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
Items 201–307 of 307
NG2 cells generate oligodendrocytes and gray matter astrocytes in the spinal cord
Zhu, X., Hill, R. A., & Nishiyama, A. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09000015 · Cited by 171
A Radial Glia-Specific Role of RhoA in Double Cortex Formation
Cappello, S., Böhringer, C. R. J., Bergami, M., Conzelmann, K.-K., Ghanem, A., Tomassy, G. S., Arlotta, P., Mainardi, M., Allegra, M., Caleo, M., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.030 · Cited by 169
Self-citationComparative aspects of adult neural stem cell activity in vertebrates
Grandel, H., & Brand, M. (2012) · Development Genes and Evolution · doi:10.1007/s00427-012-0425-5 · Cited by 168
Windrem, M. S., Roy, N. S., Wang, J., Nunes, M., Benraiss, A., Goodman, R., McKhann, G. M., & Goldman, S. A. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10397 · Cited by 167
Schnapp, E., Kragl, M., Rubin, L., & Tanaka, E. M. (2005) · Development · doi:10.1242/dev.01906 · Cited by 167
Polydendrocytes: NG2 Cells with Many Roles in Development and Repair of the CNS
Nishiyama, A. (2007) · The Neuroscientist · doi:10.1177/1073858406295586 · Cited by 162
The biology of CNS remyelination: The key to therapeutic advances
Franklin, R. J. M., & Kotter, M. R. (2008) · Journal of Neurology · doi:10.1007/s00415-008-1004-6 · Cited by 160
Growth and differentiation properties of O‐2A Progenitors purified from rat cerebral hemispheres
Behar, T. N., McMorris, F. A., Novotny, E. A., Barker, J. L., & Dubois-Dalcq, M. E. (1988) · Journal of Neuroscience Research · doi:10.1002/jnr.490210209 · Cited by 157
The Brain’s Extracellular Matrix and Its Role in Synaptic Plasticity
Frischknecht, R., & Gundelfinger, E. D. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-7091-0932-8_7 · Cited by 156
Perivascular instruction of cell genesis and fate in the adult brain
Goldman, S. A., & Chen, Z. (2011) · Nature Neuroscience · doi:10.1038/nn.2963 · Cited by 156
Clonal Identity Determines Astrocyte Cortical Heterogeneity
García‐Marqués, J., & López‐Mascaraque, L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs134 · Cited by 156
Astroglial structures in the zebrafish brain
Grupp, L., Wolburg, H., & Mack, A. F. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22481 · Cited by 155
Mekki-Dauriac, S., Agius, E., Kan, P., & Cochard, P. (2002) · Development · doi:10.1242/dev.129.22.5117 · Cited by 154
Requirements for schwann cell migration within cns environments: A viewpoint
Franklin, R. J. M., & Blakemore, W. F. (1993) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(93)90052-f · Cited by 154
Misson, J., Edwards, M. A., Yamamoto, M., & Caviness, V. S. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90043-0 · Cited by 152
Split-Cre Complementation Indicates Coincident Activity of Different Genes In Vivo
Hirrlinger, J., Scheller, A., Hirrlinger, P. G., Kellert, B., Tang, W., Wehr, M. C., Goebbels, S., Reichenbach, A., Sprengel, R., Rossner, M. J., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004286 · Cited by 151
NG2+/Olig2+ Cells are the Major Cycle‐Related Cell Population of the Adult Human Normal Brain
Geha, S., Pallud, J., Junier, M., Devaux, B. C., Léonard, N., Chassoux, F., Chneiweiss, H., Daumas‐Duport, C., & Varlet, P. (2009) · Brain Pathology · doi:10.1111/j.1750-3639.2009.00295.x · Cited by 146
Molecular Diversity Subdivides the Adult Forebrain Neural Stem Cell Population
Giachino, C., Başak, O., Lugert, S., Knuckles, P., Obernier, K., Fiorelli, R., Frank, S., Raineteau, O., Álvarez-Buylla, A., & Taylor, V. (2013) · Stem Cells · doi:10.1002/stem.1520 · Cited by 145
Alunni, A., Krecsmarik, M., Bosco, A., Galant, S., Pan, L., Moens, C. B., & Bally‐Cuif, L. (2013) · Development · doi:10.1242/dev.095018 · Cited by 145
Heterogeneity and Fgf dependence of adult neural progenitors in the zebrafish telencephalon
Ganz, J., Kaslin, J., Hochmann, S., Freudenreich, D., & Brand, M. (2010) · Glia · doi:10.1002/glia.21012 · Cited by 145
Lifelong learning: ocular dominance plasticity in mouse visual cortex
Hofer, S. B., Mrsic‐Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.06.007 · Cited by 144
Sonic Hedgehog Is a Polarized Signal for Motor Neuron Regeneration in Adult Zebrafish
Reimer, M. M., Kuscha, V., Wyatt, C., Sörensen, I., Frank, R. E., Knüwer, M., Becker, T., & Becker, C. G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4748-09.2009 · Cited by 143
Experience-dependent regulation of NG2 progenitors in the developing barrel cortex
Mangin, J., Li, P., Scafidi, J., & Gallo, V. (2012) · Nature Neuroscience · doi:10.1038/nn.3190 · Cited by 139
Differential cell proliferation in the cortex of the appsweps1de9 alzheimer's disease mouse model
Kamphuis, W., Orre, M., Kooijman, L., Dahmen, M., & Hol, E. M. (2012) · Glia · doi:10.1002/glia.22295 · Cited by 137
Reimer, M. M., Norris, A., Ohnmacht, J., Patani, R., Zhong, Z., Dias, T. B., Kuscha, V., Scott, A. L. M., Chen, Y., Rozov, S. V., et al. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.04.012 · Cited by 137
Glial cells are born with synapses
Kukley, M., Kiladze, M., Tognatta, R., Hans, M., Swandulla, D., Schramm, J., & Dietrich, D. (2008) · The FASEB Journal · doi:10.1096/fj.07-090985 · Cited by 137
Identification of midbrain floor plate radial glia-like cells as dopaminergic progenitors
Bonilla, S., Hall, A. C., Pinto, L., Attardo, A., Götz, M., Huttner, W. B., & Arenas, E. (2008) · Glia · doi:10.1002/glia.20654 · Cited by 136
Self-citationTan, A. M., Colletti, M., Rorai, A. T., Skene, J. H. P., & Levine, J. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3900-05.2006 · Cited by 136
No evidence for chronic demyelination in spared axons after spinal cord injury in a mouse
Lasiene, J., Shupe, L., Perlmutter, S., & Horner, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4756-07.2008 · Cited by 133
Hill, C. E., Pröschel, C., Noble, M., Mayer-Pröschel, M., Gensel, J. C., Beattie, M. S., & Bresnahan, J. C. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.05.043 · Cited by 133
NG2: a component of the glial scar that inhibits axon growth
Tan, A. M., Zhang, W., & Levine, J. M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00452.x · Cited by 131
Axonal dystrophy as a consequence of long-term demyelination.
Raine, C. S., & Cross, A. H. (1989) · PubMed · Cited by 131
The transcription factor Otx2 regulates choroid plexus development and function
Johansson, P. A., Irmler, M., Acampora, D., Beckers, J., Simeone, A., & Götz, M. (2013) · Development · doi:10.1242/dev.090860 · Cited by 130
Self-citationDuque, A., & RAKIC, P. T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3092-11.2011 · Cited by 129
Gregori, N. Z., Pröschel, C., Noble, M., & Mayer‐Pröschel, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00248.2002 · Cited by 123
Spassky, N., Heydon, K., Mangatal, A., Jankovski, A., Olivier, C., Quéraud-LeSaux, F., Goujet‐Zalc, C., Thomas, J., & Zalc, B. (2001) · Development · doi:10.1242/dev.128.24.4993 · Cited by 122
Tatsumi, K., Takebayashi, H., Manabe, T., Tanaka, K. F., Makinodan, M., Yamauchi, T., Makinodan, E., Matsuyoshi, H., Okuda, H., Ikenaka, K., et al. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21862 · Cited by 117
Generation of oligodendroglial progenitors from neural stem cells
Zhang, S., Lundberg, C. G., Lipsitz, D., O’Connor, L. T., & Duncan, I. D. (1998) · Journal of Neurocytology · doi:10.1023/a:1006953023845 · Cited by 113
Walton, N. M., Sutter, B. M., Chen, H., Chang, L., Roper, S. N., Scheffler, B., & Steindler, D. A. (2006) · Development · doi:10.1242/dev.02541 · Cited by 113
Single or multiple oligodendroglial lineages: A controversy
Spassky, N., Olivier, C., Pérez-Villegas, E. M., Goujet-Zalc, C., Martı́nez, S., Thomas, J.-L., & Zalc, B. (2000) · Glia · doi:10.1002/(sici)1098-1136(20000115)29:2<143::aid-glia7>3.0.co;2-d · Cited by 112
Ge, W., Zhou, W., Luo, Q., Jan, L. Y., & Jan, Y. N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811353106 · Cited by 109
Platelet‐derived growth factor receptor is expressed by cells in the early oligodendrocyte lineage
Ellison, J. A., & de Vellis, J. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490370116 · Cited by 108
Tamura, Y., Kataoka, Y., Cui, Y., Takamori, Y., Watanabe, Y., & Yamada, H. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05617.x · Cited by 107
Ventral Neurogenesis and the Neuron-Glial Switch
Kessaris, N., Pringle, N. P., & Richardson, W. D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00430-5 · Cited by 105
Park, H., Shin, J., Roberts, R. K., & Appel, B. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21365 · Cited by 104
Pinto, L., Mader, M. T., Irmler, M., Gentilini, M., Santoni, F. A., Drechsel, D., Blum, R., Stahl, R., Bulfone, A., Malatesta, P., et al. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.01.012 · Cited by 103
Self-citationStegmüller, J., Werner, H. B., Nave, K., & Trotter, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210010200 · Cited by 100
AP2γ regulates basal progenitor fate in a region- and layer-specific manner in the developing cortex
Pinto, L., Drechsel, D., Schmid, M.-T., Ninkovic, J., Irmler, M., Brill, M. S., Restani, L., Gianfranceschi, L., Cerri, C., Weber, S. N., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2399 · Cited by 100
Self-citationNG2 cells are not a major source of reactive astrocytes after neocortical stab wound injury
Komitova, M., Serwanski, D. R., Lu, Q. R., & Nishiyama, A. (2011) · Glia · doi:10.1002/glia.21152 · Cited by 98
Pihlaja, R., Koistinaho, J., Kauppinen, R., Sandholm, J., Tanila, H., & Koistinaho, M. (2011) · Glia · doi:10.1002/glia.21212 · Cited by 96
Hampton, D. W., Asher, R. A., Kondo, T., Steeves, J. D., Ramer, M. S., & Fawcett, J. W. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05940.x · Cited by 95
Robel, S., Bardehle, S., Lepier, A., Brakebusch, C., & Götz, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2696-11.2011 · Cited by 95
Self-citationFleisch, V. C., Fraser, B., & Allison, W. T. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.10.012 · Cited by 94
Bansal, R., & Pfeiffer, S. E. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490320303 · Cited by 92
Increasing Internodal Distance in Myelinated Nerves Accelerates Nerve Conduction to a Flat Maximum
Wu, L. M. N., Williams, A., Delaney, A., Sherman, D. L., & Brophy, P. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.025 · Cited by 90
Radial glia – from boring cables to stem cell stars
Malatesta, P., & Götz, M. (2013) · Development · doi:10.1242/dev.085852 · Cited by 89
Self-citationMangin, J., Kunze, A., Chittajallu, R., & Gallo, V. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1355-08.2008 · Cited by 87
Shibata, S., Yasuda, A., Renault-Mihara, F., Suyama, S., Katoh, H., Inoue, T., Inoue, Y., Nagoshi, N., Sato, M., Nakamura, M., et al. (2010) · Molecular Brain · doi:10.1186/1756-6606-3-31 · Cited by 87
Berg, D. A., Kirkham, M., Wang, H., Frisén, J., & Simon, A. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.02.001 · Cited by 86
Physiological characteristics of NG2-expressing glial cells
Lin, S.-C., & Bergles, D. E. (2002) · Journal of Neurocytology · doi:10.1023/a:1025799816285 · Cited by 84
Evidence for a second wave of oligodendrogenesis in the postnatal cerebral cortex of the mouse
Ivanova, A., Nakahira, E., Kagawa, T., Oba, A., Wada, T., Takebayashi, H., Spassky, N., Levine, J. M., Zalc, B., & Ikenaka, K. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10717 · Cited by 81
Chapouton, P., Webb, K. J., Stigloher, C., Alunni, A., Adolf, B., Hesl, B., Topp, S., Kremmer, E., & Bally‐Cuif, L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22599 · Cited by 81
Inducible Gene Expression and Gene Modification in Transgenic Mice
JAISSER, F. A. A. A. A. (2000) · Journal of the American Society of Nephrology · doi:10.1681/asn.v11suppl_2s95 · Cited by 81
Ascl1 is a required downstream effector of Gsx gene function in the embryonic mouse telencephalon
Wang, B., Waclaw, R. R., Allen, Z. J., Guillemot, F., & Campbell, K. (2009) · Neural Development · doi:10.1186/1749-8104-4-5 · Cited by 79
Bahia, P. K., Suzuki, R., Benton, D. C. H., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0597-05.2005 · Cited by 77
Early Neuronal and Glial Fate Restriction of Embryonic Neural Stem Cells
Delaunay, D., Heydon, K., Cumano, A., Schwab, M. H., Thomas, J., Suter, U., Nave, K., Zalc, B., & Spassky, N. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5497-07.2008 · Cited by 75
In vivo characterization of endogenous proliferating cells in adult rat subcortical white matter
Gensert, J. M., & Goldman, J. E. (1996) · Glia · doi:10.1002/(sici)1098-1136(199605)17:1<39::aid-glia4>3.0.co;2-2 · Cited by 73
Increase of oligodendrocyte progenitor cells after spinal cord injury
Ishii, K., Toda, M., Nakai, Y., Asou, H., Watanabe, M., Nakamura, M., Yato, Y., Fujimura, Y., Kawakami, Y., Toyama, Y., et al. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.1180 · Cited by 71
Role of radial glia in cytogenesis, patterning and boundary formation in the developing spinal cord
McDermott, K. W. G., Barry, D., & McMahon, S. S. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00462.x · Cited by 70
CNS‐irrelevant T‐cells enter the brain, cause blood–brain barrier disruption but no glial pathology
Тихоновна, С. А., Wuerfel, J. T., Pohl, E. E., Vogt, J., Tysiak, E., Glumm, R., Hendrix, S., Nitsch, R., Zipp, F., & Infante‐Duarte, C. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05792.x · Cited by 66
Sirko, S., Neitz, A., Mittmann, T., Horvat-Broecker, A., von Holst, A., Eysel, U. T., & Faissner, A. (2009) · Brain · doi:10.1093/brain/awp043 · Cited by 66
Synapses between NG2 glia and neurons
Sakry, D., Karram, K., & Trotter, J. (2011) · Journal of Anatomy · doi:10.1111/j.1469-7580.2011.01359.x · Cited by 65
Franklin, R. J. M., Zhao, C., & Sim, F. J. (2002) · Neuroreport · doi:10.1097/00001756-200205240-00001 · Cited by 63
Spassky, N., Olivier, C., Cobos, I., Bras, B. L., Goujet‐Zalc, C., Martínez, S., Zalc, B., & Thomas, J. (2001) · Developmental Neuroscience · doi:10.1159/000048715 · Cited by 63
The Curious Case of NG2 Cells: Transient Trend or Game Changer?
Mangin, J., & Gallo, V. (2011) · ASN NEURO · doi:10.1042/an20110001 · Cited by 62
Clonal Astrocytic Response to Cortical Injury
Martín-López, E., García-Marqués, J., Núñez-Llaves, R., & López-Mascaraque, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074039 · Cited by 62
Myelination of cultured dorsal root ganglion neurons by oligodendrocytes obtained from adult rats
Wood, P. M., & Bunge, R. P. (1986) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(86)90101-2 · Cited by 62
Hayakawa, K., Seo, J. H., Pham, L. D., Miyamoto, N., Som, A. T., Guo, S., Kim, K., Lo, E. H., & Arai, K. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.02.004 · Cited by 61
Do Action Potentials Regulate Myelination?
Zalc, B., & Fields, R. D. (2000) · The Neuroscientist · doi:10.1177/107385840000600109 · Cited by 58
Targeted gene disruption: applications in neurobiology
van der Neut, R. (1997) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(96)00123-9 · Cited by 57
Prokineticin 2 Expression Is Associated with Neural Repair of Injured Adult Zebrafish Telencephalon
Ayari, B., Hachimi, K. H. E., Yanicostas, C., Landoulsi, A., & Soussi‐Yanicostas, N. (2010) · Journal of Neurotrauma · doi:10.1089/neu.2009.0972 · Cited by 56
Kronenberg, G., Gertz, K. R., Cheung, G. T. Y., Buffo, A., Kettenmann, H., Götz, M., & Endres, M. (2010) · Stroke · doi:10.1161/strokeaha.110.583039 · Cited by 56
Self-citationOlig2 + neuroepithelial motoneuron progenitors are not multipotent stem cells in vivo
Mukouyama, Y., Deneen, B., Lukaszewicz, A. I., Novitch, B. G., Wichterle, H., Jessell, T. M., & Anderson, D. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510658103 · Cited by 55
Seifert‐Held, T., Bauer, J., Weissert, R., Fazekas, F., & Storch, M. K. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.5.404 · Cited by 54
A Phox2b::FLPo transgenic mouse line suitable for intersectional genetics
Hirsch, M., D’Autréaux, F., Dymecki, S. M., Brunet, J., & Goridis, C. (2013) · genesis · doi:10.1002/dvg.22393 · Cited by 53
Hirrlinger, J., Requardt, R. P., Winkler, U., Wilhelm, F., Schulze, C., & Hirrlinger, P. G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008354 · Cited by 53
März, M., Viales, R. R., Rastegar, S., & Strähle, U. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22455 · Cited by 52
Regeneration and reprogramming
Knapp, D., & Tanaka, E. M. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2012.09.006 · Cited by 50
Stem cells niches during development — lessons from the cerebral cortex
Johansson, P. A., Cappello, S., & Götz, M. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.04.003 · Cited by 49
Self-citationZhu, Q., Whittemore, S. R., DeVries, W. H., Zhao, X., Kuypers, N. J., & Qiu, M. S. (2011) · Glia · doi:10.1002/glia.21203 · Cited by 47
Embryonic Stem Cell‐Derived Neural Stem Cells Fuse with Microglia and Mature Neurons
Cusulin, C., Monni, E., Ahlenius, H., Wood, J. C., Brune, J. C., Lindvall, O., & Kokaia, Z. (2012) · Stem Cells · doi:10.1002/stem.1227 · Cited by 45
Fate specification in the adult brain – lessons for eliciting neurogenesis from glial cells
Ninkovic, J., & Götz, M. (2013) · BioEssays · doi:10.1002/bies.201200108 · Cited by 44
Self-citationLang, C. C. V., Guo, X., Kerschensteiner, M., & Bareyre, F. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030461 · Cited by 42
Berger, C., HIESTAND, P. C., Kindler, D., Rudin, M., & Rausch, M. (2006) · NMR in Biomedicine · doi:10.1002/nbm.1007 · Cited by 41
Sox appeal – Sox10 attracts epigenetic and transcriptional regulators in myelinating glia
Weider, M., Reiprich, S., & Wegner, M. (2013) · Biological Chemistry · doi:10.1515/hsz-2013-0146 · Cited by 39
Macroglial cells of the teleost central nervous system: a survey of the main types
Cuoghi, B., & Mola, L. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0870-2 · Cited by 39
Sublethal Transient Global Ischemia Stimulates Migration of Neuroblasts and Neurogenesis in Mice
Li, Y., Yu, S. P., Mohamad, O., Genetta, T. L., & Wei, L. (2010) · Translational Stroke Research · doi:10.1007/s12975-010-0016-6 · Cited by 38
Fiorelli, R., Cebrián‐Silla, A., García‐Verdugo, J. M., & Raineteau, O. (2013) · Glia · doi:10.1002/glia.22579 · Cited by 37
Opposing Roles forHoxa2andHoxb2in Hindbrain Oligodendrocyte Patterning
Miguez, A., Ducret, S., Meglio, T. D., Parras, C. M., Hmidan, H., Haton, C., Sekizar, S., Mannioui, A., Vidal, M., Kerever, A., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0885-12.2012 · Cited by 36
Glial Cell Lineages in the Rat Optic NervePreprint
RAFF, M. C., Miller, R. H., & Noble, M. (1983) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1983.048.01.061 · Cited by 36
In Vivo Targeting of Adult Neural Stem Cells in the Dentate Gyrus by a Split-Cre Approach
Beckervordersandforth, R., Deshpande, A., Schäffner, I., Huttner, H. B., Lepier, A., Lie, D. C., & Götz, M. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.01.004 · Cited by 35
Self-citationSkripuletz, T., Miller, E., Grote, L., Gudi, V., Pul, R., Voss, E., Škuljec, J., Moharregh-Khiabani, D., Trebst, C., & Stangel, M. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2011.05.009 · Cited by 31
Kainate receptors and signal integration by NG2 glial cells
Kukley, M., & Dietrich, D. (2009) · Neuron Glia Biology · doi:10.1017/s1740925x09990081 · Cited by 29
Neural Stem Cells Engrafted in the Adult Brain Fuse with Endogenous Neurons
Brilli, E., Reitano, E., Conti, L., Conforti, P., Gulino, R., Consalez, G. G., Cesana, E., Smith, A. G., Rossi, F., & Cattaneo, E. F. (2012) · Stem Cells and Development · doi:10.1089/scd.2012.0530 · Cited by 25
Jászai, J., Graupner, S., Tanaka, E. M., Funk, R. H. W., Huttner, W. Β., Brand, M., & Corbeil, D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063457 · Cited by 19
Shaping barrels: activity moves NG2+ glia
Dimou, L., & Götz, M. (2012) · Nature Neuroscience · doi:10.1038/nn.3191 · Cited by 9
Self-citationChapter 36 Glial cell development and function in the rat optic nerve
RAFF, M. C., Temple, S., & ffrench‐Constant, C. (1987) · Progress in brain research · doi:10.1016/s0079-6123(08)61844-0 · Cited by 8
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.