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

NG2 Glia: Novel Roles beyond Re-/Myelination

Parolisi, R., & Boda, E. (2018) · Neuroglia · doi:10.3390/neuroglia1010011 · Cited by 23

Oligodendrocyte progenitors as environmental biosensors

Dansu, D. K., Sauma, S., & Casaccia, P. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.09.012 · Cited by 21

Retinoid X receptor activation promotes re-myelination in a very old triple transgenic mouse model of Alzheimer’s disease

Santos-Gil, D. F., Arboleda, G., & Sandoval-Hernández, A. G. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135764 · Cited by 22

Stem Cell and Gene-Based Therapy

Battler, A., & Leor, J. (2006) · Springer eBooks · doi:10.1007/1-84628-142-3 · Cited by 21

Role of NG2 expressing cells in addiction: a new approach for an old problem

Somkuwar, S. S., Staples, M. C., Galinato, M. H., Fannon, M. J., & Mandyam, C. D. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00279 · Cited by 21

NG2 ‐glia crosstalk with microglia in health and disease

Zhang, Z., Li, X., Zhou, H., & Zhou, J. (2022) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13948 · Cited by 21

Median eminence myelin continuously turns over in adult mice

Buller, S. A., Kohnke, S., Hansford, R., Shimizu, T., Richardson, W. D., & Blouet, C. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101690 · Cited by 20

Role of Oligodendrocyte Lineage Cells in Multiple System Atrophy

Hsiao, J.-H. T., Tanglay, O., Li, A. A., Strobbe, A. Y. G., Kim, W. S., Halliday, G. M., & Fu, Y. (2023) · Cells · doi:10.3390/cells12050739 · Cited by 20

Signals that regulate the oncogenic fate of neural stem cells and progenitors

Swartling, F. J., Bolin, S., Phillips, J. J., & Persson, A. I. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.01.027 · Cited by 22

Altered gene transcription linked to astrocytes and oligodendrocytes in frontal cortex in Creutzfeldt-Jakob disease

Andrés‐Benito, P., Domínguez-González, M., & Ferrer, I. (2018) · Prion · doi:10.1080/19336896.2018.1500076 · Cited by 20

Prdm8 regulates pMN progenitor specification for motor neuron and oligodendrocyte fates by modulating Shh signaling response

Scott, K., O’Rourke, R., Gillen, A. E., & Appel, B. (2020) · Development · doi:10.1242/dev.191023 · Cited by 21

Subacute metformin treatment reduces inflammation and improves functional outcome following neonatal hypoxia ischemia

Livingston, J. M., Syeda, T., Christie, T., Gilbert, E. A. B., & Morshead, C. M. (2020) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2020.100119 · Cited by 20

Neuroprotection and neuroregeneration: roles for the white matter

Calzà, L., Baldassarro, V. A., Stanzani, A., Giardino, L., & Lorenzini, L. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.335834 · Cited by 20

Oligodendrogenesis in the fornix of adult mouse brain; the effect of LPS-induced inflammatory stimulation

Fukushima, S., Nishikawa, K., Furube, E., Muneoka, S., Ono, K., Takebayashi, H., & Miyata, S. (2015) · Brain Research · doi:10.1016/j.brainres.2015.09.011 · Cited by 21

Nexilin Regulates Oligodendrocyte Progenitor Cell Migration and Remyelination and Is Negatively Regulated by Protease-Activated Receptor 1/Ras-Proximate-1 Signaling Following Subarachnoid Hemorrhage

Li, Q., Zhao, H., Pan, P., Ru, X., Zuo, S., Qu, J., Liao, B., Chen, Y., Ruan, H., & Feng, H. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00282 · Cited by 20

Glycolipid and Glycoprotein Expression During Neural Development

Yu, R. K., & Itokazu, Y. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1154-7_9 · Cited by 20

What Are the Roles of Oligodendrocyte Precursor Cells in Normal and Pathologic Conditions?

Benarroch, E. E. (2023) · Neurology · doi:10.1212/wnl.0000000000208000 · Cited by 21

Autophagy in Oligodendrocyte Lineage Cells Controls Oligodendrocyte Numbers and Myelin Integrity in an Age-dependent Manner

Chen, H., Yang, G., Xu, D.-E., Du, Y.-T., Zhu, C., Hu, H., Luo, L., Feng, L., Huang, W., Sun, Y., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01292-1 · Cited by 19

CD44 correlates with longevity and enhances basal ATF6 activity and ER stress resistance

Takasugi, M., Ohtani, N., Takemura, K., Emmrich, S., Zakusilo, F. T., Yoshida, Y., Kutsukake, N., Mariani, J. N., Windrem, M. S., Chandler-Militello, D., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113130 · Cited by 19

Grafted human-induced pluripotent stem cells-derived oligodendrocyte progenitor cells combined with human umbilical vein endothelial cells contribute to functional recovery following spinal cord injury

Li, Q., Liu, S., Zheng, T., Li, M., Qi, B., Zhou, L., Liu, B., Ma, D., Zhao, C., & Chen, Z. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03651-1 · Cited by 19

Collapsin response mediator protein‐2 phosphorylation promotes the reversible retraction of oligodendrocyte processes in response to non‐lethal oxidative stress

Fernández-Gamba, A. C., Leal, M. C., Maarouf, C. L., Richter‐Landsberg, C., Wu, T., Morelli, L., Roher, A. E., & Castaño, E. M. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07742.x · Cited by 21

Remyelination by Resident Oligodendrocyte Precursor Cells in a Xenopus laevis Inducible Model of Demyelination

Sekizar, S., Mannioui, A., Azoyan, L., Colin, C., Thomas, J., Pasquier, D. D., Mallat, M., & Zalc, B. (2015) · Developmental Neuroscience · doi:10.1159/000380817 · Cited by 19

Myelin plasticity, neural activity, and traumatic neural injury

Kondiles, B. R., & Horner, P. J. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22540 · Cited by 21

Myelination of the developing lateral olfactory tract and anterior commissure

Collins, L. N., Hill, D. L., & Brunjes, P. C. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24452 · Cited by 20

BDNF haploinsufficiency exerts a transient and regionally different influence upon oligodendroglial lineage cells during postnatal development

Nicholson, M., Wood, R. J., Fletcher, J. L., van den Buuse, M., Murray, S. S., & Xiao, J. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.05.005 · Cited by 19

Spinal Glia Division Contributes to Conditioning Lesion–Induced Axon Regeneration Into the Injured Spinal Cord

Liu, H., Angert, M., Nishihara, T., Shubayev, I., Dolkas, J., & Shubayev, V. I. (2015) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000192 · Cited by 19

Maternal arachidonic acid supplementation improves neurodevelopment of offspring from healthy and diabetic rats

Zhao, J., Bigio, M. R. D., & Weiler, H. A. (2009) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2009.09.005 · Cited by 19

Cellular proliferation in the cerebral cortex following neural excitation in rats

Tamura, Y., Kataoka, Y., Cui, Y., & Yamada, H. (2004) · Neuroscience Research · doi:10.1016/j.neures.2004.06.011 · Cited by 19

Neuron-Glial Interactions

Pittà, M. D. (2020) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_100691-1 · Cited by 21

The Impact of Fixation on the Detection of Oligodendrocyte Precursor Cell Morphology and Vascular Associations

Pfeiffer, F., Sherafat, A., & Nishiyama, A. (2021) · Cells · doi:10.3390/cells10061302 · Cited by 19

Intrinsic organization of the corpus callosum

Barbaresi, P., Fabri, M., Lorenzi, T., Sagrati, A., & Morroni, M. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1393000 · Cited by 20

Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX

Singh, R., Yu, S. J., Osman, M., Inde, Z., Fraser, C. S., Cleveland, A. H., Almanzar, N., Lim, C. B., Joshi, G. N., Spetz, J. K. E., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-1337 · Cited by 18

Gliomas: a reflection of temporal gliogenic principles

Sojka, C., & Sloan, S. A. (2024) · Communications Biology · doi:10.1038/s42003-024-05833-2 · Cited by 18

Novel roles of oligodendrocyte precursor cells in the developing and damaged brain

Maki, T. (2017) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12358 · Cited by 18

In Vivo Conversion of Astrocytes to Oligodendrocyte Lineage Cells Using Chemicals: Targeting Gliosis for Myelin Repair

Zare, L., Baharvand, H., & Javan, M. (2018) · Regenerative Medicine · doi:10.2217/rme-2017-0155 · Cited by 18

High Vulnerability of Oligodendrocytes to Oxidative Stress Induced by Ultrafine Urban Particles

Kim, J. Y., Kim, J.-H., Kim, Y., & Seo, J. H. (2020) · Antioxidants · doi:10.3390/antiox10010004 · Cited by 18

Polyunsaturated Fatty Acid-Enriched Lipid Fingerprint of Glioblastoma Proliferative Regions Is Differentially Regulated According to Glioblastoma Molecular Subtype

Maimó‐Barceló, A., Martín‐Saíz, L., Fernández, J. A., Pérez‐Romero, K., Arjona, S. G., Lara-Almúnia, M., Lopetegui, J. P., Bestard-Escalas, J., & Barceló‐Coblijn, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23062949 · Cited by 18

Cortical Spreading Depression Shifts Cell Fate Determination of Progenitor Cells in the Adult Cortex

Tamura, Y., Eguchi, A., Jin, G., Sami, M. M., & Kataoka, Y. (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.98 · Cited by 18

Oligodendrocyte‐myelin glycoprotein is present in lipid rafts and caveolin‐1‐enriched membranes

Boyanapalli, M., Kottis, V., Lahoud, O. B., Bamri‐Ezzine, S., Braun, P. E., & Mikol, D. D. (2005) · Glia · doi:10.1002/glia.20237 · Cited by 18

Progenies of NG2 glia: what do we learn from transgenic mouse models ?

Huang, W., Guo, Q., & Scheller, A. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.286950 · Cited by 20

The contribution of DNA methylation to the (dys)function of oligodendroglia in neurodegeneration

Fodder, K., de Silva, R., Warner, T. T., & Bettencourt, C. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01607-9 · Cited by 22

Age-dependent changes on fractalkine forms and their contribution to neurodegenerative diseases

Eugenín, J. L., Bernhardi, L. E.-V., & Rommy von Bernhardi, M. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1249320 · Cited by 19

Enhanced oxidative phosphorylation, re-organized intracellular signaling, and epigenetic de-silencing as revealed by oligodendrocyte translatome analysis after contusive spinal cord injury

Forston, M. D., Wei, G. Z., Chariker, J. H., Stephenson, T., Andres, K. R., Glover, C., Rouchka, E. C., Whittemore, S. R., & Hetman, M. (2023) · Scientific Reports · doi:10.1038/s41598-023-48425-6 · Cited by 17

Heterogeneity in oligodendrocyte precursor cell proliferation is dynamic and driven by passive bioelectrical properties

Pivoňková, H., Sitnikov, S., Kamen, Y., Vanhaesebrouck, A. E., Matthey, M., Spitzer, S. O., Ng, Y. T., Tao, C., de Faria, O., Varga, B. V., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114873 · Cited by 22

Crucial role of the local micro‐environment in fate decision of neonatal rat NG2 progenitors

Sypecka, J., Sarnowska, A., & Domańska‐Janik, K. (2009) · Cell Proliferation · doi:10.1111/j.1365-2184.2009.00618.x · Cited by 17

NG2 cells are uniformly distributed and NG2 is not required for barrel formation in the somatosensory cortex

Hill, R., Natsume, R., Sakimura, K., & Nishiyama, A. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.01.010 · Cited by 17

Embracing oligodendrocyte diversity in the context of perinatal injury

Cunningham, L. A., Newville, J., & Jantzie, L. L. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.217320 · Cited by 20

Revisit the Candidacy of Brain Cell Types as the Cell(s) of Origin for Human High-Grade Glioma

Shao, F., & Liu, C. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00048 · Cited by 17

DNA methylation in Schwann cells and in oligodendrocytes

Arthur‐Farraj, P., & Moyon, S. (2020) · Glia · doi:10.1002/glia.23784 · Cited by 17

How neurogenesis finds its place in a hardwired sensory system

Oboti, L., & Peretto, P. M. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00102 · Cited by 17

Chronic lithium treatment decreases NG2 cell proliferation in rat dentate hilus, amygdala and corpus callosum

Orre, K., Wennström, M., & Tingström, A. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.01.015 · Cited by 17

Expression of NG2 and platelet-derived growth factor receptor alpha in the developing neonatal rat brain

Lai, J., Li, P., Li, H., Jiang, H., Zhu, L., Wu, H., & Li, J. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.219045 · Cited by 17

Modulating myelination: knowing when to say Wnt: Figure 1.Preprint

Rosenberg, S., & Chan, J. R. (2009) · Genes & Development · doi:10.1101/gad.1824009 · Cited by 17

Asymmetric cell division: Implications for glioma development and treatment

Lewis, K., & Petritsch, C. K. (2013) · Translational Neuroscience · doi:10.2478/s13380-013-0148-8 · Cited by 16

A review of the role of stem cells in the development and treatment of glioma

Heywood, R. M., Marcus, H. J., Ryan, D. J., Piccirillo, S. G. M., Al-Mayhani, T. M. F., & Watts, C. (2012) · Acta Neurochirurgica · doi:10.1007/s00701-012-1338-9 · Cited by 16

Cortical Spreading Depolarization Stimulates Gliogenesis in the Rat Entorhinal Cortex

Urbach, A., Brueckner, J., & Witte, O. W. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.232 · Cited by 16

Quetiapine has an additive effect to triiodothyronine in inducing differentiation of oligodendrocyte precursor cells through induction of cholesterol biosynthesis

Cardona, J. G., Smith, M. D., Wang, J., Kirby, L. A., Schott, J. T., Davidson, T. S., Karnell, J. L., Whartenby, K. A., & Calabresi, P. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221747 · Cited by 16

Effects of the transcription factor Olig1 on the differentiation and remyelination of oligodendrocyte precursor cells after focal cerebral ischemia in rats

Zhao, H., Gao, X., Liu, Z., Lin, J., Wang, S., Wang, D., & Zhang, Y. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10713 · Cited by 16

Diffuse Axonal Injury in the Rat Brain: Axonal Injury and Oligodendrocyte Activity Following Rotational Injury

Losurdo, M., Davidsson, J., & Sköld, M. K. (2020) · Brain Sciences · doi:10.3390/brainsci10040229 · Cited by 16

An Iatrogenic Model of Brain Small-Vessel Disease: Post-Radiation Encephalopathy

Moretti, R., & Caruso, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186506 · Cited by 16

Essential roles of plexin-B3+ oligodendrocyte precursor cells in the pathogenesis of Alzheimer’s disease

Nihonmatsu-Kikuchi, N., Yu, X., Matsuda, Y., Ozawa, N., Ito, T., Satou, K., Kaname, T., Iwasaki, Y., Akagi, A., Yoshida, M., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02404-7 · Cited by 16

Oligodendrogenesis is a key process for cognitive performance improvement induced by voluntary physical activity

von Bernhardi, J. E., & Dimou, L. (2022) · Glia · doi:10.1002/glia.24155 · Cited by 17

The (Real) Neurogenic/Gliogenic Potential of the Postnatal and Adult Brain Parenchyma

Bonfanti, L. (2013) · ISRN Neuroscience · doi:10.1155/2013/354136 · Cited by 18

New dimensions of asymmetric division in vertebrates

Vertii, A., Kaufman, P. D., Hehnly, H., & Doxsey, S. (2018) · Cytoskeleton · doi:10.1002/cm.21434 · Cited by 16

White Matter Changes in Cervical Dystonia Relate to Clinical Effectiveness of Botulinum Toxin Treatment

Blood, A. J., Kuster, J. K., Waugh, J. L., Levenstein, J. M., Multhaupt‐Buell, T., Sudarsky, L. R., Breiter, H. C., & Sharma, N. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00265 · Cited by 17

Enriched Environment Effects on Myelination of the Central Nervous System: Role of Glial Cells

Gao, Z.-K., Shen, X.-Y., Han, Y., Guo, Y., Yuan, M., & Bi, X. (2022) · Neural Plasticity · doi:10.1155/2022/5766993 · Cited by 15

Utilizing hiPSC-derived oligodendrocytes to study myelin pathophysiology in neuropsychiatric and neurodegenerative disorders.

Shim, G., Romero-Morales, A. I., Sripathy, S. R., & Maher, B. J. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1322813 · Cited by 16

Modeling the dynamics of oligodendrocyte precursor cells and the genesis of gliomas

Dufour, A., Gontran, E., Deroulers, C., Varlet, P., Pallud, J., Grammaticos, B., & Badoual, M. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005977 · Cited by 15

Novel Tools and Investigative Approaches for the Study of Oligodendrocyte Precursor Cells (NG2-Glia) in CNS Development and Disease

Galichet, C., Clayton, R. W., & Lovell-Badge, R. H. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.673132 · Cited by 16

Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve

Jennings, A. R., & Carroll, W. M. (2014) · Brain Pathology · doi:10.1111/bpa.12193 · Cited by 15

Quantal transmission: not just for neurons

Overstreet‐Wadiche, L. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.11.010 · Cited by 15

Leukemia Inhibitory Factor Participates in the Formation of Stress Adaptation via Hippocampal Myelination in Mice

Kurokawa, K., Tsuji, M., Takahashi, K., Miyagawa, K., Mochida-Saito, A., & Takeda, H. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.08.030 · Cited by 15

Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq

Darr, A. J., Danzi, M. C., Brady, L., Emig-Agius, D., Hackett, A., Golshani, R., Warner, N., Lee, J., Lemmon, V. P., & Tsoulfas, P. (2017) · PLOS ONE · doi:10.1371/journal.pone.0186091 · Cited by 14

Cannabinoids as Glial Cell Modulators in Ischemic Stroke: Implications for Neuroprotection

Vicente-Acosta, A., Ceprián, M., Sobrino, P., Pazos, M. R., & Loría, F. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.888222 · Cited by 15

Fmrp regulates oligodendrocyte lineage cell specification and differentiation

Doll, C. A., Scott, K., & Appel, B. (2021) · Glia · doi:10.1002/glia.24041 · Cited by 15

L-Type Ca2+ Channels of NG2 Glia Determine Proliferation and NMDA Receptor-Dependent Plasticity

Zhao, N., Huang, W., Cătălin, B., Scheller, A., & Kirchhoff, F. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.759477 · Cited by 15

Mechanisms and Medicines for Remyelination

Bothwell, M. A. (2016) · Annual Review of Medicine · doi:10.1146/annurev-med-050715-104400 · Cited by 14

Neurodegeneration, Myelin Loss and Glial Response in the Three-Vessel Global Ischemia Model in Rat

Anan’ina, T. V., Kisel, A. A., Kudabaeva, M., Чернышева, Г. А., Smol’yakova, V. I., Усов, К. Е., Павловна, К. Е., Плотников, М. Б., & Khodanovich, M. Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176246 · Cited by 14

Development of Functional Neurons from Postnatal Stem Cells In Vitro

Rowe, E., Jeftinija, D. M., Jeftinija, K., & Jeftinija, S. (2005) · Stem Cells · doi:10.1634/stemcells.2005-0037 · Cited by 14

Comparative postnatal development of spinal, trigeminal and vagal sensory root entry zones

Toma, J. S., McPhail, L. T., & Ramer, M. S. (2006) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2006.06.001 · Cited by 14

Hedgehog Signaling in CNS Remyelination

Fang, M., Tang, T., Qiu, M. S., & Xu, X. (2022) · Cells · doi:10.3390/cells11142260 · Cited by 14

Uncovering cilia function in glial development

Bear, R. M., & Caspary, T. (2023) · Annals of Human Genetics · doi:10.1111/ahg.12519 · Cited by 13

Oligodendrocyte progenitor cells differentiation induction with MAPK / ERK inhibitor fails to support repair processes in the chronically demyelinated CNS

Ganz, T., Zveik, O., Fainstein, N., Lachish, M., Rechtman, A., Sofer, L., Brill, L., Ben‐Hur, T., & Vaknin‐Dembinsky, A. (2023) · Glia · doi:10.1002/glia.24453 · Cited by 13

Cellular and Molecular Characterization of Multipolar Map5-Expressing Cells: A Subset of Newly Generated, Stage-Specific Parenchymal Cells in the Mammalian Central Nervous System

Crociara, P., Parolisi, R., Conte, D., Fumagalli, M., & Bonfanti, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063258 · Cited by 13

Intertwining extracellular nucleotides and their receptors with Ca 2+ in determining adult neural stem cell survival, proliferation and final fate

Lecca, D., Fumagalli, M., Ceruti, S., & Abbracchio, M. P. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0433 · Cited by 14

The influence of retinoic acid on the human oligodendrocyte precursor cells by RNA-sequencing

Kim, S. Y., Kelland, E. E., Kim, J. H., Lund, B. T., Chang, X., Wang, K., & Weiner, L. P. (2017) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2016.12.004 · Cited by 13

A Novel Three-Dimensional Culture System for Oligodendrocyte Precursor Cells

Egawa, N., Shindo, A., Liang, A. C., Du, Y., Xing, C., Lo, E. K., Itoh, K., Kinoshita, H., Maki, T., Takahashi, R., et al. (2017) · Stem Cells and Development · doi:10.1089/scd.2016.0306 · Cited by 13

Encapsulated oligodendrocyte precursor cell fate is dependent on PDGF‐AA release kinetics in a 3D microparticle‐hydrogel drug delivery system

Pinezich, M. R., Russell, L. N., Murphy, N. P., & Lampe, K. J. (2018) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36432 · Cited by 13

Localization of NG2 immunoreactive neuroglia cells in the rat locus coeruleus and their plasticity in response to stress

Seifi, M., Corteen, N. L., van der Want, J. J. L., Metzger, F., & Swinny, J. D. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00031 · Cited by 13

Stem Cells in Spinal Cord Injury

Wrathall, J. R., & Lytle, J. M. (2008) · Disease Markers · doi:10.1155/2008/292160 · Cited by 16

Analysis of the GPR17 receptor in NG2 ‐glia under physiological conditions unravels a new subset of oligodendrocyte progenitor cells with distinct functions

Miralles, A. J., Unger, N., Kannaiyan, N. R., Rossner, M. J., & Dimou, L. (2023) · Glia · doi:10.1002/glia.24356 · Cited by 12

Demyelination and impaired oligodendrogenesis in the corpus callosum following lead exposure

Liu, L. L., Emir, U. E., Gu, H., Sang, L. T., Sawiak, S. J., Cannon, J. R., Du, Y., & Zheng, W. (2024) · Toxicological Sciences · doi:10.1093/toxsci/kfae100 · Cited by 12

Low-Intensity Pulsed Ultrasound Promotes Oligodendrocyte Maturation and Remyelination by Down-regulating the Interleukin-17A/Notch1 Signaling Pathway in Mice with Ischemic Stroke

Wang, J., Gao, Y., Wang, B., Zhang, C., Yuan, Y., Xu, R., Ji, H., & Zhang, X. (2025) · Research · doi:10.34133/research.0676 · Cited by 15

Comparative Anatomy of Glial Cells in Mammals

Reichenbach, A., & Bringmann, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00050-6 · Cited by 12

Unraveling the adult cell progeny of early postnatal progenitor cells

Sánchez‐González, R., Salvador, N., & López‐Mascaraque, L. (2020) · Scientific Reports · doi:10.1038/s41598-020-75973-y · Cited by 12

Epigenetic Regulation of the Hippocampus, with Special Reference to Radiation Exposure

Saw, G., & Tang, F. R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249514 · Cited by 13

Transcriptomic reprogramming for neuronal age reversal

Pleşa, A. M., Shadpour, M., Boyden, E. S., & Church, G. M. (2023) · Human Genetics · doi:10.1007/s00439-023-02529-1 · Cited by 13

Opposite modulation of functional recovery following contusive spinal cord injury in mice with oligodendrocyte-selective deletions of Atf4 and Chop/Ddit3

Gao, Y., Wei, G. Z., Forston, M. D., Rood, B. R., Hodges, E. R., Burke, D. A., Andres, K. R., Morehouse, J. R., Armstrong, C., Glover, C., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-36258-2 · Cited by 12

Perineuronal germinal cells in the rat cerebral cortex

Kataoka, Y., Tamura, Y., Takamori, Y., Cui, Y., & Yamada, H. (2006) · Medical Molecular Morphology · doi:10.1007/s00795-006-0307-x · Cited by 12

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

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

NG2‐expressing cells as oligodendrocyte progenitors in the normal and demyelinated adult central nervous system

Polito, A., & Reynolds, R. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00454.x · Cited by 231

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

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

Defining the NG2-expressing cell of the adult CNS

Horner, P. J., Thallmair, M., & Gage, F. H. (2002) · Journal of Neurocytology · doi:10.1023/a:1025739630398 · Cited by 133

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