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

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

A2B Adenosine Receptors and Sphingosine 1-Phosphate Signaling Cross-Talk in Oligodendrogliogenesis

Coppi, E., Cencetti, F., Cherchi, F., Venturini, M., Donati, C., Bruni, P., Pedata, F., & Pugliese, A. M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.677988 · Cited by 5

Identifying mRNAs Residing in Myelinating Oligodendrocyte Processes as a Basis for Understanding Internode Autonomy

Gould, R. M., & Brady, S. T. (2023) · Life · doi:10.3390/life13040945 · Cited by 5

Simplified protocol for isolation of multipotential NG2 cells from postnatal mouse

Wang, Y., Tan, Z., Qin, L., & Yu, Y. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.08.001 · Cited by 5

[Glial cells function as neural stem cells and progenitor cells].

Tan, Z., Ju, S.-H., Huang, X., Gu, Y., & Su, Z. (2017) · PubMed · Cited by 5

Disturbance of oligodendrocyte differentiation in schizophrenia in relation to main hypothesis of the disease

Kolomeets, N. S. (2017) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro201711781108-117 · Cited by 5

Age-related changes in NG2-expressing telocytes of rat stomach

Tamura, Y., Takata, K., Eguchi, A., Maeda, M., & Kataoka, Y. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249729 · Cited by 5

Ecotropic Murine Leukemia Virus Infection of Glial Progenitors Interferes with Oligodendrocyte Differentiation: Implications for Neurovirulence

Li, Y., Dunphy, J. M., Pedraza, C. E., Lynch, C. R., Cardona, S. M., Macklin, W. B., & Lynch, W. P. (2016) · Journal of Virology · doi:10.1128/jvi.03156-15 · Cited by 5

The epigenetic landscape of oligodendrocyte progenitors changes with timePreprint

Dansu, D. K., Sauma, S., Huang, D., Li, M., Moyon, S., & Casaccia, P. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.06.579145 · Cited by 5

Neotenic transcriptomic features in the adult turquoise killifish brainPreprint

Burgos-Ruiz, A. M., Naranjo, S., Hernández-Pérez, M. D. V., Ardila‐García, L., Moreno-Oñate, M., Fernández‐Miñán, A., Reyes-Benitez, A. D. L., López-Rı́os, J., Nusspaumer, G., & Tena, J. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.24.645095 · Cited by 5

Clusterin induced by OPC phagocytosis blocks IL-9 secretion to inhibit myelination in a model of Alzheimer's disease

Beiter, R. M., Raghavan, T. P., Suchocki, O., Ennerfelt, H. E., Rivet-Noor, C. R., Merchak, A. R., Phillips, J. L., Bathe, T., Lukens, J. R., Prokop, S., et al. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e41635 · Cited by 4

Decoding senescent drivers in Alzheimer's disease: From bench to bedside

Zhou, R., Lin, X., Liao, Z., Lin, J., Zheng, R., Ni, H., Liu, W., Feng, Z., He, Q., Lin, X., et al. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102978 · Cited by 4

Increased oligodendrogenesis and myelination in the subventricular zone of aged mice and gray mouse lemurs

Butruille, L., Sébillot, A., Avila‐Gutierrez, K., Vancamp, P., DEMENEIX, B. A., Pifferi, F., & Remaud, S. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.12.015 · Cited by 4

Oligodendroglial physiology and function

Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00017-1 · Cited by 3

Synaptic vesicle release regulates pre-myelinating oligodendrocyte-axon interactions in a neuron subtype-specific manner

Gronseth, J. R., Nelson, H. N., Johnson, T. L., Mallon, T. A., Martell, M. R., Pfaffenbach, K. A., Duxbury, B. B., Henke, J. T., Treichel, A. J., & Hines, J. H. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1386352 · Cited by 4

Histone H4 acetylation differentially modulates proliferation in adult oligodendrocyte progenitors

Dansu, D. K., Selcen, I., Sauma, S., Prentice, E., Huang, D., Li, M., Moyon, S., & Casaccia, P. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202308064 · Cited by 4

Pathology and Molecular Pathology of Brain Cancer

Ligon, K. L., Wilkinson, K., & Stiles, C. D. (2016) · Springer eBooks · doi:10.1007/978-3-319-35153-7_16 · Cited by 4

Novel Toolboxes for the Investigation of Activity-Dependent Myelination in the Central Nervous System

Heflin, J. K., & Sun, W. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.769809 · Cited by 4

Oligodendrocyte: Structure, Function and Pathology

Patro, N., Patro, I. K., & Tandon, P. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_3 · Cited by 5

Comparative Anatomy of Glial Cells in Mammals

Reichenbach, A., & Bringmann, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820584-6.00016-7 · Cited by 4

Mini-review: Aplastic myelin following chemotherapy

Savchuk, S., & Monje, M. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136861 · Cited by 4

Oligodendrocyte‐selective deletion of the eIF2α kinase Perk/Eif2ak3 limits functional recovery after spinal cord injury

Ohri, S. S., Forston, M. D., Myers, S. A., Brown, B. L., Andres, K. R., Howard, R. M., Gao, Y., Liu, Y., Cavener, D. R., Hetman, M., et al. (2024) · Glia · doi:10.1002/glia.24525 · Cited by 4

White Matter Injury: An Emerging Potential Target for Treatment after Subarachnoid Hemorrhage

Liu, Y., He, Y., Zhang, J., Wang, X., Zhang, A., Yu, Q., Wang, K., Fang, Y., Jiang, Q., & Chen, S. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/3842493 · Cited by 4

NG2 expressing cells in hippocampal cultures survive neurotoxic insult and retain the ability to divide

Dzwonek, K. (2005) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2005-1551 · Cited by 4

Retrovirally delivered Islet-1 increases recruitment of Ng2 expressing cells from the postnatal SVZ into the striatum

Rogelius, N., JENSEN, J., Lundberg, C., & Parmar, M. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.04.022 · Cited by 4

Future of Multiple Sclerosis Therapy: Combining Antigen-Specific Immunotherapy With Strategies to Promote Myelin Repair

Frederick, T. J., & Miller, S. D. (2006) · Future Neurology · doi:10.2217/14796708.1.4.489 · Cited by 4

Neural Activity-Dependent Cellular Proliferation in the Rat Cerebral Cortex

Kataoka, Y., Tamura, Y., Cui, Y., & Yamada, H. (2005) · ACTA HISTOCHEMICA ET CYTOCHEMICA · doi:10.1267/ahc.38.93 · Cited by 4

Sequential Specification of Oligodendrocyte Lineage Cells by Distinct Levels of Hedgehog and Notch SignalingPreprint

Ravanelli, A. M., Kearns, C. A., Powers, R. K., Wang, Y., Hines, J. H., Donaldson, M. J., & Appel, B. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/377671 · Cited by 4

Editorial: Tenascins – Key Players in Tissue Homeostasis and Defense

Yoshida, K. I., Midwood, K. S., & Orend, G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.834353 · Cited by 4

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 · Cited by 5

Physiology of neuroglia of the central nervous system

Verkhratsky, A., & Semyanov, A. V. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00005-x · Cited by 4

Adaptive oligodendrogenesis regulates blood-hypothalamus barrier permeability, hypothalamic glucose sensing and systemic glucose homeostasis in male mice

Buller, S. A., Staricoff, E. O., Riches, C. H., Tsang, A., Giavara, G., Josipović, M., Ikemura, K., Opoku, G., Sato, I., Hirohata, S., et al. (2026) · Molecular Metabolism · doi:10.1016/j.molmet.2026.102428 · Cited by 3

Remyelination in Multiple Sclerosis: The Therapeutic Potential of Neural and Mesenchymal Stem/Progenitor Cells

Rivera, F. J., Kraus, J., Steffenhagen, C., Küry, P., Weidner, N., & Aigner, L. (2011) · Current Signal Transduction Therapy · doi:10.2174/157436211797483994 · Cited by 3

Inhibiting microglia exacerbates the early effects of cuprizone in males in a rat model of multiple sclerosis, with no effect in females

Xavier, S., Younesi, S., Sominsky, L., & Spencer, S. J. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.989132 · Cited by 3

Membrane properties and coupling of macroglia in the optic nerve

Kompier, N. F., Semtner, M., Walter, S., Kakabadze, N., Steinhäuser, C., Nolte, C., & Kettenmann, H. (2024) · Current Research in Neurobiology · doi:10.1016/j.crneur.2024.100137 · Cited by 3

Notch Signaling in Central Nervous System: From Cellular Development to Multiple Sclerosis Disease

Askari, H., Rabiei, F., Yahyazadeh, M., Biagini, G., & Ghasemi‐Kasman, M. (2024) · Current Neuropharmacology · doi:10.2174/1570159x22666240731114906 · Cited by 3

Exploratory study of the dysregulation of age-related changes in neural/glial antigen 2 and neuroinflammation markers in individuals with major depression

Vargas‐Medrano, J., Sotelo, D., Vidal-Martínez, G., & Thompson, P. M. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.101107 · Cited by 3

Hypoxic White Matter Injury and Recovery After Reoxygenation in Adult Mice: Magnetic Resonance Imaging Findings and Histological Studies

Liu, Y., Qiao, H., Du, W., Xu, L., Yuan, F., Lin, J., Li, M., Zhu, L., Li, S., & Zhang, J. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-022-01305-5 · Cited by 3

Transcriptional and bioinformatic analysis of GABAA receptors expressed in oligodendrocyte progenitor cells from the human brain

Gutierrez, B. A., González-Coronel, J. M., Arellano, R. O., & Limón, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1279232 · Cited by 3

White Matter Repair in Subcortical Stroke

Sözmen, E. G., & Carmichael, S. T. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_12 · Cited by 3

Stem Cell Based Therapies for Glaucoma

Jayaram, H., Becker, S., & Limb, G. A. (2011) · InTech eBooks · doi:10.5772/21726 · Cited by 3

Glial progenitor cells in the adult brain reveal their alternate fate

Kang, S. H., & Bergles, D. E. (2008) · Nature Neuroscience · doi:10.1038/nn1208-1365 · Cited by 3

Deciphering Adult Neural Stem Cells with Single-Cell Sequencing

Liu, Y., Zhu, Y., Shi, Y., Liu, X., Su, W., & Zhuo, Y. (2023) · Stem Cells and Development · doi:10.1089/scd.2022.0234 · Cited by 3

Oligodendrocyte Progenitor Cell Culture

Nishiyama, A., Suzuki, R., Zuo, H., & Zhu, X. (2009) · Springer protocols handbooks/Springer protocols · doi:10.1007/978-1-60761-292-6_12 · Cited by 3

Chemokine Receptors and NeuroAIDS

Meucci, O. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0793-6 · Cited by 3

Neuron–glial interactions and neurotransmitter signaling to cells of the oligodendrocyte lineage

Call, C. L., Biase, L. M. D., & Bergles, D. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00036-9 · Cited by 3

Neuron–Glial Interactions

Biase, L. M. D., & Bergles, D. E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00133-7 · Cited by 3

A COMPARATIVE ANALYSIS OF CONVECTIVE HEAT TRANSFER IN A NUCLEAR ROCKET NOZZLE

Neumann, H., & Bettinger, P. J. (1963) · University of Michigan Library Repository · Cited by 3

Oligomeric amyloid beta prevents myelination in a clusterin-dependent mannerPreprint

Beiter, R. M., Raghavan, T. P., Suchocki, O., Ennerfelt, H. E., Rivet-Noor, C. R., Merchak, A. R., Phillips, J. L., Bathe, T., Lukens, J. R., Prokop, S., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4415143/v1 · Cited by 3

Terra incognita of glial cell dynamics in the etiology of leukodystrophies: Broadening disease and therapeutic perspectives

Chaudhary, R., Rehman, M., Agarwal, V., Kumar, A., Kaushik, A. S., Srivastava, S., Srivastava, S., Verma, R., Rajinikanth, P. S., & Mishra, V. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122953 · Cited by 3

Human mesenchymal stem cells-derived microvesicles increase oligodendrogenesis and neurogenesis of cultured adult neural stem cells

Ghanbari, A., Rad, F., Shahraki, M. H., Hosseini, E., Barmak, M. J., & Zibara, K. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.137951 · Cited by 2

Developing a minimally invasive gene therapy for multiple sclerosis

Nijhuis, P. J. H., Romijn, M., Honing, R., van Zon, G., Huitinga, I., de Winter, F., & Verhaagen, J. (2025) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2025.101504 · Cited by 2

Human oligodendrocyte progenitor cells mediate synapse elimination through TAM receptor activation

Gkogka, A., Malwade, S., Koskuvi, M., Ohtonen, S., Molnar, E., Bose, R., Ceccatelli, S., Koıstınaho, J., Tiihonen, J., Schalling, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66521-1 · Cited by 3

Design of hydrogel biomaterial interfaces for the injured spinal cord

McKay, C. A., & Gilbert, R. J. (2013) · Surface Innovations · doi:10.1680/si.13.00016 · Cited by 2

Sensitive timing of undifferentiation in oligodendrocyte progenitor cells and their enhanced maturation in primary visual cortex of binocularly enucleated mice

Shin, H., & Kawai, H. (2021) · PLoS ONE · doi:10.1371/journal.pone.0257395 · Cited by 1

Mechanisms of Plasticity Remodeling and Recovery

Zheng, Z., Chen, J., & Chopp, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-69424-7.00011-9 · Cited by 2

Organization of the ventricular zone of the cerebellum

Gómez-González, G. B., Becerra-González, M., Martínez-Mendoza, M. L., Rodríguez-Arzate, C. A., & Martínez‐Torres, A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.955550 · Cited by 2

IGFBP-2 and IGF-II: Key Components of the Neural Stem Cell Niche? Implications for Glioblastoma Pathogenesis

Harland, A. J., & Perks, C. M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104749 · Cited by 2

Immune System Modulation of Germinal and Parenchymal Neural Progenitor Cells in Physiological and Pathological Conditions

Rolando, C., Boda, E., & Buffo, A. (2012) · InTech eBooks · doi:10.5772/31823 · Cited by 2

The Potential Role of Nonneuronal Cells in the Deep Brain Stimulation Mechanism

Vedam‐Mai, V., Okun, M. S., & Hol, E. M. (2012) · Springer eBooks · doi:10.1007/978-3-642-30991-5_19 · Cited by 2

Modeling Gliomas Using PDGF-Expressing Retroviruses

Assanah, M. C., Lopez, K. A., Bruce, J. N., & Canoll, P. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-553-8_1 · Cited by 2

"NG2 Proteoglycan in the Diagnosis, Prognosis and Therapy of Gliomas"

Schiffer, D. (2017) · International Journal of Cell Science & Molecular Biology · doi:10.19080/ijcsmb.2017.02.555582 · Cited by 2

NEUROPROTECTIVE EFFECT OF THYROID HORMONES IN CEREBRAL HYPOPERFUSION

Криштоп, В. В., Rumyantseva, T. А., & Nikonorova, V. G. (2021) · Ulyanovsk Medico-biological Journal · doi:10.34014/2227-1848-2021-1-6-25 · Cited by 2

Oligodendrogenesis After Cerebral Ischaemia and Traumatic Brain Injury

Zhang, Z. G., & Chopp, M. (2013) · EMJ Neurology · doi:10.33590/emjneurol/10314620 · Cited by 2

Visualization of the membrane surface and cytoskeleton of oligodendrocyte progenitor cell growth cones using a combination of scanning ion conductance and four times expansion microscopy

Haak, A., Leßlich, H. M., & Dietzel, I. D. (2023) · Biological Chemistry · doi:10.1515/hsz-2023-0217 · Cited by 2

Oligodeoxynucleotide IMT504: Effects on Central Nervous System Repair Following Demyelination

Mathieu, P., Sampertegui, Y. R., Elı́as, F., Silva, A. S., Calcagno, M. D. L., López, R. A., & Adamo, A. M. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03825-7 · Cited by 2

The role of induced pluripotent stem cell (IPs) in the transplantation of glaucoma.

Fu, M., Zhu, B., Sun, X., & Luo, D. (1957) · PubMed · Cited by 2

Remyelination in Multiple Sclerosis

Stangel, M., Pul, R., Skripuletz, T., Trebst, C., Voß, E. V., & Gudi, V. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-384913-7.00009-5 · Cited by 3

Visual deprivation induces transient upregulation of oligodendrocyte progenitor cells in the subcortical white matter of mouse visual cortex

Shin, H., & Kawai, H. D. (2021) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2021.06.004 · Cited by 2

Basic mechanisms

Kesselring, J., Comı, G., & Thompson, A. J. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781698.002 · Cited by 2

Sparse interaction between oligodendrocyte precursor cells (NG2 + cells) and nodes of Ranvier in the central nervous systemPreprint

Biase, L. M. D., Pucak, M. L., Kang, S. H., Rodriguez, S. N., & Bergles, D. E. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/185801 · Cited by 2

Age-linked heterogeneity among oligodendrocyte precursor cells in the cerebral cortex of mice and humanPreprint

Bribián, A., Medina-Rodriguez, E. M., Josa‐Prado, F., García‐Álvarez, I., Machín-Díaz, I., Murcia‐Belmonte, V., Vega-Zelaya, L., Pastor, J., Garrido, L., & de Castro, F. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/799544 · Cited by 2

TCF12 controls oligodendroglial cell proliferation and regulates signaling pathways conserved in gliomasPreprint

Archontidi, S., Marie, C., Gyorgy, B., Guégan, J., Sanson, M., Parras, C. M., & Huillard, E. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.26.453859 · Cited by 2

Impaired Macroautophagy in Oligodendrocyte Precursor Cells Exacerbates Aging-related Cognitive Deficits via a Senescence Associated SignalingPreprint

Ma, Q., Chen, H., Sun, Y., Li, Q., Du, Y.-T., Hu, N., Huang, X., Zhu, C., Yang, G., Tang, Y., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3926942/v1 · Cited by 2

Single-cell omics and heterogeneity of neuroglial cells

Lahaie, S. C., Brezner, N., & Murai, K. K. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00013-9 · Cited by 1

Oligodendrocyte arrangement, identification and morphology in the developing superior olivary complex

Zacher, A., Grabinski, M., Console‐Meyer, L., Felmy, F., & Pätz, C. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1561312 · Cited by 1

4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione rescues oligodendrocytes ferroptosis leading to myelin loss and ameliorates neuronal injury facilitating memory in neonatal hypoxic-ischemic brain damage

Huang, Q., Tang, J., Xiang, Y., Shang, X., Li, K., Chen, L., Hu, J., Li, H., Pi, Y., Yang, H., et al. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115262 · Cited by 1

Alterations in Both Caliber and Myelination of Callosal Axons Elicited by Ubiquitous Genetic Ablation of c‐Jun Amino‐Terminal Kinase 3 ( JNK3 )

Bardile, C. F., Priego, M., Sidik, H., Tano, V., Langley, S. R., Pouladi, M. A., & Morfini, G. A. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70356 · Cited by 1

Functional Role of DDR1 in Oligodendrocyte Signaling Mechanism in Association with Myelination and Remyelination Process in the Central Nerve System

Anand, M. A. V., Manjula, K. S., & Wang, C. (2024) · Journal of physiological investigation. · doi:10.4103/ejpi.ejpi-d-24-00043 · Cited by 1

Genetic Tools in Rodents to Study Cannabinoid Functions

Monory, K., de Azúa, I. R., & Lutz, B. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_550 · Cited by 1

The role of autophagy in ischemic brain injury

Osterli, E., Park, Y., Hu, K., Kasof, G. M., Wiederhold, T., Liu, C., & Hu, B. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2486445 · Cited by 3

Cellular Origin of Glioblastoma: Current Evidence, Challenges, and Implications

Qian, G., Fu, Y., & Kim, A. (2025) · International journal of high school research · doi:10.36838/v7i8.13 · Cited by 1

Glia Are Bussin’: How Single‐Cell and Spatial Transcriptomics Enlighten the Role of Neuroglia in Spinal Cord Injury and Regeneration

Mejia, J., & Horner, P. J. (2026) · Glia · doi:10.1002/glia.70139 · Cited by 1

RXR Gamma Enables Oligodendrocyte Differentiation by Suppressing Sonic Hedgehog Signaling

Baldassarro, V. A., Brassart, Q., Fraulob, V., Calzà, L., & Krężel, W. (2026) · Glia · doi:10.1002/glia.70151 · Cited by 1

NG2 Glia and Cellular Crosstalk in Health and Disease: Focus on Spinal Cord Injury

Kabdesh, I. M., Bilalova, A., Mukhamedshina, Y. O., & Chelyshev, Y. A. (2026) · Pathophysiology · doi:10.3390/pathophysiology33020038 · Cited by 1

Early Developmental Neuronal Activity Impacts Oligodendrocyte Differentiation Through AMPA Receptors

Allen, T. E., Peet, G. C., Wulschner, L. E. G., Oh, W. C., & Macklin, W. B. (2026) · Glia · doi:10.1002/glia.70157 · Cited by 1

Mechanically Compliant, Precision‐Porous Brain Implants Reduce the Foreign Body Reaction and Guide Regeneration

Dryg, I. D., Zhen, L., Darrow, R., Lawton, S., Crawford, L., Robinson, R., Perlmutter, S. I., Bryers, J. D., & Ratner, B. D. (2026) · Advanced Healthcare Materials · doi:10.1002/adhm.71522 · Cited by 1

Human spinal cord organoids recapitulate developmental and disease-associated oligodendrocyte lineage signatures

Pio, T., Bettaiah, M., Zhao, R., Wariyar, S. S., Mouhi, S., Hill, E. J., Sloan, S. A., Ou, Z., Yu, A. J. R., Adams, C., et al. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.103114 · Cited by 1

Neural Stem Cells and Demyelinating Disease

Crawford, A. H., & Franklin, R. J. M. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4939-1908-6_8 · Cited by 1

Oligodendrocyte Progenitors in Schizophrenia: The Role in Pathogenesis and Potential Treatment Target

Kolomeets, N. S. (2024) · Psikhiatriya · doi:10.30629/2618-6667-2023-21-7-46-64 · Cited by 1

VIII. The Neuroglia of the CNS

Pannese, E. (2014) · Springer eBooks · doi:10.1007/978-3-319-06856-5_8 · Cited by 1

Parenchymal Neuro-Glio-Genesis Versus Germinal Layer- Derived Neurogenesis: Two Faces of Central Nervous System Structural Plasticity

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Les hormones thyroïdiennes régulent le destin des cellules souches neurales

Remaud, S., & DEMENEIX, B. A. (2019) · Biologie Aujourd hui · doi:10.1051/jbio/2019007 · Cited by 1

Specific Functions of ERK/MAPK Signaling in Brain Development and Neurocognition

Holter, M. C. (2019) · Cited by 1

Generation and Maturation of Macroglia in the Central Nervous System

Patro, N., & Patro, I. K. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_6 · Cited by 1

Application of Plasma to Humans (Blood Coagulation and Regenerative Medicine)

(2018) · Elsevier eBooks · doi:10.1016/b978-0-12-815004-7.00006-8 · Cited by 1

Neural Stem Cells

Kempermann, G. (2010) · Oxford University Press eBooks · doi:10.1093/med/9780199729692.003.0003 · Cited by 1

The role of amphoterin-induced gene and open reading frame (AMIGO) family in myelination and neurodegeneration and Investigating the roles of mesenchymal and hematopoieticstem cell conditioned media on neutrophil recruitment in amodel of inflammation

Tickle, J. (2013) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1

Promouvoir la remyélinisation dans le cadre de la sclérose en plaque à l’aide des cellules neurales/précurseurs et/ou souches endogènes adultes

Roulois, A., Zhao, C., Zawadzka, M., Bruce, C. C., & Franklin, R. J. M. (2007) · Revue Neurologique · doi:10.1016/s0035-3787(07)90477-4 · Cited by 1

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Ben‐Hur, T., & Einstein, O. (2006) · Springer eBooks · doi:10.1007/1-84628-142-3_6 · Cited by 1

4: NG2-expressing cells as oligodendrocyte progenitors in the normal and demyelinated adult CNS

Polito, A., & Reynolds, R. (2004) · Journal of Anatomy

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NG2 cells in the brain: a novel glial cell population.

Nishiyama, A. (2001) · PubMed · Cited by 57

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NG2+ Glial Cells: A Novel Glial Cell Population in the Adult Brain

Nishiyama, A., Chang, A., & Trapp, B. D. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199911000-00001 · Cited by 297