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Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein
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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/(sici)1097-0169(1997)36:3<276::aid-cm8>3.0.co;2-5openalex-snapshot
Centrosomal deployment of γ-tubulin and pericentrin: Evidence for a microtubule-nucleating domain and a minus-end docking domain in certain mouse epithelial cells
inferredcites →https://doi.org/10.1002/cm.970320404openalex-snapshot
Polarity and nucleation of microtubules in polarized epithelial cells
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb06972.xopenalex-snapshot
Gamma‐tubulin is required for the structure and function of the microtubule organizing centre in Drosophila neuroblasts.
inferredcites →https://doi.org/10.1006/dbio.1993.1119openalex-snapshot
Apical Orientation of the Microtubule Organizing Center and Associated γ-Tubulin during the Polarization of the Retinal Pigment Epithelium in Vivo
inferredcites →https://doi.org/10.1007/978-3-662-08650-6_2openalex-snapshot
Membrane structure and function
inferredcites →https://doi.org/10.1016/0092-8674(91)90390-kopenalex-snapshot
γ-Tubulin is a highly conserved component of the centrosome
inferredcites →https://doi.org/10.1016/0092-8674(94)90503-7openalex-snapshot
In vitro reconstitution of centrosome assembly and function: The central role of γ-tubulin
inferredcites →https://doi.org/10.1016/0092-8674(94)90504-5openalex-snapshot
Pericentrin, a highly conserved centrosome protein involved in microtubule organization
inferredcites →https://doi.org/10.1016/0309-1651(82)90001-7openalex-snapshot
A model for the microtubule organizing activity of the centrosomes and kinetochores in mammalian cells
inferredcites →https://doi.org/10.1016/1047-8477(92)90011-xopenalex-snapshot
Centrosome organization and centriole architecture: Their sensitivity to divalent cations
inferredcites →https://doi.org/10.1016/b978-0-12-394770-3.50006-1openalex-snapshot
Structure and Functions of Isolated Centrosomes
inferredcites →https://doi.org/10.1016/s0248-4900(99)80094-xopenalex-snapshot
Microtubule release and capture in epithelial cells
inferredcites →https://doi.org/10.1016/s0248-4900(99)80095-1openalex-snapshot
Centrosome structure and microbubule nucleation in animal cells
inferredcites →https://doi.org/10.1016/s0891-0618(98)00012-xopenalex-snapshot
The role of motor proteins in establishing the microtubule arrays of axons and dendrites
inferredcites →https://doi.org/10.1038/338662a0openalex-snapshot
Identification of γ-tubulin, a new member of the tubulin superfamily encoded by mipA gene of Aspergillus nidulans
inferredcites →https://doi.org/10.1038/356080a0openalex-snapshot
γ-Tubulin is a centrosomal protein required for cell cycle-dependent microtubule nucleation
inferredcites →https://doi.org/10.1038/378578a0openalex-snapshot
Nucleation of microtubule assembly by a γ-tubulin-containing ring complex
inferredcites →https://doi.org/10.1038/378638a0openalex-snapshot
Microtubule nucleation by γ-tubulin-containing rings in the centrosome
inferredcites →https://doi.org/10.1073/pnas.94.10.5078openalex-snapshot
Microtubule release from the centrosome
inferredcites →https://doi.org/10.1083/jcb.105.3.1283openalex-snapshot
Control of microtubule nucleation and stability in Madin-Darby canine kidney cells: the occurrence of noncentrosomal, stable detyrosinated microtubules.
inferredcites →https://doi.org/10.1083/jcb.107.4.1461openalex-snapshot
The unusual microtubule polarity in teleost retinal pigment epithelial cells.
inferredcites →https://doi.org/10.1083/jcb.109.1.179openalex-snapshot
Role of microtubules in polarized delivery of apical membrane proteins to the brush border of the intestinal epithelium.
inferredcites →https://doi.org/10.1083/jcb.111.6.3013openalex-snapshot
Regulation of microtubule dynamics and nucleation during polarization in MDCK II cells.
inferredcites →https://doi.org/10.1083/jcb.113.2.275openalex-snapshot
Microtubular organization and its involvement in the biogenetic pathways of plasma membrane proteins in Caco-2 intestinal epithelial cells.
inferredcites →https://doi.org/10.1083/jcb.119.1.171openalex-snapshot
Gamma-tubulin distribution in the neuron: implications for the origins of neuritic microtubules.
inferredcites →https://doi.org/10.1083/jcb.123.6.1761openalex-snapshot
WIF-B cells: an in vitro model for studies of hepatocyte polarity.
inferredcites →https://doi.org/10.1083/jcb.130.5.1137openalex-snapshot
Gamma-tubulin can both nucleate microtubule assembly and self-assemble into novel tubular structures in mammalian cells.
inferredcites →https://doi.org/10.1083/jcb.134.1.165openalex-snapshot
The adenomatous polyposis coli tumor suppressor protein localizes to plasma membrane sites involved in active cell migration.
inferredcites →https://doi.org/10.1083/jcb.137.1.193openalex-snapshot
Centrosomes Isolated from Spisula solidissima Oocytes Contain Rings and an Unusual Stoichiometric Ratio of α/β Tubulin
inferredcites →https://doi.org/10.1083/jcb.141.1.163openalex-snapshot
Pericentrin and γ-Tubulin Form a Protein Complex and Are Organized into a Novel Lattice at the Centrosome
inferredcites →https://doi.org/10.1083/jcb.142.3.775openalex-snapshot
Recruitment of the γ-Tubulin Ring Complex to Drosophila Salt-stripped Centrosome Scaffolds
inferredcites →https://doi.org/10.1083/jcb.147.3.481openalex-snapshot
Direct Interaction of Pericentrin with Cytoplasmic Dynein Light Intermediate Chain Contributes to Mitotic Spindle Organization
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.73.3.601openalex-snapshot
The pericentriolar material in Chinese hamster ovary cells nucleates microtubule formation
inferredcites →https://doi.org/10.1083/jcb.75.3.977openalex-snapshot
Continuation of mitosis after selective laser microbeam destruction of the centriolar region.
inferredcites →https://doi.org/10.1083/jcb.98.2.525openalex-snapshot
Tubulin hooks as probes for microtubule polarity: an analysis of the method and an evaluation of data on microtubule polarity in the mitotic spindle.
inferredcites →https://doi.org/10.1146/annurev.bi.63.070194.003231openalex-snapshot
THE CENTROSOME AND CELLULAR ORGANIZATION
inferredcites →https://doi.org/10.1146/annurev.cb.01.110185.001045openalex-snapshot
Microtubule Organizing Centers
inferredcites →https://doi.org/10.1242/jcs.102.2.215openalex-snapshot
A cell surface-associated centrosomal layer of microtubule-organizing material in the inner pillar cell of the mouse cochlea
inferredcites →https://doi.org/10.1242/jcs.107.2.589openalex-snapshot
Reorganization of the centrosome and associated microtubules during the morphogenesis of a mouse cochlear epithelial cell
inferredcites →https://doi.org/10.1242/jcs.108.4.1333openalex-snapshot
Formation of two microtubule-nucleating sites which perform differently during centrosomal reorganization in a mouse cochlear epithelial cell
inferredcites →https://doi.org/10.1242/jcs.109.1.179openalex-snapshot
Molecular characterisation of ninein, a new coiled-coil protein of the centrosome
inferredcites →https://doi.org/10.1242/jcs.109.4.875openalex-snapshot
γ-Tubulin in mammalian cells: the centrosomal and the cytosolic forms
inferredcites →https://doi.org/10.1242/jcs.99.4.693openalex-snapshot
The fission yeast γ-tubulin is essential for mitosis and is localized at microtubule organizing centers
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Targeted Localization of the Mother Centrosome in CD8 T Cells Undergoing Asymmetric Cell Division Promotes Memory Formation
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Differential expression of centrosome‐associated proteins in human brain tumors: A possible role of hNinein isoform 6 in cell differentiation
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Higher order structure of the PCM adjacent to the centriole
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Structural and functional effects of hydrostatic pressure on centrosomes from vertebrate cells
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The centrosome: The centriole‐PCM coalition
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Positioning and capture of cell surface‐associated microtubules in epithelial tendon cells that differentiate in primary embryonic Drosophila cell cultures
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Glutamylated and glycylated tubulin isoforms in the aberrant sperm axoneme of the gall‐midge fly, Asphondylia ruebsaameni
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Reorganization of microtubule nucleation during muscle differentiation
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Detection of the centriole tyr- or acet-tubulin changes in endothelial cells treated with thrombin using microscopic immunocytochemistry
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Microtubule plus‐end and minus‐end capture at adherens junctions is involved in the assembly of apico‐basal arrays in polarised epithelial cells
inferred← citeshttps://doi.org/10.1002/cm.20540openalex-snapshot
Shaping microtubules into diverse patterns: Molecular connections for setting up both ends
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Emerging roles of the centrosome in neuronal development
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CEP72 Emerges as a Key Centriolar Satellite Protein in Health and Disease
inferred← citeshttps://doi.org/10.1002/cne.22001openalex-snapshot
Patterns of expression of Bardet‐Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions
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Molecular Regulation of Sprouting Angiogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.20770openalex-snapshot
Microtubule polarity and axis formation in the Drosophila oocyte
inferred← citeshttps://doi.org/10.1002/dvdy.21390openalex-snapshot
Multicellular rosette formation during cell ingression in the avian primitive streak
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Noncentrosomal microtubules in C. elegans epithelia
inferred← citeshttps://doi.org/10.1002/em.20493openalex-snapshot
The functional significance of centrosomes in mammalian meiosis, fertilization, development, nuclear transfer, and stem cell differentiation
inferred← citeshttps://doi.org/10.1002/embr.201337929openalex-snapshot
Msd1/SSX2IP‐dependent microtubule anchorage ensures spindle orientation and primary cilia formation
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2012.tb00413.xopenalex-snapshot
The Ciliary Cytoskeleton
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2018.tb00003.xopenalex-snapshot
Molecular Regulation of Sprouting Angiogenesis
inferred← citeshttps://doi.org/10.1002/jcb.21117openalex-snapshot
What is the function of centrioles?
inferred← citeshttps://doi.org/10.1002/jcb.25160openalex-snapshot
Cell Cycle‐Dependent Localization of Dynactin Subunit p150glued at Centrosome
inferred← citeshttps://doi.org/10.1006/bbrc.2000.4050openalex-snapshot
Genomic Organization and Molecular Characterization of the Human Ninein Gene
inferred← citeshttps://doi.org/10.1007/978-1-4020-8843-8_2openalex-snapshot
Gamma-Tubulins And Their Functions In Plant Cells
inferred← citeshttps://doi.org/10.1007/978-1-4419-6199-0_6openalex-snapshot
Centrosomes, Polyploidy and Cancer
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The Impact of Centrosome Abnormalities on Breast Cancer Development and Progression with a Focus on Targeting Centrosomes for Breast Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_18openalex-snapshot
Centrosome Amplification and Tumorigenesis: Cause or Effect?
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_5openalex-snapshot
Virus Exploitation (Hijacking) of Centrosomes
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The Impact of Centrosome Pathologies on Ovarian Cancer Development and Progression with a Focus on Centrosomes as Therapeutic Target
inferred← citeshttps://doi.org/10.1007/978-3-211-76310-0_17openalex-snapshot
The role of the cytoskeleton in the structure and function of the Golgi apparatus
inferred← citeshttps://doi.org/10.1007/978-3-319-95693-0_4openalex-snapshot
The Impact of Centrosome Pathologies on Prostate Cancer Development and Progression
inferred← citeshttps://doi.org/10.1007/978-3-7091-1903-7_2openalex-snapshot
Non-centrosomal Microtubule Organization in Differentiated Cells
inferred← citeshttps://doi.org/10.1007/978-3-7091-1903-7_3openalex-snapshot
Organizational Properties of the Pericentriolar Material
inferred← citeshttps://doi.org/10.1007/978-94-007-2004-6openalex-snapshot
Mechanical Stretch and Cytokines
inferred← citeshttps://doi.org/10.1007/978-94-007-2004-6_9openalex-snapshot
Primary Cilia are Mechanosensory Organelles with Chemosensory Roles
inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_1openalex-snapshot
Primary and Motile Cilia: Their Ultrastructure and Ciliogenesis
inferred← citeshttps://doi.org/10.1007/s00018-004-4039-6openalex-snapshot
Scaffolds, levers, rods and springs: diverse cellular functions of long coiled-coil proteins
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/s00018-019-03181-7openalex-snapshot
Requirement of NPHP5 in the hierarchical assembly of basal feet associated with basal bodies of primary cilia
inferred← citeshttps://doi.org/10.1007/s00018-025-05714-9openalex-snapshot
Mechanisms of cortical microtubule organization in epidermal keratinocytes
inferred← citeshttps://doi.org/10.1007/s00418-008-0427-6openalex-snapshot
The mammalian centrosome and its functional significance
inferred← citeshttps://doi.org/10.1007/s00418-009-0631-zopenalex-snapshot
Relocalization of a microtubule-anchoring protein, ninein, from the centrosome to dendrites during differentiation of mouse neurons
inferred← citeshttps://doi.org/10.1007/s00418-013-1119-4openalex-snapshot
Golgi as an MTOC: making microtubules for its own good
inferred← citeshttps://doi.org/10.1007/s00418-018-1698-1openalex-snapshot
Functions and dysfunctions of the mammalian centrosome in health, disorders, disease, and aging
inferred← citeshttps://doi.org/10.1007/s00441-016-2508-5openalex-snapshot
Orchestrating cellular signaling pathways—the cellular “conductor” protein tyrosine phosphatase interacting protein 51 (PTPIP51)
inferred← citeshttps://doi.org/10.1007/s00709-016-1070-zopenalex-snapshot
Regulation of microtubule nucleation mediated by γ-tubulin complexes
inferred← citeshttps://doi.org/10.1007/s10495-008-0200-2openalex-snapshot
The tubulin-depolymerising agent combretastatin-4 induces ectopic aster assembly and mitotic catastrophe in lung cancer cells H460
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/s41745-020-00213-1openalex-snapshot
Centrosome: A Microtubule Nucleating Cellular Machinery
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.20054-0openalex-snapshot
Microtubules and Microtubule-Associated Proteins (MAPs)
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/b978-0-12-815389-5.00021-6openalex-snapshot
Renal cilia structure, function, and physiology
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00173-5openalex-snapshot
Microtubules and Microtubule Associated Proteins (MAPs)
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00240-6openalex-snapshot
Microtubules in Differentiated Cells
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.03.002openalex-snapshot
Analysis of centrosomes in human cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.01.129openalex-snapshot
Asymmetric spindle pole formation in CPAP-depleted mitotic cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.05.030openalex-snapshot
Modeling reveals cortical dynein-dependent fluctuations in bipolar spindle length
inferred← citeshttps://doi.org/10.1016/j.ceb.2006.12.008openalex-snapshot
γ-tubulin complexes and microtubule organization
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.05.007openalex-snapshot
Formation and functions of asymmetric microtubule organization in polarized cells
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.09.003openalex-snapshot
Microtubule-organizing centers: from the centrosome to non-centrosomal sites
inferred← citeshttps://doi.org/10.1016/j.cell.2008.09.040openalex-snapshot
Anchorage of Microtubule Minus Ends to Adherens Junctions Regulates Epithelial Cell-Cell Contacts
inferred← citeshttps://doi.org/10.1016/j.cell.2013.08.060openalex-snapshot
Asymmetric Inheritance of Centrosome-Associated Primary Cilium Membrane Directs Ciliogenesis after Cell Division
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.02.043openalex-snapshot
CEP128 Localizes to the Subdistal Appendages of the Mother Centriole and Regulates TGF-β/BMP Signaling at the Primary Cilium
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108495openalex-snapshot
Talpid3-Mediated Centrosome Integrity Restrains Neural Progenitor Delamination to Sustain Neurogenesis by Stabilizing Adherens Junctions
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115127openalex-snapshot
Targeted localization of the mother centrosome in CD8+ T cells undergoing asymmetric cell division promotes memory formation
inferred← citeshttps://doi.org/10.1016/j.cub.2007.05.055openalex-snapshot
EB1 Is Required for Primary Cilia Assembly in Fibroblasts
inferred← citeshttps://doi.org/10.1016/j.cub.2009.05.016openalex-snapshot
Control of Centriole Length by CPAP and CP110
inferred← citeshttps://doi.org/10.1016/j.cub.2009.05.018openalex-snapshot
Overly Long Centrioles and Defective Cell Division upon Excess of the SAS-4-Related Protein CPAP
inferred← citeshttps://doi.org/10.1016/j.cub.2014.12.027openalex-snapshot
Microtubule Minus-End-Targeting Proteins
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.021openalex-snapshot
Proximity labeling reveals non-centrosomal microtubule-organizing center components required for microtubule growth and localization
inferred← citeshttps://doi.org/10.1016/j.cub.2026.03.064openalex-snapshot
Microtubule organization and molecular architecture of ciliary basal bodies in multiciliated airway cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.08.004openalex-snapshot
Centrosome Duplication and Nematodes: Recent Insights from an Old Relationship
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.09.003openalex-snapshot
Cdk1/Erk2- and Plk1-Dependent Phosphorylation of a Centrosome Protein, Cep55, Is Required for Its Recruitment to Midbody and Cytokinesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.02.004openalex-snapshot
Plk1-Dependent and -Independent Roles of an ODF2 Splice Variant, hCenexin1, at the Centrosome of Somatic Cells
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.2010.07.009openalex-snapshot
MIM and Cortactin Antagonism Regulates Ciliogenesis and Hedgehog Signaling
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.06.010openalex-snapshot
Patronin/Shot Cortical Foci Assemble the Noncentrosomal Microtubule Array that Specifies the Drosophila Anterior-Posterior Axis
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.10.006openalex-snapshot
Spatial Control of Primary Ciliogenesis by Subdistal Appendages Alters Sensation-Associated Properties of Cilia
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.09.015openalex-snapshot
Comparative Super-Resolution Mapping of Basal Feet Reveals a Modular but Distinct Architecture in Primary and Motile Cilia
inferred← citeshttps://doi.org/10.1016/j.ejcb.2011.07.007openalex-snapshot
Centriolar satellites: Busy orbits around the centrosome
inferred← citeshttps://doi.org/10.1016/j.ejcb.2012.03.009openalex-snapshot
Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition
inferred← citeshttps://doi.org/10.1016/j.exer.2007.07.022openalex-snapshot
Reorganization of centrosomal marker proteins coincides with epithelial cell differentiation in the vertebrate lens
inferred← citeshttps://doi.org/10.1016/j.isci.2026.117062openalex-snapshot
The Odf2 status contributes to asymmetric inheritance of CD133-positive recycling endosomes during cytokinesis in SK-N-DZ human neuroblastoma cells
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.108419openalex-snapshot
Ninein isoform contributions to intracellular processes and macrophage immune function
inferred← citeshttps://doi.org/10.1016/j.jgg.2018.08.001openalex-snapshot
Mid1ip1b modulates apical reorientation of non-centrosomal microtubule organizing center in epithelial cells
inferred← citeshttps://doi.org/10.1016/j.mcn.2006.03.003openalex-snapshot
GSK3β and PKCζ function in centrosome localization and process stabilization during Slit-mediated neuronal repolarization
inferred← citeshttps://doi.org/10.1016/j.mib.2003.10.016openalex-snapshot
Long-lost relatives reappear: identification of new members of the tubulin superfamily
inferred← citeshttps://doi.org/10.1016/j.neuron.2015.01.018openalex-snapshot
Sip1 Downstream Effector ninein Controls Neocortical Axonal Growth, Ipsilateral Branching, and Microtubule Growth and Stability
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2004.07.016openalex-snapshot
Distribution of the microtubule-related protein ninein in developing neurons
inferred← citeshttps://doi.org/10.1016/j.sbi.2020.08.008openalex-snapshot
The structure of the γ-TuRC: a 25-years-old molecular puzzle
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.06.006openalex-snapshot
The PCM–basal body/primary cilium coalition
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.07.002openalex-snapshot
Centriole maturation and transformation to basal body
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.04.019openalex-snapshot
Centrosome dysfunction in human diseases
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.2017.10.005openalex-snapshot
Microtubule-Organizing Centers: Towards a Minimal Parts List
inferred← citeshttps://doi.org/10.1016/j.virol.2019.11.018openalex-snapshot
Zika virus NS5 localizes at centrosomes during cell division
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.03.031openalex-snapshot
Gene knockout analysis of two γ-tubulin isoforms in mice
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.08.003openalex-snapshot
Three Tctn proteins are functionally conserved in the regulation of neural tube patterning and Gli3 processing but not ciliogenesis and Hedgehog signaling 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.yexcr.2006.09.023openalex-snapshot
Cyclin G2 is a centrosome-associated nucleocytoplasmic shuttling protein that influences microtubule stability and induces a p53-dependent cell cycle arrest
inferred← citeshttps://doi.org/10.1016/j.yexcr.2006.12.022openalex-snapshot
Regulation of multiple cell cycle events by Cdc14 homologues in vertebrates
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.02.023openalex-snapshot
hNinein is required for targeting spindle-associated protein Astrin to the centrosome during the S and G2 phases
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.02.030openalex-snapshot
Intermediate filaments: A role in epithelial polarity
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.09.022openalex-snapshot
The microtubule plus end-binding protein EB1 is involved in Sertoli cell plasticity in testicular seminiferous tubules
inferred← citeshttps://doi.org/10.1016/j.ymeth.2017.05.017openalex-snapshot
CeFra-seq: Systematic mapping of RNA subcellular distribution properties through cell fractionation coupled to deep-sequencing
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)01510-9openalex-snapshot
Molecular characterization of human ninein protein: two distinct subdomains required for centrosomal targeting and regulating signals in cell cycle
inferred← citeshttps://doi.org/10.1016/s0014-4827(03)00033-8openalex-snapshot
The architecture of microtubular network and Golgi orientation in osteoclasts—major differences between avian and mammalian species
inferred← citeshttps://doi.org/10.1016/s0074-7696(04)38003-4openalex-snapshot
The Centrosome in Higher Organisms: Structure, Composition, and Duplication
inferred← citeshttps://doi.org/10.1016/s0955-0674(00)00179-4openalex-snapshot
Microtubules don and doff their caps: dynamic attachments at plus and minus ends
inferred← citeshttps://doi.org/10.1016/s0955-0674(01)00290-3openalex-snapshot
Centrosome composition and microtubule anchoring mechanisms
inferred← citeshttps://doi.org/10.1016/s0955-0674(01)00291-5openalex-snapshot
Integration of the centrosome in cell cycle control, stress response and signal transduction pathways
inferred← citeshttps://doi.org/10.1016/s1534-5807(03)00193-xopenalex-snapshot
Polo-like Kinase 1 Regulates Nlp, a Centrosome Protein Involved in Microtubule Nucleation
inferred← citeshttps://doi.org/10.1017/cbo9780511529825openalex-snapshot
Development of the Ocular Lens
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.002openalex-snapshot
The Lens: Historical and Comparative Perspectives
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.003openalex-snapshot
Lens Induction and Determination
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.004openalex-snapshot
Transcription Factors in Early Lens Development
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.005openalex-snapshot
The Structure of the Vertebrate Lens
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.009openalex-snapshot
Lens Cell Proliferation: The Cell Cycle
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.010openalex-snapshot
Lens Fiber Differentiation
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.011openalex-snapshot
Role of Matrix and Cell Adhesion Molecules in Lens Differentiation
inferred← citeshttps://doi.org/10.1017/cbo9780511529825.012openalex-snapshot
Growth Factors in Lens Development
inferred← citeshttps://doi.org/10.1021/pr200338dopenalex-snapshot
Identification of hnRNPH1, NF45, and C14orf166 as Novel Host Interacting Partners of the Mature Hepatitis C Virus Core Protein
inferred← citeshttps://doi.org/10.1023/a:1011312808421openalex-snapshot
The Contribution of Epigenetic Changes to Abnormal Centrosomes and Genomic Instability in Breast Cancer
inferred← citeshttps://doi.org/10.1023/a:1025477807393openalex-snapshot
Microtubule assembly in cultured myoblasts and myotubes following nocodazole induced microtubule depolymerisation
inferred← citeshttps://doi.org/10.1034/j.1600-0854.2003.00104.xopenalex-snapshot
Elucidation of Basal Body and Centriole Functions in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1038/emboj.2009.161openalex-snapshot
Cep72 regulates the localization of key centrosomal proteins and proper bipolar spindle formation
inferred← citeshttps://doi.org/10.1038/emboj.2013.3openalex-snapshot
Kif3a interacts with Dynactin subunit p150Glued to organize centriole subdistal appendages
inferred← citeshttps://doi.org/10.1038/jid.2014.79openalex-snapshot
TIG3: An Important Regulator of Keratinocyte Proliferation and Survival
inferred← citeshttps://doi.org/10.1038/nature08435openalex-snapshot
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
inferred← citeshttps://doi.org/10.1038/ncb1251openalex-snapshot
Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia
inferred← citeshttps://doi.org/10.1038/ncb1474openalex-snapshot
The Plk1 target Kizuna stabilizes mitotic centrosomes to ensure spindle bipolarity
inferred← citeshttps://doi.org/10.1038/ncb2597openalex-snapshot
Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization
inferred← citeshttps://doi.org/10.1038/ncb2958openalex-snapshot
Mitotic spindle multipolarity without centrosome amplification
inferred← citeshttps://doi.org/10.1038/ncb900openalex-snapshot
ɛ-Tubulin is required for centriole duplication and microtubule organization
inferred← citeshttps://doi.org/10.1038/ncomms15057openalex-snapshot
Hierarchical assembly of centriole subdistal appendages via centrosome binding proteins CCDC120 and CCDC68
inferred← citeshttps://doi.org/10.1038/ncomms5207openalex-snapshot
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis
inferred← citeshttps://doi.org/10.1038/ng.3031openalex-snapshot
The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation
inferred← citeshttps://doi.org/10.1038/ng2069openalex-snapshot
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
inferred← citeshttps://doi.org/10.1038/nrg1557openalex-snapshot
The centrosome in human genetic disease
inferred← citeshttps://doi.org/10.1038/nrm2100openalex-snapshot
Microtubule-organizing centres: a re-evaluation
inferred← citeshttps://doi.org/10.1038/nrm2524openalex-snapshot
Organelle positioning and cell polarity
inferred← citeshttps://doi.org/10.1038/nrm3175openalex-snapshot
Deconstructing the skin: cytoarchitectural determinants of epidermal morphogenesis
inferred← citeshttps://doi.org/10.1038/nrm4084openalex-snapshot
Control of microtubule organization and dynamics: two ends in the limelight
inferred← citeshttps://doi.org/10.1038/onc.2015.332openalex-snapshot
Structural centrosome aberrations favor proliferation by abrogating microtubule-dependent tissue integrity of breast epithelial mammospheres
inferred← citeshttps://doi.org/10.1038/onc.2017.92openalex-snapshot
Regulation of spindle integrity and mitotic fidelity by BCCIP
inferred← citeshttps://doi.org/10.1038/s41419-019-1778-8openalex-snapshot
Cep131 overexpression promotes centrosome amplification and colon cancer progression by regulating Plk4 stability
inferred← citeshttps://doi.org/10.1038/s41420-024-02093-1openalex-snapshot
Pyroptosis leads to loss of centrosomal integrity in macrophages
inferred← citeshttps://doi.org/10.1038/s41467-018-07664-2openalex-snapshot
Microtubule asters anchored by FSD1 control axoneme assembly and ciliogenesis
inferred← citeshttps://doi.org/10.1038/s41467-019-09413-5openalex-snapshot
Asymmetric division events promote variability in cell cycle duration in animal cells and Escherichia coli
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/s41556-020-0470-7openalex-snapshot
A perinuclear microtubule-organizing centre controls nuclear positioning and basement membrane secretion
inferred← citeshttps://doi.org/10.1038/s41580-018-0004-3openalex-snapshot
The cytoplasmic dynein transport machinery and its many cargoes
inferred← citeshttps://doi.org/10.1038/s41598-022-22871-0openalex-snapshot
The apical ciliary adhesion complex is established at the basal foot of motile cilia and depends on the microtubule network
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601459openalex-snapshot
GSK‐3β‐regulated interaction of BICD with dynein is involved in microtubule anchorage at centrosome
inferred← citeshttps://doi.org/10.1038/sj.leu.2402454openalex-snapshot
Centrosome replication, genomic instability and cancer
inferred← citeshttps://doi.org/10.1038/srep26580openalex-snapshot
14-3-3γ Prevents Centrosome Amplification and Neoplastic Progression
inferred← citeshttps://doi.org/10.1042/bst0371007openalex-snapshot
Regulation of microtubule dynamic instability
inferred← citeshttps://doi.org/10.1074/jbc.m113.492066openalex-snapshot
Centrosomal Protein DZIP1 Regulates Hedgehog Signaling by Promoting Cytoplasmic Retention of Transcription Factor GLI3 and Affecting Ciliogenesis
inferred← citeshttps://doi.org/10.1074/jbc.m114.575100openalex-snapshot
TACC3 Protein Regulates Microtubule Nucleation by Affecting γ-Tubulin Ring Complexes
inferred← citeshttps://doi.org/10.1080/15384101.2014.1000197openalex-snapshot
Centrosomal nucleolin is required for microtubule network organization
inferred← citeshttps://doi.org/10.1083/jcb.200108088openalex-snapshot
Characterization of Cep135, a novel coiled-coil centrosomal protein involved in microtubule organization in mammalian cells
inferred← citeshttps://doi.org/10.1083/jcb.200203001openalex-snapshot
The adenomatous polyposis coli protein unambiguously localizes to microtubule plus ends and is involved in establishing parallel arrays of microtubule bundles in highly polarized epithelial cells
inferred← citeshttps://doi.org/10.1083/jcb.200203034openalex-snapshot
The Rho-associated protein kinase p160ROCK is required for centrosome positioning
inferred← citeshttps://doi.org/10.1083/jcb.200203089openalex-snapshot
Distinct cell cycle–dependent roles for dynactin and dynein at centrosomes
inferred← citeshttps://doi.org/10.1083/jcb.200204023openalex-snapshot
Assembly of centrosomal proteins and microtubule organization depends on PCM-1
inferred← citeshttps://doi.org/10.1083/jcb.200207076openalex-snapshot
Microtubule release from the centrosome in migrating cells
inferred← citeshttps://doi.org/10.1083/jcb.200301105openalex-snapshot
A novel human protein of the maternal centriole is required for the final stages of cytokinesis and entry into S phase
inferred← citeshttps://doi.org/10.1083/jcb.200308104openalex-snapshot
Mammalian PAR-1 determines epithelial lumen polarity by organizing the microtubule cytoskeleton
inferred← citeshttps://doi.org/10.1083/jcb.200409153openalex-snapshot
Centrosome fragments and microtubules are transported asymmetrically away from division plane in anaphase
inferred← citeshttps://doi.org/10.1083/jcb.200510028openalex-snapshot
NEDD1-dependent recruitment of the γ-tubulin ring complex to the centrosome is necessary for centriole duplication and spindle assembly
inferred← citeshttps://doi.org/10.1083/jcb.200609109openalex-snapshot
Desmoplakin: an unexpected regulator of microtubule organization in the epidermis
inferred← citeshttps://doi.org/10.1083/jcb.200707181openalex-snapshot
Cep164, a novel centriole appendage protein required for primary cilium formation
inferred← citeshttps://doi.org/10.1083/jcb.201103160openalex-snapshot
A PAR-1–dependent orientation gradient of dynamic microtubules directs posterior cargo transport in the Drosophila oocyte
inferred← citeshttps://doi.org/10.1083/jcb.201104009openalex-snapshot
Lis1 is essential for cortical microtubule organization and desmosome stability in the epidermis
inferred← citeshttps://doi.org/10.1083/jcb.201111146openalex-snapshot
Scoring a backstage pass: Mechanisms of ciliogenesis and ciliary access
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.201303071openalex-snapshot
Two appendages homologous between basal bodies and centrioles are formed using distinct Odf2 domains
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.201506140openalex-snapshot
Sliding of centrosome-unattached microtubules defines key features of neuronal phenotype
inferred← citeshttps://doi.org/10.1083/jcb.201507046openalex-snapshot
Ndel1 suppresses ciliogenesis in proliferating cells by regulating the trichoplein–Aurora A pathway
inferred← citeshttps://doi.org/10.1083/jcb.201601099openalex-snapshot
Divergent regulation of functionally distinct γ-tubulin complexes during differentiation
inferred← citeshttps://doi.org/10.1083/jcb.201709041openalex-snapshot
BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone
inferred← citeshttps://doi.org/10.1083/jcb.201808176openalex-snapshot
The Drosophila Ninein homologue Bsg25D cooperates with Ensconsin in myonuclear positioning
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