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Ninein is essential for the maintenance of the cortical progenitor character by anchoring the centrosome to microtubules
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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/dvdy.21351openalex-snapshot
Survey of the morphogenetic dynamics of the ventricular surface of the developing mouse neocortex
inferredcites →https://doi.org/10.1002/stem.1124openalex-snapshot
The Effects of Fabp7 and Fabp5 on Postnatal Hippocampal Neurogenesis in the Mouse
inferredcites →https://doi.org/10.1006/dbio.2000.9616openalex-snapshot
Fate Mapping of the Mouse Prosencephalic Neural Plate
inferredcites →https://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
inferredcites →https://doi.org/10.1016/0092-8674(95)90035-7openalex-snapshot
Cleavage orientation and the asymmetric inheritance of notchl immunoreactivity in mammalian neurogenesis
inferredcites →https://doi.org/10.1016/j.brainresbull.2005.02.006openalex-snapshot
Role of Pax6 in forebrain regionalization
inferredcites →https://doi.org/10.1016/j.cell.2008.07.017openalex-snapshot
Regulation of Neurogenesis by Interkinetic Nuclear Migration through an Apical-Basal Notch Gradient
inferredcites →https://doi.org/10.1016/j.cell.2009.06.032openalex-snapshot
Actomyosin Is the Main Driver of Interkinetic Nuclear Migration in the Retina
inferredcites →https://doi.org/10.1016/j.mcn.2006.10.008openalex-snapshot
Loss- and gain-of-function analyses reveal targets of Pax6 in the developing mouse telencephalon
inferredcites →https://doi.org/10.1016/j.mod.2011.04.001openalex-snapshot
Pax6 regulates boundary-cell specification in the rat hindbrain
inferredcites →https://doi.org/10.1016/j.neures.2006.03.004openalex-snapshot
Transcription factors in glutamatergic neurogenesis: Conserved programs in neocortex, cerebellum, and adult hippocampus
inferredcites →https://doi.org/10.1016/j.neures.2009.01.006openalex-snapshot
Rac is involved in the interkinetic nuclear migration of cortical progenitor cells
inferredcites →https://doi.org/10.1016/j.neuron.2007.08.026openalex-snapshot
Cep120 and TACCs Control Interkinetic Nuclear Migration and the Neural Progenitor Pool
inferredcites →https://doi.org/10.1016/j.neuron.2009.08.018openalex-snapshot
SUN1/2 and Syne/Nesprin-1/2 Complexes Connect Centrosome to the Nucleus during Neurogenesis and Neuronal Migration in Mice
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.011openalex-snapshot
Hook3 Interacts with PCM1 to Regulate Pericentriolar Material Assembly and the Timing of Neurogenesis
inferredcites →https://doi.org/10.1016/j.ydbio.2006.07.045openalex-snapshot
Pax6 is required for delta-catenin/neurojugin expression during retinal, cerebellar and cortical development in mice
inferredcites →https://doi.org/10.1016/j.ydbio.2012.06.031openalex-snapshot
Apical movement during interkinetic nuclear migration is a two-step process
inferredcites →https://doi.org/10.1038/emboj.2011.81openalex-snapshot
Regulation of interkinetic nuclear migration by cell cycle‐coupled active and passive mechanisms in the developing brain
inferredcites →https://doi.org/10.1038/emboj.2012.43openalex-snapshot
Cyclin D2 in the basal process of neural progenitors is linked to non‐equivalent cell fates
inferredcites →https://doi.org/10.1038/nature08435openalex-snapshot
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
inferredcites →https://doi.org/10.1038/nature08845openalex-snapshot
Neurogenic radial glia in the outer subventricular zone of human neocortex
inferredcites →https://doi.org/10.1038/ncb1673openalex-snapshot
Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis
inferredcites →https://doi.org/10.1038/nn.2665openalex-snapshot
Kinesin 3 and cytoplasmic dynein mediate interkinetic nuclear migration in neural stem cells
inferredcites →https://doi.org/10.1038/nn1172openalex-snapshot
Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases
inferredcites →https://doi.org/10.1038/sj.emboj.7600223openalex-snapshot
Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells
inferredcites →https://doi.org/10.1046/j.1432-0436.2002.700405.xopenalex-snapshot
Manipulating gene expressions by electroporation in the developing brain of mammalian embryos
inferredcites →https://doi.org/10.1073/pnas.0308600100openalex-snapshot
Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: A major site of neurogenesis
inferredcites →https://doi.org/10.1073/pnas.0437969100openalex-snapshot
Mitotic spindle rotation and mode of cell division in the developing telencephalon
inferredcites →https://doi.org/10.1073/pnas.082243699openalex-snapshot
A monomeric red fluorescent protein
inferredcites →https://doi.org/10.1073/pnas.0908928106openalex-snapshot
Myosin II is required for interkinetic nuclear migration of neural progenitors
inferredcites →https://doi.org/10.1074/jbc.m108495200openalex-snapshot
Pax6 Controls the Expression of Lewis x Epitope in the Embryonic Forebrain by Regulating α1,3-Fucosyltransferase IX Expression
inferredcites →https://doi.org/10.1083/jcb.121.3.491openalex-snapshot
The 220-kD protein colocalizing with cadherins in non-epithelial cells is identical to ZO-1, a tight junction-associated protein in epithelial cells: cDNA cloning and immunoelectron microscopy.
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.200505166openalex-snapshot
LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages
inferredcites →https://doi.org/10.1111/j.1365-2443.2007.01113.xopenalex-snapshot
Pax6 transcription factor is required for the interkinetic nuclear movement of neuroepithelial cells
inferredcites →https://doi.org/10.1128/mcb.02021-07openalex-snapshot
Downregulation of Protein 4.1R, a Mature Centriole Protein, Disrupts Centrosomes, Alters Cell Cycle Progression, and Perturbs Mitotic Spindles and Anaphase
inferredcites →https://doi.org/10.1186/1471-213x-10-6openalex-snapshot
Downstream genes of Pax6 revealed by comprehensive transcriptome profiling in the developing rat hindbrain
inferredcites →https://doi.org/10.1242/dev.01173openalex-snapshot
Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells
inferredcites →https://doi.org/10.1242/dev.074591openalex-snapshot
The role of Pax6 in regulating the orientation and mode of cell division of progenitors in the mouse cerebral cortex
inferredcites →https://doi.org/10.1242/dev.124.15.2961openalex-snapshot
Pax-6 is involved in the specification of hindbrain motor neuron subtype
inferredcites →https://doi.org/10.1242/dev.129.7.1553openalex-snapshot
Comparison of the generic neuronal differentiation and neuron subtype specification functions of mammalianachaete-scuteandatonalhomologs in cultured neural progenitor cells
inferredcites →https://doi.org/10.1242/dev.30.3.661openalex-snapshot
Inhibition of nuclear migration in the absence of microtubules in the chick embryo
inferredcites →https://doi.org/10.1242/jcs.010322openalex-snapshot
Ninein is released from the centrosome and moves bi-directionally along microtubules
inferredcites →https://doi.org/10.1242/jcs.02302openalex-snapshot
Microtubule nucleation and anchoring at the centrosome are independent processes linked by ninein function
inferredcites →https://doi.org/10.1242/jcs.057851openalex-snapshot
FAK-mediated extracellular signals are essential for interkinetic nuclear migration and planar divisions in the neuroepithelium
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.113.17.3013openalex-snapshot
Microtubule minus-end anchorage at centrosomal and non-centrosomal sites: the role of ninein
inferredcites →https://doi.org/10.1371/journal.pbio.0050297openalex-snapshot
Fabp7 Maps to a Quantitative Trait Locus for a Schizophrenia Endophenotype
inferredcites →https://doi.org/10.1523/jneurosci.12-11-04565.1992openalex-snapshot
A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes
inferredcites →https://doi.org/10.1523/jneurosci.2512-05.2005openalex-snapshot
Role of Fabp7 , a Downstream Gene of Pax6, in the Maintenance of Neuroepithelial Cells during Early Embryonic Development of the Rat Cortex
inferredcites →https://doi.org/10.1634/stemcells.2007-0884openalex-snapshot
Concise Review: Pax6 Transcription Factor Contributes to both Embryonic and Adult Neurogenesis as a Multifunctional Regulator
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4692176openalex-extracted
Targeted Localization of the Mother Centrosome in CD8 T Cells Undergoing Asymmetric Cell Division Promotes Memory Formation
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_14openalex-snapshot
MTOC Organization and Competition During Neuron Differentiation
inferred← citeshttps://doi.org/10.1007/s00018-014-1766-1openalex-snapshot
Pax6 controls centriole maturation in cortical progenitors through Odf2
inferred← citeshttps://doi.org/10.1007/s10571-025-01616-3openalex-snapshot
In Utero Electroporation Uncovers an Early-Differentiating Subset of Dentate Gyrus Progenitors
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.jbc.2025.108419openalex-snapshot
Ninein isoform contributions to intracellular processes and macrophage immune function
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.sbi.2020.10.023openalex-snapshot
Centrosomes in asymmetric cell division
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.09.004openalex-snapshot
RNA processing in neurological tissue: development, aging and disease
inferred← citeshttps://doi.org/10.1016/j.tcb.2022.03.004openalex-snapshot
Centrosome heterogeneity in stem cells regulates cell diversity
inferred← citeshttps://doi.org/10.1038/s41467-026-68428-xopenalex-snapshot
Dynamic allele usage of X-linked genes ameliorates neurodevelopmental disease phenotypes in brain organoids
inferred← citeshttps://doi.org/10.1038/s41583-025-00906-5openalex-snapshot
Early spinal cord development: from neural tube formation to neurogenesis
inferred← citeshttps://doi.org/10.1038/s41586-024-07081-0openalex-snapshot
Autonomous transposons tune their sequences to ensure somatic suppression
inferred← citeshttps://doi.org/10.1038/s41598-017-05738-7openalex-snapshot
Dynamics and function of CXCR4 in formation of the granule cell layer during hippocampal development
inferred← citeshttps://doi.org/10.1038/s44318-024-00327-7openalex-snapshot
Kinesin-like motor protein KIF23 maintains neural stem and progenitor cell pools in the developing cortex
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.201808176openalex-snapshot
The Drosophila Ninein homologue Bsg25D cooperates with Ensconsin in myonuclear positioning
inferred← citeshttps://doi.org/10.1091/mbc.e23-06-0245openalex-snapshot
Ninein domains required for its localization, association with partners dynein and ensconsin, and microtubule organization
inferred← citeshttps://doi.org/10.1098/rsob.200399openalex-snapshot
A centriole's subdistal appendages: contributions to cell division, ciliogenesis and differentiation
inferred← citeshttps://doi.org/10.1098/rsob.220229openalex-snapshot
Emerging roles of centrosome cohesion
inferred← citeshttps://doi.org/10.1098/rstb.2013.0466openalex-snapshot
When fate follows age: unequal centrosomes in asymmetric cell division
inferred← citeshttps://doi.org/10.1101/2022.10.07.511381openalex-snapshot
Pantr2 , a trans-acting lncRNA, modulates the differentiation potential of neural progenitors in vivo
inferred← citeshttps://doi.org/10.1101/2023.06.17.545424openalex-snapshot
Dynamic X-chromosomal reactivation enhances female brain resilience
inferred← citeshttps://doi.org/10.1101/2023.10.27.564302openalex-snapshot
Kinesin family member Kif23 regulates cytokinetic division and maintains neural stem/progenitor cell pool in the developing neocortex
inferred← citeshttps://doi.org/10.1101/gad.351337.123openalex-snapshot
Pan-cellular organelles and suborganelles—from common functions to cellular diversity?
inferred← citeshttps://doi.org/10.1111/dgd.12135openalex-snapshot
Asymmetric inheritance of Cyclin D2 maintains proliferative neural stem/progenitor cells: A critical event in brain development and evolution
inferred← citeshttps://doi.org/10.1111/joa.13709openalex-snapshot
The subcommissural organ maintains features of neuroepithelial cells in the adult mouse
inferred← citeshttps://doi.org/10.1128/mcb.01138-14openalex-snapshot
JAK2 Tyrosine Kinase Phosphorylates and Is Negatively Regulated by Centrosomal Protein Ninein
inferred← citeshttps://doi.org/10.1242/bio.019638openalex-snapshot
Loss of function of theDrosophilaNinein-related centrosomal protein Bsg25D causes mitotic defects and impairs embryonic development
inferred← citeshttps://doi.org/10.1242/dev.138271openalex-snapshot
mTORC1 signaling and primary cilia are required for brain ventricle morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.204829openalex-snapshot
In preprints: unraveling a new non-canonical role of Cyclin D1 in corticogenesis
inferred← citeshttps://doi.org/10.21769/bioprotoc.4812openalex-snapshot
Spatial Centrosome Proteomic Profiling of Human iPSC-derived Neural Cells
inferred← citeshttps://doi.org/10.26508/lsa.201900373openalex-snapshot
Epidermal development requires ninein for spindle orientation and cortical microtubule organization
inferred← citeshttps://doi.org/10.33612/diss.674227669openalex-snapshot
Investigating cellular aspects of neural progenitor cells in zebrafish forebrain development
inferred← citeshttps://doi.org/10.3389/fcell.2022.867870openalex-snapshot
Microtubule Anchoring: Attaching Dynamic Polymers to Cellular Structures
inferred← citeshttps://doi.org/10.3389/fnins.2021.789583openalex-snapshot
Multiple Functions of the Dmrt Genes in the Development of the Central Nervous System
inferred← citeshttps://doi.org/10.3389/fnins.2021.803107openalex-snapshot
Evolution of the Neocortex Through RNA-Binding Proteins and Post-transcriptional Regulation
inferred← citeshttps://doi.org/10.3390/cells15060537openalex-snapshot
Architects of the Developing Brain: Cytoskeleton-Organizing Molecules in Neurodevelopmental Disorders
inferred← citeshttps://doi.org/10.3390/ijms20051010openalex-snapshot
An RNA Switch of a Large Exon of Ninein Is Regulated by the Neural Stem Cell Specific-RNA Binding Protein, Qki5
inferred← citeshttps://doi.org/10.3390/ijms21197354openalex-snapshot
Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3390/ijms23116115openalex-snapshot
Thirty Years’ History since the Discovery of Pax6: From Central Nervous System Development to Neurodevelopmental Disorders
inferred← citeshttps://doi.org/10.3803/enm.2015.30.1.53openalex-snapshot
Determination of Mother Centriole Maturation in CPAP-Depleted Cells Using the Ninein Antibody
inferred← citeshttps://doi.org/10.53846/goediss-4855openalex-snapshot
Transcriptional control of the establishment of neocortical projections in the mammalian telencephalon
inferred← citeshttps://doi.org/10.70675/00a59d8fzc81cz4ee3zabc6zd0f36c15e0f2openalex-snapshot
Mécanismes de développement des cellules épendymaires : origine et lignage des cellules épendymaires dans le cerveau des mammifères
inferred← citeshttps://doi.org/10.70675/31292d91ze225z4d77zb626zcb3377a74f23openalex-snapshot
Study of the coupling between interkinetic nuclear migration and cell-cycle progression in the mouse developing cortex
inferred← citeshttps://doi.org/10.7554/elife.77892openalex-snapshot
Self-assembly of pericentriolar material in interphase cells lacking centrioles
inferred← citeshttps://doi.org/10.7554/elife.93457openalex-snapshot
Loss of ninein interferes with osteoclast formation and causes premature ossification
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