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

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What this work says

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

inferredcites →https://doi.org/10.1016/0012-1606(75)90295-xopenalex-snapshot

Developmental defects of female-sterile mutants of Drosophila melanogaster

inferredcites →https://doi.org/10.1016/0092-8674(89)90130-xopenalex-snapshot

Centrosomes, and not nuclei, initiate pole cell formation in Drosophila embryos

inferredcites →https://doi.org/10.1016/0168-9525(90)90017-zopenalex-snapshot

The development of Drosophila melanogaster

inferredcites →https://doi.org/10.1016/0955-0674(95)80040-9openalex-snapshot

The cytoskeleton and morphogenesis of the early Drosophila embryo

inferredcites →https://doi.org/10.1016/j.cub.2004.03.042openalex-snapshot

Microtubule Nucleation at Non-Spindle Pole Body Microtubule-Organizing Centers Requires Fission Yeast Centrosomin-Related Protein mod20p

inferredcites →https://doi.org/10.1016/j.cub.2006.01.053openalex-snapshot

Making Microtubules and Mitotic Spindles in Cells without Functional Centrosomes

inferredcites →https://doi.org/10.1016/j.yexcr.2004.04.052openalex-snapshot

Drosophila Nek2 protein kinase knockdown leads to centrosome maturation defects while overexpression causes centrosome fragmentation and cytokinesis failure

inferredcites →https://doi.org/10.1016/s0006-3495(03)74895-4openalex-snapshot

A Force Balance Model of Early Spindle Pole Separation in Drosophila Embryos

inferredcites →https://doi.org/10.1016/s0070-2153(99)49003-9openalex-snapshot

γ-Tubulin

inferredcites →https://doi.org/10.1016/s0070-2153(99)49004-0openalex-snapshot

γ-Tubulin complexes and their role in microtubule nucleation

inferredcites →https://doi.org/10.1016/s0070-2153(99)49020-9openalex-snapshot

The centrosome in early drosophila embryogenesis

inferredcites →https://doi.org/10.1016/s0248-4900(02)01202-9openalex-snapshot

Centrosome separation: respective role of microtubules and actin filaments

inferredcites →https://doi.org/10.1016/s0960-9822(01)00017-3openalex-snapshot

Zygotic development without functional mitotic centrosomes

inferredcites →https://doi.org/10.1016/s0960-9822(01)00561-9openalex-snapshot

Organized microtubule arrays in γ-tubulin-depleted Drosophila spermatocytes

inferredcites →https://doi.org/10.1016/s0960-9822(02)01033-3openalex-snapshot

XMAP215 Is Required for the Microtubule-Nucleating Activity of Centrosomes

inferredcites →https://doi.org/10.1016/s0960-9822(03)00577-3openalex-snapshot

TAC-1, a Regulator of Microtubule Length in the C. elegans Embryo

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/s0960-9822(03)00597-9openalex-snapshot

Caenorhabditis elegans TAC-1 and ZYG-9 Form a Complex that Is Essential for Long Astral and Spindle Microtubules

inferredcites →https://doi.org/10.1016/s0960-9822(99)80393-5openalex-snapshot

Mutations in centrosomin reveal requirements for centrosomal function during early Drosophila embryogenesis

inferredcites →https://doi.org/10.1038/35050579openalex-snapshot

Centrosomes and the Scrambled protein coordinate microtubule-independent actin reorganization

inferredcites →https://doi.org/10.1038/35083025openalex-snapshot

Msps protein is localized to acentrosomal poles to ensure bipolarity of Drosophila meiotic spindles

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/10.1038/9025openalex-snapshot

Antagonistic microtubule-sliding motors position mitotic centrosomes in Drosophila early embryos

inferredcites →https://doi.org/10.1038/nature02825openalex-snapshot

Centrosomes direct cell polarity independently of microtubule assembly in C. elegans embryos

inferredcites →https://doi.org/10.1038/ng1352openalex-snapshot

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

inferredcites →https://doi.org/10.1038/ng1539openalex-snapshot

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

inferredcites →https://doi.org/10.1074/jbc.m004358200openalex-snapshot

Identification of a Common Protein Association Region in the Neuronal Cdk5 Activator

inferredcites →https://doi.org/10.1074/jbc.m006546200openalex-snapshot

Myomegalin Is a Novel Protein of the Golgi/Centrosome That Interacts with a Cyclic Nucleotide Phosphodiesterase

inferredcites →https://doi.org/10.1083/jcb.146.3.597openalex-snapshot

Cytoplasmic Dynein Is Required for the Nuclear Attachment and Migration of Centrosomes during Mitosis inDrosophila

inferredcites →https://doi.org/10.1083/jcb.146.5.1005openalex-snapshot

mini spindles

inferredcites →https://doi.org/10.1083/jcb.147.1.135openalex-snapshot

Cytoplasmic Dynein Is Required for Distinct Aspects of Mtoc Positioning, Including Centrosome Separation, in the One Cell Stage Caenorhabditis elegans Embryo

inferredcites →https://doi.org/10.1083/jcb.147.2.351openalex-snapshot

The Kinesin-Related Protein, Hset, Opposes the Activity of Eg5 and Cross-Links Microtubules in the Mammalian Mitotic Spindle

inferredcites →https://doi.org/10.1083/jcb.147.5.969openalex-snapshot

Centriolar Satellites

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.200202047openalex-snapshot

The kinetically dominant assembly pathway for centrosomal asters in Caenorhabditis elegans is γ-tubulin dependent

inferredcites →https://doi.org/10.1083/jcb.200204023openalex-snapshot

Assembly of centrosomal proteins and microtubule organization depends on PCM-1

inferredcites →https://doi.org/10.1083/jcb.200305048openalex-snapshot

Interaction of Aurora-A and centrosomin at the microtubule-nucleating site in Drosophila and mammalian cells

inferredcites →https://doi.org/10.1083/jcb.200410119openalex-snapshot

Efficient formation of bipolar microtubule bundles requires microtubule-bound γ-tubulin complexes

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.200504037openalex-snapshot

Function and regulation of Maskin, a TACC family protein, in microtubule growth during 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.200511071openalex-snapshot

Drosophila melanogaster γ-TuRC is dispensable for targeting γ-tubulin to the centrosome and microtubule nucleation

inferredcites →https://doi.org/10.1091/mbc.12.6.1751openalex-snapshot

Spindle Dynamics and the Role of γ-Tubulin in Early Caenorhabditis elegans Embryos

inferredcites →https://doi.org/10.1091/mbc.e03-10-0728openalex-snapshot

Identification and Characterization of Two Novel Proteins Affecting Fission Yeast γ-tubulin Complex Function

inferredcites →https://doi.org/10.1091/mbc.e04-08-0676openalex-snapshot

Effects of γ-Tubulin Complex Proteins on Microtubule Nucleation and Catastrophe in Fission Yeast

inferredcites →https://doi.org/10.1091/mbc.e04-08-0688openalex-snapshot

Dynamic Recruitment of Nek2 Kinase to the Centrosome Involves Microtubules, PCM-1, and Localized Proteasomal Degradation

inferredcites →https://doi.org/10.1091/mbc.e05-04-0338openalex-snapshot

Live Imaging ofDrosophilaBrain Neuroblasts Reveals a Role for Lis1/Dynactin in Spindle Assembly and Mitotic Checkpoint Control

inferredcites →https://doi.org/10.1091/mbc.e05-08-0722openalex-snapshot

TheDrosophilaγ-Tubulin Small Complex Subunit Dgrip84 Is Required for Structural and Functional Integrity of the Spindle Apparatus

inferredcites →https://doi.org/10.1093/emboj/19.2.241openalex-snapshot

D‐TACC: a novel centrosomal protein required for normal spindle function in the early Drosophila embryo

inferredcites →https://doi.org/10.1093/genetics/144.4.1623openalex-snapshot

Flanking Duplications and Deletions Associated With P-Induced Male Recombination in Drosophila

inferredcites →https://doi.org/10.1093/genetics/157.4.1623openalex-snapshot

Identification of Chromosome Inheritance Modifiers in Drosophila melanogaster

inferredcites →https://doi.org/10.1101/gad.182800openalex-snapshot

Mutation of a Drosophila gamma tubulin ring complex subunit encoded by discs degenerate-4 differentially disrupts centrosomal protein localization

inferredcites →https://doi.org/10.1242/dev.121.11.3861openalex-snapshot

The Drosophila homeotic target gene centrosomin (cnn) encodes a novel centrosomal protein with leucine zippers and maps to a genomic region required for midgut morphogenesis

inferredcites →https://doi.org/10.1242/dev.126.13.2829openalex-snapshot

The Centrosomin protein is required for centrosome assembly and function during cleavage in Drosophila

inferredcites →https://doi.org/10.1242/jcs.00134openalex-snapshot

The centrosome is a dynamic structure that ejects PCM flares

inferredcites →https://doi.org/10.1242/jcs.01344openalex-snapshot

lis-1is required for dynein-dependent cell division processes inC. elegansembryos

inferredcites →https://doi.org/10.1242/jcs.03039openalex-snapshot

α4-Tubulin is involved in rapid formation of long microtubules to push apart the daughter centrosomes during earlyxDrosophilaembryogenesis

inferredcites →https://doi.org/10.1242/jcs.03226openalex-snapshot

Microtubule nucleation: γ-tubulin and beyond

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.4520143openalex-extracted

A Distinct Gamma-Tubulin Complex Supports Mitochondrial Structural Resilience for Spermiogenesis

inferred← citeshttps://doi.org/10.1002/cm.20440openalex-snapshot

Detachment of the basal body from the sperm tail is not required to organize functional centrosomes during Drosophila embryogenesis

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/cm.70006openalex-snapshot

Noncentrosomal Microtubule Assembly and Its Regulation

inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_12openalex-snapshot

Coordination of Embryogenesis by the Centrosome in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1007/978-3-032-16833-7_12openalex-snapshot

Insights into Microtubule Nucleation at the Golgi Apparatus

inferred← citeshttps://doi.org/10.1007/s00018-011-0635-4openalex-snapshot

What’s the hype about CDK5RAP2?

inferred← citeshttps://doi.org/10.1007/s00018-021-03928-1openalex-snapshot

Centrosome instability: when good centrosomes go bad

inferred← citeshttps://doi.org/10.1007/s41745-020-00213-1openalex-snapshot

Centrosome: A Microtubule Nucleating Cellular Machinery

inferred← citeshttps://doi.org/10.1016/b978-0-12-407699-0.00002-9openalex-snapshot

A Hypothesis on the Origin and Evolution of Tubulin

inferred← citeshttps://doi.org/10.1016/j.celrep.2016.12.074openalex-snapshot

Germ Cell-less Promotes Centrosome Segregation to Induce Germ Cell Formation

inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117260openalex-snapshot

The endoplasmic reticulum protein Erg28 restrains Mto1-Mto2-γ-TuSC-mediated microtubule assembly

inferred← citeshttps://doi.org/10.1016/j.cub.2009.04.037openalex-snapshot

Centrocortin Cooperates with Centrosomin to Organize Drosophila Embryonic Cleavage Furrows

inferred← citeshttps://doi.org/10.1016/j.cub.2010.10.006openalex-snapshot

Fission Yeast Mto1 Regulates Diversity of Cytoplasmic Microtubule Organizing Centers

inferred← citeshttps://doi.org/10.1016/j.cub.2014.03.006openalex-snapshot

Activation of the γ-Tubulin Complex by the Mto1/2 Complex

inferred← citeshttps://doi.org/10.1016/j.cub.2014.08.062openalex-snapshot

Pericentrin: Critical for Spindle Orientation

inferred← citeshttps://doi.org/10.1016/j.cub.2017.05.090openalex-snapshot

A Splice Variant of Centrosomin Converts Mitochondria to Microtubule-Organizing Centers

inferred← citeshttps://doi.org/10.1016/j.cub.2018.05.044openalex-snapshot

γ-TuRC Heterogeneity Revealed by Analysis of Mozart1

inferred← citeshttps://doi.org/10.1016/j.cub.2019.05.058openalex-snapshot

Reconstitution of Microtubule Nucleation In Vitro Reveals Novel Roles for Mzt1

inferred← citeshttps://doi.org/10.1016/j.devcel.2021.05.017openalex-snapshot

Polyploid mitosis and depolyploidization promote chromosomal instability and tumor progression in a Notch-induced tumor model

inferred← citeshttps://doi.org/10.1016/j.devcel.2024.09.002openalex-snapshot

Partial closure of the γ-tubulin ring complex by CDK5RAP2 activates microtubule nucleation

inferred← citeshttps://doi.org/10.1016/j.febslet.2014.06.027openalex-snapshot

Targeting Alp7/TACC to the spindle pole body is essential for mitotic spindle assembly in fission yeast

inferred← citeshttps://doi.org/10.1016/j.isci.2019.02.002openalex-snapshot

Spatiotemporally Controlled Myosin Relocalization and Internal Pressure Generate Sibling Cell Size Asymmetry

inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.03.020openalex-snapshot

Human centrosome organization and function in interphase and mitosis

inferred← citeshttps://doi.org/10.1016/j.tcb.2008.06.005openalex-snapshot

The TACC proteins: TACC-ling microtubule dynamics and centrosome function

inferred← citeshttps://doi.org/10.1016/j.tcb.2011.04.007openalex-snapshot

Cdk5rap2 exposes the centrosomal root of microcephaly syndromes

inferred← citeshttps://doi.org/10.1016/j.tig.2009.09.011openalex-snapshot

Primary microcephaly: do all roads lead to Rome?

inferred← citeshttps://doi.org/10.1016/j.xpro.2022.101493openalex-snapshot

Live imaging of Drosophila melanogaster neural stem cells with photo-ablated centrosomes

inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60166-6openalex-snapshot

From ultrastructural flagellar sperm defects to the health of babies conceived by ICSI

inferred← citeshttps://doi.org/10.1038/emboj.2009.331openalex-snapshot

Fission yeast Pcp1 links polo kinase‐mediated mitotic entry to γ‐tubulin‐dependent spindle formation

inferred← citeshttps://doi.org/10.1038/ncb3204openalex-snapshot

PLK1-dependent activation of LRRK1 regulates spindle orientation by phosphorylating CDK5RAP2

inferred← citeshttps://doi.org/10.1038/ncomms11005openalex-snapshot

A CEP215–HSET complex links centrosomes with spindle poles and drives centrosome clustering in cancer

inferred← citeshttps://doi.org/10.1038/ncomms8929openalex-snapshot

Mto2 multisite phosphorylation inactivates non-spindle microtubule nucleation complexes during mitosis

inferred← citeshttps://doi.org/10.1038/onc.2008.254openalex-snapshot

PP2A-dependent disruption of centrosome replication and cytoskeleton organization in Drosophila by SV40 small tumor antigen

inferred← citeshttps://doi.org/10.1038/s41467-021-24332-0openalex-snapshot

A release-and-capture mechanism generates an essential non-centrosomal microtubule array during tube budding

inferred← citeshttps://doi.org/10.1038/s41467-023-35955-wopenalex-snapshot

Microtubule nucleation and γTuRC centrosome localization in interphase cells require ch-TOG

inferred← citeshttps://doi.org/10.1038/s41467-024-55778-7openalex-snapshot

Structural insights into the interplay between microtubule polymerases, γ-tubulin complexes and their receptors

inferred← citeshttps://doi.org/10.1038/s44318-026-00878-xopenalex-snapshot

Polo/PLK1 phosphorylation relieves Centrosomin/Cnn autoinhibition to promote centrosome scaffold assembly

inferred← citeshttps://doi.org/10.1042/ebc20180028openalex-snapshot

Microtubule nucleation by γ-tubulin complexes and beyond

inferred← citeshttps://doi.org/10.1042/ebc20180036openalex-snapshot

Bridging centrioles and PCM in proper space and time

inferred← citeshttps://doi.org/10.1074/jbc.m110.105965openalex-snapshot

Conserved Motif of CDK5RAP2 Mediates Its Localization to Centrosomes and the Golgi Complex

inferred← citeshttps://doi.org/10.1083/jcb.200912163openalex-snapshot

CDK5RAP2 functions in centrosome to spindle pole attachment and DNA damage response

inferred← citeshttps://doi.org/10.1083/jcb.201001144openalex-snapshot

Aurora A contributes to p150glued phosphorylation and function during mitosis

inferred← citeshttps://doi.org/10.1083/jcb.201502032openalex-snapshot

Rootletin organizes the ciliary rootlet to achieve neuron sensory function in Drosophila

inferred← citeshttps://doi.org/10.1083/jcb.201503117openalex-snapshot

Interphase centrosome organization by the PLP-Cnn scaffold is required for centrosome function

inferred← citeshttps://doi.org/10.1083/jcb.202006010openalex-snapshot

Centriole-independent mitotic spindle assembly relies on the PCNT–CDK5RAP2 pericentriolar matrix

inferred← citeshttps://doi.org/10.1083/jcb.202007101openalex-snapshot

Autoinhibitory mechanism controls binding of centrosomin motif 1 to γ-tubulin ring complex

inferred← citeshttps://doi.org/10.1083/jcb.202009083openalex-snapshot

Polo-like kinase 1 independently controls microtubule-nucleating capacity and size of the centrosome

inferred← citeshttps://doi.org/10.1083/jcb.202010020openalex-snapshot

Autoinhibition of Cnn binding to γ-TuRCs prevents ectopic microtubule nucleation and cell division defects

inferred← citeshttps://doi.org/10.1083/jcb.202212043openalex-snapshot

Multifaceted modes of γ-tubulin complex recruitment and microtubule nucleation at mitotic centrosomes

inferred← citeshttps://doi.org/10.1083/jcb.202605160openalex-snapshot

A structural model for the autoinhibition of the γ-TuRC–activating CM1 domain

inferred← citeshttps://doi.org/10.1091/mbc.e13-05-0235openalex-snapshot

Fission yeast MOZART1/Mzt1 is an essential γ-tubulin complex component required for complex recruitment to the microtubule organizing center, but not its assembly

inferred← citeshttps://doi.org/10.1091/mbc.e13-10-0617openalex-snapshot

Drosophilapericentrin requires interaction with calmodulin for its function at centrosomes and neuronal basal bodies but not at sperm basal bodies

inferred← citeshttps://doi.org/10.1091/mbc.e14-03-0786openalex-snapshot

Csi1p recruits alp7p/TACC to the spindle pole bodies for bipolar spindle formation

inferred← citeshttps://doi.org/10.1091/mbc.e15-09-0655openalex-snapshot

The Seckel syndrome and centrosomal protein Ninein localizes asymmetrically to stem cell centrosomes but is not required for normal development, behavior, or DNA damage response inDrosophila

inferred← citeshttps://doi.org/10.1091/mbc.e24-05-0220openalex-snapshot

The core spindle pole body scaffold Ppc89 links the pericentrin orthologue Pcp1 to the fission yeast spindle pole body via an evolutionarily conserved interface

inferred← citeshttps://doi.org/10.1093/genetics/iyac178openalex-snapshot

Mitotic progression and dual spindle formation caused by spindle association of de novo–formed microtubule-organizing centers in parthenogenetic embryos of Drosophila ananassae

inferred← citeshttps://doi.org/10.1096/fj.202401541ropenalex-snapshot

Roles of Cep215/Cdk5rap2 in establishing testicular architecture for mouse male germ cell development

inferred← citeshttps://doi.org/10.1098/rsob.170266openalex-snapshot

Assembly and regulation of γ-tubulin complexes

inferred← citeshttps://doi.org/10.1101/2022.09.23.509043openalex-snapshot

Multifaceted modes of γ-tubulin complex recruitment and microtubule nucleation at mitotic centrosomes

inferred← citeshttps://doi.org/10.1101/2023.12.14.571518openalex-snapshot

Closure of the γ-tubulin ring complex by CDK5RAP2 activates microtubule nucleation

inferred← citeshttps://doi.org/10.1101/2025.10.03.680336openalex-snapshot

Structural insights into mitotic-centrosome assembly

inferred← citeshttps://doi.org/10.1101/754457openalex-snapshot

Architecture of the Mto1/2 microtubule nucleation complex

inferred← citeshttps://doi.org/10.1101/cshperspect.a015800openalex-snapshot

The Centrosome and Its Duplication Cycle

inferred← citeshttps://doi.org/10.1111/j.1600-0854.2009.00880.xopenalex-snapshot

Centrosome Function: Sometimes Less Is More

inferred← citeshttps://doi.org/10.1117/12.2214275openalex-snapshot

Non-iterative adaptive optical microscopy using wavefront sensing

inferred← citeshttps://doi.org/10.1126/sciadv.adq9549openalex-snapshot

Centrioles generate two scaffolds with distinct biophysical properties to build mitotic centrosomes

inferred← citeshttps://doi.org/10.1126/sciadv.aed6539openalex-snapshot

Phosphorylation remodels the mitotic centrosome matrix to generate bipartite γ-tubulin complex docking sites

inferred← citeshttps://doi.org/10.1242/bio.20123392openalex-snapshot

Myomegalin is necessary for the formation of centrosomal and Golgi-derived microtubules

inferred← citeshttps://doi.org/10.1242/bio.2012596openalex-snapshot

Dgp71WD is required for the assembly of the acentrosomal Meiosis I spindle, and is not a general targeting factor for the γ-TuRC

inferred← citeshttps://doi.org/10.1242/dev.040410openalex-snapshot

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

inferred← citeshttps://doi.org/10.1242/dev.201917openalex-snapshot

Dysregulation of the endoplasmic reticulum blocks recruitment of centrosome-associated proteins resulting in mitotic failure

inferred← citeshttps://doi.org/10.1242/jcs.038414openalex-snapshot

Two distinct regions of Mto1 are required for normal microtubule nucleation and efficient association with the γ-tubulin complex in vivo

inferred← citeshttps://doi.org/10.1242/jcs.201350openalex-snapshot

Sequential activities of Dynein, Mud and Asp in centrosome–spindle coupling maintain centrosome number upon mitosis

inferred← citeshttps://doi.org/10.1242/jcs.240267openalex-snapshot

A novel mitosis-specific Cep215 domain interacts with Cep192 and phosphorylated Aurora A for organization of spindle poles

inferred← citeshttps://doi.org/10.1242/jcs.245464openalex-snapshot

Molecular insight into how γ-TuRC makes microtubules

inferred← citeshttps://doi.org/10.1242/jcs.259025openalex-snapshot

Centrosome maturation requires phosphorylation-mediated sequential domain interactions of SPD-5

inferred← citeshttps://doi.org/10.1364/oe.20.015969openalex-snapshot

Live imaging using adaptive optics with fluorescent protein guide-stars

inferred← citeshttps://doi.org/10.1371/journal.pone.0030045openalex-snapshot

Wolbachia-Mediated Male Killing Is Associated with Defective Chromatin Remodeling

inferred← citeshttps://doi.org/10.1371/journal.pone.0068523openalex-snapshot

Dynamic Recruitment of CDK5RAP2 to Centrosomes Requires Its Association with Dynein

inferred← citeshttps://doi.org/10.1371/journal.pone.0076613openalex-snapshot

Fodrin in Centrosomes: Implication of a Role of Fodrin in the Transport of Gamma-Tubulin Complex in Brain

inferred← citeshttps://doi.org/10.1371/journal.pone.0087016openalex-snapshot

Importance of the CEP215-Pericentrin Interaction for Centrosome Maturation during Mitosis

inferred← citeshttps://doi.org/10.1371/journal.pone.0096933openalex-snapshot

Luna, a Drosophila KLF6/KLF7, Is Maternally Required for Synchronized Nuclear and Centrosome Cycles in the Preblastoderm Embryo

inferred← citeshttps://doi.org/10.1371/journal.pone.0190530openalex-snapshot

The centrosomin CM2 domain is a multi-functional binding domain with distinct cell cycle roles

inferred← citeshttps://doi.org/10.1534/genetics.109.103887openalex-snapshot

Centrosomin: A Complex Mix of Long and Short Isoforms Is Required for Centrosome Function During Early Development in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1534/genetics.113.152546openalex-snapshot

Probing the Boundaries of Orthology: The Unanticipated Rapid Evolution ofDrosophila centrosomin

inferred← citeshttps://doi.org/10.1534/genetics.116.198168openalex-snapshot

The Centrioles,Centrosomes, Basal Bodies, and Cilia ofDrosophila melanogaster

inferred← citeshttps://doi.org/10.3389/fcell.2021.727264openalex-snapshot

Microtubule Organizing Centers Contain Testis-Specific γ-TuRC Proteins in Spermatids of Drosophila

inferred← citeshttps://doi.org/10.3390/biom9010028openalex-snapshot

Aurora A Protein Kinase: To the Centrosome and Beyond

inferred← citeshttps://doi.org/10.3390/cells10040776openalex-snapshot

γ-Tubulin Complexes and Fibrillar Arrays: Two Conserved High Molecular Forms with Many Cellular Functions

inferred← citeshttps://doi.org/10.3390/cells7090121openalex-snapshot

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

inferred← citeshttps://doi.org/10.3390/cells9102156openalex-snapshot

Principal Postulates of Centrosomal Biology. Version 2020

inferred← citeshttps://doi.org/10.3390/ijms221910387openalex-snapshot

Dynamic Changes of Brain Cilia Transcriptomes across the Human Lifespan

inferred← citeshttps://doi.org/10.4161/cc.29083openalex-snapshot

Inhibition of Polo kinase by BI2536 affects centriole separation duringDrosophilamale meiosis

inferred← citeshttps://doi.org/10.4161/cc.9.4.10667openalex-snapshot

CEP215 is involved in the dynein-dependent accumulation of pericentriolar matrix proteins for spindle pole formation

inferred← citeshttps://doi.org/10.70675/1b6f8da8za1a4z43b1z8867zc4b4762ea99copenalex-snapshot

Identification of the molecular mechanisms generating genetic instability in polyploid cells

inferred← citeshttps://doi.org/10.70675/aef9b7dfz28ebz494bzb882zeb50332186e8openalex-snapshot

Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20

inferred← citeshttps://doi.org/10.70675/b4589585zfb4bz4275zb365z57520fcda476openalex-snapshot

Mechanisms of non-centrosomal MTOC formation at the nucleus in muscle cells

inferred← citeshttps://doi.org/10.7554/elife.02208openalex-snapshot

Cell-cycle dependent phosphorylation of yeast pericentrin regulates γ-TuSC-mediated microtubule nucleation

inferred← citeshttps://doi.org/10.7554/elife.33465openalex-snapshot

Exportin Crm1 is repurposed as a docking protein to generate microtubule organizing centers at the nuclear pore

inferred← citeshttps://doi.org/10.7554/elife.65168openalex-snapshot

CM1-driven assembly and activation of yeast γ-tubulin small complex underlies microtubule nucleation

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