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A Mesenchymal-Like ZEB1+ Niche Harbors Dorsal Radial Glial Fibrillary Acidic Protein-Positive Stem Cells in the Spinal Cord
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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)1097-0029(19980401)41:1<2::aid-jemt2>3.0.co;2-zopenalex-snapshot
Ependymal development, proliferation, and functions: A review
inferredcites →https://doi.org/10.1002/1098-1136(20010101)33:1<72::aid-glia1007>3.0.co;2-aopenalex-snapshot
GFAP promoter-controlled EGFP-expressing transgenic mice: A tool to visualize astrocytes and astrogliosis in living brain tissue
inferredcites →https://doi.org/10.1002/ar.1092110112openalex-snapshot
Spinal tanycytes in the adult rat : A correlative Golgi gold‐toning study
inferredcites →https://doi.org/10.1002/cne.10481openalex-snapshot
Molecular mapping of the origin of postnatal spinal cord ependymal cells: Evidence that adult ependymal cells are derived from Nkx6.1+ ventral neural progenitor cells
inferredcites →https://doi.org/10.1002/glia.20243openalex-snapshot
Adult human subventricular, subgranular, and subpial zones contain astrocytes with a specialized intermediate filament cytoskeleton
inferredcites →https://doi.org/10.1002/jnr.21646openalex-snapshot
Adult human spinal cord harbors neural precursor cells that generate neurons and glial cells in vitro
inferredcites →https://doi.org/10.1002/stem.24openalex-snapshot
Activated Spinal Cord Ependymal Stem Cells Rescue Neurological Function
inferredcites →https://doi.org/10.1006/dbio.2002.0779openalex-snapshot
Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators
inferredcites →https://doi.org/10.1006/exnr.1997.6697openalex-snapshot
FGF-2 Is Sufficient to Isolate Progenitors Found in the Adult Mammalian Spinal Cord
inferredcites →https://doi.org/10.1007/bf00209966openalex-snapshot
Ependyma and meninges of the spinal cord of the mouse
inferredcites →https://doi.org/10.1016/j.cell.2008.03.027openalex-snapshot
The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells
inferredcites →https://doi.org/10.1016/j.conb.2007.04.006openalex-snapshot
Signaling in adult neurogenesis: from stem cell niche to neuronal networks
inferredcites →https://doi.org/10.1016/j.devcel.2006.05.011openalex-snapshot
δEF1 Mediates TGF-β Signaling in Vascular Smooth Muscle Cell Differentiation
inferredcites →https://doi.org/10.1016/j.stem.2008.05.001openalex-snapshot
Zfh-1 Controls Somatic Stem Cell Self-Renewal in the Drosophila Testis and Nonautonomously Influences Germline Stem Cell Self-Renewal
inferredcites →https://doi.org/10.1016/j.stem.2008.06.011openalex-snapshot
Stem Cells for Spinal Cord Repair
inferredcites →https://doi.org/10.1016/j.stem.2008.07.004openalex-snapshot
Neural Stem Cells Confer Unique Pinwheel Architecture to the Ventricular Surface in Neurogenic Regions of the Adult Brain
inferredcites →https://doi.org/10.1016/j.stem.2008.07.025openalex-snapshot
A Specialized Vascular Niche for Adult Neural Stem Cells
inferredcites →https://doi.org/10.1016/j.stem.2008.07.026openalex-snapshot
Adult SVZ Stem Cells Lie in a Vascular Niche: A Quantitative Analysis of Niche Cell-Cell Interactions
inferredcites →https://doi.org/10.1016/j.tins.2008.05.006openalex-snapshot
Origin and function of olfactory bulb interneuron diversity
inferredcites →https://doi.org/10.1016/j.ydbio.2005.12.030openalex-snapshot
LeX is expressed by principle progenitor cells in the embryonic nervous system, is secreted into their environment and binds Wnt-1
inferredcites →https://doi.org/10.1016/s0092-8674(00)80956-3openalex-snapshot
Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System
inferredcites →https://doi.org/10.1016/s0896-6273(02)01133-9openalex-snapshot
EGF Converts Transit-Amplifying Neurogenic Precursors in the Adult Brain into Multipotent Stem Cells
inferredcites →https://doi.org/10.1016/s0896-6273(04)00140-0openalex-snapshot
Radial Glia Serve as Neuronal Progenitors in All Regions of the Central Nervous System
inferredcites →https://doi.org/10.1038/nn.2268openalex-snapshot
Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke
inferredcites →https://doi.org/10.1038/nrc2131openalex-snapshot
Snail, Zeb and bHLH factors in tumour progression: an alliance against the epithelial phenotype?
inferredcites →https://doi.org/10.1038/nrn1955openalex-snapshot
Therapeutic interventions after spinal cord injury
inferredcites →https://doi.org/10.1038/nrn2571openalex-snapshot
Identity crisis for adult periventricular neural stem cells: subventricular zone astrocytes, ependymal cells or both?
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02181.xopenalex-snapshot
In vivo infusions of exogenous growth factors into the fourth ventricle of the adult mouse brain increase the proliferation of neural progenitors around the fourth ventricle and the central canal of the spinal cord
inferredcites →https://doi.org/10.1073/pnas.96.20.11619openalex-snapshot
Regeneration of a germinal layer in the adult mammalian brain
inferredcites →https://doi.org/10.1093/emboj/16.13.3935openalex-snapshot
ZEB, a vertebrate homolog of Drosophila Zfh‐1, is a negative regulator of muscle differentiation
inferredcites →https://doi.org/10.1093/hmg/ddi446openalex-snapshot
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1
inferredcites →https://doi.org/10.1101/gad.1302105openalex-snapshot
Brain lipid-binding protein is a direct target of Notch signaling in radial glial cells
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04563.xopenalex-snapshot
Neurogenesis in the adult spinal cord in an experimental model of multiple sclerosis
inferredcites →https://doi.org/10.1126/science.276.5312.586openalex-snapshot
Neurogenesis in Postnatal Rat Spinal Cord: A Study in Primary Culture
inferredcites →https://doi.org/10.1159/000064943openalex-snapshot
Hox Genes and Spinal Cord Development
inferredcites →https://doi.org/10.1369/jhc.2008.951814openalex-snapshot
Region-specific Differentiation Potential of Adult Rat Spinal Cord Neural Stem/Precursors and Their Plasticity in Response to In Vitro Manipulation
inferredcites →https://doi.org/10.1371/journal.pbio.0060182openalex-snapshot
Spinal Cord Injury Reveals Multilineage Differentiation of Ependymal Cells
inferredcites →https://doi.org/10.1371/journal.pone.0002888openalex-snapshot
Generation of Breast Cancer Stem Cells through Epithelial-Mesenchymal Transition
inferredcites →https://doi.org/10.14670/hh-19.607openalex-snapshot
The system of cerebrospinal fluid-contacting neurons. Its supposed role in the nonsynaptic signal transmission of the brain.
inferredcites →https://doi.org/10.1523/jneurosci.0809-04.2004openalex-snapshot
Gene Expression Changes in the Course of Neural Progenitor Cell Differentiation
inferredcites →https://doi.org/10.1523/jneurosci.16-23-07599.1996openalex-snapshot
Multipotent CNS Stem Cells Are Present in the Adult Mammalian Spinal Cord and Ventricular Neuroaxis
inferredcites →https://doi.org/10.1523/jneurosci.6183-08.2009openalex-snapshot
Enigmatic Central Canal Contacting Cells: Immature Neurons in “Standby Mode”?
inferredcites →https://doi.org/10.1634/stemcells.2005-0076openalex-snapshot
Motor Neuron Degeneration Promotes Neural Progenitor Cell Proliferation, Migration, and Neurogenesis in the Spinal Cords of Amyotrophic Lateral Sclerosis Mice
inferredcites →https://doi.org/10.1634/stemcells.2005-0138openalex-snapshot
Exogenous and Fibroblast Growth Factor 2/Epidermal Growth Factor–Regulated Endogenous Cytokines Regulate Neural Precursor Cell Growth and Differentiation
inferredcites →https://doi.org/10.1634/stemcells.2005-0249openalex-snapshot
Early Response of Endogenous Adult Neural Progenitor Cells to Acute Spinal Cord Injury in Mice
inferredcites →https://doi.org/10.1634/stemcells.2005-0556openalex-snapshot
NG2 and Olig2 Expression Provides Evidence for Phenotypic Deregulation of Cultured Central Nervous System and Peripheral Nervous System Neural Precursor Cells
inferredcites →https://doi.org/10.1634/stemcells.2006-0705openalex-snapshot
New GABAergic Interneurons Supported by Myelin-Specific T Cells Are Formed in Intact Adult Spinal Cord
inferredcites →https://doi.org/10.1634/stemcells.2007-0867openalex-snapshot
Enumeration of Neural Stem and Progenitor Cells in the Neural Colony-Forming Cell Assay
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.4693677openalex-extracted
Ezrin, a novel marker of ependymal cells, can be used to demonstrate their proliferation regulation after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1002/1878-0261.12085openalex-snapshot
EMT‐ and MET‐related processes in nonepithelial tumors: importance for disease progression, prognosis, and therapeutic opportunities
inferred← citeshttps://doi.org/10.1002/biof.1505openalex-snapshot
Nodal increases the malignancy of childhood neuroblastoma cells via regulation of Zeb1
inferred← citeshttps://doi.org/10.1002/cne.23029openalex-snapshot
SPARC‐like 1 (SC1) is a diversely expressed and developmentally regulated matricellular protein that does not compensate for the absence of SPARC in the CNS
inferred← citeshttps://doi.org/10.1002/cne.23104openalex-snapshot
Biciliated ependymal cell proliferation contributes to spinal cord growth
inferred← citeshttps://doi.org/10.1002/cne.23184openalex-snapshot
A cell population that strongly expresses the CB1 cannabinoid receptor in the ependyma of the rat spinal cord
inferred← citeshttps://doi.org/10.1002/cne.23590openalex-snapshot
Evidence that the central canal lining of the spinal cord contributes to oligodendrogenesis during postnatal development and adulthood in intact rats
inferred← citeshttps://doi.org/10.1002/cne.24091openalex-snapshot
Quantitative analyses of cellularity and proliferative activity reveals the dynamics of the central canal lining during postnatal development of the rat
inferred← citeshttps://doi.org/10.1002/cne.24441openalex-snapshot
Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis
inferred← citeshttps://doi.org/10.1002/dneu.22238openalex-snapshot
Akhirin regulates the proliferation and differentiation of neural stem cells in intact and injured mouse spinal cord
inferred← citeshttps://doi.org/10.1002/dneu.22942openalex-snapshot
Comparative model of minimal spinal cord injury reveals a rather anti‐inflammatory response in the lesion site as well as increased proliferation in the central canal lining in the neonates compared to the adult rats
inferred← citeshttps://doi.org/10.1002/glia.22579openalex-snapshot
The adult spinal cord harbors a population of GFAP-positive progenitors with limited self-renewal potential
inferred← citeshttps://doi.org/10.1002/jnr.24918openalex-snapshot
The ependymal cell cytoskeleton in the normal and injured spinal cord of mice
inferred← citeshttps://doi.org/10.1002/stem.1175openalex-snapshot
Spatial Domains of Progenitor-Like Cells and Functional Complexity of a Stem Cell Niche in the Neonatal Rat Spinal Cord
inferred← citeshttps://doi.org/10.1002/stem.2488openalex-snapshot
Myelin Basic Protein Regulates Primitive and Definitive Neural Stem Cell Proliferation from the Adult Spinal Cord
inferred← citeshttps://doi.org/10.1002/stem.3107openalex-snapshot
Unlocking the paradoxical endogenous stem cell response after spinal cord injury
inferred← citeshttps://doi.org/10.1007/978-1-0716-1783-0_4openalex-snapshot
Isolate and Culture Neural Stem Cells from the Mouse Adult Spinal Cord
inferred← citeshttps://doi.org/10.1007/978-1-4939-1908-6_1openalex-snapshot
Adult Neurogenesis and Regeneration: Focus on Nonmammalian Vertebrates
inferred← citeshttps://doi.org/10.1007/978-1-62703-574-3_5openalex-snapshot
Isolate and Culture Neural Stem Cells from the Mouse Adult Spinal Cord
inferred← citeshttps://doi.org/10.1007/978-3-031-39558-1_3openalex-snapshot
Development of the Spinal Cord
inferred← citeshttps://doi.org/10.1007/978-3-319-62817-2_13openalex-snapshot
Progenitors in the Ependyma of the Spinal Cord: A Potential Resource for Self-Repair After Injury
inferred← citeshttps://doi.org/10.1007/978-3-319-69194-7_5openalex-snapshot
Spinal Cord Stem Cells In Their Microenvironment: The Ependyma as a Stem Cell Niche
inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_7openalex-snapshot
Motile Cilia and Brain Function: Ependymal Motile Cilia Development, Organization, Function and Their Associated Pathologies
inferred← citeshttps://doi.org/10.1007/978-94-017-7273-0_20openalex-snapshot
Stem Cells and Spinal Cord Regeneration
inferred← citeshttps://doi.org/10.1007/s00018-023-04811-xopenalex-snapshot
Persistence of FoxJ1+ Pax6+ Sox2+ ependymal cells throughout life in the human spinal cord
inferred← citeshttps://doi.org/10.1007/s00429-014-0965-8openalex-snapshot
Systematic expression analysis of Hox genes at adulthood reveals novel patterns in the central nervous system
inferred← citeshttps://doi.org/10.1007/s11060-016-2240-8openalex-snapshot
ZEB1 expression is increased in IDH1-mutant lower-grade gliomas
inferred← citeshttps://doi.org/10.1007/s11064-013-1048-6openalex-snapshot
Differential Expression of Micro-Heterogeneous LewisX-Type Glycans in the Stem Cell Compartment of the Developing Mouse Spinal Cord
inferred← citeshttps://doi.org/10.1007/s12015-025-10995-5openalex-snapshot
Region-Specific Adult Neural Stem Cell Niches of the Mediobasal Hypothalamus and Medulla Oblongata
inferred← citeshttps://doi.org/10.1007/s12035-016-0132-8openalex-snapshot
Wnts Are Expressed in the Ependymal Region of the Adult Spinal Cord
inferred← citeshttps://doi.org/10.1016/b978-0-08-102807-0.00010-7openalex-snapshot
Functional properties of progenitor-like cells in the spinal cord
inferred← citeshttps://doi.org/10.1016/b978-0-12-817986-4.00015-8openalex-snapshot
Effects of extrinsic factors and intracellular signaling and transcription factors regulating the development and cell fate of spinal cord ependymal cells
inferred← citeshttps://doi.org/10.1016/j.acthis.2013.08.004openalex-snapshot
Enigmatic cerebrospinal fluid-contacting neurons arise even after the termination of neurogenesis in the rat spinal cord during embryonic development and retain their immature-like characteristics until adulthood
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.04.081openalex-snapshot
ZEB1 Represses Neural Differentiation and Cooperates with CTBP2 to Dynamically Regulate Cell Migration during Neocortex Development
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110440openalex-snapshot
Identification of a discrete subpopulation of spinal cord ependymal cells with neural stem cell properties
inferred← citeshttps://doi.org/10.1016/j.coph.2019.11.008openalex-snapshot
Ependymal cells in the spinal cord as neuronal progenitors
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.03.021openalex-snapshot
Zeb Family Members and Boundary Cap Cells Underlie Developmental Plasticity of Sensory Nociceptive Neurons
inferred← citeshttps://doi.org/10.1016/j.devcel.2023.01.003openalex-snapshot
An ependymal cell census identifies heterogeneous and ongoing cell maturation in the adult mouse spinal cord that changes dynamically on injury
inferred← citeshttps://doi.org/10.1016/j.diff.2025.100913openalex-snapshot
Mesenchymal phenotype as a hallmark of undifferentiated states
inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.01.026openalex-snapshot
Neural stem cells in the adult spinal cord
inferred← citeshttps://doi.org/10.1016/j.nbd.2024.106746openalex-snapshot
Ezrin, a novel marker of ependymal cells, can be used to demonstrate their proliferation regulation after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1016/j.neures.2022.11.004openalex-snapshot
Analysis of a cell niche with proliferative potential at the roof of the aqueduct of Sylvius
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2022.109326openalex-snapshot
GABAergic regulation of cell proliferation within the adult mouse spinal cord
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.10.013openalex-snapshot
Spinal cord injury induces a long-lasting upregulation of interleukin-1β in astrocytes around the central canal
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2016.11.028openalex-snapshot
Postnatal maturation of mouse medullo-spinal cerebrospinal fluid-contacting neurons
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.04.002openalex-snapshot
The spinal ependymal zone as a source of endogenous repair cells across vertebrates
inferred← citeshttps://doi.org/10.1016/j.scr.2014.03.006openalex-snapshot
ATF3 is a novel nuclear marker for migrating ependymal stem cells in the rat spinal cord
inferred← citeshttps://doi.org/10.1016/j.stemcr.2019.04.001openalex-snapshot
RNA Profiling of the Human and Mouse Spinal Cord Stem Cell Niches Reveals an Embryonic-like Regionalization with MSX1+ Roof-Plate-Derived Cells
inferred← citeshttps://doi.org/10.1016/j.stemcr.2022.10.002openalex-snapshot
Satellite glia of the adult dorsal root ganglia harbor stem cells that yield glia under physiological conditions and neurons in response to injury
inferred← citeshttps://doi.org/10.1038/s41420-025-02492-yopenalex-snapshot
Pkd2l1 deletion inhibits the neurogenesis of cerebrospinal fluid-contacting neurons and impedes spinal cord injury repair
inferred← citeshttps://doi.org/10.1038/srep17745openalex-snapshot
CB1 cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord
inferred← citeshttps://doi.org/10.1074/jbc.m116.771493openalex-snapshot
The zinc finger E-box-binding homeobox 1 (Zeb1) promotes the conversion of mouse fibroblasts into functional neurons
inferred← citeshttps://doi.org/10.1074/jbc.ra118.005498openalex-snapshot
Zinc finger E-box–binding homeobox 1 (ZEB1) is required for neural differentiation of human embryonic stem cells
inferred← citeshttps://doi.org/10.1080/01677063.2017.1359833openalex-snapshot
Light on a sensory interface linking the cerebrospinal fluid to motor circuits in vertebrates
inferred← citeshttps://doi.org/10.1080/23262133.2017.1300037openalex-snapshot
Building a central nervous system: The neural stem cell lineage revealed
inferred← citeshttps://doi.org/10.1093/brain/awv089openalex-snapshot
The ependymal region of the adult human spinal cord differs from other species and shows ependymoma-like features
inferred← citeshttps://doi.org/10.1101/2022.03.07.483249openalex-snapshot
Ependymal cell maturation is heterogeneous and ongoing in the mouse spinal cord and dynamically regulated in response to injury
inferred← citeshttps://doi.org/10.1101/2023.03.29.534787openalex-snapshot
In Rhesus monkeys, CSF-contacting neurons are the only neurons present in the medullo-spinal peri-ependymal zone
inferred← citeshttps://doi.org/10.1101/2025.10.01.677488openalex-snapshot
Hippo/YAP1 Signaling Regulates the Oligodendrocyte–Astrocyte Fate Switch and Ependymal Gene Expression in Adult Spinal Cord Stem Cells
inferred← citeshttps://doi.org/10.1111/dgd.12284openalex-snapshot
Regulation of the neural niche by the soluble molecule Akhirin
inferred← citeshttps://doi.org/10.1111/dgd.12546openalex-snapshot
Intracellular signaling similarity reveals neural stem cell‐like properties of ependymal cells in the adult rat spinal cord
inferred← citeshttps://doi.org/10.1111/ejn.15342openalex-snapshot
Evidence for PKD2L1‐positive neurons distant from the central canal in the ventromedial spinal cord and medulla of the adult mouse
inferred← citeshttps://doi.org/10.1111/joa.13094openalex-snapshot
Multiple steps characterise ventricular layer attrition to form the ependymal cell lining of the adult mouse spinal cord central canal
inferred← citeshttps://doi.org/10.1134/s1990519x24600595openalex-snapshot
The Role of Ciliated Cells of the Spinal Canal
inferred← citeshttps://doi.org/10.1155/2019/1958631openalex-snapshot
Employing Endogenous NSCs to Promote Recovery of Spinal Cord Injury
inferred← citeshttps://doi.org/10.1186/s12915-025-02203-0openalex-snapshot
Blueprints for healing: central nervous system regeneration in zebrafish and neonatal mice
inferred← citeshttps://doi.org/10.1186/s13064-021-00152-2openalex-snapshot
Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis
inferred← citeshttps://doi.org/10.1186/s13287-023-03395-4openalex-snapshot
The activation of dormant ependymal cells following spinal cord injury
inferred← citeshttps://doi.org/10.1242/dev.129254openalex-snapshot
The late and dual origin of cerebrospinal fluid-contacting neurons in the mouse spinal cord
inferred← citeshttps://doi.org/10.1242/dev.194415openalex-snapshot
Defining the signalling determinants of a posterior ventral spinal cord identity in human neuromesodermal progenitor derivatives
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000470openalex-snapshot
Crumbs2 mediates ventricular layer remodelling to form the spinal cord central canal
inferred← citeshttps://doi.org/10.1371/journal.pone.0024538openalex-snapshot
Adult Spinal Cord Radial Glia Display a Unique Progenitor Phenotype
inferred← citeshttps://doi.org/10.1371/journal.pone.0087748openalex-snapshot
Morphology, Distribution and Phenotype of Polycystin Kidney Disease 2-like 1-Positive Cerebrospinal Fluid Contacting Neurons in The Brainstem of Adult Mice
inferred← citeshttps://doi.org/10.1371/journal.pone.0122337openalex-snapshot
OCAM Regulates Embryonic Spinal Cord Stem Cell Proliferation by Modulating ErbB2 Receptor
inferred← citeshttps://doi.org/10.1371/journal.pone.0151274openalex-snapshot
Asymmetric Distribution of GFAP in Glioma Multipotent Cells
inferred← citeshttps://doi.org/10.1523/jneurosci.2056-19.2020openalex-snapshot
Connexin Signaling Is Involved in the Reactivation of a Latent Stem Cell Niche after Spinal Cord Injury
inferred← citeshttps://doi.org/10.2478/s11535-012-0027-2openalex-snapshot
Regional differences of proliferation activity in the spinal cord ependyma of adult rats
inferred← citeshttps://doi.org/10.2741/3734openalex-snapshot
The spinal cord ependymal region: A stem cell niche in the caudal central nervous system
inferred← citeshttps://doi.org/10.3389/fbioe.2022.966866openalex-snapshot
The roles and applications of neural stem cells in spinal cord injury repair
inferred← citeshttps://doi.org/10.3389/fcell.2024.1426395openalex-snapshot
Roles of cerebrospinal fluid-contacting neurons as potential neural stem cells in the repair and regeneration of spinal cord injuries
inferred← citeshttps://doi.org/10.3389/fncel.2021.630882openalex-snapshot
The Neural Stem Cell Properties of PKD2L1+ Cerebrospinal Fluid-Contacting Neurons in vitro
inferred← citeshttps://doi.org/10.3389/fncel.2023.1288676openalex-snapshot
P2X7 receptor activation awakes a dormant stem cell niche in the adult spinal cord
inferred← citeshttps://doi.org/10.3389/fnins.2024.1425849openalex-snapshot
Differentiation stage-specific expression of transcriptional regulators for epithelial mesenchymal transition in dentate granule progenitors
inferred← citeshttps://doi.org/10.3389/fnmol.2013.00023openalex-snapshot
Differential regulation of proliferation and neuronal differentiation in adult rat spinal cord neural stem/progenitors by ERK1/2, Akt, and PLCγ
inferred← citeshttps://doi.org/10.3389/fphys.2013.00340openalex-snapshot
Adult spinal cord ependymal layer: a promising pool of quiescent stem cells to treat spinal cord injury
inferred← citeshttps://doi.org/10.3390/cells10040925openalex-snapshot
Expression and Function of ZEB1 in the Cornea
inferred← citeshttps://doi.org/10.3390/cells10092235openalex-snapshot
The Structure of the Spinal Cord Ependymal Region in Adult Humans Is a Distinctive Trait among Mammals
inferred← citeshttps://doi.org/10.3390/cells10123332openalex-snapshot
RNA Profiling of Mouse Ependymal Cells after Spinal Cord Injury Identifies the Oncostatin Pathway as a Potential Key Regulator of Spinal Cord Stem Cell Fate
inferred← citeshttps://doi.org/10.3390/jdb9030029openalex-snapshot
Regulation of the Brain Neural Niche by Soluble Molecule Akhirin
inferred← citeshttps://doi.org/10.3390/jdb9030030openalex-snapshot
Morphological and Functional Changes of Roof Plate Cells in Spinal Cord Development
inferred← citeshttps://doi.org/10.3410/f.735638130.793562488openalex-snapshot
Faculty Opinions recommendation of RNA Profiling of the Human and Mouse Spinal Cord Stem Cell Niches Reveals an Embryonic-like Regionalization with MSX1+ Roof-Plate-Derived Cells.
inferred← citeshttps://doi.org/10.37175/stemedicine.v1i1.19openalex-snapshot
Spinal cord neural stem cells heterogeneity in postnatal development
inferred← citeshttps://doi.org/10.4172/2157-7633.1000184openalex-snapshot
Unconventional Neurogenic Niches and Neurogenesis Modulation by Vitamins
inferred← citeshttps://doi.org/10.4172/2165-7939.1000e113openalex-snapshot
The Differential Intracellular Expression of the Novel Marker ATF-3 Characterizes the Quiescent or Activated State of Endogenous Spinal Stem Cells: A Tool to Study up Neurorepair?
inferred← citeshttps://doi.org/10.5772/58599openalex-snapshot
Typical and Atypical Stem Cell Niches of the Adult Nervous System in Health and Inflammatory Brain and Spinal Cord Diseases
inferred← citeshttps://doi.org/10.64898/2026.01.16.699895openalex-snapshot
Connexins are essential for the contribution of latent progenitors to self-repair after spinal cord injury
inferred← citeshttps://doi.org/10.70675/109d0ff4z6678z4088zb318z4ce95cacf339openalex-snapshot
Influence des processus inflammatoires sur la neuroplasticité et sur les récupérations fonctionnelles après lésion spinale chez le rat adulte
inferred← citeshttps://doi.org/10.70675/131710fezef59z4eb9za19bz5e24cb31410dopenalex-snapshot
Human and mouse spinal cord : a territory of diverse neural stem/progenitor cells, identification and functionality
inferred← citeshttps://doi.org/10.70675/21469ecczdd09z40efza3e9ze2532dc07f8bopenalex-snapshot
Étude de la transmission GABAergique et des propriétés des canaux PKD2L1 dans les neurones au contact du liquide cérébro-spinal chez la souris
inferred← citeshttps://doi.org/10.70675/33fcdb63z50cdz44fczabf8ze0c1aa826f87openalex-snapshot
Caractérisation des neurones bulbo-spinaux PKD2L1+ qui contactent le liquide céphalo-rachidien
inferred← citeshttps://doi.org/10.70675/44244bd9z7ce5z477bzada2z9720ad170d42openalex-snapshot
Effet de la stimulation magnétique répétitive trans-spinale comme thérapie non invasive dans le cadre des lésions médullaires.
inferred← citeshttps://doi.org/10.70675/462a9646z2946z42bfzb142z0572d8cd6805openalex-snapshot
Implication des voies de différenciation épithéliale précoce dans la morphogenèse mammaire et la progression des cancers du sein
inferred← citeshttps://doi.org/10.70675/8b7a9f65z9bb1z4beezb266z3249784928caopenalex-snapshot
Biologie des cellules souches cochléaires : perspectives dans le traitement de la surdité sensorielle
inferred← citeshttps://doi.org/10.70675/d43a0790z3457z40b4z9ebfzbd65741a771fopenalex-snapshot
Cellules souches et biomarqueurs cochléaires : perspectives thérapeutiques des surdités neurosensorielles
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