The DOI matches its Crossref record; 307 of the 307 references it cites were found in a registry or an index.
Glial Cells as Progenitors and Stem Cells: New Roles in the Healthy and Diseased Brain
Abstract
The diverse functions of glial cells prompt the question to which extent specific subtypes may be devoted to a specific function. We discuss this by reviewing one of the most recently discovered roles of glial cells, their function as neural stem cells (NSCs) and progenitor cells. First we give an overview of glial stem and progenitor cells during development; these are the radial glial cells that act as NSCs and other glial progenitors, highlighting the distinction between the lineage of cells in vivo and their potential when exposed to a different environment, e.g., in vitro. We then proceed to the adult stage and discuss the glial cells that continue to act as NSCs across vertebrates and others that are more lineage-restricted, such as the adult NG2-glia, the most frequent progenitor type in the adult mammalian brain, that remain within the oligodendrocyte lineage. Upon certain injury conditions, a distinct subset of quiescent astrocytes reactivates proliferation and a larger potential, clearly demonstrating the concept of heterogeneity with distinct subtypes of, e.g., astrocytes or NG2-glia performing rather different roles after brain injury. These new insights not only highlight the importance of glial cells for brain repair but also their great potential in various aspects of regeneration.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Reynolds, B. A., & Weiss, S. (1992) · Science · doi:10.1126/science.1553558 · Cited by 4,482
Microglia: Active sensor and versatile effector cells in the normal and pathologic brain
Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676
Kettenmann, H., Hanisch, U.-K., Noda, M., & Verkhratsky, A. (2011) · Physiological Reviews · doi:10.1152/physrev.00011.2010 · Cited by 3,547
Neuronal replacement from endogenous precursors in the adult brain after stroke
Arvidsson, A., Collin, T., Kirik, D., Kokaia, Z., & Lindvall, O. (2002) · Nature Medicine · doi:10.1038/nm747 · Cited by 2,799
Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions
Ming, G.-L., & Song, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.001 · Cited by 2,651
Molecular dissection of reactive astrogliosis and glial scar formation
Sofroniew, M. V. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.08.002 · Cited by 2,594
The Glial Nature of Embryonic and Adult Neural Stem Cells
Kriegstein, A., & Alvarez-Buylla, A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135600 · Cited by 2,475
Genomic analysis of reactive astrogliosis
Zamanian, J. L., Xu, L., Foo, L. C., Nouri, N., Zhou, L., Giffard, R. G., & Barres, B. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6221-11.2012 · Cited by 2,404
The cell biology of neurogenesis
Götz, M., & Huttner, W. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1739 · Cited by 2,130
Self-citationRaff, M. C., Miller, R. H., & Noble, M. (1983) · Nature · doi:10.1038/303390a0 · Cited by 2,030
Neurons derived from radial glial cells establish radial units in neocortex
Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016
Dynamics of hippocampal neurogenesis in adult humans
Spalding, K. L., Bergmann, O., Alkass, K., Bernard, S., Salehpour, M., Huttner, H. B., Boström, E., Westerlund, I., Vial, C., Buchholz, B. A., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.002 · Cited by 1,841
M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination
Miron, V. E., Boyd, A., Zhao, J.-W., Yuen, T. J., Ruckh, J. M., Shadrach, J. L., van Wijngaarden, P., Wagers, A. J., Williams, A., Franklin, R. J. M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3469 · Cited by 1,777
Chen, M. S., Huber, A. B., van der Haar, M. E., Frank, M., Schnell, L., Spillmann, A. A., Christ, F., & Schwab, M. E. (2000) · Nature · doi:10.1038/35000219 · Cited by 1,445
Multipotent CNS Stem Cells Are Present in the Adult Mammalian Spinal Cord and Ventricular Neuroaxis
Weiss, S., Dunne, C., Hewson, J., Wohl, C., Wheatley, M., Peterson, A. C., & Reynolds, B. A. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07599.1996 · Cited by 1,220
Induction of neurogenesis in the neocortex of adult mice
Magavi, S. S., Leavitt, B. R., & Macklis, J. D. (2000) · Nature · doi:10.1038/35016083 · Cited by 1,216
Kessaris, N., Fogarty, M., Iannarelli, P., Grist, M., Wegner, M., & Richardson, W. D. (2006) · Nature Neuroscience · doi:10.1038/nn1620 · Cited by 1,195
Extensive piano practicing has regionally specific effects on white matter development
Bengtsson, S. L., Nagy, Z., Skare, S., Forsman, L., Forssberg, H., & Ullén, F. (2005) · Nature Neuroscience · doi:10.1038/nn1516 · Cited by 1,193
The Immunopathology of Multiple Sclerosis: An Overview
Lassmann, H., Brück, W., & Lucchinetti, C. F. (2007) · Brain Pathology · doi:10.1111/j.1750-3639.2007.00064.x · Cited by 1,182
Microglia: new roles for the synaptic stripper
Kettenmann, H., Kirchhoff, F., & Verkhratsky, A. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.023 · Cited by 1,173
Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage
Malatesta, P., Hartfuss, E., & Götz, M. (2000) · Development · doi:10.1242/dev.127.24.5253 · Cited by 1,157
Self-citationSommer, I., & Schachner, M. (1981) · Developmental Biology · doi:10.1016/0012-1606(81)90477-2 · Cited by 1,134
The injured spinal cord spontaneously forms a new intraspinal circuit in adult rats
Bareyre, F. M., Kerschensteiner, M., Raineteau, O., Mettenleiter, T. C., Weinmann, O., & Schwab, M. E. (2004) · Nature Neuroscience · doi:10.1038/nn1195 · Cited by 1,086
Retinal Stem Cells in the Adult Mammalian Eye
Tropepe, V., Coles, B. L. K., Chiasson, B. J., Horsford, D. J., Elia, A. J., McInnes, R. R., & van der Kooy, D. (2000) · Science · doi:10.1126/science.287.5460.2032 · Cited by 1,081
Lu, Q. R., Sun, T., Zhu, Z., Ma, N., Garcia, M., Stiles, C. D., & Rowitch, D. H. (2002) · Cell · doi:10.1016/s0092-8674(02)00678-5 · Cited by 1,073
The bHLH Transcription Factors OLIG2 and OLIG1 Couple Neuronal and Glial Subtype Specification
Zhou, Q., & Anderson, D. J. (2002) · Cell · doi:10.1016/s0092-8674(02)00677-3 · Cited by 1,059
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 1,059
Mirzadeh, Z., Merkle, F. T., Soriano-Navarro, M., Garcia-Verdugo, J. M., & Alvarez-Buylla, A. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.07.004 · Cited by 1,015
Okada, S., Nakamura, M., Katoh, H., Miyao, T., Shimazaki, T., Ishii, K., Yamane, J., Yoshimura, A., Iwamoto, Y., Toyama, Y., et al. (2006) · Nature Medicine · doi:10.1038/nm1425 · Cited by 968
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961
STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury
Herrmann, J. E., Imura, T., Song, B., Qi, J., Ao, Y., Nguyen, T. K., Korsak, R. A., Takeda, K., Akira, S., & Sofroniew, M. V. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1709-08.2008 · Cited by 958
Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth
Wang, K. C., Koprivica, V., Kim, J. A., Sivasankaran, R., Guo, Y., Neve, R. L., & He, Z. (2002) · Nature · doi:10.1038/nature00867 · Cited by 955
Neurogenesis in the striatum of the adult human brain
Ernst, A., Alkass, K., Bernard, S., Salehpour, M., Perl, S., Tisdale, J., Possnert, G., Druid, H., & Frisén, J. (2014) · Cell · doi:10.1016/j.cell.2014.01.044 · Cited by 937
Dawson, M. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00210-0 · Cited by 927
Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling
Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 919
Palmer, T. D., Markakis, E. A., Willhoite, A. R., Safar, F., & Gage, F. H. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08487.1999 · Cited by 909
Asymmetric Inheritance of Radial Glial Fibers by Cortical Neurons
Miyata, T., Kawaguchi, A., Okano, H., & Ogawa, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00420-2 · Cited by 892
Oligodendrocyte Precursor Cells Reprogrammed to Become Multipotential CNS Stem Cells
Kondo, T., & Raff, M. (2000) · Science · doi:10.1126/science.289.5485.1754 · Cited by 878
Polydendrocytes (NG2 cells): multifunctional cells with lineage plasticity
Nishiyama, A., Komitova, M., Suzuki, R., & Zhu, X. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2495 · Cited by 865
A Pericyte Origin of Spinal Cord Scar Tissue
Göritz, C., Dias, D. O., Tomilin, N., Barbacid, M., Shupliakov, O., & Frisén, J. (2011) · Science · doi:10.1126/science.1203165 · Cited by 858
Lu, Q. R., Yuk, D.-I., Alberta, J. A., Zhu, Z., Pawlitzky, I., Chan, J., McMahon, A. P., Stiles, C. D., & Rowitch, D. H. (2000) · Neuron · doi:10.1016/s0896-6273(00)80897-1 · Cited by 852
Wanner, I. B., Anderson, M. A., Song, B., Levine, J., Fernandez, A., Gray-Thompson, Z., Ao, Y., & Sofroniew, M. V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2121-13.2013 · Cited by 839
Noble, M., Murray, K., Stroobant, P., Waterfield, M. D., & Riddle, P. (1988) · Nature · doi:10.1038/333560a0 · Cited by 830
Eyes Wide Open: A Critical Review of Sphere-Formation as an Assay for Stem Cells
Pastrana, E., Silva-Vargas, V., & Doetsch, F. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.04.007 · Cited by 828
Hughes, E. G., Kang, S. H., Fukaya, M., & Bergles, D. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3390 · Cited by 808
Kang, S. H., Fukaya, M., Yang, J. K., Rothstein, J. D., & Bergles, D. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.009 · Cited by 787
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
Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain
Buffo, A., Rite, I., Tripathi, P., Lepier, A., Colak, D., Horn, A.-P., Mori, T., & Götz, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709002105 · Cited by 765
Self-citationMalatesta, P., Hack, M. A., Hartfuss, E., Kettenmann, H., Klinkert, W., Kirchhoff, F., & Götz, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00116-8 · Cited by 746
Self-citationRegeneration of adult axons in white matter tracts of the central nervous system
Davies, S. J. A., Fitch, M. T., Memberg, S. P., Hall, A. K., Raisman, G., & Silver, J. (1997) · Nature · doi:10.1038/37776 · Cited by 737
The oligodendrocyte and its many cellular processes
PFEIFFER, S., WARRINGTON, A., & BANSAL, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 737
Herculano-Houzel, S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201895109 · Cited by 726
Identification of a multipotent astrocytic stem cell in the immature and adult mouse brain
Laywell, E. D., Rakic, P., Kukekov, V. G., Holland, E. C., & Steindler, D. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250471697 · Cited by 721
Persistent Production of Neurons from Adult Brain Stem Cells During Recovery after Stroke
Thored, P., Arvidsson, A., Cacci, E., Ahlenius, H., Kallur, T., Darsalia, V., Ekdahl, C. T., Kokaia, Z., & Lindvall, O. (2006) · Stem Cells · doi:10.1634/stemcells.2005-0281 · Cited by 714
NG2-Positive Oligodendrocyte Progenitor Cells in Adult Human Brain and Multiple Sclerosis Lesions
Chang, A., Nishiyama, A., Peterson, J., Prineas, J., & Trapp, B. D. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06404.2000 · Cited by 712
Adult Spinal Cord Stem Cells Generate Neurons after Transplantation in the Adult Dentate Gyrus
Shihabuddin, L. S., Horner, P. J., Ray, J., & Gage, F. H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08727.2000 · Cited by 708
Palmer, T. D., Ray, J., & Gage, F. H. (1995) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1995.1035 · Cited by 697
NG2 cells generate both oligodendrocytes and gray matter astrocytes
Zhu, X., Bergles, D. E., & Nishiyama, A. (2008) · Development · doi:10.1242/dev.004895 · Cited by 683
Induction of myelination in the central nervous system by electrical activity
Demerens, C., Stankoff, B., Logak, M., Anglade, P., Allinquant, B., Couraud, F., Zalc, B., & Lubetzki, C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9887 · Cited by 678
Proliferation of oligodendrocyte precursor cells depends on electrical activity in axons
Barres, B. A., & Raff, M. C. (1993) · Nature · doi:10.1038/361258a0 · Cited by 673
Spinal Cord Injury Reveals Multilineage Differentiation of Ependymal Cells
Meletis, K., Barnabé-Heider, F., Carlén, M., Evergren, E., Tomilin, N., Shupliakov, O., & Frisén, J. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060182 · Cited by 666
Nunes, M. C., Roy, N. S., Keyoung, H. M., Goodman, R. R., McKhann, G., Jiang, L., Kang, J., Nedergaard, M., & Goldman, S. A. (2003) · Nature Medicine · doi:10.1038/nm837 · Cited by 656
Zawadzka, M., Rivers, L. E., Fancy, S. P. J., Zhao, C., Tripathi, R., Jamen, F., Young, K., Goncharevich, A., Pohl, H., Rizzi, M., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.04.002 · Cited by 650
Murine features of neurogenesis in the human hippocampus across the lifespan from 0 to 100 years
Knoth, R., Singec, I., Ditter, M., Pantazis, G., Capetian, P., Meyer, R. P., Horvat, V., Volk, B., & Kempermann, G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008809 · Cited by 650
Myelination and the trophic support of long axons
Nave, K.-A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2797 · Cited by 648
Nishiyama, A., Lin, X.-H., Giese, N., Heldin, C.-H., & Stallcup, W. B. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960201)43:3<299::aid-jnr5>3.0.co;2-e · Cited by 630
Origin of New Glial Cells in Intact and Injured Adult Spinal Cord
Barnabé-Heider, F., Göritz, C., Sabelström, H., Takebayashi, H., Pfrieger, F. W., Meletis, K., & Frisén, J. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.07.014 · Cited by 628
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
Fode, C., Ma, Q., Casarosa, S., Ang, S.-L., Anderson, D. J., & Guillemot, F. (2000) · Genes & Development · doi:10.1101/gad.14.1.67 · Cited by 624
Myelin-Associated Glycoprotein Interacts with the Nogo66 Receptor to Inhibit Neurite Outgrowth
Domeniconi, M., Cao, Z., Spencer, T., Sivasankaran, R., Wang, K. C., Nikulina, E., Kimura, N., Cai, H., Deng, K., Gao, Y., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00770-5 · Cited by 593
NG2 proteoglycan is expressed exclusively by mural cells during vascular morphogenesis
Ozerdem, U., Grako, K. A., Dahlin‐Huppe, K., Monosov, E., & Stallcup, W. B. (2001) · Developmental Dynamics · doi:10.1002/dvdy.1200 · Cited by 593
Gesammelte Abhandlungen zur wissenschaftlichen Medicin
Virchow, R. (1862) · Cited by 590
Microtubule Stabilization Reduces Scarring and Causes Axon Regeneration After Spinal Cord Injury
Hellal, F., Hurtado, A., Ruschel, J., Flynn, K. C., Laskowski, C. J., Umlauf, M., Kapitein, L. C., Strikis, D., Lemmon, V., Bixby, J., et al. (2011) · Science · doi:10.1126/science.1201148 · Cited by 588
In vivo imaging of axonal degeneration and regeneration in the injured spinal cord
Kerschensteiner, M., Schwab, M. E., Lichtman, J. W., & Misgeld, T. (2005) · Nature Medicine · doi:10.1038/nm1229 · Cited by 580
The “quad‐partite” synapse: Microglia‐synapse interactions in the developing and mature CNS
Schafer, D. P., Lehrman, E. K., & Stevens, B. (2013) · Glia · doi:10.1002/glia.22389 · Cited by 570
Dimou, L., Simon, C., Kirchhoff, F., Takebayashi, H., & Götz, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2831-08.2008 · Cited by 551
Endogenous progenitors remyelinate demyelinated axons in the adult CNS
Gensert, J. M., & Goldman, J. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)80359-1 · Cited by 544
De novo generation of neuronal cells from the adult mouse brain.
Richards, L. J., Kilpatrick, T. J., & Bartlett, P. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.18.8591 · Cited by 544
Regional Astrocyte Allocation Regulates CNS Synaptogenesis and Repair
Tsai, H.-H., Li, H., Fuentealba, L. C., Molofsky, A. V., Taveira-Marques, R., Zhuang, H., Tenney, A., Murnen, A. T., Fancy, S. P. J., Merkle, F., et al. (2012) · Science · doi:10.1126/science.1222381 · Cited by 533
Acute Inflammation Initiates the Regenerative Response in the Adult Zebrafish Brain
Kyritsis, N., Kizil, C., Zocher, S., Kroehne, V., Kaslin, J., Freudenreich, D., Iltzsche, A., & Brand, M. (2012) · Science · doi:10.1126/science.1228773 · Cited by 517
The stem cell potential of glia: lessons from reactive gliosis
Robel, S., Berninger, B., & Götz, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2978 · Cited by 515
Self-citationPringle, N. P., & Richardson, W. D. (1993) · Development · doi:10.1242/dev.117.2.525 · Cited by 510
Local generation of glia is a major astrocyte source in postnatal cortex
Ge, W.-P., Miyawaki, A., Gage, F. H., Jan, Y. N., & Jan, L. Y. (2012) · Nature · doi:10.1038/nature10959 · Cited by 507
Protective Role of Reactive Astrocytes in Brain Ischemia
Li, L., Lundkvist, A., Andersson, D., Wilhelmsson, U., Nagai, N., Pardo, A. C., Nodin, C., Ståhlberg, A., Aprico, K., Larsson, K., et al. (2008) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600546 · Cited by 505
The role of mononuclear phagocytes in wound healing after traumatic injury to adult mammalian brain
Giulian, D., Chen, J., Ingeman, J., George, J., & Noponen, M. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-12-04416.1989 · Cited by 498
Takebayashi, H., Nabeshima, Y., Yoshida, S., Chisaka, O., Ikenaka, K., & Nabeshima, Y.-I. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00926-0 · Cited by 494
Belachew, S., Chittajallu, R., Aguirre, A. A., Yuan, X., Kirby, M., Anderson, S., & Gallo, V. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200210110 · Cited by 488
In vivo reprogramming of astrocytes to neuroblasts in the adult brain
Niu, W., Zang, T., Zou, Y., Fang, S., Smith, D. K., Bachoo, R., & Zhang, C.-L. (2013) · Nature Cell Biology · doi:10.1038/ncb2843 · Cited by 482
Wallerian Degeneration, WldS, and Nmnat
Coleman, M. P., & Freeman, M. R. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153248 · Cited by 473
Age-dependent fate and lineage restriction of single NG2 cells
Zhu, X., Hill, R. A., Dietrich, D., Komitova, M., Suzuki, R., & Nishiyama, A. (2011) · Development · doi:10.1242/dev.047951 · Cited by 464
Dayer, A. G., Cleaver, K. M., Abouantoun, T., & Cameron, H. A. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200407053 · Cited by 454
Regeneration of the adult zebrafish brain from neurogenic radial glia-type progenitors
Kroehne, V., Freudenreich, D., Hans, S., Kaslin, J., & Brand, M. (2011) · Development · doi:10.1242/dev.072587 · Cited by 452
Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke
Carlén, M., Meletis, K., Göritz, C., Darsalia, V., Evergren, E., Tanigaki, K., Amendola, M., Barnabé-Heider, F., Yeung, M. S. Y., Naldini, L., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2268 · Cited by 452
The Adult Substantia Nigra Contains Progenitor Cells with Neurogenic Potential
Lie, D. C., Dziewczapolski, G., Willhoite, A. R., Kaspar, B. K., Shults, C. W., & Gage, F. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06639.2002 · Cited by 449
Repair of demyelinated lesions by transplantation of purified 0-2A progenitor cells
Groves, A. K., Barnett, S. C., Franklin, R. J. M., Crang, A. J., Mayer, M., Blakemore, W. F., & Noble, M. (1993) · Nature · doi:10.1038/362453a0 · Cited by 444
Pringle, N. P., Mudhar, H. S., Collarini, E. J., & Richardson, W. D. (1992) · Development · doi:10.1242/dev.115.2.535 · Cited by 443
Extensive elongation of axons from rat brain into peripheral nerve grafts
Benfey, M., & Aguayo, A. J. (1982) · Nature · doi:10.1038/296150a0 · Cited by 442
Apoptosis after traumatic human spinal cord injury
Emery, E., Aldana, P., Bunge, M. B., Puckett, W., Srinivasan, A., Keane, R. W., Bethea, J., & Levi, A. D. O. (1998) · Journal of Neurosurgery · doi:10.3171/jns.1998.89.6.0911 · Cited by 440
Mizuguchi, R., Sugimori, M., Takebayashi, H., Kosako, H., Nagao, M., Yoshida, S., Nabeshima, Y.-I., Shimamura, K., & Nakafuku, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00413-5 · Cited by 436
Matthias, K., Kirchhoff, F., Seifert, G., Hüttmann, K., Matyash, M., Kettenmann, H., & Steinhäuser, C. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01750.2003 · Cited by 431
Origin and function of olfactory bulb interneuron diversity
Lledo, P.-M., Merkle, F. T., & Alvarez-Buylla, A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.05.006 · Cited by 427
Glial specification in the vertebrate neural tube
Rowitch, D. H. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1389 · Cited by 426
Live imaging of astrocyte responses to acute injury reveals selective juxtavascular proliferation
Bardehle, S., Krüger, M., Buggenthin, F., Schwausch, J., Ninkovic, J., Clevers, H., Snippert, H. J., Theis, F. J., Meyer-Luehmann, M., Bechmann, I., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3371 · Cited by 426
Self-citationFallon, J., Reid, S., Kinyamu, R., Opole, I., Opole, R., Baratta, J., Korc, M., Endo, T. L., Duong, A., Nguyen, G., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.26.14686 · Cited by 425
Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon
Adolf, B., Chapouton, P., Lam, C. S., Topp, S., Tannhäuser, B., Strähle, U., Götz, M., & Bally-Cuif, L. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.03.023 · Cited by 424
Self-citationMcTigue, D. M., Wei, P., & Stokes, B. T. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03392.2001 · Cited by 423
Astrocyte intermediate filaments in CNS pathologies and regeneration
Pekny, M., & Pekna, M. (2004) · The Journal of Pathology · doi:10.1002/path.1645 · Cited by 420
Generation of induced neurons via direct conversion in vivo
Torper, O., Pfisterer, U., Wolf, D. A., Pereira, M., Lau, S., Jakobsson, J., Björklund, A., Grealish, S., & Parmar, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303829110 · Cited by 417
Buffo, A., Vosko, M. R., Ertürk, D., Hamann, G. F., Jucker, M., Rowitch, D., & Götz, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506535102 · Cited by 394
Self-citationIncreased expression of the NG2 chondroitin-sulfate proteoglycan after brain injury
Levine, J. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-08-04716.1994 · Cited by 393
Functional regeneration of respiratory pathways after spinal cord injury
Alilain, W. J., Horn, K. P., Hu, H., Dick, T. E., & Silver, J. (2011) · Nature · doi:10.1038/nature10199 · Cited by 390
Radial glia: multi-purpose cells for vertebrate brain development
Campbell, K., & Götz, M. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02156-2 · Cited by 388
Self-citationThallmair, M., Metz, G. A. S., Z'Graggen, W. J., Raineteau, O., Kartje, G. L., & Schwab, M. E. (1998) · Nature Neuroscience · doi:10.1038/373 · Cited by 382
Reactive Glia in the Injured Brain Acquire Stem Cell Properties in Response to Sonic Hedgehog
Sirko, S., Behrendt, G., Johansson, P. A., Tripathi, P., Costa, M. R., Bek, S., Heinrich, C., Tiedt, S., Colak, D., Dichgans, M., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.01.019 · Cited by 381
Self-citationThe Age of Olfactory Bulb Neurons in Humans
Bergmann, O., Liebl, J., Bernard, S., Alkass, K., Yeung, M. S. Y., Steier, P., Kutschera, W., Johnson, L., Landén, M., Druid, H., et al. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.030 · Cited by 374
The perineuronal net and the control of CNS plasticity
Wang, D., & Fawcett, J. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1375-y · Cited by 373
Spinal cord injury is accompanied by chronic progressive demyelination
Totoiu, M. O., & Keirstead, H. S. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20517 · Cited by 372
Spiking and nonspiking classes of oligodendrocyte precursor glia in CNS white matter
Káradóttir, R., Hamilton, N. B., Bakiri, Y., & Attwell, D. (2008) · Nature Neuroscience · doi:10.1038/nn2060 · Cited by 370
Adult generation of glutamatergic olfactory bulb interneurons
Brill, M. S., Ninkovic, J., Winpenny, E., Hodge, R. D., Ozen, I., Yang, R., Lepier, A., Gascón, S., Erdelyi, F., Szabo, G., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2416 · Cited by 368
Self-citationKokovay, E., Goderie, S., Wang, Y., Lotz, S., Lin, G., Sun, Y., Roysam, B., Shen, Q., & Temple, S. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.05.019 · Cited by 359
Adult neurogenesis and brain regeneration in zebrafish
Kizil, C., Kaslin, J., Kroehne, V., & Brand, M. (2012) · Developmental Neurobiology · doi:10.1002/dneu.20918 · Cited by 349
Keirstead, H. S., Levine, J. M., & Blakemore, W. F. (1998) · Glia · doi:10.1002/(sici)1098-1136(199802)22:2<161::aid-glia7>3.0.co;2-a · Cited by 345
Beckervordersandforth, R., Tripathi, P., Ninkovic, J., Bayam, E., Lepier, A., Stempfhuber, B., Kirchhoff, F., Hirrlinger, J., Haslinger, A., Lie, D. C., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.11.017 · Cited by 335
Self-citationHochstim, C., Deneen, B., Lukaszewicz, A., Zhou, Q., & Anderson, D. J. (2008) · Cell · doi:10.1016/j.cell.2008.02.046 · Cited by 331
Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice
Kraft, A. W., Hu, X., Yoon, H., Yan, P., Xiao, Q., Wang, Y., Gil, S. C., Brown, J., Wilhelmsson, U., Restivo, J. L., et al. (2013) · The FASEB Journal · doi:10.1096/fj.12-208660 · Cited by 324
Denis-Donini, S., Glowinski, J., & Prochiantz, A. (1984) · Nature · doi:10.1038/307641a0 · Cited by 324
Simon, C., Götz, M., & Dimou, L. (2011) · Glia · doi:10.1002/glia.21156 · Cited by 313
Self-citationRobins, S. C., Stewart, I., McNay, D. E., Taylor, V., Giachino, C., Goetz, M., Ninkovic, J., Briancon, N., Maratos-Flier, E., Flier, J. S., et al. (2013) · Nature Communications · doi:10.1038/ncomms3049 · Cited by 306
Resident Neural Stem Cells Restrict Tissue Damage and Neuronal Loss After Spinal Cord Injury in Mice
Sabelström, H., Stenudd, M., Réu, P., Dias, D. O., Elfineh, M., Zdunek, S., Damberg, P., Göritz, C., & Frisén, J. (2013) · Science · doi:10.1126/science.1242576 · Cited by 305
Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth
Benson, M. D., Romero, M. I., Lush, M. E., Lu, Q. R., Henkemeyer, M., & Parada, L. F. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504021102 · Cited by 305
Loss of astrocytic domain organization in the epileptic brain
Oberheim, N. A., Tian, G.-F., Han, X., Peng, W., Takano, T., Ransom, B., & Nedergaard, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4980-07.2008 · Cited by 303
Timsit, S., Martinez, S., Allinquant, B., Peyron, F., Puelles, L., & Zalc, B. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-02-01012.1995 · Cited by 302
Multiple restricted origin of oligodendrocytes
Spassky, N., Goujet-Zalc, C., Parmantier, E., Olivier, C., Martinez, S., Ikenaka, K., Macklin, W., Zalc, B., & Thomas, J.-L. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)91253-x · Cited by 301
Neuroglia: the 150 years after
Kettenmann, H., & Verkhratsky, A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.003 · Cited by 300
RAFF, M., ABNEY, E., & FOKSEANG, J. (1985) · Cell · doi:10.1016/s0092-8674(85)80101-x · Cited by 294
Excitability and synaptic communication within the oligodendrocyte lineage
De Biase, L. M., Nishiyama, A., & Bergles, D. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.6000-09.2010 · Cited by 286
Glial-Restricted Precursors Are Derived from Multipotent Neuroepithelial Stem Cells
Rao, M. S., & Mayer-Proschel, M. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8597 · Cited by 284
FGF-2 Is Sufficient to Isolate Progenitors Found in the Adult Mammalian Spinal Cord
Shihabuddin, L. S., Ray, J., & Gage, F. H. (1997) · Experimental Neurology · doi:10.1006/exnr.1997.6697 · Cited by 283
Protective astrogenesis from the SVZ niche after injury is controlled by Notch modulator Thbs4
Benner, E. J., Luciano, D., Jo, R., Abdi, K., Paez-Gonzalez, P., Sheng, H., Warner, D. S., Liu, C., Eroglu, C., & Kuo, C. T. (2013) · Nature · doi:10.1038/nature12069 · Cited by 282
Pellegrini, E., Mouriec, K., Anglade, I., Menuet, A., Le Page, Y., Gueguen, M., Marmignon, M., Brion, F., Pakdel, F., & Kah, O. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21222 · Cited by 277
Motor Neuron Regeneration in Adult Zebrafish
Reimer, M. M., Sörensen, I., Kuscha, V., Frank, R. E., Liu, C., Becker, C. G., & Becker, T. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1189-08.2008 · Cited by 276
Sternberger, N. H., Itoyama, Y., Kies, M. W., & Webster, H. D. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.5.2521 · Cited by 270
Evidence for the ventral origin of oligodendrocyte precursors in the rat spinal cord
Warf, B., Fok-Seang, J., & Miller, R. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02477.1991 · Cited by 269
NG2 cells: Properties, progeny and origin
Trotter, J., Karram, K., & Nishiyama, A. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.006 · Cited by 264
Differentiation of proliferated NG2-positive glial progenitor cells in a remyelinating lesion
Watanabe, M., Toyama, Y., & Nishiyama, A. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10338 · Cited by 261
Radial glial cell heterogeneity—The source of diverse progeny in the CNS
PINTO, L., & GOTZ, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.02.010 · Cited by 260
Chapouton, P., Skupien, P., Hesl, B., Coolen, M., Moore, J. C., Madelaine, R., Kremmer, E., Faus-Kessler, T., Blader, P., Lawson, N. D., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6170-09.2010 · Cited by 259
Roy, N. S., Wang, S., Harrison-Restelli, C., Benraiss, A., Fraser, R. A. R., Gravel, M., Braun, P. E., & Goldman, S. A. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09986.1999 · Cited by 258
Cell cycle dynamics of NG2 cells in the postnatal and ageing brain
Psachoulia, K., Jamen, F., Young, K. M., & Richardson, W. D. (2009) · Neuron Glia Biology · doi:10.1017/s1740925x09990354 · Cited by 257
März, M., Chapouton, P., Diotel, N., Vaillant, C., Hesl, B., Takamiya, M., Lam, C. S., Kah, O., Bally‐Cuif, L., & Strähle, U. (2010) · Glia · doi:10.1002/glia.20971 · Cited by 257
Myelination: An Overlooked Mechanism of Synaptic Plasticity?
Fields, R. D. (2005) · The Neuroscientist · doi:10.1177/1073858405282304 · Cited by 256
Proliferation of Parenchymal Neural Progenitors in Response to Injury in the Adult Rat Spinal Cord
Yamamoto, S.-I., Yamamoto, N., Kitamura, T., Nakamura, K., & Nakafuku, M. (2001) · Experimental Neurology · doi:10.1006/exnr.2001.7798 · Cited by 253
The foxa2 gene controls the birth and spontaneous degeneration of dopamine neurons in old age
Kittappa, R., Chang, W. W., Awatramani, R. B., & McKay, R. D. G. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050325 · Cited by 251
Neurogenesis of corticospinal motor neurons extending spinal projections in adult mice
Chen, J., Magavi, S. S. P., & Macklis, J. D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406795101 · Cited by 241
Hohlfeld, R., & Wekerle, H. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0404874101 · Cited by 239
Haan, N., Goodman, T., Najdi-Samiei, A., Stratford, C. M., Rice, R., El Agha, E., Bellusci, S., & Hajihosseini, M. K. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2437-12.2013 · Cited by 239
Polito, A., & Reynolds, R. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00454.x · Cited by 231
Environmental impact on direct neuronal reprogramming in vivo in the adult brain
Grande, A., Sumiyoshi, K., López-Juárez, A., Howard, J., Sakthivel, B., Aronow, B., Campbell, K., & Nakafuku, M. (2013) · Nature Communications · doi:10.1038/ncomms3373 · Cited by 227
Shechter, R., & Schwartz, M. (2013) · The Journal of Pathology · doi:10.1002/path.4106 · Cited by 225
Aguirre, A., & Gallo, V. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3572-04.2004 · Cited by 224
Neurotransmitter-mediated control of neurogenesis in the adult vertebrate brain
Berg, D. A., Belnoue, L., Song, H., & Simon, A. (2013) · Development · doi:10.1242/dev.088005 · Cited by 224
De Novo Neurogenesis in Adult Hypothalamus as a Compensatory Mechanism to Regulate Energy Balance
Pierce, A. A., & Xu, A. W. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2479-09.2010 · Cited by 223
Transplantation reveals regional differences in oligodendrocyte differentiation in the adult brain
Viganò, F., Möbius, W., Götz, M., & Dimou, L. (2013) · Nature Neuroscience · doi:10.1038/nn.3503 · Cited by 221
Self-citationPrior experience enhances plasticity in adult visual cortex
Hofer, S. B., Mrsic-Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2006) · Nature Neuroscience · doi:10.1038/nn1610 · Cited by 220
Behrendt, G., Baer, K., Buffo, A., Curtis, M. A., Faull, R. L., Rees, M. I., Götz, M., & Dimou, L. (2013) · Glia · doi:10.1002/glia.22432 · Cited by 219
Self-citationXu, Q., Guo, L., Moore, H., Waclaw, R. R., Campbell, K., & Anderson, S. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.004 · Cited by 218
Ninkovic, J., Steiner-Mezzadri, A., Jawerka, M., Akinci, U., Masserdotti, G., Petricca, S., Fischer, J., von Holst, A., Beckers, J., Lie, C. D., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.07.002 · Cited by 214
Self-citationMason, J. L., Toews, A., Hostettler, J. D., Morell, P., Suzuki, K., Goldman, J. E., & Matsushima, G. K. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63726-1 · Cited by 212
Identity, distribution, and development of polydendrocytes: NG2-expressing glial cells
Nishiyama, A., Watanabe, M., Yang, Z., & Bu, J. (2002) · Journal of Neurocytology · doi:10.1023/a:1025783412651 · Cited by 210
Amplification of progenitors in the mammalian telencephalon includes a new radial glial cell type
Pilz, G.-A., Shitamukai, A., Reillo, I., Pacary, E., Schwausch, J., Stahl, R., Ninkovic, J., Snippert, H. J., Clevers, H., Godinho, L., et al. (2013) · Nature Communications · doi:10.1038/ncomms3125 · Cited by 210
Self-citationLong-Term Potentiation of Neuron-Glia Synapses Mediated by Ca 2+ -Permeable AMPA Receptors
Ge, W.-P., Yang, X.-J., Zhang, Z., Wang, H.-K., Shen, W., Deng, Q.-D., & Duan, S. (2006) · Science · doi:10.1126/science.1124669 · Cited by 209
Ohori, Y., Yamamoto, S.-I., Nagao, M., Sugimori, M., Yamamoto, N., Nakamura, K., & Nakafuku, M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3127-06.2006 · Cited by 209
Development of NG2 neural progenitor cells requires Olig gene function
Ligon, K. L., Kesari, S., Kitada, M., Sun, T., Arnett, H. A., Alberta, J. A., Anderson, D. J., Stiles, C. D., & Rowitch, D. H. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511001103 · Cited by 205
Restricted growth of Schwann cells lacking Cajal bands slows conduction in myelinated nerves
Court, F. A., Sherman, D. L., Pratt, T., Garry, E. M., Ribchester, R. R., Cottrell, D. F., Fleetwood-Walker, S. M., & Brophy, P. J. (2004) · Nature · doi:10.1038/nature02841 · Cited by 205
Regenerative medicine for retinal diseases: activating endogenous repair mechanisms
Karl, M. O., & Reh, T. A. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.02.003 · Cited by 203
Stem Cells in the Adult Zebrafish Cerebellum: Initiation and Maintenance of a Novel Stem Cell Niche
Kaslin, J., Ganz, J., Geffarth, M., Grandel, H., Hans, S., & Brand, M. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0072-09.2009 · Cited by 203
ELECTRON MICROSCOPIC FEATURES OF MULTIPLE SCLEROSIS LESIONS
PÉRIER, O., & GRÉGOIRE, A. (1965) · Brain · doi:10.1093/brain/88.5.937 · Cited by 203
Adult neurogenesis in non‐mammalian vertebrates
Chapouton, P., Jagasia, R., & Bally‐Cuif, L. (2007) · BioEssays · doi:10.1002/bies.20615 · Cited by 201
Kokovay, E., Wang, Y., Kusek, G., Wurster, R., Lederman, P., Lowry, N., Shen, Q., & Temple, S. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.06.016 · Cited by 201
Synantocytes: the fifth element
Butt, A. M., Hamilton, N., Hubbard, P., Pugh, M., & Ibrahim, M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00458.x · Cited by 201
Neuron-glia synapses in the brain
Bergles, D. E., Jabs, R., & Steinhäuser, C. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.003 · Cited by 197
Rothenaigner, I., Krecsmarik, M., Hayes, J. A., Bahn, B., Lepier, A., Fortin, G., Götz, M., Jagasia, R., & Bally-Cuif, L. (2011) · Development · doi:10.1242/dev.058156 · Cited by 197
Self-citationBaumgart, E. V., Barbosa, J. S., Bally‐cuif, L., Götz, M., & Ninkovic, J. (2012) · Glia · doi:10.1002/glia.22269 · Cited by 196
Self-citationWu, S., Wu, Y., & Capecchi, M. R. (2006) · Development · doi:10.1242/dev.02236 · Cited by 193
Scar-mediated inhibition and CSPG receptors in the CNS
Sharma, K., Selzer, M. E., & Li, S. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.07.009 · Cited by 188
Shimada, I. S., LeComte, M. D., Granger, J. C., Quinlan, N. J., & Spees, J. L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4303-11.2012 · Cited by 187
Regenerative response following stab injury in the adult zebrafish telencephalon
März, M., Schmidt, R., Rastegar, S., & Strähle, U. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22710 · Cited by 187
The cerebrospinal fluid: regulator of neurogenesis, behavior, and beyond
Zappaterra, M. W., & Lehtinen, M. K. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0957-x · Cited by 185
Lam, C. S., März, M., & Strähle, U. (2009) · Developmental Dynamics · doi:10.1002/dvdy.21853 · Cited by 184
Plasticity of developing cerebellar cells in vitro studied with antibodies against the NG2 antigen
Levine, J., & Stallcup, W. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-09-02721.1987 · Cited by 184
Clarke, L. E., Young, K. M., Hamilton, N. B., Li, H., Richardson, W. D., & Attwell, D. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0928-12.2012 · Cited by 182
Huang, W., Zhao, N., Bai, X., Karram, K., Trotter, J., Goebbels, S., Scheller, A., & Kirchhoff, F. (2014) · Glia · doi:10.1002/glia.22648 · Cited by 181
Axonal pathology in myelin disorders
Bjartmar, C., Yin, X., & Trapp, B. D. (1999) · Journal of Neurocytology · doi:10.1023/a:1007010205037 · Cited by 180
Adult zebrafish as a model for successful central nervous system regeneration
Becker, C. G., & Becker, T. (2008) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2008-00443 · Cited by 180
Di Bello, I. C., Dawson, M. R. L., Levine, J. M., & Reynolds, R. (1999) · Journal of Neurocytology · doi:10.1023/a:1007069815302 · Cited by 179
VEGF-C is a trophic factor for neural progenitors in the vertebrate embryonic brain
Le Bras, B., Barallobre, M.-J., Homman-Ludiye, J., Ny, A., Wyns, S., Tammela, T., Haiko, P., Karkkainen, M. J., Yuan, L., Muriel, M.-P., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1646 · Cited by 178
Battiste, J., Helms, A. W., Kim, E. J., Savage, T. K., Lagace, D. C., Mandyam, C. D., Eisch, A. J., Miyoshi, G., & Johnson, J. E. (2007) · Development · doi:10.1242/dev.02727 · Cited by 177
Early development and dispersal of oligodendrocyte precursors in the embryonic chick spinal cord
Ono, K., Bansal, R., Payne, J., Rutishauser, U., & Miller, R. H. (1995) · Development · doi:10.1242/dev.121.6.1743 · Cited by 172
Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2
Meijer, D. H., Kane, M. F., Mehta, S., Liu, H., Harrington, E., Taylor, C. M., Stiles, C. D., & Rowitch, D. H. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3386 · Cited by 172
Levine, J., & Nishiyama, A. (1996) · PubMed · Cited by 171
Cited by
Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system
Marques, S., Zeisel, A., Codeluppi, S., van Bruggen, D., Mendanha Falcão, A., Xiao, L., Li, H., Häring, M., Hochgerner, H., Romanov, R. A., et al. (2016) · Science · doi:10.1126/science.aaf6463 · Cited by 1,132
Glia as architects of central nervous system formation and function
Allen, N. J., & Lyons, D. A. (2018) · Science · doi:10.1126/science.aat0473 · Cited by 1,001
Brain Cell Type Specific Gene Expression and Co-expression Network Architectures
McKenzie, A. T., Wang, M., Hauberg, M. E., Fullard, J. F., Kozlenkov, A., Keenan, A., Hurd, Y. L., Dracheva, S., Casaccia, P., Roussos, P., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-27293-5 · Cited by 481
Elusive roles for reactive astrocytes in neurodegenerative diseases
Ben Haim, L., Carrillo-de Sauvage, M.-A., Ceyzériat, K., & Escartin, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00278 · Cited by 453
Sox2-mediated conversion of NG2 glia into induced neurons in the injured adult cerebral cortex
Heinrich, C., Bergami, M., Gascón, S., Lepier, A., Viganò, F., Dimou, L., Sutor, B., Berninger, B., & Götz, M. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.10.007 · Cited by 323
Self-citation
Metadata
- Authors
- Dimou, L., & Götz, M.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2014-07
- Volume
- 94
- Issue
- 3
- Pages
- 709-737
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2117122511
- Cited by
- 264
- References
- 307
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- closed
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.