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Ependymal cell contribution to scar formation after spinal cord injury is minimal, local and dependent on direct ependymal injury
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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/cne.23104openalex-snapshot
Biciliated ependymal cell proliferation contributes to spinal cord growth
inferredcites →https://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
inferredcites →https://doi.org/10.1002/dvg.22753openalex-snapshot
A Knock‐in Foxj1CreERT2::GFP mouse for recombination in epithelial cells with motile cilia
inferredcites →https://doi.org/10.1002/glia.20176openalex-snapshot
Cell proliferation and replacement following contusive spinal cord injury
inferredcites →https://doi.org/10.1002/glia.21077openalex-snapshot
Prospectively isolated CD133/CD24‐positive ependymal cells from the adult spinal cord and lateral ventricle wall differ in their long‐term in vitro self‐renewal and in vivo gene expression
inferredcites →https://doi.org/10.1002/glia.21089openalex-snapshot
Molecular comparison of GLT1 + and ALDH1L1 + astrocytes in vivo in astroglial reporter mice
inferredcites →https://doi.org/10.1002/glia.22538openalex-snapshot
Expression profiling of Aldh1l1‐precursors in the developing spinal cord reveals glial lineage‐specific genes and direct Sox9‐Nfe2l1 interactions
inferredcites →https://doi.org/10.1007/bf00993263openalex-snapshot
Quantitative aspects of reactive gliosis: A review
inferredcites →https://doi.org/10.1007/s00401-009-0619-8openalex-snapshot
Astrocytes: biology and pathology
inferredcites →https://doi.org/10.1016/j.cell.2012.08.020openalex-snapshot
Long-Distance Growth and Connectivity of Neural Stem Cells after Severe Spinal Cord Injury
inferredcites →https://doi.org/10.1016/j.expneurol.2013.01.026openalex-snapshot
Neural stem cells in the adult spinal cord
inferredcites →https://doi.org/10.1016/j.neuron.2013.12.034openalex-snapshot
Reactive Gliosis and the Multicellular Response to CNS Damage and Disease
inferredcites →https://doi.org/10.1016/j.stem.2010.07.014openalex-snapshot
Origin of New Glial Cells in Intact and Injured Adult Spinal Cord
inferredcites →https://doi.org/10.1016/j.stemcr.2014.04.008openalex-snapshot
Primitive Neural Stem Cells in the Adult Mammalian Brain Give Rise to GFAP-Expressing Neural Stem Cells
inferredcites →https://doi.org/10.1016/j.tins.2009.08.002openalex-snapshot
Molecular dissection of reactive astrogliosis and glial scar formation
inferredcites →https://doi.org/10.1016/s0006-8993(01)02574-4openalex-snapshot
Localisation of the SRY-related HMG box protein, SOX9, in rodent brain
inferredcites →https://doi.org/10.1016/s0092-8674(00)81571-8openalex-snapshot
Fulminant Jejuno-Ileitis following Ablation of Enteric Glia in Adult Transgenic Mice
inferredcites →https://doi.org/10.1016/s0896-6273(00)80781-3openalex-snapshot
Leukocyte Infiltration, Neuronal Degeneration, and Neurite Outgrowth after Ablation of Scar-Forming, Reactive Astrocytes in Adult Transgenic Mice
inferredcites →https://doi.org/10.1016/s0896-6273(02)00835-8openalex-snapshot
LeX/ssea-1 Is Expressed by Adult Mouse CNS Stem Cells, Identifying Them as Nonependymal
inferredcites →https://doi.org/10.1021/acsbiomaterials.5b00153openalex-snapshot
Thermoresponsive Copolypeptide Hydrogel Vehicles for Central Nervous System Cell Delivery
inferredcites →https://doi.org/10.1038/35102174openalex-snapshot
The development of neural stem cells
inferredcites →https://doi.org/10.1038/nature17623openalex-snapshot
Astrocyte scar formation aids central nervous system axon regeneration
inferredcites →https://doi.org/10.1038/nn.2467openalex-snapshot
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
inferredcites →https://doi.org/10.1038/nrn3898openalex-snapshot
Astrocyte barriers to neurotoxic inflammation
inferredcites →https://doi.org/10.1038/sj.jcbfm.9600546openalex-snapshot
Protective Role of Reactive Astrocytes in Brain Ischemia
inferredcites →https://doi.org/10.1089/089771504323004575openalex-snapshot
The Pathology of Human Spinal Cord Injury: Defining the Problems
inferredcites →https://doi.org/10.1093/brain/awl165openalex-snapshot
Essential protective roles of reactive astrocytes in traumatic brain injury
inferredcites →https://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
inferredcites →https://doi.org/10.1093/cercor/bhs049openalex-snapshot
Ependymal Ciliary Dysfunction and Reactive Astrocytosis in a Reorganized Subventricular Zone after Stroke
inferredcites →https://doi.org/10.1096/fj.12-208660openalex-snapshot
Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice
inferredcites →https://doi.org/10.1111/j.1750-3639.1994.tb00838.xopenalex-snapshot
GFAP and Astrogliosis
inferredcites →https://doi.org/10.1126/science.1242576openalex-snapshot
Resident Neural Stem Cells Restrict Tissue Damage and Neuronal Loss After Spinal Cord Injury in Mice
inferredcites →https://doi.org/10.1242/dev.041129openalex-snapshot
FoxJ1-dependent gene expression is required for differentiation of radial glia into ependymal cells and a subset of astrocytes in the postnatal brain
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.0033529openalex-snapshot
Tamoxifen-Induced Cre-loxP Recombination Is Prolonged in Pancreatic Islets of Adult Mice
inferredcites →https://doi.org/10.1523/jneurosci.0171-11.2011openalex-snapshot
Specification of a Foxj1-Dependent Lineage in the Forebrain Is Required for Embryonic-to-Postnatal Transition of Neurogenesis in the Olfactory Bulb
inferredcites →https://doi.org/10.1523/jneurosci.1514-09.2009openalex-snapshot
Reactive Astrocytes Form Scar-Like Perivascular Barriers to Leukocytes during Adaptive Immune Inflammation of the CNS
inferredcites →https://doi.org/10.1523/jneurosci.1709-08.2008openalex-snapshot
STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.1759-11.2011openalex-snapshot
Macroglial Plasticity and the Origins of Reactive Astroglia in Experimental Autoimmune Encephalomyelitis
inferredcites →https://doi.org/10.1523/jneurosci.2121-13.2013openalex-snapshot
Glial Scar Borders Are Formed by Newly Proliferated, Elongated Astrocytes That Interact to Corral Inflammatory and Fibrotic Cells via STAT3-Dependent Mechanisms after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.2510-13.2013openalex-snapshot
Short Hairpin RNA against PTEN Enhances Regenerative Growth of Corticospinal Tract Axons after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.3547-03.2004openalex-snapshot
Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.3579-11.2011openalex-snapshot
The Role of Attenuated Astrocyte Activation in Infantile Neuronal Ceroid Lipofuscinosis
inferredcites →https://doi.org/10.1523/jneurosci.4178-07.2008openalex-snapshot
A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function
inferredcites →https://doi.org/10.1523/jneurosci.4531-07.2007openalex-snapshot
Mosaic Removal of Hedgehog Signaling in the Adult SVZ Reveals That the Residual Wild-Type Stem Cells Have a Limited Capacity for Self-Renewal
inferredcites →https://doi.org/10.2307/1005004openalex-snapshot
An Account of the Transit of Venus over the Sun, June 3d, 1769, and of the Transit of Mercury Nov. 9th, Both as Observed in the State-House Square, Philadelphia. By the Committee Appointed for Those Observations. Drawn up, and Communicated, in Behalf of the Committee, by Rev. John Ewing, A. M.
inferredcites →https://doi.org/10.3758/bf03193146openalex-snapshot
G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences
inferredcites →https://doi.org/10.4049/jimmunol.1001135openalex-snapshot
Gp130-Dependent Astrocytic Survival Is Critical for the Control of Autoimmune Central Nervous System Inflammation
inferredcites →https://doi.org/10.4049/jimmunol.181.4.2683openalex-snapshot
Astrocyte gp130 Expression Is Critical for the Control of Toxoplasma Encephalitis
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/adfm.202508435openalex-snapshot
Engineering Topographical Cues to Enhance Neural Regeneration in Spinal Cord Injury: Overcoming Challenges and Advancing Therapies
inferred← citeshttps://doi.org/10.1002/adhm.202301662openalex-snapshot
Functional Hydrogel Co‐Remolding Migration and Differentiation Microenvironment for Severe Spinal Cord Injury Repair
inferred← citeshttps://doi.org/10.1002/biot.202100167openalex-snapshot
Spinal cord regeneration: A brief overview of the present scenario and a sneak peek into the future
inferred← citeshttps://doi.org/10.1002/cne.24335openalex-snapshot
Neural stem/progenitor cells are activated during tail regeneration in the leopard gecko (Eublepharis macularius)
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.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.23687openalex-snapshot
Questions and (some) answers on reactive astrocytes
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/path.5151openalex-snapshot
Cells in the adult human spinal cord ependymal region do not proliferate after injury
inferred← citeshttps://doi.org/10.1002/smtd.202301173openalex-snapshot
Hydrogel and Nanomedicine‐Based Multimodal Therapeutic Strategies for Spinal Cord Injury
inferred← citeshttps://doi.org/10.1002/stem.3097openalex-snapshot
Epidermal growth factor receptor-extracellular-regulated kinase blockade upregulates TRIM32 signaling cascade and promotes neurogenesis after spinal cord injury
inferred← citeshttps://doi.org/10.1002/stem.3107openalex-snapshot
Unlocking the paradoxical endogenous stem cell response after spinal cord injury
inferred← citeshttps://doi.org/10.1002/stem.3366openalex-snapshot
Direct Neuronal Differentiation of Neural Stem Cells for Spinal Cord Injury Repair
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Nanofibers and Nanostructured Scaffolds for Nervous System Lesions
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/10.1007/978-3-319-69194-7_5openalex-snapshot
Spinal Cord Stem Cells In Their Microenvironment: The Ependyma as a Stem Cell Niche
inferred← citeshttps://doi.org/10.1007/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/s10571-020-01006-xopenalex-snapshot
p75NTR Promotes Astrocyte Proliferation in Response to Cortical Stab Wound
inferred← citeshttps://doi.org/10.1007/s10571-024-01519-9openalex-snapshot
The Role of Inflammatory Cascade and Reactive Astrogliosis in Glial Scar Formation Post-spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/s11064-026-04674-1openalex-snapshot
Harnessing Endogenous Neural Stem Cells: A New Frontier in Spinal Cord Injury Repair
inferred← citeshttps://doi.org/10.1007/s11427-020-1901-4openalex-snapshot
Lineage tracing reveals the origin of Nestin-positive cells are heterogeneous and rarely from ependymal cells after spinal cord injury
inferred← citeshttps://doi.org/10.1007/s11427-020-1930-0openalex-snapshot
Single-cell RNA sequencing reveals Nestin+ active neural stem cells outside the central canal after spinal cord injury
inferred← citeshttps://doi.org/10.1007/s12035-026-05670-wopenalex-snapshot
Targeting Reactive Astrocytes with Flavonoids to Alleviate Neuroinflammation and Promote Synaptic Function
inferred← citeshttps://doi.org/10.1007/s12264-022-00897-8openalex-snapshot
Spatiotemporal Dynamics of the Molecular Expression Pattern and Intercellular Interactions in the Glial Scar Response to Spinal Cord Injury
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/bs.irn.2024.04.005openalex-snapshot
The role of glial cells in amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1016/j.actbio.2021.04.017openalex-snapshot
Tissue-specific parameters for the design of ECM-mimetic biomaterials
inferred← citeshttps://doi.org/10.1016/j.actbio.2024.10.017openalex-snapshot
Glia in tissue engineering: From biomaterial tools to transplantation
inferred← citeshttps://doi.org/10.1016/j.bbr.2019.112209openalex-snapshot
Functions of subventricular zone neural precursor cells in stroke recovery
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120479openalex-snapshot
Small molecules combined with collagen hydrogel direct neurogenesis and migration of neural stem cells after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107834openalex-snapshot
Zeb2 Is a Regulator of Astrogliosis and Functional Recovery after CNS Injury
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111705openalex-snapshot
Myostatin is a negative regulator of adult neurogenesis after spinal cord injury in zebrafish
inferred← citeshttps://doi.org/10.1016/j.conb.2017.10.025openalex-snapshot
Glial control of neurogenesis
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.2022.07.012openalex-snapshot
DNGR-1-tracing marks an ependymal cell subset with damage-responsive neural stem cell potential
inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113556openalex-snapshot
Spatiotemporal dynamic changes, proliferation, and differentiation characteristics of Sox9-positive cells after severe complete transection spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114147openalex-snapshot
Retinal ganglion cell expression of cytokine enhances occupancy of NG2 cell-derived astrocytes at the nerve injury site: Implication for axon regeneration
inferred← citeshttps://doi.org/10.1016/j.gde.2023.102090openalex-snapshot
In vivo cell fate reprogramming for spinal cord repair
inferred← citeshttps://doi.org/10.1016/j.it.2020.07.004openalex-snapshot
Astrocyte Reactivity: Subtypes, States, and Functions in CNS Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.jtcms.2022.04.002openalex-snapshot
Effects of electroacupuncture combined with hydrogel on the formation and changes in the glial scar in rats with spinal cord injury
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.nec.2021.03.011openalex-snapshot
Targeting Central Nervous System Regeneration with Cell Type Specificity
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.spinee.2025.07.028openalex-snapshot
NG2 glia promote injured spinal cord repair through neuronal transdifferentiation and keratins expression in juvenile mice
inferred← citeshttps://doi.org/10.1016/j.stem.2021.02.009openalex-snapshot
In vivo reprogramming of NG2 glia enables adult neurogenesis and functional recovery following spinal cord injury
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.2025.102574openalex-snapshot
Ependymal and neural stem cells are close relatives
inferred← citeshttps://doi.org/10.1016/j.wneu.2022.02.012openalex-snapshot
Strategies for Effective Neural Circuit Reconstruction After Spinal Cord Injury: Use of Stem Cells and Biomaterials
inferred← citeshttps://doi.org/10.1016/j.yexcr.2018.04.017openalex-snapshot
FoxJ1 regulates spinal cord development and is required for the maintenance of spinal cord stem cell potential
inferred← citeshttps://doi.org/10.1016/j.ymthe.2021.04.027openalex-snapshot
Gsx1 promotes locomotor functional recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1038/nm.4502openalex-snapshot
Restorative effects of human neural stem cell grafts on the primate spinal cord
inferred← citeshttps://doi.org/10.1038/nn.4541openalex-snapshot
Cell transplantation therapy for spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41392-022-00885-4openalex-snapshot
Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury
inferred← citeshttps://doi.org/10.1038/s41392-023-01477-6openalex-snapshot
Spinal cord injury: molecular mechanisms and therapeutic interventions
inferred← citeshttps://doi.org/10.1038/s41419-021-04064-1openalex-snapshot
Interleukin-17A regulates ependymal cell proliferation and functional recovery after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1038/s41419-023-06003-8openalex-snapshot
UCHL1 facilitates protein aggregates clearance to enhance neural stem cell activation in spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41467-019-11707-7openalex-snapshot
Moving beyond the glial scar for spinal cord repair
inferred← citeshttps://doi.org/10.1038/s41467-024-50628-yopenalex-snapshot
Single-cell analysis of innate spinal cord regeneration identifies intersecting modes of neuronal repair
inferred← citeshttps://doi.org/10.1038/s41586-024-07889-wopenalex-snapshot
Endogenous opioid signalling regulates spinal ependymal cell proliferation
inferred← citeshttps://doi.org/10.1038/s41593-017-0033-9openalex-snapshot
The diversity and disparity of the glial scar
inferred← citeshttps://doi.org/10.1038/s41593-024-01684-6openalex-snapshot
Derivation and transcriptional reprogramming of border-forming wound repair astrocytes after spinal cord injury or stroke in mice
inferred← citeshttps://doi.org/10.1038/s41598-018-19913-xopenalex-snapshot
Foxj1 expressing ependymal cells do not contribute new cells to sites of injury or stroke in the mouse forebrain
inferred← citeshttps://doi.org/10.1038/s41598-019-39551-1openalex-snapshot
Mouse mast cell protease 4 suppresses scar formation after traumatic spinal cord injury
inferred← citeshttps://doi.org/10.1073/pnas.1803297115openalex-snapshot
Wnt/β-catenin signaling regulates ependymal cell development and adult homeostasis
inferred← citeshttps://doi.org/10.1073/pnas.2413140122openalex-snapshot
Characterizing progenitor cells in developing and injured spinal cord: Insights from single-nucleus transcriptomics and lineage tracing
inferred← citeshttps://doi.org/10.1080/17590914.2026.2673257openalex-snapshot
CD44 Knockout Alters the Cellular Response and Improves Locomotor Outcome After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1084/jem.20210040openalex-snapshot
Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord
inferred← citeshttps://doi.org/10.1089/scd.2021.0297openalex-snapshot
Identification of Novel Multipotent Stem Cells in Mouse Spinal Cord Following Traumatic Injury
inferred← citeshttps://doi.org/10.1093/brain/awaf148openalex-snapshot
Astrocyte regeneration via FGF8-DBX1 signalling facilitates recovery in neuromyelitis optica rats
inferred← citeshttps://doi.org/10.1093/burnst/tkab035openalex-snapshot
Deciphering glial scar after spinal cord injury
inferred← citeshttps://doi.org/10.1101/2021.02.12.428106openalex-snapshot
Reaction of ependymal cells to spinal cord injury: a potential role for oncostatin pathway and microglial cells
inferred← citeshttps://doi.org/10.1101/2021.08.18.456778openalex-snapshot
Myostatin is a negative regulator of adult neurogenesis in zebrafish
inferred← citeshttps://doi.org/10.1101/2021.09.23.461600openalex-snapshot
UCHL1 facilitates aggregates clearance and enhances neural stem cell activation in spinal cord injury
inferred← citeshttps://doi.org/10.1101/2021.12.20.473346openalex-snapshot
Spatiotemporal dynamics of molecular expression pattern and intercellular interactions in glial scar responding to spinal cord injury
inferred← citeshttps://doi.org/10.1101/2023.09.07.556726openalex-snapshot
Endogenous Opioid Signaling Regulates Proliferation of Spinal Cord Ependymal Cells
inferred← citeshttps://doi.org/10.1111/apha.70147openalex-snapshot
Ependymal Yes‐Associated Protein Promotes the Neural Regeneration Through Enhancing the Ependymal Cell‐Derived Perilesional Glial Borders in Mice After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1111/cpr.13275openalex-snapshot
The PI3K / AKT signalling pathway in inflammation, cell death and glial scar formation after traumatic spinal cord injury: Mechanisms and therapeutic opportunities
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/10.1134/s0006297922090012openalex-snapshot
Astrocyte Activation Markers
inferred← citeshttps://doi.org/10.1134/s1990519x24600595openalex-snapshot
The Role of Ciliated Cells of the Spinal Canal
inferred← citeshttps://doi.org/10.1152/physrev.00017.2017openalex-snapshot
The Biology of Regeneration Failure and Success After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1155/2019/1958631openalex-snapshot
Employing Endogenous NSCs to Promote Recovery of Spinal Cord Injury
inferred← citeshttps://doi.org/10.1172/jci90608openalex-snapshot
Cell biology of spinal cord injury and repair
inferred← citeshttps://doi.org/10.1186/s12987-020-00213-4openalex-snapshot
Chronic extradural compression of spinal cord leads to syringomyelia in rat model
inferred← citeshttps://doi.org/10.1186/s12987-025-00631-2openalex-snapshot
Ependymal cilia decline and AQP4 upregulation in young adult rats with syringomyelia
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.204421openalex-snapshot
Sox9 and nuclear factor I transcription factors regulate the timing of neurogenesis and ependymal maturation in dopamine progenitors
inferred← citeshttps://doi.org/10.1360/ssv-2021-0065openalex-snapshot
Pathological changes and repair strategies for spinal cord injury
inferred← citeshttps://doi.org/10.14336/ad.2022.0826-1openalex-snapshot
Roles of Ependymal Cells in the Physiology and Pathology of the Central Nervous System
inferred← citeshttps://doi.org/10.14739/2310-1210.2020.5.214723openalex-snapshot
Clinical-anamnestic characteristic of first-year children with CNS hipoxyc-ischemic injury
inferred← citeshttps://doi.org/10.1523/jneurosci.0585-18.2018openalex-snapshot
A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute to Schwann Cell Remyelination in the Central Nervous System
inferred← citeshttps://doi.org/10.15252/embr.201745294openalex-snapshot
Cross‐talk between monocyte invasion and astrocyte proliferation regulates scarring in brain injury
inferred← citeshttps://doi.org/10.17816/morph.628591openalex-snapshot
Secondary reagents for immunohistochemical research of rat brain
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1210885/v1openalex-snapshot
Spatiotemporal dynamics of molecular expression pattern and intercellular interactions in glial scar responding to spinal cord injury
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2320747/v1openalex-snapshot
UCHL1 inhibited by reactive astrocytes facilitates aggregates clearance to promote neural stem cell activation
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8134246/v1openalex-snapshot
Proteomic profile of Laser-dissected Motoneurons and Ependymal Cell Layer and of Dorsal Root Ganglia after Spinal Cord Injury in Rat
inferred← citeshttps://doi.org/10.26724/2079-8334-2023-4-86-206-211openalex-snapshot
ASTROCYTE RESPONSE TO INTRACEREBRAL HEMORRHAGE IN VARIOUS BRAIN REGIONS AND PHARMACOLOGICAL CORRECTION
inferred← citeshttps://doi.org/10.31083/j.jin2310192openalex-snapshot
Alterations in Endogenous Stem Cell Populations in the Acute Phase of Blast-Induced Spinal Cord Injury
inferred← citeshttps://doi.org/10.3389/ebm.2024.10266openalex-snapshot
Bridging the gap: a translational perspective in spinal cord injury
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1276445openalex-snapshot
Regulation of the JAK/STAT signaling pathway in spinal cord injury: an updated review
inferred← citeshttps://doi.org/10.3389/fnagi.2021.769548openalex-snapshot
Dynamic Diversity of Glial Response Among Species in Spinal Cord Injury
inferred← citeshttps://doi.org/10.3389/fnana.2017.00094openalex-snapshot
The BAF45D Protein Is Preferentially Expressed in Adult Neurogenic Zones and in Neurons and May Be Required for Retinoid Acid Induced PAX6 Expression
inferred← citeshttps://doi.org/10.3389/fncel.2017.00398openalex-snapshot
Spinal Cord Cells from Pre-metamorphic Stages Differentiate into Neurons and Promote Axon Growth and Regeneration after Transplantation into the Injured Spinal Cord of Non-regenerative Xenopus laevis Froglets
inferred← citeshttps://doi.org/10.3389/fncel.2018.00045openalex-snapshot
Musashi and Plasticity of Xenopus and Axolotl Spinal Cord Ependymal Cells
inferred← citeshttps://doi.org/10.3389/fncel.2020.00078openalex-snapshot
Dissecting the Dual Role of the Glial Scar and Scar-Forming Astrocytes in Spinal Cord Injury
inferred← citeshttps://doi.org/10.3389/fncel.2020.00107openalex-snapshot
Regeneration Through in vivo Cell Fate Reprogramming for Neural Repair
inferred← citeshttps://doi.org/10.3389/fncel.2021.703810openalex-snapshot
Diversity of Reactive Astrogliosis in CNS Pathology: Heterogeneity or Plasticity?
inferred← citeshttps://doi.org/10.3389/fncel.2022.1049562openalex-snapshot
Neurogenesis potential of oligodendrocyte precursor cells from oligospheres and injured spinal cord
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.2022.955598openalex-snapshot
Capacity of astrocytes to promote axon growth in the injured mammalian central nervous system
inferred← citeshttps://doi.org/10.3390/biom13050754openalex-snapshot
Ependyma in Neurodegenerative Diseases, Radiation-Induced Brain Injury and as a Therapeutic Target for Neurotrophic Factors
inferred← citeshttps://doi.org/10.3390/cells10081943openalex-snapshot
Activation of Neuroprotective Microglia and Astrocytes at the Lesion Site and in the Adjacent Segments Is Crucial for Spontaneous Locomotor Recovery after Spinal Cord Injury
inferred← citeshttps://doi.org/10.3390/cells10082045openalex-snapshot
Diversity of Adult Neural Stem and Progenitor Cells in Physiology and Disease
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/cells10102783openalex-snapshot
Role of Aldynoglia Cells in Neuroinflammatory and Neuroimmune Responses after Spinal Cord Injury
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/cells11050846openalex-snapshot
Regulating Endogenous Neural Stem Cell Activation to Promote Spinal Cord Injury Repair
inferred← citeshttps://doi.org/10.3390/cells13020148openalex-snapshot
Astroglial Cells: Emerging Therapeutic Targets in the Management of Traumatic Brain Injury
inferred← citeshttps://doi.org/10.3390/cells8091025openalex-snapshot
Potential of Adult Endogenous Neural Stem/Progenitor Cells in the Spinal Cord to Contribute to Remyelination in Experimental Autoimmune Encephalomyelitis
inferred← citeshttps://doi.org/10.3390/ijms23073728openalex-snapshot
Neurogenesis as a Tool for Spinal Cord Injury
inferred← citeshttps://doi.org/10.3410/f.727835419.793573252openalex-snapshot
Faculty Opinions recommendation of Cell biology of spinal cord injury and repair.
inferred← citeshttps://doi.org/10.3410/f.732753027.793557616openalex-snapshot
Faculty Opinions recommendation of Restorative effects of human neural stem cell grafts on the primate spinal cord.
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/10.3410/f.736508557.793573253openalex-snapshot
Faculty Opinions recommendation of Moving beyond the glial scar for spinal cord repair.
inferred← citeshttps://doi.org/10.36468/pharmaceutical-sciences.spl.300openalex-snapshot
To Investigate the Effect of Nerve Growth Factor on Neurons by Establishing the Animal Model of Spinal Cord Injury
inferred← citeshttps://doi.org/10.3791/57727openalex-snapshot
A Neurosphere Assay to Evaluate Endogenous Neural Stem Cell Activation in a Mouse Model of Minimal Spinal Cord Injury
inferred← citeshttps://doi.org/10.4103/1673-5374.338993openalex-snapshot
Purinergic signaling systems across comparative models of spinal cord injury
inferred← citeshttps://doi.org/10.4103/1673-5374.350234openalex-snapshot
Corrigendum: Purinergic signaling systems across comparative models of spinal cord injury
inferred← citeshttps://doi.org/10.4103/1673-5374.380903openalex-snapshot
Visualizing Wallerian degeneration in the corticospinal tract after sensorimotor cortex ischemia in mice
inferred← citeshttps://doi.org/10.4103/1673-5374.389630openalex-snapshot
Resident immune responses to spinal cord injury: role of astrocytes and microglia
inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-24-00068openalex-snapshot
Exosomes originating from neural stem cells undergoing necroptosis participate in cellular communication by inducing TSC2 upregulation of recipient cells following spinal cord injury
inferred← citeshttps://doi.org/10.4103/regenmed.regenmed-d-26-00004openalex-snapshot
AMPA receptor signaling as a driver of ependymal cell activation after spinal cord injury with future directions toward repair
inferred← citeshttps://doi.org/10.47093/2218-7332.2023.14.3.19-27openalex-snapshot
Features of neuroglia at the epicenter of spinal cord contusion injury and at distant areas in mini-pigs
inferred← citeshttps://doi.org/10.5607/en19078openalex-snapshot
Alternatively Polarized Macrophages Regulate the Growth and Differentiation of Ependymal Stem Cells through the SIRT2 Pathway
inferred← citeshttps://doi.org/10.64898/2026.06.17.733052openalex-snapshot
Ciliary integrity defines a central canal repair checkpoint linking microtubule stabilization to spinal cord regeneration
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/10.70675/038d98c5z55ccz4754z9af9z417e3826d282openalex-snapshot
Hétérogénéité de la réactivité astrocytaire dans la maladie d'Alzheimer
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/10.70675/1622b534z9107z40c2z85eez2caf8cc3454copenalex-snapshot
Guidage axonal des cellules ganglionnaires de la rétine en cours de régénération dans le noyau suprachiasmatique
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/10.7150/thno.84133openalex-snapshot
Recent advances in endogenous neural stem/progenitor cell manipulation for spinal cord injury repair
inferred← citeshttps://doi.org/10.7554/elife.95672openalex-snapshot
Targeting resident astrocytes attenuates neuropathic pain after spinal cord injury
inferred← citeshttps://doi.org/10.7554/elife.95672.1openalex-snapshot
Targeting resident astrocytes attenuates neuropathic pain after spinal cord injury
inferred← citeshttps://doi.org/10.7554/elife.95672.2openalex-snapshot
Targeting resident astrocytes attenuates neuropathic pain after spinal cord injury
inferred← citeshttps://doi.org/10.7554/elife.95672.3openalex-snapshot
Targeting resident astrocytes attenuates neuropathic pain after spinal cord injury
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