple myeloma: mechanistic insights and therapeutic potential

inferred← citeshttps://doi.org/10.1083/jcb.202104114openalex-snapshot

Microtubule-associated proteins promote microtubule generation in the absence of γ-tubulin in human colon cancer cells

inferred← citeshttps://doi.org/10.1093/plcell/koaf065openalex-snapshot

The unconventional TPX2 family protein TPXL3 regulates α Aurora kinase function in spindle morphogenesis in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plphys/kiac409openalex-snapshot

Mutation of histone H3 serine 28 to alanine influences H3K27me3-mediated gene silencing in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1101/2021.01.04.425196openalex-snapshot

Aurora kinases promote mitotic progression and asymmetric cell division through activation of Polo kinase

inferred← citeshttps://doi.org/10.1101/2021.03.10.433854openalex-snapshot

A Focused Small-Molecule Screen Identifies PHA-680626 as an Amphosteric Inhibitor Disrupting the Interaction between Aurora-A and N-Myc

inferred← citeshttps://doi.org/10.1101/2023.03.05.531163openalex-snapshot

The Golgi checkpoint: Golgi unlinking during G2 is required for correct spindle formation and cytokinesis

inferred← citeshttps://doi.org/10.1101/2023.03.13.532472openalex-snapshot

High prevalence and dependence of centrosome clustering in mesenchymal tumors and leukemia

inferred← citeshttps://doi.org/10.1101/2024.02.10.579770openalex-snapshot

Identification of a motif in TPX2 that regulates spindle architecture in Xenopus egg extracts

inferred← citeshttps://doi.org/10.1101/2025.04.23.650020openalex-snapshot

Efficiency and localisation of AURKA degradation by PROTACs is modulated by deubiquitinases UCHL5 and target-selective OTUD6A

inferred← citeshttps://doi.org/10.1126/scisignal.abb6707openalex-snapshot

Redox priming promotes Aurora A activation during mitosis

inferred← citeshttps://doi.org/10.1134/s0026893324700304openalex-snapshot

Microtubule-Associated Protein 9 Is a Potential Tumor Suppressor That Is Inactivated by Methylation in Cervical Cancer

inferred← citeshttps://doi.org/10.1158/0008-5472.can-21-0259openalex-snapshot

Autocrine GMCSF Signaling Contributes to Growth of HER2+ Breast Leptomeningeal Carcinomatosis

inferred← citeshttps://doi.org/10.11606/t.46.2019.tde-26042022-080615openalex-snapshot

Identificação de alvos da KRAS oncogênica com potencial terapêutico para câncer de pâncreas

inferred← citeshttps://doi.org/10.1163/15685403-bja10440openalex-snapshot

Molecular identification and expression pattern of three novel Aurora kinases in Macrobrachium rosenbergii (Decapoda, Caridea)

inferred← citeshttps://doi.org/10.1186/s12943-025-02353-3openalex-snapshot

Aurora kinases signaling in cancer: from molecular perception to targeted therapies

inferred← citeshttps://doi.org/10.1186/s12958-021-00847-5openalex-snapshot

Effects of Aurora kinase A on mouse decidualization via Stat3-plk1-cdk1 pathway

inferred← citeshttps://doi.org/10.1242/dev.202479openalex-snapshot

Temporally distinct roles of Aurora A in polarization of the C. elegans zygote

inferred← citeshttps://doi.org/10.1242/jcs.256297openalex-snapshot

Loss of acentriolar MTOCs disrupts spindle pole Aurora A and assembly of the liquid-like meiotic spindle domain in oocytes

inferred← citeshttps://doi.org/10.1371/journal.pgen.1008913openalex-snapshot

Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells

inferred← citeshttps://doi.org/10.1371/journal.pgen.1010145openalex-snapshot

The spindle assembly checkpoint and the spatial activation of Polo kinase determine the duration of cell division and prevent tumor formation

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1233138/v1openalex-snapshot

Predictive Value of Serum Aurora A, Thymidine Kinase 1, and HER3/ErbB3 in Breast Cancer Patients Before Neoadjuvant Treatment

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1575751/v1openalex-snapshot

A Study on the Shh-related signal factor in mouse embryonic palatal process by dexamethasone and vitamin B12

inferred← citeshttps://doi.org/10.21203/rs.3.rs-519922/v1openalex-snapshot

Acentrosomal spindle morphogenesis is dependent on the unconventional TPX2 family protein TPXL3 and a Aurora kinase in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.21203/rs.3.rs-65694/v1openalex-snapshot

GM-CSF signaling is critical for HER2+ breast leptomeningeal carcinomatosis

inferred← citeshttps://doi.org/10.21203/rs.3.rs-7001456/v1openalex-snapshot

Aurka orchestrates colorectal cancer progression through dual regulation of tumor proliferation and immune microenvironment

inferred← citeshttps://doi.org/10.21873/cdp.10016openalex-snapshot

The Relevance of Aurora Kinase Inhibition in Hematological Malignancies

inferred← citeshttps://doi.org/10.26508/lsa.202201726openalex-snapshot

AurkA nuclear localization is promoted by TPX2 and counteracted by protein degradation

inferred← citeshttps://doi.org/10.26508/lsa.202302469openalex-snapshot

The Golgi checkpoint: Golgi unlinking during G2 is necessary for spindle formation and cytokinesis

inferred← citeshttps://doi.org/10.33590/emjoncol/20-00251openalex-snapshot

Emerging Role of Aurora A in Radioresistance: A Comprehensive Review

inferred← citeshttps://doi.org/10.3389/fcell.2024.1513472openalex-snapshot

The role of Golgi complex proteins in cell division and consequences of their dysregulation

inferred← citeshttps://doi.org/10.3389/fonc.2026.1857128openalex-snapshot

Aurora kinase B as a therapeutic target in HPV-induced cervical cancer: mechanisms and future perspectives

inferred← citeshttps://doi.org/10.3389/fphar.2025.1658493openalex-snapshot

Mechanisms and advantages of natural derived small molecule compounds in the prevention and treatment of colorectal cancer: a review

inferred← citeshttps://doi.org/10.3390/biology15141105openalex-snapshot

New Roles of Chk1 in Spindle Formation and Genome Integrity

inferred← citeshttps://doi.org/10.3390/cancers13112655openalex-snapshot

Chromosomal Instability in Acute Myeloid Leukemia

inferred← citeshttps://doi.org/10.3390/cancers14051345openalex-snapshot

CK1 Is a Druggable Regulator of Microtubule Dynamics and Microtubule-Associated Processes

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

Estrogens—Origin of Centrosome Defects in Human Cancer?

inferred← citeshttps://doi.org/10.3390/cells12202434openalex-snapshot

Aurora Kinase A Regulates Cell Transitions in Glucocorticoid-Induced Bone Loss

inferred← citeshttps://doi.org/10.3390/cells13161397openalex-snapshot

Contribution of AurkA/TPX2 Overexpression to Chromosomal Imbalances and Cancer

inferred← citeshttps://doi.org/10.3390/diagnostics16010160openalex-snapshot

The Role of Aurora Kinase A in HBV-Associated Hepatocellular Carcinomas: A Molecular and Immunohistochemical Study

inferred← citeshttps://doi.org/10.3390/ijerph17197350openalex-snapshot

Impact of Aurora Kinase A Polymorphism and Epithelial Growth Factor Receptor Mutations on the Clinicopathological Characteristics of Lung Adenocarcinoma

inferred← citeshttps://doi.org/10.3390/ijms22041906openalex-snapshot

Inflammatory Microenvironment and Specific T Cells in Myeloproliferative Neoplasms: Immunopathogenesis and Novel Immunotherapies

inferred← citeshttps://doi.org/10.3390/ijms22168818openalex-snapshot

Aurora B Tension Sensing Mechanisms in the Kinetochore Ensure Accurate Chromosome Segregation

inferred← citeshttps://doi.org/10.3390/ijms222313122openalex-snapshot

PHA-680626 Is an Effective Inhibitor of the Interaction between Aurora-A and N-Myc

inferred← citeshttps://doi.org/10.3390/molecules25204632openalex-snapshot

Mitotic Poisons in Research and Medicine

inferred← citeshttps://doi.org/10.70675/551b43b1zd937z4c11z920dzf3963c9bf07bopenalex-snapshot

Role of the protein kinase MPS1 in the regulation of chromosome segregation in budding yeast mitosis

inferred← citeshttps://doi.org/10.70675/a76902caz0ba4z4a7ez9c29zd59a2d9da247openalex-snapshot

Etude des conséquences d’une surexpression de la protéine Cycline A2 sur la croissance cellulaire et le maintien de l’intégrité du génome

inferred← citeshttps://doi.org/10.70675/c3838112z117cz48d9zbdcaz32c664616ba4openalex-snapshot

Deciphering the role of ALMS domaincontaining proteins in centrioles biogenesis

inferred← citeshttps://doi.org/10.7554/elife.107362openalex-snapshot

Efficiency and localisation of AURKA degradation by PROTACs is modulated by deubiquitinases UCHL5 and target-selective OTUD6A

inferred← citeshttps://doi.org/10.7554/elife.107362.1openalex-snapshot

Efficiency and localisation of AURKA degradation by PROTACs is modulated by deubiquitinases UCHL5 and target-selective OTUD6A

inferred← citeshttps://doi.org/10.7554/elife.107362.2openalex-snapshot

Efficiency and localisation of AURKA degradation by PROTACs is modulated by deubiquitinases UCHL5 and target-selective OTUD6A

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