Properties of human astrocytes and NG2 glia

Tripartite synapses: glia, the unacknowledged partner

Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529 · see citing works

Physiology of Astroglia

Verkhratsky, A., & Nedergaard, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00042.2016 · Cited by 1,678 · see citing works

Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains

Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578 · see citing works

Uniquely Hominid Features of Adult Human Astrocytes

Oberheim, N. A., Takano, T., Han, X., He, W., Lin, J. H. C., Wang, F., Xu, Q., Wyatt, J. D., Pilcher, W., Ojemann, J. G., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4707-08.2009 · Cited by 1,488 · see citing works

Long-term potentiation depends on release of d-serine from astrocytes

Henneberger, C., Papouin, T., Oliet, S. H. R., & Rusakov, D. A. (2010) · Nature · doi:10.1038/nature08673 · Cited by 1,389 · see citing works

Gliotransmitters Travel in Time and Space

Araque, A., Carmignoto, G., Haydon, P. G., Oliet, S. H. R., Robitaille, R., & Volterra, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.007 · Cited by 1,308 · see citing works

Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.

Orkand, R. K., Nicholls, J. G., & Kuffler, S. W. (1966) · Journal of Neurophysiology · doi:10.1152/jn.1966.29.4.788 · Cited by 1,213 · see citing works

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 · see citing works

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 · see citing works

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery

Blümcke, I., Spreafico, R., Haaker, G., Coras, R., Kobow, K., Bien, C. G., Pfäfflin, M., Elger, C. E., Widman, G., Schramm, J., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1703784 · Cited by 935 · see citing works

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

Dawson, M. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00210-0 · Cited by 927 · see citing works

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 · see citing works

The tripartite synapse: roles for gliotransmission in health and disease

Halassa, M. M., Fellin, T., & Haydon, P. G. (2007) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2006.12.005 · Cited by 852 · see citing works

Potassium buffering in the central nervous system

Kofuji, P., & Newman, E. A. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.008 · Cited by 847 · see citing works

Oligodendrocyte progenitors balance growth with self-repulsion to achieve homeostasis in the adult brain

Hughes, E. G., Kang, S. H., Fukaya, M., & Bergles, D. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3390 · Cited by 808 · see citing works

Astrocyte dysfunction in neurological disorders: a molecular perspective

Seifert, G., Schilling, K., & Steinhäuser, C. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1870 · Cited by 798 · see citing works

Astroglial networks: a step further in neuroglial and gliovascular interactions

Giaume, C., Koulakoff, A., Roux, L., Holcman, D., & Rouach, N. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2757 · Cited by 781 · see citing works

NG2+ CNS glial progenitors remain committed to the oligodendrocyte lineage in postnatal life and following neurodegeneration

Kang, S., Fukaya, M., Yang, J. K., Rothstein, J., & Bergles, D. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.009 · Cited by 778 · see citing works

Astrocytic complexity distinguishes the human brain

Oberheim, N. A., Wang, X., Goldman, S., & Nedergaard, M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.08.004 · Cited by 739 · see citing works

Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate

Bezzi, P., Gundersen, V., Galbete, J. L., Seifert, G., Steinhäuser, C., Pilati, E., & Volterra, A. (2004) · Nature Neuroscience · doi:10.1038/nn1246 · Cited by 737 · see citing works

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 · see citing works

NG2 cells generate both oligodendrocytes and gray matter astrocytes

Zhu, X., Bergles, D. E., & Nishiyama, A. (2007) · Development · doi:10.1242/dev.004895 · Cited by 678 · see citing works

Hippocampal AstrocytesIn SituRespond to Glutamate Released from Synaptic Terminals

Porter, J. T., & McCarthy, K. D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05073.1996 · Cited by 672 · see citing works

Gesammelte Abhandlungen zur wissenschaftlichen Medicin

Virchow, R. (1862) · Cited by 590 · see citing works

Astrocyte calcium waves: What they are and what they do

Scemes, E., & Giaume, C. (2006) · Glia · doi:10.1002/glia.20374 · Cited by 588 · see citing works

The Impact of Astrocytic Gap Junctional Coupling on Potassium Buffering in the Hippocampus

Wallraff, A., Köhling, R., Heinemann, U., Theis, M., Willecke, K., & Steinhäuser, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0037-06.2006 · Cited by 582 · see citing works

Hippocampal Astrocytes In Situ Respond to Glutamate Released from Synaptic Terminals

Porter, J. T., & McCarthy, K. D. (2021) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/s4kv-rg05 · Cited by 561 · see citing works

Glial cells in (patho)physiology

Parpura, V., Heneka, M. T., Montana, V., Oliet, S. H. R., Schousboe, A., Haydon, P. G., Stout, R. F., Spray, D. C., Reichenbach, A., Pannicke, T., et al. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07664.x · Cited by 561 · see citing works

Progeny of Olig2-expressing progenitors in the gray and white matter of the adult mouse cerebral cortex

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 · see citing works

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 · see citing works

Role of astrocytes in the clearance of excess extracellular potassium

Walz, W. (2000) · Neurochemistry International · doi:10.1016/s0197-0186(99)00137-0 · Cited by 464 · see citing works

Connexin channel permeability to cytoplasmic molecules

Harris, A. L. (2007) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2007.03.011 · Cited by 457 · see citing works

Synaptic signaling between GABAergic interneurons and oligodendrocyte precursor cells in the hippocampus

Lin, S.-C., & Bergles, D. (2004) · Nature Neuroscience · doi:10.1038/nn1162 · Cited by 449 · see citing works

Segregated Expression of AMPA-Type Glutamate Receptors and Glutamate Transporters Defines Distinct Astrocyte Populations in the Mouse Hippocampus

Matthias, K., Kirchhoff, F., Seifert, G., Hüttmann, K., Matyash, M., Kettenmann, H., & Steinhäuser, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01750.2003 · Cited by 431 · see citing works

Human astrocytes: structure and functions in the healthy brain

Vasile, F., Dossi, E., & Rouach, N. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1383-5 · Cited by 428 · see citing works

Proliferation of NG2-Positive Cells and Altered Oligodendrocyte Numbers in the Contused Rat Spinal Cord

McTigue, D. M., Wei, P., & Stokes, B. T. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03392.2001 · Cited by 423 · see citing works

Heterogeneity in astrocyte morphology and physiology

Matyash, V., & Kettenmann, H. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.001 · Cited by 413 · see citing works

Glutamate Metabolism in the Brain Focusing on Astrocytes

Schousboe, A., Scafidi, S., Bak, L. K., Waagepetersen, H. S., & McKenna, M. C. (2014) · Advances in neurobiology · doi:10.1007/978-3-319-08894-5_2 · Cited by 366 · see citing works

Mechanisms of Glutamate Transport

Vandenberg, R. J., & Ryan, R. M. (2013) · Physiological Reviews · doi:10.1152/physrev.00007.2013 · Cited by 349 · see citing works

Three-dimensional Ca ²⁺ imaging advances understanding of astrocyte biology

Bindocci, E., Savtchouk, I., Liaudet, N., Becker, D., Carriero, G., & Volterra, A. (2017) · Science · doi:10.1126/science.aai8185 · Cited by 342 · see citing works

Astrocyte uncoupling as a cause of human temporal lobe epilepsy

Bedner, P., Dupper, A., Hüttmann, K., Müller, J., Herde, M. K., Dublin, P., Deshpande, T., Schramm, J., Häussler, U., Haas, C. A., et al. (2015) · Brain · doi:10.1093/brain/awv067 · Cited by 328 · see citing works

Gliotransmission: Beyond Black-and-White

Savtchouk, I., & Volterra, A. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0017-17.2017 · Cited by 325 · see citing works

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 · see citing works

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 · see citing works

Activation and Proliferation of Endogenous Oligodendrocyte Precursor Cells during Ethidium Bromide-Induced Demyelination

Levine, J. M., & Reynolds, R. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7224 · Cited by 282 · see citing works

Astrocytes in the hippocampus of patients with temporal lobe epilepsy display changes in potassium conductances

Hinterkeuser, S., Schröder, W., Hager, G., Seifert, G., Blümcke, I., Elger, C. E., Schramm, J., & Steinhäuser, C. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00104.x · Cited by 266 · see citing works

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 · see citing works

Large-Scale Calcium Waves Traveling through Astrocytic Networks In Vivo

Kuga, N., Sasaki, T., Takahara, Y., Matsuki, N., & Ikegaya, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5319-10.2011 · Cited by 262 · see citing works

NG2‐positive cells in the mouse white and grey matter display distinct physiological properties

Chittajallu, R., Aguirre, A., & Gallo, V. (2004) · Journal of Physiology · doi:10.1113/jphysiol.2004.074252 · Cited by 248 · see citing works

Interaction between NG2 proteoglycan and PDGF ?-receptor on O2A progenitor cells is required for optimal response to PDGF

Nishiyama, A., Lin, X., Giese, N. A., Heldin, C., & Stallcup, W. B. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960201)43:3 · Cited by 239 · see citing works

Analysis of Astroglial K+ Channel Expression in the Developing Hippocampus Reveals a Predominant Role of the Kir4.1 Subunit

Seifert, G., Hüttmann, K., Binder, D. K., Hartmann, C. J., Wyczynski, A., Neusch, C., & Steinhäuser, C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3790-08.2009 · Cited by 236 · see citing works

Differential Role of KIR Channel and Na+/K+-Pump in the Regulation of Extracellular K+ in Rat Hippocampus

D’Ambrosio, R., Gordon, D., & Winn, H. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00240.2001 · Cited by 235 · see citing works

Long-Term Potentiation of Neuron-Glia Synapses Mediated by Ca 2+ -Permeable AMPA Receptors

Ge, W., Yang, X.-J., Zhang, Z., Wang, H.-K., Shen, W., Deng, Q.-D., & Duan, S. (2006) · Science · doi:10.1126/science.1124669 · Cited by 208 · see citing works

Neuron-glia synapses in the brain

Bergles, D. E., Jabs, R., & Steinhäuser, C. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.003 · Cited by 199 · see citing works

Activity‐dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps

Ransom, C. B., Ransom, B. R., & Sontheimer, H. W. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00427.x · Cited by 197 · see citing works

Astrocyte dysfunction in temporal lobe epilepsy: K + channels and gap junction coupling

Steinhäuser, C., Seifert, G., & Bedner, P. (2012) · Glia · doi:10.1002/glia.22313 · Cited by 197 · see citing works

Multiple Lines of Evidence Indicate That Gliotransmission Does Not Occur under Physiological Conditions

Fiacco, T. A., & McCarthy, K. D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0016-17.2017 · Cited by 194 · see citing works

Distinct types of astroglial cells in the hippocampus differ in gap junction coupling

Wallraff, A., Odermatt, B., Willecke, K., & Steinhäuser, C. (2004) · Glia · doi:10.1002/glia.20040 · Cited by 191 · see citing works

Phenotypic Heterogeneity and Plasticity of Isocortical and Hippocampal Astrocytes in the Human Brain

Sosunov, A. A., Wu, X., Tsankova, N. M., Guilfoyle, E., McKhann, G. M., & Goldman, J. E. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4037-13.2014 · Cited by 185 · see citing works

Upregulation in astrocytic connexin 43 gap junction levels may exacerbate generalized seizures in mesial temporal lobe epilepsy

Fonseca, C. G., Green, C. R., & Nicholson, L. F. B. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03289-9 · Cited by 181 · see citing works

Properties of GABA and glutamate responses in identified glial cells of the mouse hippocampal slice

Steinhäser, C., Jabs, R., & Kettenmann, H. (1994) · Hippocampus · doi:10.1002/hipo.450040105 · Cited by 174 · see citing works

Expression of connexin 43 and connexin 32 gap-junction proteins in epilepsy-associated brain tumors and in the perilesional epileptic cortex

Aronica, E., Gorter, J. A., Jansen, G. H., Leenstra, S., Yankaya, B., & Troost, D. (2001) · Acta Neuropathologica · doi:10.1007/s004010000305 · Cited by 164 · see citing works

Der feinere Bau des Nervensystems im Lichte neuester Forschungen

Lenhossék, M. (1893) · Cited by 161 · see citing works

Postnatal Development of Ionic Currents in Rat Hippocampal Astrocytes In Situ

Bordey, A., & Sontheimer, H. W. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.1.461 · Cited by 159 · see citing works

Electroconvulsive seizures induce proliferation of NG2-expressing glial cells in adult rat hippocampus

Wennström, M., Hellsten, J., Ekdahl, C. T., & Tingström, A. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00693-0 · Cited by 158 · see citing works

Synaptic transmission onto hippocampal glial cells with hGFAP promoter activity

Jabs, R., Pivneva, T. A., Hüttmann, K., Wyczynski, A., Nolte, C., Kettenmann, H., & Steinhäuser, C. (2005) · Journal of Cell Science · doi:10.1242/jcs.02515 · Cited by 153 · see citing works

Astrocyte Calcium Signal and Gliotransmission in Human Brain Tissue

Navarrete, M., Perea, G., Maglio, L. E., Pastor, J., de Sola, R. G., & Araque, A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs122 · Cited by 152 · see citing works

Functional and Molecular Properties of Human Astrocytes in Acute Hippocampal Slices Obtained from Patients with Temporal Lobe Epilepsy

Schröder, W., Hinterkeuser, S., Seifert, G., Schramm, J., Jabs, R., Wilkin, G. P., & Steinhäuser, C. (2000) · Epilepsia · doi:10.1111/j.1528-1157.2000.tb01578.x · Cited by 150 · see citing works

Developmental regulation of Na+ and K+ conductances in glial cells of mouse hippocampal brain slices

Kressin, K., Kuprijanova, E., Jabs, R., Seifert, G., & Steinhäuser, C. (1995) · Glia · doi:10.1002/glia.440150210 · Cited by 148 · see citing works

Connexin expression by radial glia-like cells is required for neurogenesis in the adult dentate gyrus

Kunze, A., Congreso, M. R., Hartmann, C. J., Wallraff, A., Hüttmann, K., Bedner, P., Requardt, R. P., Seifert, G., Redecker, C., Willecke, K., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813160106 · Cited by 143 · see citing works

Gap junction gene expression in human seizure disorder

Naus, C. C. G., Bechberger, J. F., & Paul, D. L. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90007-y · Cited by 143 · see citing works

The homeostatic astroglia emerges from evolutionary specialization of neural cells

Verkhratsky, A., & Nedergaard, M. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0428 · Cited by 133 · see citing works

Characterization of Panglial Gap Junction Networks in the Thalamus, Neocortex, and Hippocampus Reveals a Unique Population of Glial Cells

Griemsmann, S., Höft, S. P., Bedner, P., Zhang, J., von Staden, E., Beinhauer, A., Degen, J., Dublin, P., Cope, D. W., Richter, N., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu157 · Cited by 132 · see citing works

Interlaminar astroglia of the cerebral cortex: a marker of the primate brain

Colombo, J. A., & Reisin, H. D. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.003 · Cited by 132 · see citing works

A fourth type of neuroglial cell in the adult central nervous system

Peters, A. (2004) · Journal of Neurocytology · doi:10.1023/b:neur.0000044195.64009.27 · Cited by 131 · see citing works

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 129 · see citing works

NG2‐expressing cells in the nervous system revealed by the NG2‐EYFP‐knockin mouse

Karram, K., Goebbels, S., Schwab, M. H., Jennissen, K., Seifert, G., Steinhäuser, C., Nave, K., & Trotter, J. (2008) · genesis · doi:10.1002/dvg.20440 · Cited by 126 · see citing works

Astrocytes and NG2‐glia: what's in a name?

Nishiyama, A., Yang, Z., & Butt, A. M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00489.x · Cited by 126 · see citing works

Co-expression of PDGF α receptor and NG2 by oligodendrocyte precursors in human CNS and multiple sclerosis lesions

Wilson, H., Scolding, N. J., & Raine, C. S. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.04.014 · Cited by 122 · see citing works

Astrocytic function and its alteration in the epileptic brain

Jabs, R., Seifert, G., & Steinhäuser, C. (2008) · Epilepsia · doi:10.1111/j.1528-1167.2008.01488.x · Cited by 116 · see citing works

Effects of barium on stimulus‐induced rises of [K+]o in human epileptic non‐sclerotic and sclerotic hippocampal area CA1

Kivi, A., Lehmann, T., Kovács, R., Eilers, A., Jauch, R., Meencke, H. J., von Deimling, A., Heinemann, U., & Gabriel, S. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00103.x · Cited by 116 · see citing works

AMPA Receptor-Mediated Modulation of Inward Rectifier K+ Channels in Astrocytes of Mouse Hippocampus

Schröder, W., Seifert, G., Hüttmann, K., Hinterkeuser, S., & Steinhäuser, C. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1080 · Cited by 113 · see citing works

Electrophysiological Properties of Human Astrocytic Tumor Cells In Situ: Enigma of Spiking Glial Cells

Bordey, A., & Sontheimer, H. W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.5.2782 · Cited by 111 · see citing works

Gray Matter NG2 Cells Display Multiple Ca2+-Signaling Pathways and Highly Motile Processes

Haberlandt, C., Derouiche, A., Wyczynski, A., Haseleu, J., Pohle, J., Karram, K., Trotter, J., Seifert, G., Frotscher, M., Steinhäuser, C., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017575 · Cited by 107 · see citing works

Alterations of Glial Cell Function in Temporal Lobe Epilepsy

Heinemann, U., Gabriel, S., Jauch, R., Schulze, K., Kivi, A., Eilers, A., Kovacs, R., & Lehmann, T. N. (2000) · Epilepsia · doi:10.1111/j.1528-1157.2000.tb01579.x · Cited by 105 · see citing works

Electrophysiological properties of NG2 + cells: Matching physiological studies with gene expression profiles

Larson, V. A., Zhang, Y., & Bergles, D. E. (2015) · Brain Research · doi:10.1016/j.brainres.2015.09.010 · Cited by 102 · see citing works

Altered expression of connexin subtypes in mesial temporal lobe epilepsy in humans

Collignon, F. P., Wetjen, N. M., Cohen‐Gadol, A., Cascino, G. D., Parisi, J. E., Meyer, F. B., Marsh, W. R., Roche, P. C., & Weigand, S. D. (2006) · Journal of neurosurgery · doi:10.3171/jns.2006.105.1.77 · Cited by 97 · see citing works

Adult glial precursor proliferation in mutant SOD1G93A mice

Magnus, T., Carmen, J., Deleon, J., Xue, H., Pardo, A. C., Lepore, A., Mattson, M. P., Rao, M. S., & Maragakis, N. (2008) · Glia · doi:10.1002/glia.20604 · Cited by 93 · see citing works

Oligodendrocyte Precursor Cells Are Accurate Sensors of Local K+in Mature Gray Matter

Maldonado, P. P., Vélez‐Fort, M., Levavasseur, F., & Angulo, M. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1961-12.2013 · Cited by 93 · see citing works

Subcellular reorganization and altered phosphorylation of the astrocytic gap junction protein connexin43 in human and experimental temporal lobe epilepsy

Deshpande, T., Li, T., Herde, M. K., Becker, A., Vatter, H., Schwarz, M. K., Henneberger, C., Steinhäuser, C., & Bedner, P. (2017) · Glia · doi:10.1002/glia.23196 · Cited by 87 · see citing works

Enhanced Relative Expression of Glutamate Receptor 1 Flip AMPA Receptor Subunits in Hippocampal Astrocytes of Epilepsy Patients with Ammon's Horn Sclerosis

Seifert, G., Hüttmann, K., Schramm, J., & Steinhäuser, C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3904-03.2004 · Cited by 85 · see citing works

Role of astroglial connexin30 in hippocampal gap junction coupling

Gosejacob, D., Dublin, P., Bedner, P., Hüttmann, K., Zhang, J., Tress, O., Willecke, K., Pfrieger, F. W., Steinhäuser, C., & Theis, M. (2010) · Glia · doi:10.1002/glia.21120 · Cited by 80 · see citing works

Properties of voltage-activated Na+ and K+ currents in mouse hippocampal glial cells in situ and after acute isolation from tissue slices

Steinh�user, C., Kressin, K., Kuprijanova, E., Weber, M., & Seifert, G. (1994) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374585 · Cited by 79 · see citing works

Localization of excitatory amino acid transporters EAAT1 and EAAT2 in human postmortem cortex: A light and electron microscopic study

Roberts, R. C., Roche, J. K., & McCullumsmith, R. E. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.019 · Cited by 76 · see citing works

Heterogeneity of Kir4.1 channel expression in glia revealed by mouse transgenesis

Tang, X., Taniguchi, K., & Kofuji, P. (2009) · Glia · doi:10.1002/glia.20882 · Cited by 76 · see citing works

Glial membrane potentials and their relationship to [K+]o in man and guinea pig

Picker, S., Pieper, C. F., & Goldring, S. (1981) · Journal of neurosurgery · doi:10.3171/jns.1981.55.3.0347 · Cited by 74 · see citing works

Changes in glial glutamate transporters in human epileptogenic hippocampus: Inadequate explanation for high extracellular glutamate during seizures

Bjørnsen, L. P., Eid, T., Holmseth, S., Danbolt, N. C., Spencer, D. D., & de Lanerolle, N. C. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.09.014 · Cited by 74 · see citing works

Long, interlaminar astroglial cell processes in the cortex of adult monkeys

Colombo, J. A., Yáñez, A., Puissant, V., & Lipina, S. (1995) · Journal of Neuroscience Research · doi:10.1002/jnr.490400414 · Cited by 72 · see citing works

Analysis of AMPA Receptor Properties During Postnatal Development of Mouse Hippocampal Astrocytes

Seifert, G., Zhou, M., & Steinhäuser, C. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.6.2916 · Cited by 67 · see citing works

Diversity of astrocyte potassium channels: An update

Seifert, G., Henneberger, C., & Steinhäuser, C. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.12.002 · Cited by 66 · see citing works

Albumin is taken up by hippocampal NG2 cells and astrocytes and decreases gap junction coupling

Braganza, O., Bedner, P., Hüttmann, K., von Staden, E., Friedman, A., Seifert, G., & Steinhäuser, C. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03665.x · Cited by 64 · see citing works

Effects of barium, furosemide, ouabaine and 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid (DIDS) on ionophoretically-induced changes in extracellular potassium concentration in hippocampal slices from rats and from patients with epilepsy

Jauch, R., Windmüller, O., Lehmann, T., Heinemann, U., & Gabriel, S. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03254-1 · Cited by 62 · see citing works

Hippocampal Connexin 43 Expression in Human Complex Partial Seizure Disorder

Elisevich, K. V., Rempel, S. A., Smith, B. J., & Edvardsen, K. (1997) · Experimental Neurology · doi:10.1006/exnr.1997.6467 · Cited by 58 · see citing works

Spontaneous Glial Calcium Waves in the Retina Develop over Early Adulthood

Kurth-Nelson, Z. L., Mishra, A., & Newman, E. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2493-09.2009 · Cited by 48 · see citing works

Dual patch voltage clamp study of low membrane resistance astrocytes in situ

Ma, B., Xu, G., Wang, W., Enyeart, J. J., & Zhou, M. (2014) · Molecular Brain · doi:10.1186/1756-6606-7-18 · Cited by 48 · see citing works

Changes in Flip/Flop Splicing of Astroglial AMPA Receptors in Human Temporal Lobe Epilepsy

Seifert, G., Schröder, W., Hinterkeuser, S., Schumacher, T. B., Schramm, J., & Steinhäuser, C. (2002) · Epilepsia · doi:10.1046/j.1528-1157.43.s.5.10.x · Cited by 47 · see citing works

Increased intercellular communication in mouse astrocytes exposed to hyposmotic shocks

Scemes, E., & Spray, D. C. (1998) · Glia · doi:10.1002/(sici)1098-1136(199809)24:1 · Cited by 33 · see citing works

Dual reporter approaches for identification of Cre efficacy and astrocyte heterogeneity

Degen, J., Dublin, P., Zhang, J., Dobrowolski, R., Jokwitz, M., Karram, K., Trotter, J., Jabs, R., Willecke, K., Steinhäuser, C., et al. (2012) · The FASEB Journal · doi:10.1096/fj.12-207183 · Cited by 31 · see citing works

Sodium channel currents in rat hippocampal NG2 glia: Characterization and contribution to resting membrane potential

Xie, M., Lynch, D., Schools, G. P., Feustel, P. J., Kimelberg, H. K., & Zhou, M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.09.057 · Cited by 29 · see citing works

Changes in splice variant expression and subunit assembly of AMPA receptors during maturation of hippocampal astrocytes

Seifert, G., Weber, M., Schramm, J., & Steinhäuser, C. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00039-3 · Cited by 27 · see citing works

Changes in the proliferative capacity of NG2 cell subpopulations during postnatal development of the mouse hippocampus

Moshrefi-Ravasdjani, B., Dublin, P., Seifert, G., Jennissen, K., Steinhäuser, C., Kafitz, K. W., & Rose, C. R. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1249-2 · Cited by 27 · see citing works

Astrocyte Networks and Intercellular Calcium Propagation

Lallouette, J., Pittà, M. D., & Berry, H. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_7 · Cited by 27 · see citing works

Heterogeneity and function of hippocampal macroglia

Seifert, G., & Steinhäuser, C. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2746-1 · Cited by 23 · see citing works

The NG2 Protein Is Not Required for Glutamatergic Neuron–NG2 Cell Synaptic Signaling

Passlick, S., Trotter, J., Seifert, G., Steinhäuser, C., & Jabs, R. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu171 · Cited by 22 · see citing works

Do Evolutionary Changes in Astrocytes Contribute to the Computational Power of the Hominid Brain?

Bush, N. A. O., & Nedergaard, M. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2363-0 · Cited by 22 · see citing works

Protein synthesis‐dependent but Bcl‐2‐independent cytochrome C release in zinc depletion‐induced neuronal apoptosis

Ahn, Y.-H., Koh, J., & Hong, S. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20000901)61:5 · Cited by 21 · see citing works

Physiology of Astroglia: Channels, Receptors, Transporters, Ion Signaling and Gliotransmission

Verkhratsky, A., & Parpura, V. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00123ed1v01y201501ngl004 · Cited by 13 · see citing works

Glucose transporter proteins in brain: Delivery of glucose to neurons and glia

Vannucci, S. J., Maher, F., & Simpson, I. A. (1997) · Glia · doi:10.1002/(sici)1098-1136(199709)21:1

Reactive astrocyte nomenclature, definitions, and future directions

Escartin, C., Galea, E., Lakatos, A., O’Callaghan, J. P., Petzold, G. C., Serrano-Pozo, A., Steinhäuser, C., Volterra, A., Carmignoto, G., Agarwal, A., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00783-4 · Cited by 2,533 · see citing works

Making sense of astrocytic calcium signals — from acquisition to interpretation

Semyanov, A., Henneberger, C., & Agarwal, A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0361-8 · Cited by 269 · see citing works

Astrocytes in the initiation and progression of epilepsy

Vezzani, A., Ravizza, T., Bedner, P., Aronica, E., Steinhäuser, C., & Boison, D. (2022) · Nature Reviews Neurology · doi:10.1038/s41582-022-00727-5 · Cited by 272 · see citing works

Ion Channels and Electrophysiological Properties of Astrocytes: Implications for Emergent Stimulation Technologies

McNeill, J., Rudyk, C., Hildebrand, M. E., & Salmaso, N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.644126 · Cited by 121 · see citing works

Astrocytes in the central nervous system and their functions in health and disease: A review

Gradišnik, L., & Velnar, T. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i15.3385 · Cited by 91 · see citing works

Metabolic compartmentalization between astroglia and neurons in physiological and pathophysiological conditions of the neurovascular unit

Takahashi, S. (2020) · Neuropathology · doi:10.1111/neup.12639 · Cited by 75 · see citing works

Astrocytes and major depression: The purinergic avenue

Zhao, Y. F., Verkhratsky, A., Tang, Y. C., & Illés, P. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109252 · Cited by 73 · see citing works

Glial smog: Interplay between air pollution and astrocyte-microglia interactions

Gómez‐Budia, M., Konttinen, H., Saveleva, L., Korhonen, P., Jalava, P., Kanninen, K. M., & Malm, T. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104715 · Cited by 59 · see citing works

Human Astrocytes Model Derived from Induced Pluripotent Stem Cells

Leventoux, N., Morimoto, S., Imaizumi, K., Sato, Y., Takahashi, S., Mashima, K., Ishikawa, M., Sonn, I., Kondo, T., Watanabe, H., et al. (2020) · Cells · doi:10.3390/cells9122680 · Cited by 60 · see citing works

Astrocytic and Oligodendrocytic P2X7 Receptors Determine Neuronal Functions in the CNS

Zhao, Y., Tang, Y., & Illés, P. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.641570 · Cited by 59 · see citing works

Na+-dependent transporters: The backbone of astroglial homeostatic function

Verkhratsky, A., & Rose, C. R. (2019) · Cell Calcium · doi:10.1016/j.ceca.2019.102136 · Cited by 55 · see citing works

A perspective on astrocyte regulation of neural circuit function and animal behavior

Hirrlinger, J., & Nimmerjahn, A. (2022) · Glia · doi:10.1002/glia.24168 · Cited by 55 · see citing works

Tuberous Sclerosis Complex as Disease Model for Investigating mTOR-Related Gliopathy During Epileptogenesis

Zimmer, T. S., Broekaart, D. W. M., Gruber, V.-E., van Vliet, E. A., Mühlebner, A., & Aronica, E. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01028 · Cited by 48 · see citing works

Acute brain injuries trigger microglia as an additional source of the proteoglycan NG2

Huang, W., Bai, X., Meyer, E., & Scheller, A. (2020) · Acta Neuropathologica Communications · doi:10.1186/s40478-020-01016-2 · Cited by 47 · see citing works

Constitutive deletion of astrocytic connexins aggravates kainate‐induced epilepsy

Deshpande, T., Li, T., Henning, L., Wu, Z., Müller, J., Seifert, G., Steinhäuser, C., & Bedner, P. (2020) · Glia · doi:10.1002/glia.23832 · Cited by 44 · see citing works

Glial Interfaces: Advanced Materials and Devices to Uncover the Role of Astroglial Cells in Brain Function and Dysfunction

Maiolo, L., Guarino, V., Saracino, E., Convertino, A., Melucci, M., Muccini, M., Ambrosio, L., Zamboni, R., & Benfenati, V. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.202001268 · Cited by 47 · see citing works

Astrocytic GABA Accumulation in Experimental Temporal Lobe Epilepsy

Müller, J., Timmermann, A., Henning, L., Müller, H., Steinhäuser, C., & Bedner, P. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.614923 · Cited by 42 · see citing works

High, in Contrast to Low Levels of Acute Stress Induce Depressive-like Behavior by Involving Astrocytic, in Addition to Microglial P2X7 Receptors in the Rodent Hippocampus

Zhao, Y.-F., Ren, W.-J., Zhang, Y., He, J., Yin, H., Liao, Y., Rubini, P., Deussing, J. M., Verkhratsky, A., Yuan, Z., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031904 · Cited by 40 · see citing works

NG2 cells and their neurogenic potential

Kirdajová, D., & Anděrová, M. (2019) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2019.11.005 · Cited by 37 · see citing works

The Structure and Function of Glial Networks: Beyond the Neuronal Connections

Peng, H.-R., Zhang, Y.-K., & Zhou, J. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00992-w · Cited by 35 · see citing works

Many roles for oligodendrocyte precursor cells in physiology and pathology

Nishiyama, A., Serwanski, D. R., & Pfeiffer, F. (2021) · Neuropathology · doi:10.1111/neup.12732 · Cited by 29 · see citing works

Cell death of hippocampal CA1 astrocytes during early epileptogenesis

Wu, Z., Deshpande, T., Henning, L., Bedner, P., Seifert, G., & Steinhäuser, C. (2021) · Epilepsia · doi:10.1111/epi.16910 · Cited by 34 · see citing works

Impaired myelin production due to an intrinsic failure of oligodendrocytes in mTORpathies

Gruber, V., Lang, J., Endmayr, V., Diehm, R., Pimpel, B., Glatter, S., Anink, J. J., Bongaarts, A., Luinenburg, M. J., Reinten, R. J. A., et al. (2021) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12744 · Cited by 31 · see citing works

Overview Article Astrocytes as Initiators of Epilepsy

Henning, L., Unichenko, P., Bedner, P., Steinhäuser, C., & Henneberger, C. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03773-z · Cited by 31 · see citing works

Role of Impaired Astrocyte Gap Junction Coupling in Epileptogenesis

Bedner, P., & Steinhäuser, C. (2023) · Cells · doi:10.3390/cells12121669 · Cited by 31 · see citing works

Reprogramming cellular identity in vivo

Leaman, S., Marichal, N., & Berninger, B. (2022) · Development · doi:10.1242/dev.200433 · Cited by 22 · see citing works

Astrocytes: new evidence, new models, new roles

Brazhe, A., Verisokin, A. Y., Вячеславовна, В. Д., & Postnov, D. E. (2023) · Biophysical Reviews · doi:10.1007/s12551-023-01145-7 · Cited by 23 · see citing works

Gut microbiota-related neuroinflammation at the crossroad of food reward alterations: implications for eating disorders

Huwart, S. J. P., Morales‐Puerto, N., & Everard, A. (2025) · Gut · doi:10.1136/gutjnl-2024-333397 · Cited by 26 · see citing works

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 17 · see citing works

Reciprocal Interactions between Oligodendrocyte Precursor Cells and the Neurovascular Unit in Health and Disease

Pfeiffer, F. (2022) · Cells · doi:10.3390/cells11121954 · Cited by 17 · see citing works

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 · see citing works

Distinctive biophysical features of human cell-types: insights from studies of neurosurgically resected brain tissue

Chameh, H. M., Falby, M. R., Movahed, M., Arbabi, K., Rich, S., Zhang, L., Lefebvre, J., Tripathy, S. J., Pittà, M. D., & Valiante, T. A. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2023.1250834 · Cited by 14 · see citing works

Alterations in brain fluid physiology during the early stages of development of ischaemic oedema

Hladky, S. B., & Barrand, M. A. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00534-8 · Cited by 18 · see citing works

The orphan G protein‐coupled receptor GPR149 is a negative regulator of myelination and remyelination

Suo, N., He, B., Cui, S.-H., Yang, Y., Wang, M., Yuan, Q., & Xie, X. (2022) · Glia · doi:10.1002/glia.24233 · Cited by 15 · see citing works

Diversity, Functional Complexity, and Translational Potential of Glial Cells in the Central Nervous System

Wawrzyniak, A., Krawczyk-Marć, I., Żuryń, A., Walocha, J. A., & Balawender, K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26189080 · Cited by 16 · see citing works

Optimised isolation and characterisation of adult human astrocytes from neurotrauma patients

Gradišnik, L., Maver, U., Bošnjak, R., & Velnar, T. (2020) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2020.108796 · Cited by 14 · see citing works

Glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor regulate the interaction between astrocytes and Schwann cells at the trigeminal root entry zone

Wang, F., Luo, D., Adam, M. I., Lin, L., Makin, A., Zhang, X., Zhou, L.-X., Liao, X., & Zhao, L. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.354517 · Cited by 13 · see citing works

Computational modeling of neuron–glia signaling interactions to unravel cellular and neural circuit functioning

Linne, M. (2024) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102838 · Cited by 12 · see citing works

Interferon-Beta Induces Major Histocompatibility Complex of Class I (MHC-I) Expression and a Proinflammatory Phenotype in Cultivated Human Astrocytes

Ignarro, R. S., Bombeiro, A. L., Chiarotto, G. B., Cartarozzi, L. P., Coser, L. D. O., Ghizoni, E., Tedeschi, H., Cendes, F., Lopes-Cendes, I., Rogerio, F., et al. (2022) · Differentiation · doi:10.1016/j.diff.2022.10.004 · Cited by 13 · see citing works

Advanced Bio-Based Polymers for Astrocyte Cell Models

Gradišnik, L., Bošnjak, R., Maver, T., & Velnar, T. (2021) · Materials · doi:10.3390/ma14133664 · Cited by 13 · see citing works

ATP indirectly stimulates hippocampal CA1 and CA3 pyramidal neurons via the activation of neighboring P2X7 receptor-bearing astrocytes and NG2 glial cells, respectively

Zhang, Y., Yin, H., Rubini, P., Illés, P., & Tang, Y. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.944541 · Cited by 13 · see citing works

Therapeutic Potential of GABAergic Signaling in Myelin Plasticity and Repair

Reyes‐Haro, D., Cisneros-Mejorado, A., & Arellano, R. O. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.662191 · Cited by 11 · see citing works

Translational neuroscience: the state of the nation (a PhD student perspective)

Davies, C., Hamilton, O. K., Hooley, M., Ritakari, T. E., Stevenson, A. J., & Wheater, E. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa038 · Cited by 11 · see citing works

Glial Populations in the Human Brain Following Ischemic Injury

Mihailova, V., Stoyanova, I. I., & Tonchev, A. B. (2023) · Biomedicines · doi:10.3390/biomedicines11092332 · Cited by 10 · see citing works

GLIPR1 and SPARC expression profile reveals a signature associated with prostate Cancer Brain metastasis

Barros, E. G. D. O., Branco, L. A. C., Costa, N. M. D., Nicolau‐Neto, P., Palmero, C. Y., Pontes, B., do Amaral, R. F., Alves‐Leon, S. V., de Souza, J. M., Romão, L. F., et al. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111230 · Cited by 9 · see citing works

Seizure-Induced Acute Glial Activation in the in vitro Isolated Guinea Pig Brain

Verde, D. V., de Curtis, M., & Librizzi, L. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.607603 · Cited by 8 · see citing works

Do astrocytes act as immune cells after pediatric TBI?

Panchenko, P. E., Hippauf, L., Konsman, J. P., & Badaut, J. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106231 · Cited by 8 · see citing works

The Concept of Neuroglia ‐ the State of the Art Circa 1900

Kettenmann, H., Ugursu, B., Ransom, B. R., & Steinhäuser, C. (2025) · Glia · doi:10.1002/glia.24678 · Cited by 7 · see citing works

The aminosteroid U73122 promotes oligodendrocytes generation and myelin formation

Cui, S.-H., Suo, N., Yang, Y., Wu, X., Guo, S., & Xie, X. (2023) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01183-7 · Cited by 6 · see citing works

Age‐Related Alterations in Hippocampal Microstructure Quantified Using High‐Gradient Diffusion MRI ( dMRI ) in an Unfolded Hippocampal Space

Ma, Y., Lee, H., Chan, K., Eskandarian, L., Gaudet, K., Tian, Q., Bhatt, A., Gerold, J., Russo, A. W., Salat, D. H., et al. (2025) · Aging Cell · doi:10.1111/acel.70274 · Cited by 5 · see citing works

A companion to the preclinical common data elements and case report forms for neuropathology studies in epilepsy research. A report of the TASK3 WG2 Neuropathology Working Group of the ILAE / AES Joint Translational Task Force

Aronica, E., Binder, D. K., Drexel, M., Ikonomidou, C., Kadam, S. D., Sperk, G., & Steinhäuser, C. (2022) · Epilepsia Open · doi:10.1002/epi4.12638 · Cited by 4 · see citing works

Neuron-Glial2 (NG2) cells: A promising target for neuroinflammation-related neurodegeneration

Hein, Z. M., Nassir, C. M. N. C. M., Ramli, M. D. C., Serafi, I. E., & Chetsawang, B. (2025) · Translational Research in Anatomy · doi:10.1016/j.tria.2025.100395 · Cited by 3 · see citing works

The 5-HT and PLC Signaling Pathways Regulate the Secretion of IL-1β, TNF-α and BDNF from NG2 Cells

Yang, T., Li, Y., Wang, H., Shi, P., Liu, T., Guo, H., Tu, X., & Yao, X. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/7425538 · Cited by 3 · see citing works

Non-trivial dynamics in a model of glial membrane voltage driven by open potassium pores

Janjić, P., Solev, D., & Kocarev, L. (2023) · Biophysical Journal · doi:10.1016/j.bpj.2023.03.013 · Cited by 3 · see citing works

Membrane properties and coupling of macroglia in the optic nerve

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

A Crucial Role for Astrocytes in Epileptogenesis

Bedner, P., Peterson, A. R., Binder, D. K., & Steinhäuser, C. (2024) · doi:10.1093/med/9780197549469.003.0026 · Cited by 2 · see citing works

Cancer: A bioelectric disease?

Desoyer, C., Šupe, R., Ghorbanpour, S. M., Goswami, D., Khalaj, M., Karami, N., Brislinger, D., Hauser, C. A. E., & Baumgärtner, C. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70701 · Cited by 2 · see citing works

Bipolar disorder as a gliopathy

Stertz, L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819182-8.00015-6 · Cited by 2 · see citing works

PD-1 deficiency aggravates spinal cord injury by regulating the reprogramming of NG2 glia and activating the NgR/RhoA/ROCK signaling pathway

Liu, Y., Zhao, Y., Liao, X., Zhou, S., Guo, X., Yang, L., & Lv, B. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110978 · Cited by 2 · see citing works

Morphological and physiological features of human cerebral cortical astrocytes in regenerative medicine: a narrative review

Tyurikova, O. (2024) · Regenerative medicine reports . · doi:10.4103/regenmed.regenmed-d-24-00003 · Cited by 2 · see citing works

Non-neuronal targets for migraine therapy

Gliga, O., Feliu‐Soler, A., & Vila‐Pueyo, M. (2026) · Neurotherapeutics · doi:10.1016/j.neurot.2026.e00845 · Cited by 1 · see citing works

Diffusion‐weighted GRASE sequence with 3D navigator for high‐resolution time‐dependent diffusion MRI in the human cortical gray matter

Li, H., Zhu, Q., Lu, J., Shen, Y., Zhao, Z., Hsu, Y., Xu, Y., Zhang, Y., & Wu, D. (2025) · Magnetic Resonance in Medicine · doi:10.1002/mrm.30587 · Cited by 1 · see citing works

Generation and Maturation of Macroglia in the Central Nervous System

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

Astrocyte heterogeneity under physiological conditions and after brain injury

Mihailova, V., Morfov, S., Velikov, I., Spasov, R., Stoyanova, I. I., & Tonchev, A. B. (2023) · Varna Medical Forum · doi:10.14748/vmf.v12i1.8763

Additional file 1 of Acute brain injuries trigger microglia as an additional source of the proteoglycan NG2

Huang, W., Bai, X., Meyer, E., & Scheller, A. (2020) · Figshare · doi:10.6084/m9.figshare.12864347

APOE Gene Editing as a Therapeutic Target Toward Precision Medicine in AD

Teter, B., Campagna, J. J., Spilman, P. R., & John, V. (2025) · Springer eBooks · doi:10.1007/978-3-031-52641-1_73-1 · Cited by 1 · see citing works

Ontogenesis and diversification of cerebellar glia: A developmental perspective

Turrini, G., Bianciotto, O. T., Cerrato, V., & Buffo, A. (2026) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2026.01.008

Investigating the molecular signature of reactive astrocytes mediated by the JAK2- STAT3 pathway using different omics : transcriptomics and proteomics insights

Riquelme‐Perez, M. (2023) · theses.fr (ABES) · doi:10.70675/72aad0d8z36a8z4a7azb1eaze65fa79463da

APOE Gene Editing as a Therapeutic Target Toward Precision Medicine in AD

Teter, B., Campagna, J. J., Spilman, P., & John, V. (2026) · Springer eBooks · doi:10.1007/978-3-031-96089-5_73

Diversity of glutamate receptors in glial cells of the mouse optic nerve

Kompier, N. F., Semtner, M., Walter, S., Steinhäuser, C., Nolte, C., & Kettenmann, H. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1911068

Progenitor Timing Shapes NG2 ‐Glia Fate and Oligodendrocyte Differentiation

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Vasile, F., Dossi, E., & Rouach, N. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1383-5 · Cited by 428 · see citing works

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Bush, N. A. O., & Nedergaard, M. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2363-0 · Cited by 22 · see citing works

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