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CD133 + neural stem cells in the ependyma of mammalian postnatal forebrain

https://doi.org/10.1073/pnas.0710000105
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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/cm.970250104openalex-snapshot
βIV is the major β‐tubulin isotype in bovine cilia
inferredcites →https://doi.org/10.1016/0306-4522(96)00042-5openalex-snapshot
mCD24 expression in the developing mouse brain and in zones of secondary neurogenesis in the adult
inferredcites →https://doi.org/10.1016/0896-6273(93)90281-uopenalex-snapshot
Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone
inferredcites →https://doi.org/10.1016/j.cell.2004.08.012openalex-snapshot
Self-Renewal, Multipotency, and the Existence of Two Cell Populations within an Epithelial Stem Cell Niche
inferredcites →https://doi.org/10.1016/s0092-8674(00)80783-7openalex-snapshot
Subventricular Zone Astrocytes Are Neural Stem Cells in the Adult Mammalian Brain
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)00835-8openalex-snapshot
LeX/ssea-1 Is Expressed by Adult Mouse CNS Stem Cells, Identifying Them as Nonependymal
inferredcites →https://doi.org/10.1038/35102167openalex-snapshot
Stem cells, cancer, and cancer stem cells
inferredcites →https://doi.org/10.1038/nature03128openalex-snapshot
Identification of human brain tumour initiating cells
inferredcites →https://doi.org/10.1038/nature06090openalex-snapshot
Differential Notch signalling distinguishes neural stem cells from intermediate progenitors
inferredcites →https://doi.org/10.1038/nmeth758openalex-snapshot
Neural stem cells and neurospheres—re-evaluating the relationship
inferredcites →https://doi.org/10.1038/nn1473openalex-snapshot
Isolation of neural stem cells from the postnatal cerebellum
inferredcites →https://doi.org/10.1038/nrg952openalex-snapshot
The stem-cell niche theory: lessons from flies
inferredcites →https://doi.org/10.1073/pnas.0510419103openalex-snapshot
Coupling of cell migration with neurogenesis by proneural bHLH factors
inferredcites →https://doi.org/10.1073/pnas.97.26.14720openalex-snapshot
Direct isolation of human central nervous system stem cells
inferredcites →https://doi.org/10.1097/00001756-200006260-00037openalex-snapshot
Visualization of neurogenesis in the central nervous system using nestin promoter-GFP transgenic mice
inferredcites →https://doi.org/10.1126/science.287.5457.1433openalex-snapshot
Mammalian Neural Stem Cells
inferredcites →https://doi.org/10.1126/science.8178174openalex-snapshot
Long-Distance Neuronal Migration in the Adult Mammalian Brain
inferredcites →https://doi.org/10.1146/annurev.cb.11.110195.000343openalex-snapshot
The Biology of Hematopoietic Stem Cells
inferredcites →https://doi.org/10.1182/blood-2003-06-1881openalex-snapshot
Alternative promoters regulate transcription of the gene that encodes stem cell surface protein AC133
inferredcites →https://doi.org/10.1182/blood.v90.12.5013openalex-snapshot
A Novel Five-Transmembrane Hematopoietic Stem Cell Antigen: Isolation, Characterization, and Molecular Cloning
inferredcites →https://doi.org/10.1242/jcs.02439openalex-snapshot
Release of extracellular membrane particles carrying the stem cell marker prominin-1 (CD133) from neural progenitors and other epithelial cells
inferredcites →https://doi.org/10.1523/jneurosci.1108-04.2005openalex-snapshot
Adult Ependymal Cells Are Postmitotic and Are Derived from Radial Glial Cells during Embryogenesis
inferredcites →https://doi.org/10.1523/jneurosci.19-11-04462.1999openalex-snapshot
Adult Mammalian Forebrain Ependymal and Subependymal Cells Demonstrate Proliferative Potential, but only Subependymal Cells Have Neural Stem Cell Characteristics
inferredcites →https://doi.org/10.1523/jneurosci.21-09-03092.2001openalex-snapshot
The Expression Pattern of the Cell Cycle Inhibitor p19INK4dby Progenitor Cells of the Rat Embryonic Telencephalon and Neonatal Anterior Subventricular Zone
inferredcites →https://doi.org/10.1634/stemcells.2004-0232openalex-snapshot
Somatic Stem Cell Marker Prominin‐1/CD133 Is Expressed in Embryonic Stem Cell–Derived Progenitors

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/dvdy.22307openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.20741openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.20812openalex-snapshot
Expression of distinct splice variants of the stem cell marker prominin‐1 (CD133) in glial cells
inferred← citeshttps://doi.org/10.1002/glia.21074openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.21077openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.22413openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.22521openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/glia.22768openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hipo.22200openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jcp.22436openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jnr.23040openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jnr.23480openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/stem.462openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/stem.644openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/stem.699openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wdev.248openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wdev.369openalex-snapshot
Developmental dynamics of neurogenesis and gliogenesis in the postnatal mammalian brain in health and disease: Historical and future perspectives
inferred← citeshttps://doi.org/10.1007/978-1-4614-5894-4_1openalex-snapshot
Prominin-1 (CD133): Molecular and Cellular Features Across Species
inferred← citeshttps://doi.org/10.1007/978-1-4614-5894-4_5openalex-snapshot
Gene Regulation of Prominin-1 (CD133) in Normal and Cancerous Tissues
inferred← citeshttps://doi.org/10.1007/978-1-4614-7696-2_24openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4939-1908-6_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-60761-130-1_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-61779-002-7_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-21030-8_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-007-1709-1_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-10-2723-9_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-13-6325-2_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-99-0846-2_24-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-99-7119-0_24openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-008-8544-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00418-009-0605-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00418-012-1008-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00418-012-1053-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00441-019-03132-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00701-012-1338-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10014-008-0237-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11010-021-04339-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11055-010-9333-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11055-011-9535-1openalex-snapshot
Glial Reaction of the Subventricular Zone of the Telencephalon of the Rat Brain on Modeling of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/s11055-013-9776-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11055-014-9960-zopenalex-snapshot
Extraependymal Ependymocytes in the Rat Brain
inferred← citeshttps://doi.org/10.1007/s11055-015-0160-2openalex-snapshot
Nestin Expression in the Ependymal Cells of the Lateral Ventricles of the Rat Brain during Aging
inferred← citeshttps://doi.org/10.1007/s11055-016-0230-0openalex-snapshot
Structural Organization of the Processes of Ependymocytes Paving the Lateral Ventricles of the Brain
inferred← citeshttps://doi.org/10.1007/s11064-008-9723-8openalex-snapshot
Stem Cell Markers in Gliomas
inferred← citeshttps://doi.org/10.1007/s11064-011-0539-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11427-016-0205-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11427-021-2007-8openalex-snapshot
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Neural stem cell heterogeneity through time and space in the ventricular-subventricular zone
inferred← citeshttps://doi.org/10.1007/s12015-024-10698-3openalex-snapshot
Single-cell Profiling of Reprogrammed Human Neural Stem Cells Unveils High Similarity to Neural Progenitors in the Developing Central Nervous System
inferred← citeshttps://doi.org/10.1007/s12035-019-01777-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12975-017-0556-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13258-010-1001-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-380928-5.10015-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00074-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00079-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00086-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-416012-5.00004-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-416022-4.00012-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-800102-8.00029-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-800781-5.00010-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-800781-5.00015-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-803892-5.00018-8openalex-snapshot
Targeted Therapies for Glioma Stem Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00023-0openalex-snapshot
Neurogenesis in the damaged mammalian brain
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00042-4openalex-snapshot
Ependyma
inferred← citeshttps://doi.org/10.1016/bs.asn.2020.07.001openalex-snapshot
Aging of the ventricular-subventricular zone neural stem cell niche
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.01.004openalex-snapshot
Ependymal cell differentiation, from monociliated to multiciliated cells
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.12.008openalex-snapshot
Gangliosides in Nerve Cell Specification
inferred← citeshttps://doi.org/10.1016/j.acthis.2009.09.007openalex-snapshot
Novel observations on the origin of ependymal cells in the ventricular zone of the rat spinal cord
inferred← citeshttps://doi.org/10.1016/j.addr.2017.07.016openalex-snapshot
Gene regulation in adult neural stem cells. Current challenges and possible applications
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.09.002openalex-snapshot
Signaling mechanisms regulating adult neural stem cells and neurogenesis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.04.181openalex-snapshot
Deficiency of Ttyh1 downstream to Notch signaling results in precocious differentiation of neural stem cells
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.04.014openalex-snapshot
Neural repair by NT3-chitosan via enhancement of endogenous neurogenesis after adult focal aspiration brain injury
inferred← citeshttps://doi.org/10.1016/j.brainres.2010.01.056openalex-snapshot
Endothelinergic cells in the subependymal region of mice
inferred← citeshttps://doi.org/10.1016/j.brainres.2010.11.040openalex-snapshot
EGF induces CREB and ERK activation at the wall of the mouse lateral ventricles
inferred← citeshttps://doi.org/10.1016/j.brainres.2012.10.047openalex-snapshot
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An Integrated In Vitro and In Vivo High-Throughput Screen Identifies Treatment Leads for Ependymoma
inferred← citeshttps://doi.org/10.1016/j.cell.2015.04.001openalex-snapshot
Single-Cell Transcriptome Analyses Reveal Signals to Activate Dormant Neural Stem Cells
inferred← citeshttps://doi.org/10.1016/j.cell.2018.03.063openalex-snapshot
Single-Cell Transcriptomics and Fate Mapping of Ependymal Cells Reveals an Absence of Neural Stem Cell Function
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.03.037openalex-snapshot
Neonatal Subventricular Zone Neural Stem Cells Release Extracellular Vesicles that Act as a Microglial Morphogen
inferred← citeshttps://doi.org/10.1016/j.clbc.2017.01.007openalex-snapshot
Expression Profiling of Clinical Specimens Supports the Existence of Neural Progenitor-Like Stem Cells in Basal Breast Cancers
inferred← citeshttps://doi.org/10.1016/j.conb.2008.04.001openalex-snapshot
Development of neural stem cell in the adult brain
inferred← citeshttps://doi.org/10.1016/j.conb.2018.07.006openalex-snapshot
Regulation of neurogenesis in the adult and aging brain
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.diff.2019.07.001openalex-snapshot
Improved differentiation of human enriched CD133+CD24+ renal progenitor cells derived from embryonic stem cell with embryonic mouse kidney-derived mesenchymal stem cells co-culture
inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2011.10.029openalex-snapshot
Increased membrane shedding – indicated by an elevation of CD133-enriched membrane particles – into the CSF in partial epilepsy
inferred← citeshttps://doi.org/10.1016/j.exer.2009.06.019openalex-snapshot
Microglia derived IL-6 suppresses neurosphere generation from adult human retinal cell suspensions
inferred← citeshttps://doi.org/10.1016/j.gendis.2024.101398openalex-snapshot
The subventricular zone structure, function and implications for neurological disease
inferred← citeshttps://doi.org/10.1016/j.gep.2009.06.002openalex-snapshot
fezf2 expression delineates cells with proliferative potential and expressing markers of neural stem cells in the adult zebrafish brain
inferred← citeshttps://doi.org/10.1016/j.isci.2026.117476openalex-snapshot
Integrated 3D light sheet and 2D multiplex imaging for deep histological characterization of somatic mouse glioblastoma
inferred← citeshttps://doi.org/10.1016/j.jfma.2013.12.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mcn.2010.04.003openalex-snapshot
Multipotent precursors in the anterior and hippocampal subventricular zone display similar transcription factor signatures but their proliferation and maintenance are differentially regulated
inferred← citeshttps://doi.org/10.1016/j.mcn.2011.02.001openalex-snapshot
Unique gene expression patterns indicate microglial contribution to neural stem cell recovery following irradiation
inferred← citeshttps://doi.org/10.1016/j.nbd.2017.07.010openalex-snapshot
Early ciliary and prominin-1 dysfunctions precede neurogenesis impairment in a mouse model of type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.neulet.2010.03.019openalex-snapshot
Heterotopically transplanted CVO neural stem cells generate neurons and migrate with SVZ cells in the adult mouse brain
inferred← citeshttps://doi.org/10.1016/j.neulet.2013.07.021openalex-snapshot
Cerebellar neural stem cells differentiate into two distinct types of astrocytes in response to CNTF and BMP2
inferred← citeshttps://doi.org/10.1016/j.neulet.2015.02.023openalex-snapshot
Long-term tracing of the BrdU label-retaining cells in adult rat brain
inferred← citeshttps://doi.org/10.1016/j.neuro.2016.03.023openalex-snapshot
Trimethyltin intoxication induces the migration of ventricular/subventricular zone cells to the injured murine hippocampus
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.05.001openalex-snapshot
Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.05.004openalex-snapshot
Lake-Front Property: A Unique Germinal Niche by the Lateral Ventricles of the Adult Brain
inferred← citeshttps://doi.org/10.1016/j.neuron.2014.02.039openalex-snapshot
Prospective Identification and Purification of Quiescent Adult Neural Stem Cells from Their In Vivo Niche
inferred← citeshttps://doi.org/10.1016/j.neuron.2014.04.025openalex-snapshot
The Quintessence of Quiescence
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.06.065openalex-snapshot
Ependymal stem cells divide asymmetrically and transfer progeny into the subventricular zone when activated by injury
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2010.04.058openalex-snapshot
Characterization of novel monoclonal antibodies able to identify neurogenic niches and arrest neurosphere proliferation and differentiation
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.01.019openalex-snapshot
Allopregnanolone enhances the neurogenesis of midbrain dopaminergic neurons in APPswe/PSEN1 mice
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2017.03.045openalex-snapshot
Newborn dopaminergic neurons are associated with the migration and differentiation of SVZ-derived neural progenitors in a 6-hydroxydopamin-injected mouse model
inferred← citeshttps://doi.org/10.1016/j.omtm.2021.09.017openalex-snapshot
Seven-year follow-up of durability and safety of AAV CNS gene therapy for a lysosomal storage disorder in a large animal
inferred← citeshttps://doi.org/10.1016/j.omtn.2018.12.009openalex-snapshot
Generation of Genetically Stable Human Direct-Conversion-Derived Neural Stem Cells Using Quantity Control of Proto-oncogene Expression
inferred← citeshttps://doi.org/10.1016/j.phrs.2016.04.009openalex-snapshot
Inhibiting angiotensin-converting enzyme promotes renal repair by modulating progenitor cell activation
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2013.07.003openalex-snapshot
Shades of gray: The delineation of marker expression within the adult rodent subventricular zone
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.06.005openalex-snapshot
Neural stem cell heterogeneity in the mammalian forebrain
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.147386openalex-snapshot
Single-cell RNA sequencing reveals adverse effects of paraquat on the fate commitment of murine neural stem cells
inferred← citeshttps://doi.org/10.1016/j.scr.2010.05.001openalex-snapshot
A novel classification of quiescent and transit amplifying adult neural stem cells by surface and metabolic markers permits a defined simultaneous isolation
inferred← citeshttps://doi.org/10.1016/j.scr.2013.09.002openalex-snapshot
Neural stem cell isolation from the whole mouse brain using the novel FABP7-binding fluorescent dye, CDr3
inferred← citeshttps://doi.org/10.1016/j.semcancer.2012.06.005openalex-snapshot
Renal stem cells and their implications for kidney cancer
inferred← citeshttps://doi.org/10.1016/j.semradonc.2008.11.001openalex-snapshot
Cancer Stem Cells in Solid Tumors: An Overview
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.stem.2008.08.011openalex-snapshot
The Niche Revealed
inferred← citeshttps://doi.org/10.1016/j.stem.2009.03.003openalex-snapshot
SSEA-1 Is an Enrichment Marker for Tumor-Initiating Cells in Human Glioblastoma
inferred← citeshttps://doi.org/10.1016/j.stem.2009.08.017openalex-snapshot
High Levels of Id1 Expression Define B1 Type Adult Neural Stem Cells
inferred← citeshttps://doi.org/10.1016/j.stem.2010.11.017openalex-snapshot
In Vivo Fate Mapping and Expression Analysis Reveals Molecular Hallmarks of Prospectively Isolated Adult Neural Stem Cells
inferred← citeshttps://doi.org/10.1016/j.stem.2011.04.007openalex-snapshot
Eyes Wide Open: A Critical Review of Sphere-Formation as an Assay for Stem Cells
inferred← citeshttps://doi.org/10.1016/j.stemcr.2014.01.004openalex-snapshot
In Vivo Targeting of Adult Neural Stem Cells in the Dentate Gyrus by a Split-Cre Approach
inferred← citeshttps://doi.org/10.1016/j.stemcr.2017.02.012openalex-snapshot
Synergic Functions of miRNAs Determine Neuronal Fate of Adult Neural Stem 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.tem.2012.09.002openalex-snapshot
Renal progenitors in non-diabetic and diabetic nephropathies
inferred← citeshttps://doi.org/10.1016/j.tins.2009.01.007openalex-snapshot
Decision by division: making cortical maps
inferred← citeshttps://doi.org/10.1016/j.tranon.2017.01.008openalex-snapshot
Analysis of Chemopredictive Assay for Targeting Cancer Stem Cells in Glioblastoma Patients
inferred← citeshttps://doi.org/10.1016/j.yexcr.2013.08.028openalex-snapshot
FoxJ1-expressing cells contribute to neurogenesis in forebrain of adult rats: Evidence from in vivo electroporation combined with piggyBac transposon
inferred← citeshttps://doi.org/10.1038/cr.2008.270openalex-snapshot
Promoter hypomethylation regulates CD133 expression in human gliomas
inferred← citeshttps://doi.org/10.1038/cr.2009.56openalex-snapshot
Adult neural stem cells in the mammalian central nervous system
inferred← citeshttps://doi.org/10.1038/eye.2008.380openalex-snapshot
Influence of microglia on retinal progenitor cell turnover and cell replacement
inferred← citeshttps://doi.org/10.1038/gt.2008.165openalex-snapshot
Neural stem cells target intracranial glioma to deliver an oncolytic adenovirus in vivo
inferred← citeshttps://doi.org/10.1038/gt.2009.58openalex-snapshot
Analysis of neuronal proliferation, migration and differentiation in the postnatal brain using equine infectious anemia virus-based lentiviral vectors
inferred← citeshttps://doi.org/10.1038/jid.2012.196openalex-snapshot
CD133 Is a Marker for Long-Term Repopulating Murine Epidermal Stem Cells
inferred← citeshttps://doi.org/10.1038/nature09631openalex-snapshot
Ependymal cells of chordate larvae are stem-like cells that form the adult nervous system
inferred← citeshttps://doi.org/10.1038/nn.2268openalex-snapshot
Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke
inferred← citeshttps://doi.org/10.1038/nn0309-243openalex-snapshot
Notch keeps ependymal cells in line
inferred← citeshttps://doi.org/10.1038/nrn2571openalex-snapshot
Identity crisis for adult periventricular neural stem cells: subventricular zone astrocytes, ependymal cells or both?
inferred← citeshttps://doi.org/10.1038/nrneph.2012.290openalex-snapshot
Renal progenitors: an evolutionary conserved strategy for kidney regeneration
inferred← citeshttps://doi.org/10.1038/nrneph.2014.1openalex-snapshot
The emergence of the glomerular parietal epithelial cell
inferred← citeshttps://doi.org/10.1038/s41467-018-03812-wopenalex-snapshot
Uncovering inherent cellular plasticity of multiciliated ependyma leading to ventricular wall transformation and hydrocephalus
inferred← citeshttps://doi.org/10.1038/s41698-019-0106-1openalex-snapshot
Off-target effect of the BMI1 inhibitor PTC596 drives epithelial-mesenchymal transition in glioblastoma multiforme
inferred← citeshttps://doi.org/10.1038/srep00250openalex-snapshot
Growth hormone responsive neural precursor cells reside within the adult mammalian brain
inferred← citeshttps://doi.org/10.1038/srep05506openalex-snapshot
Targeted gene transfer into ependymal cells through intraventricular injection of AAV1 vector and long-term enzyme replacement via the CSF
inferred← citeshttps://doi.org/10.1038/srep45656openalex-snapshot
Single-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types
inferred← citeshttps://doi.org/10.1039/c8cc08107gopenalex-snapshot
Advances in the design of cell-permeable fluorescent probes for applications in live cell imaging
inferred← citeshttps://doi.org/10.1053/j.seminoncol.2009.05.003openalex-snapshot
Understanding the Origins of Gliomas and Developing Novel Therapies: Cerebrospinal Fluid and Subventricular Zone Interplay
inferred← citeshttps://doi.org/10.1063/5.0027211openalex-snapshot
Bioengineering the neurovascular niche to study the interaction of neural stem cells and endothelial cells
inferred← citeshttps://doi.org/10.1073/pnas.0711637105openalex-snapshot
Revisiting neural stem cell identity
inferred← citeshttps://doi.org/10.1073/pnas.2014389117openalex-snapshot
High-resolution mouse subventricular zone stem-cell niche transcriptome reveals features of lineage, anatomy, and aging
inferred← citeshttps://doi.org/10.1074/jbc.m112.398834openalex-snapshot
Disruption of Wave-associated Rac GTPase-activating Protein (Wrp) Leads to Abnormal Adult Neural Progenitor Migration Associated with Hydrocephalus
inferred← citeshttps://doi.org/10.1074/jbc.m114.618686openalex-snapshot
γ-Aminobutyric A Receptor (GABAAR) Regulates Aquaporin 4 Expression in the Subependymal Zone
inferred← citeshttps://doi.org/10.1080/09553002.2022.2055802openalex-snapshot
Response of murine neural stem/progenitor cells to gamma-neutron radiation
inferred← citeshttps://doi.org/10.1088/1361-6528/aa96ebopenalex-snapshot
Engineered core–shell magnetic nanoparticle for MR dual-modal tracking and safe magnetic manipulation of ependymal cells in live rodents
inferred← citeshttps://doi.org/10.1089/biores.2015.0011openalex-snapshot
Potential Reparative Role of Resident Adult Renal Stem/Progenitor Cells in Acute Kidney Injury
inferred← citeshttps://doi.org/10.1089/scd.2008.0144openalex-snapshot
Isolation of Human Multipotent Neural Progenitors from Adult Filum Terminale
inferred← citeshttps://doi.org/10.1089/scd.2011.0274openalex-snapshot
JAM-C is an Apical Surface Marker for Neural Stem Cells
inferred← citeshttps://doi.org/10.1089/scd.2011.0279openalex-snapshot
Ischemia-Induced Neural Stem/Progenitor Cells in the Pia Mater Following Cortical Infarction
inferred← citeshttps://doi.org/10.1089/scd.2012.0660openalex-snapshot
A Novel Fluorescent Reporter CDy1 Enriches for Neural Stem Cells Derived from the Murine Brain
inferred← citeshttps://doi.org/10.1089/scd.2023.0196openalex-snapshot
R-Loop Defines Neural Stem/Progenitor Cells During Mouse Neurodevelopment
inferred← citeshttps://doi.org/10.1093/brain/awu155openalex-snapshot
Temporal dynamics of hippocampal neurogenesis in chronic neurodegeneration
inferred← citeshttps://doi.org/10.1093/braincomms/fcaa171openalex-snapshot
Isolation and culture of functional adult human neurons from neurosurgical brain specimens
inferred← citeshttps://doi.org/10.1093/glycob/cwp149openalex-snapshot
Characterization of GD3 ganglioside as a novel biomarker of mouse neural stem cells
inferred← citeshttps://doi.org/10.1093/jrr/rrs078openalex-snapshot
In vitro stemness characterization of radio-resistant clones isolated from a medulloblastoma cell line ONS-76
inferred← citeshttps://doi.org/10.1093/med/9780199729692.003.0003openalex-snapshot
Neural Stem Cells
inferred← citeshttps://doi.org/10.1093/med/9780199729692.003.0005openalex-snapshot
Neurogenesis in the Adult Subventricular Zone and Olfactory Bulb
inferred← citeshttps://doi.org/10.1093/stmcls/sxaf015openalex-snapshot
Unlocking the potential of regionally activated injury/ischemia-induced stem cells for neural regeneration
inferred← citeshttps://doi.org/10.1097/mnh.0b013e32833680dcopenalex-snapshot
Regeneration and the kidney
inferred← citeshttps://doi.org/10.1097/nen.0b013e3181b44a5aopenalex-snapshot
Disruption of the Neurogenic Niche in the Subventricular Zone of Postnatal Hydrocephalic hyh Mice
inferred← citeshttps://doi.org/10.1098/rsob.240035openalex-snapshot
Beyond amyloid and tau: rethinking Alzheimer’s disease through less explored avenues
inferred← citeshttps://doi.org/10.1100/tsw.2011.42openalex-snapshot
Glioblastoma Multiforme Stem Cells
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