Cited by 927Neurogenesis and neuroplasticity mechanismsMultiple Sclerosis Research StudiesNeuroinflammation and Neurodegeneration Mechanisms

The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.

NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS

Dawson, M·2003·Molecular and Cellular Neuroscience

DOI 10.1016/s1044-7431(03)00210-0

Open this paper in CoChat — free account

Abstract

Glial progenitor cells of the developing CNS committed to the oligodendrocyte lineage (OPCs) express the chondroitin sulfate proteoglycan, NG2. A proportion of OPCs fail to differentiate past the stage at which they express NG2 and the lipid antigen O4 and persist in the adult CNS in a phenotypically immature form. However, the physiological function of NG2(+) cells in the adult CNS is unknown. Using antibodies against NG2 we show that NG2 is expressed by a distinct cell population in the mature CNS with the homogeneous antigenic phenotype of oligodendrocyte progenitors. The morphology of NG2(+) OPCs varies from region to region, reflecting the different structural environments, but they appear to represent a homogeneous population within any one gray or white matter region. A study of nine CNS regions showed that NG2(+) OPCs are numerous throughout the CNS and numbers in the white matter are only 1.5 times that in the gray. Whereas the ratio of OPCs to myelinating oligodendrocytes in the spinal cord gray and white matter approximates 1:4, gray matter regions of the forebrain have a 1:1 ratio, a phenomenon that will have consequences for oligodendrocyte replacement following demyelination. BrdU incorporation experiments showed that NG2(+) cells are the major dividing cell population of the adult rat CNS. Since very little apoptosis was detected and BrdU became increasingly present in oligodendrocytes after a 10-day pulse chase, with a concomitant decrease in NG2(+) BrdU incorporating cells, we suggest that the size of the oligodendrocyte population may actually increase during adult life.

Integrity signals

Registry

Crossref · 10.1016/s1044-7431(03)00210-0

Cites

43 of 43 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cell death and control of cell survival in the oligodendrocyte lineage
Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345
Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus
Bergles, D. E., Roberts, J. D. B., Somogyi, P., & Jahr, C. E. (2000) · Nature · doi:10.1038/35012083 · Cited by 1,062
Why does remyelination fail in multiple sclerosis?
Franklin, R. J. M. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn917 · Cited by 862
Proliferation and Differentiation of Progenitor Cells Throughout the Intact Adult Rat Spinal Cord
Horner, P. J., Power, A. E., Kempermann, G., Kuhn, H. G., Palmer, T. D., Winkler, J., Thal, L. J., & Gage, F. H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02218.2000 · Cited by 777
NG2-Positive Oligodendrocyte Progenitor Cells in Adult Human Brain and Multiple Sclerosis Lesions
Chang, A., Nishiyama, A., Peterson, J. W., Prineas, J. W., & Trapp, B. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06404.2000 · Cited by 711
The oligodendrocyte precursor cell in health and disease
Levine, J. M., Reynolds, R., & Fawcett, J. W. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01691-x · Cited by 673
MYELINATION IN RAT BRAIN: CHANGES IN MYELIN COMPOSITION DURING BRAIN MATURATION1
Norton, W. T., & Poduslo, S. E. (1973) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1973.tb07520.x · Cited by 668
The Age-Related Decrease in CNS Remyelination Efficiency Is Attributable to an Impairment of Both Oligodendrocyte Progenitor Recruitment and Differentiation
Sim, F. J., Zhao, C., Penderis, J., & Franklin, R. J. M. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02451.2002 · Cited by 625
Oligodendrocyte Population Dynamics and the Role of PDGF In Vivo
Calver, A. R., Hall, A. C., Yu, W., Walsh, F. S., Heath, J. K., Betsholtz, C., & Richardson, W. D. (1998) · Neuron · doi:10.1016/s0896-6273(00)80469-9 · Cited by 516
A singularity of PDGF alpha-receptor expression in the dorsoventral axis of the neural tube may define the origin of the oligodendrocyte lineage
Pringle, N. P., & Richardson, W. D. (1993) · Development · doi:10.1242/dev.117.2.525 · Cited by 510

Show all 43 references

Sorted by citations

Items 801–900 of 924

FUNCTIONS OF ADULT OLIGODENDROCYTE PRECURSOR CELLS IN BRAIN INJURY AND REPAIR
Levine, J. M. (2005) · Cited by 1
Effects of Brain Injury on Primary Cilia of Glial Cells and Pericytes
Coronel, M. V. (2016) · University of North Texas Digital Library (University of North Texas) · doi:10.12794/metadc955100 · Cited by 1
Damage and Repair in Experimental Cortical Demyelination
Garea‐Rodríguez, E. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3318 · Cited by 1
Oligodendrocyte generation and maturation in the hippocampus may be a target of fluoxetine for delaying cognitive dysfunction during early Alzheimer’s diseasePreprint
Zhang, Y., Chao, F., Zhang, L., Zhou, C., Jiang, L. H., Tang, J., Liang, X., Fan, J., Dou, X., & Tang, Y. C. (2020) · doi:10.21203/rs.2.24601/v1 · Cited by 1
Functional properties of the plasma membrane of human glioma initiating cells
Barrantes‐Freer, A. (2012) · doi:10.53846/goediss-3284 · Cited by 1
Combination-Based Drug Screening for Induced Oligodendrocyte Differentiation Enables Mechanistic Insight and Identifies Optimal Drug Pairs for RemyelinationPreprint
Beyer, B. A., Sul, A., Miller, J., Neumann, B., Plaisted, W. C., Kondo, T., Franklin, R. J. M., & Lairson, L. L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.11.548469 · Cited by 1
The role of hypoxia in neuroinflammatory disease
Desai, R. (2013) · UCL Discovery (University College London) · Cited by 1
Implication du canal potassium Kv3.1 dans la lipotoxicité du 7-cétocholestérol, 24S-hydroxycholestérol et de l’acide tétracosanoïque sur des cellules nerveuses 158N et BV-2 : Etude des relations entre Kv3.1, homéostasie potassique et métabolisme peroxysomal dans la maladie d’Alzheimer
Bezine, M. (2017) · theses.fr (ABES) · doi:10.70675/a634c389z7b07z4830zb56dzbf7b53a56944 · Cited by 1
Targeting UBE3A and downstream estrogen receptor-β signaling to restore oligodendroglial homeostasis in Angelman syndromePreprint
Yang, X., Mayoral, S., Jiang, Y.-H., Marshall, J., & Huang, Y. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.21.726878 · Cited by 1
The effect of dopamine and its agonist pramipexole on oligodendrocytes in culture and in the cuprizone mouse model
Richter, J. S. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4342 · Cited by 1
The Role of Transcription Factors in Regulating Adult Neurogenesis after Excitotoxic Brain Injury
Jones, K. (2012) · ResearchSpace (University of Auckland)
Endogenous Neural Stem/Progenitor Cells and Regenerative Responses to Brain Injury
Dizon, M. L. V. (2012) · InTech eBooks · doi:10.5772/30210
Thyroid Hormone Actions on Glioma Cells
Zhou, M., Kimelberg, H. K., Davis, F. B., & Davis, P. J. (2011) · Wiley eBooks · doi:10.1002/9783527633968.ch16
Brain Regeneration - in vitro and in vivo studies of exercise-related effects on brain plasticity
Bull, C. (2008) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Charakterisierung von Astrozyten im respiratorischen Netzwerk
Graß, D. (2005) · doi:10.53846/goediss-1209
Regulation der zellulären Plastizität in der adulten Substantia nigra: Effekte von reizreicher Umgebung und physischer Aktivität
Siebert, E. (2008) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-15548
Etude de la voie de signalisation Sonic Hedgehog et du contrôle de la prolifération cellulaire dans le cerveau mature de rongeurs
Loulier, K., & Ruat, M. (2005) · OpenGrey (Institut de l'Information Scientifique et Technique)
Lithium and brain plasticity - studies on glial cell changes and electroconvulsive treatment-induced amnesia in rats
Orre, K. (2013) · Lund University Publications (Lund University)
Links Between Injury-Induced Brain Remodeling and Oncogenesis
El-Habr, E. A., & Junier, M. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4899-7399-3_10
Neural stem cells in development and cancer
Waldhuber, M. (2008) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.9221
Properties of nestin-GFP-expressing cells in different regions of adult murine brain
Wang, L. (2005) · doi:10.18452/15299
Morphological and functional studies of cells derived from post-natal neural stem cells
Rowe, E. (2005) · doi:10.31274/rtd-180813-11129
Reactive Glia and Proliferation of Ependyma in Guinea Pigs with Experimental Allergic Encephalomyelitis.
Noorulla, M., & Gc, S. (2014) · Research and reviews : journal of medical and health sciences/Research an reviews : journal of medical and health sciences
HIV Coreceptors and Their Roles in Leukocyte Trafficking During Neuroinflammatory Diseases
Klein, R. S., & McCandless, E. E. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0793-6_6
MOLECULAR SUBCLASSIFICATION, STEM CELL MARKERS AND GROWTH REGULATORY PATHWAYS IN GLIOMAS
Olausson, K. H. (2015) · Figshare
Untangling regulatory cues that control cell cycle progression and fate specification in the oligodendroglial lineage
Belachew, S. M. (2005) · Open Repository and Bibliography (University of Liège)
Challenging the Dogma: Reevaluating the Role of Astrocyte Calcium Signaling in Physiology
Petravicz, J. (2010) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/zc2z-3e62
Neuronal regeneration in forebrain ischemia model
Kawahara, N. (2014) · Nosotchu · doi:10.3995/jstroke.36.216
Biological Mechanisms of Dynamic White Matter AlterationsPreprint
Tromp, D. (2016) · doi:10.15200/winn.146135.50625
Exploring the Effect of Novel Small Molecules on Oligodendrocyte Precursor Proliferation
Sakya, S. (2016) · OpenCommons - UConn (University of Connecticut)
Stem Cell Biology in the Central Nervous System
Horner, P. J., & Nutt, S. E. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00006-x
Principles of Translation of Biologic Therapies in Spinal Cord Injury
Guest, J. D. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00270-7
Mechanisms of Plasticity, Remodeling and Recovery
Zhang, Z. G., & Chopp, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-29544-4.00011-6
The adult human oligodendrocyte precursor cell: a key player in myelin repair
Rist, J. M., & Franklin, R. J. M. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781698.007
Characterization, differentiation and therapeutic application of NG2+ progenitor cells
Ju, P. J. (2013) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/53654
Novel Oncogenic Drivers in Pediatric Gliomagenesis
Diaz, A. (2016) · doi:10.21007/etd.cghs.2016.0396
The oligodendrocyte "processosome": novel regulators of differentiation and myelination
da Silva, A. F. B. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/1zbe-vq61
Stem Cells and Neurogenesis for Brain Development, Degeneration and Therapy
Peer, J., Zhang, H., Peng, H., Vance, K. E., Huang, Y., & Zheng, J. (2016) · Springer eBooks · doi:10.1007/978-3-319-44022-4_15
Pathogenic mechanisms in multiple system atrophy: a study of oligodendroglial pathology
Asi, Y. T. (2014) · UCL Discovery (University College London)
Deficiency of Myelin Proteins during Brain Development in Fragile X Mice
Jiang, D. L. (2015) · TSpace (University of Toronto)
Post-transcriptional Regulatory Mechanisms Controlling Development of Murine Cerebral Cortical Precursors
Amadei, G. (2016) · TSpace (University of Toronto)
Conductive polymer nanofibers as a platform for both stimulating and measuring differentiation in oligodendrocyte progenitor cells
Lowe, A. L. (2017) · Wellesley College Digital RepositoryWellesley (Wellesley College)
Pten Function in Postnatal Brain Development and Tumorigenesis
Zhu, G. G. (2011) · doi:10.21007/etd.cghs.2011.0383
Modulation of remyelination by adaptive inflammation and electrical stimulation
Kunz, P. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6357
Stereological Analysis of Oligodendrocyte Progenitor Cells In the Adult Mouse Brain
Boulanger, J. J. (2017) · uO Research (University of Ottawa) · doi:10.20381/ruor-20632
The glycosyltransferase EXTL2 and its regulation of remyelination and neuroinflammation
Pu, Y. (2019) · doi:10.11575/prism/36358
Placebo Controlled Double Blind Crossover Trial of Metformin for Brain Repair in Children Treated with Cranial Radiation for Brain Tumours
Ayoub, R. (2018) · TSpace (University of Toronto)
Origin and development of oligodendroglioma
Volovetz, J., Bayık, D., & Lathia, J. D. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813158-9.00007-4 · Cited by 1
Demyelinating conditions regulated by ROS pathways outside and inside the brain
Carlström, K. E. (2020) · Figshare
Genomic Instability and the Oncohistone H3K27M Drive Gliomagenesis in a Murine Model
Pribyl, L. J. (2020) · doi:10.21007/etd.cghs.2020.0515
Investigating age and differentiation stage differences in human oligodendrocyte lineage cells via single-cell and bulk RNA sequencing analysis
Luo, J. X. X. (2021) · eScholarship@McGill (McGill) · doi:10.82308/21669
Individual roles of p53 and NF1 in OPC Competition and Gliomagenesis
Gonzalez, P. P. (2017) · doi:10.18130/v39s69
References
(2006) · Elsevier eBooks · doi:10.1016/b978-0-443-07271-0.50022-7
Bibliography
(2016) · Elsevier eBooks · doi:10.1016/b978-0-12-812972-2.50025-8
Oligodendrocyte responses after spinal cord injury.
Wei, G. (2021) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/3682
A2B Adenosine Receptor as a New and Attractive Target to Treat Brain Ischemia or Demyelination
Cherchi, F., Venturini, M., Dettori, I., Pedata, F., Coppi, E., & Pugliese, A. M. (2022) · Topics in medicinal chemistry · doi:10.1007/7355_2022_153
Data from Olig1/2-Expressing Intermediate Lineage Progenitors Are Predisposed to PTEN/p53-Loss–Induced Gliomagenesis and Harbor Specific Therapeutic Vulnerabilities
Verma, R., Chen, X., Xin, D. E., Luo, Z., Ogurek, S., Xin, M., Rao, R., Berry, K., & Lu, Q. R. (2023) · doi:10.1158/0008-5472.c.6514394.v1
Data from Olig1/2-Expressing Intermediate Lineage Progenitors Are Predisposed to PTEN/p53-Loss–Induced Gliomagenesis and Harbor Specific Therapeutic Vulnerabilities
Verma, R., Chen, X., Xin, D. E., Luo, Z., Ogurek, S., Xin, M., Rao, R., Berry, K., & Lu, Q. R. (2023) · doi:10.1158/0008-5472.c.6514394
An integrated single-cell transcriptome landscape of postnatal mouse hypothalamusPreprint
Junaid, M., Choe, H. K., Kondoh, K., Lee, E. J., & Lim, S. B. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.13.536811
Relieving the epigenetic blockade in progressive ms
Tiane, A. (2023) · Research Publications (Maastricht University) · doi:10.26481/dis.20230606at
Role of MeCP2 in oligodendrocyte lineage cells in Rett syndrome: review and inference
Zhang, Z., Li, P., & Chen, Y. (2023) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2023.13
Glial Cells During the Life Cycle
Walz, W. (2023) · Springer eBooks · doi:10.1007/978-3-031-48105-5_3
The effects of microgravity on cellular elements of the central nervous system - astrocytes, microglia, neurons, oligodendrocytes, and oligodendrocyte precursor cells
Smith, J. K. (2024) · International Journal of Frontline Research and Reviews · doi:10.56355/ijfrr.2024.2.1.0021
In Vivo Viral Gene Delivery to Manipulate Functional Properties of AMPA Receptors in Oligodendrocyte Lineage Cells
Chen, T., Kula, B., & Kukley, M. (2024) · Neuromethods · doi:10.1007/978-1-0716-3742-5_15
Directed differentiation of functional corticospinal-like neurons from endogenous SOX6+/NG2+ cortical progenitors
Özkan, A., Padmanabhan, H. K., Shipman, S. L., Azim, E., Kumar, P., Sadegh, C., Başak, A. N., & Macklis, J. D. (2026) · eLife · doi:10.1101/2024.04.21.590488
Directed differentiation of functional corticospinal-like neurons from endogenous SOX6+/NG2+ cortical progenitorsPreprint
Özkan, A., Padmanabhan, H. K., Shipman, S. L., Azim, E., Kumar, P., Sadegh, C., Başak, A. N., & Macklis, J. D. (2024) · eLife · doi:10.7554/elife.100340.1
Mutant IDH impairs chromatin binding by PDGFB to promote chromosome instabilityPreprint
Curry, R. N., McDonald, M. F., He, P., Lozzi, B., Ko, Y., O’Reilly, I., Rosenbaum, A., Kwon, W., Fahim, L. E., Marcus, J. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.20.639365
The modulation of the blood–brain barrier by focused ultrasound stimulates oligodendrogenesis
Noseworthy, K., Silburt, J., Apa, A., Rubio-Atonal, L. F., Wu, S.-K., Schuurmans, C. J., Hynynen, K., & Aubert, I. (2026) · Acta Neuropathologica Communications · doi:10.1186/s40478-026-02364-1
Morphology of Oligodendroglial Cells
Butt, A. M., Willis, A., Stevens, R., Hunter, I., & Nishiyama, A. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-87919-7_5
Directed differentiation of functional corticospinal-like neurons from endogenous SOX6+/NG2+ cortical progenitorsPreprint
Özkan, A., Padmanabhan, H. K., Shipman, S. L., Azim, E., Kumar, P., Sadegh, C., Başak, A. N., & Macklis, J. D. (2025) · eLife · doi:10.7554/elife.100340.2
Neural Stem Cells
Kempermann, G. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780197519233.003.0003
Screening for Candidate Brain Tumor Genes : Identifying Genes that Cooperate with Platelet-Derived Growth Factor in Glioma Development and Progression
Johansson, F. (2006) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Additional file 1 of Acute brain injuries trigger microglia as an additional source of the proteoglycan NG2
Huang, W., Bai, X., Meyer, E., & Scheller, A. (2020) · Figshare · doi:10.6084/m9.figshare.12864347
Additional file 1 of Single-nucleus transcriptomic analysis reveals the relationship between gene expression in oligodendrocyte lineage and major depressive disorder
Xie, Y., Chen, L., Wang, L., Liu, T., Zheng, Y., Si, L., Ge, H., Xu, H., Xiao, L., & Wang, G. (2024) · Figshare · doi:10.6084/m9.figshare.26673627
Oligodendrocyte progenitor cells are promoted in the neurogenic niches of the juvenile mouse brain during viral infectionPreprint
Kamte, Y. S., Potosnak, C. E., London, N. M., Singh, V. R., Thompson, K., Fadare, A., Chandwani, M. N., Leak, R. K., & O’Donnell, L. A. (2026) · Research Square · doi:10.21203/rs.3.rs-8563506/v1
Critical role of cell competition in gliomagenesisPreprint
Jiang, Y., Ahn, R., Huang, A., Gonzalez, P. P., Kim, J., Zhang, G., Liu, Z., He, Z., Dudley, L. A., Patel, K. S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.15.699808
Diverging routes of oligodendrocyte recruitment in adaptive and regenerative myelinationPreprint
Hoodless, L. J., Bispo, P., Collins, E. M., Baldacchino, K., Auer, F., & Czopka, T. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.04.703508
Advances in rodent oligodendrocyte precursor cells isolation and culture: From traditional methods to modern approaches
Akbari, H., Kashani, I. R., Yazdi, F. R., Pasbakhsh, P., & Mojaverrostami, S. (2026) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2026.110706
Selective Cortical Myelination Reflects Axon-Driven Progression of the BCAS1-positive Oligodendrocyte LineagePreprint
Zi, H., Goldbrunner, A., Askari, S., Eichenseer, K., Misgeld, T., & Snaidero, N. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.15.705957
Etude du rôle des héparans sulfates protéoglycanes dans la mobilisation post-lesionnelle des progéniteurs oligodendrocytaires chez la souris adulte
Macchi, M. (2015) · theses.fr (ABES) · doi:10.70675/8a0cff28z4ed8z4fffz803czec7420fd87a4
Etablissement d'un protocole haut débit d'acquisition et d'analyse d'images pour les études précliniques par microscopie bi-photonique intravitale multispectrale : application à l'étude de la neuroinflammation provoquée par un modèle murin de sclérose en plaque
Jaouën, A. (2017) · doi:10.70675/32a64946zb1b6z4f2dza493zac9994e9782d
The role of Chd7 & Chd8 chromatin remodelers in oligodendrogenesis and (re)myelination
Marie, C. (2017) · theses.fr (ABES) · doi:10.70675/01ff9606zc0a7z47a8za3f4ze4f886e3bb00
Voie Hedgehog et système VIP-récepteurs dans des cellules de glioblastome
Bensalma, S. (2013) · doi:10.70675/3bacbf21zc15cz490bz8b16z29f7306fa39f
Identification des facteurs oligodendrogliaux sécrétés impliqués dans la formation des Nœuds de Ranvier du Système Nerveux Central
Dubessy, A. (2018) · theses.fr (ABES) · doi:10.70675/016d707fz833bz4934za505z598a3d10e994
Macrophage activation profiles of multiple sclerosis patients
Fransson, J. (2019) · theses.fr (ABES) · doi:10.70675/361929ebz66c2z48dbz83a1z8955d8b54716
Dynamics of nodes of Ranvier assembly during myelination and remyelination in the central nervous system
Thétiot, M. (2018) · theses.fr (ABES) · doi:10.70675/4fd006d4z6c0ez4fe8zbcd0z0df8b8ef8d85
Régénération spontanée de la myéline dans le cerveau de souris adulte : interactions entre cellules souches, progéniteurs et microglie
Brousse, B. (2019) · theses.fr (ABES) · doi:10.70675/84a13ba7z3dc7z4ffazab9bz484310509294
Rôle de la voie de signalisation Sonic Hedgehog dans les cellules Glast positives du cerveau de souris adulte
Tirou, L. (2020) · theses.fr (ABES) · doi:10.70675/5a9de569zf953z4f2cz9ccaz89ba17ab8490
Influence de l'activateur tissulaire du plasminogène sur la lignée oligodendrocytaire et dans le processus de myélinisation
Delaunay-Piednoir, B. (2020) · theses.fr (ABES) · doi:10.70675/a754abeez40abz4036zb972zea7fa2fedbc8
Le cil primaire : une nouvelle cible pour la remyélinisation ?
Delfino, G. (2020) · theses.fr (ABES) · doi:10.70675/a62c179az64bfz4247zb041zc7cfc961677c
Myelin Matters in Schizophrenia : Neurobiological Insights from Rat Model and Human Studies
Maas, D. A. (2019) · theses.fr (ABES) · doi:10.70675/4ea9aa0azc70cz4bb4zada7z4f82cac02e1c
Characterization of cellular heterogeneity in Diffuse Low Grade Glioma
Augustus, M. (2020) · theses.fr (ABES) · doi:10.70675/037c23a4z44ddz4bb7z999ezb0c178c35170
Characterization of Tns3 molecular mechanisms in oligodendrogenesis
Merour, E. (2021) · theses.fr (ABES) · doi:10.70675/ff1209dazde97z429ez9b2az5593a14d4080
Gliogenèse hypothalamique et contrôle de la fonction de reproduction
Martin, M. J. (2021) · theses.fr (ABES) · doi:10.70675/0650653dz87dez4961z9536z23565f173f47
Mécanismes moléculaires et cellulaires impliqués dans la production de la myéline induite par les voies de signalisation Hedgehog et des androgènes dans le système nerveux central
Kassoussi, A. (2021) · theses.fr (ABES) · doi:10.70675/38265e1ez294bz4bcez8a40z0950f2d261f8
Impact of PV interneuron - OPC synapse disruption on cognitive functioning
Vidal, M. (2021) · theses.fr (ABES) · doi:10.70675/66c1e527zbd3ez49f6z8736ze9817c27856d
Fonctions de PAK1 dans la régulation du cytosquelette d’actine : implication dans la myélinisation du système nerveux central
Baudouin, L. (2021) · theses.fr (ABES) · doi:10.70675/75a319c3z246bz4800z9a27z970f7eb653f4
TCF12 roles in oligodendroglial cells and gliomas
Archontidi, S. (2021) · theses.fr (ABES) · doi:10.70675/ff2d35a7z988ez4886zbc49z95515fc3af57
Etude des conséquences des altérations de la myéline sur les fonctions cognitives à la suite d’un épisode transitoire de démyélinisation chez la souris adulte
Mercier, O. (2022) · theses.fr (ABES) · doi:10.70675/d08f6127z74b9z4df6zb55dz2fb5ac93dea2
Preclinical gene therapy using recombinant AAV vectors in mouse models of two human diseases
Günes, Y. Ö. (2022) · theses.fr (ABES) · doi:10.70675/52c9a808z1652z42c4zae82zc812b95f1723

Authors: Dawson, M.
Affiliations: Charing Cross Hospital (GB)
Corresponding author: Dawson, M
Venue: Molecular and Cellular Neuroscience
Publisher: Elsevier BV
Published: 2003-10
Volume: 24
Issue: 2
Pages: 476-488
ISSN: 1044-7431 (ISSN-L)
DOI: 10.1016/s1044-7431(03)00210-0
OpenAlex: W1985286185
Cited by: 927
References: 43
Citations by year: 2026: 25 · 2025: 27 · 2024: 56 · 2023: 54 · 2022: 38 · 2021: 71 · 2020: 57 · 2019: 46 · 2018: 51 · 2017: 59 · 2016: 40 · 2015: 48 · 2014: 43 · 2013: 52 · 2012: 28
FWCI: 5.53
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Molecular and Cellular Neuroscience (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords: NG2, oligodendrocyte precursor cells, cell cycling, oligodendrocyte lineage, myelination, demyelination, white matter, gray matter, BrdU incorporation, apoptosis, O4, chondroitin sulfate proteoglycans
MeSH terms: Chondroitin Sulfate Proteoglycan 4, Animals, Antigens, Cell Cycle, Central Nervous System, Gene Expression Regulation, Male, Neuroglia, Proteoglycans, Stem Cells, Rats, Sprague-Dawley, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks