Glia — more than just brain glue

The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease

Barres, B. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.013 · Cited by 1,352 · see citing works

Astrocyte Control of Synaptic Transmission and Neurovascular Coupling

Haydon, P. G., & Carmignoto, G. (2006) · Physiological Reviews · doi:10.1152/physrev.00049.2005 · Cited by 1,326 · see citing works

Axon-Glial Signaling and the Glial Support of Axon Function

Nave, K., & Trapp, B. D. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094309 · Cited by 659 · see citing works

The astrocyte odyssey

Wang, D. D., & Bordey, A. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.015 · Cited by 517 · see citing works

Signaling between glia and neurons: focus on synaptic plasticity

Allen, N. J., & Barres, B. A. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.08.006 · Cited by 321 · see citing works

Glial cell biology in Drosophila and vertebrates

Freeman, M. R., & Doherty, J. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2005.12.002 · Cited by 277 · see citing works

Neuroglia

(2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195152227.001.0001 · Cited by 59 · see citing works

An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex

Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875 · see citing works

Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse

Zhang, Y., Sloan, S. A., Clarke, L. E., Caneda, C., Plaza, C. A., Blumenthal, P. D., Vogel, H., Steinberg, G. K., Edwards, M. S. B., Li, G., et al. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.013 · Cited by 2,295 · see citing works

The human brain in numbers: a linearly scaled-up primate brain

Herculano-Houzel, S. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.031.2009 · Cited by 1,778 · see citing works

Diversity of astrocyte functions and phenotypes in neural circuits

Khakh, B. S., & Sofroniew, M. V. (2015) · Nature Neuroscience · doi:10.1038/nn.4043 · Cited by 1,239 · see citing works

The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting

von Bartheld, C. S., Bahney, J., & Herculano‐Houzel, S. (2016) · Journal of Comparative Neurology · doi:10.1002/cne.24040 · Cited by 1,063 · see citing works

Astrocyte Crosstalk in CNS Inflammation

Linnerbauer, M., Wheeler, M. A., & Quintana, F. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.012 · Cited by 989 · see citing works

The glia/neuron ratio: How it varies uniformly across brain structures and species and what that means for brain physiology and evolution

Herculano‐Houzel, S. (2014) · Glia · doi:10.1002/glia.22683 · Cited by 731 · see citing works

Astrocyte Pathology in Major Depressive Disorder: Insights from Human Postmortem Brain Tissue

Rajkowska, G., & Stockmeier, C. (2013) · Current Drug Targets · doi:10.2174/13894501113149990156 · Cited by 603 · see citing works

Aquaporin 4 and neuromyelitis optica

Papadopoulos, M., & Verkman, A. S. (2012) · Lancet Neurology · doi:10.1016/s1474-4422(12)70133-3 · Cited by 574 · see citing works

Quercetin hinders microglial activation to alleviate neurotoxicity via the interplay between NLRP3 inflammasome and mitophagy

Han, X., Xu, T., Fang, Q., Zhang, H., Yue, L., Hu, G., & Sun, L. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102010 · Cited by 554 · see citing works

The Indispensable Roles of Microglia and Astrocytes during Brain Development

Reemst, K., Noctor, S. C., Lucassen, P. J., & Hol, E. M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00566 · Cited by 516 · see citing works

The Emerging Nature of Astrocyte Diversity

Khakh, B. S., & Deneen, B. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050443 · Cited by 485 · see citing works

Complex I assembly into supercomplexes determines differential mitochondrial ROS production in neurons and astrocytes

López-Fabuel, I., Douce, J. L., Logan, A., James, A. M., Bonvento, G., Murphy, M. P., Almeida, Á., & Bolaños, J. P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613701113 · Cited by 474 · see citing works

Isolation and Culture of Mouse Cortical Astrocytes

Schildge, S., Bohrer, C., Beck, K., & Schachtrup, K. (2013) · Journal of Visualized Experiments · doi:10.3791/50079 · Cited by 453 · see citing works

Roles of neuropathology-associated reactive astrocytes: a systematic review

Lawrence, J. M., Schardien, K., Wigdahl, B., & Nonnemacher, M. R. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01526-9 · Cited by 433 · see citing works

The landscape of aging

Cai, Y., Song, W., Li, J., Jing, Y., Liang, C., Zhang, L., Zhang, X., Zhang, W., Liu, B., An, Y., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-022-2161-3 · Cited by 436 · see citing works

Stability of synchronization in simplicial complexes

Gambuzza, L. V., Patti, F. D., Gallo, L., Stefano Lepri, A., Romance, M., Criado, R., Frasca, M., Latora, V., & Boccaletti, S. (2021) · Nature Communications · doi:10.1038/s41467-021-21486-9 · Cited by 350 · see citing works

Astrocyte Biomarkers in Alzheimer’s Disease

Carter, S. F., Herholz, K., Rosa-Neto, P., Pellerin, L., Nordberg, A., & Zimmer, E. R. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.11.006 · Cited by 355 · see citing works

Dynamics and Mechanisms of CNS Myelination

Bercury, K. K., & Macklin, W. B. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.01.016 · Cited by 320 · see citing works

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 · see citing works

Astrocyte development: A Guide for the Perplexed

Molofsky, A. V., & Deneen, B. (2015) · Glia · doi:10.1002/glia.22836 · Cited by 305 · see citing works

Artifact versus reality—How astrocytes contribute to synaptic events

Nedergaard, M., & Verkhratsky, A. (2012) · Glia · doi:10.1002/glia.22288 · Cited by 304 · see citing works

Cellular senescence and the aging brain

Chinta, S. J., Woods, G., Rane, A., Demaria, M., Campisi, J., & Andersen, J. K. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2014.09.018 · Cited by 282 · see citing works

Improved tools to study astrocytes

Yu, X., Nagai, J., & Khakh, B. S. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0264-8 · Cited by 298 · see citing works

Glucose metabolism links astroglial mitochondria to cannabinoid effects

Jiménez-Blasco, D., Busquets-García, A., Hébert-Chatelain, É., Serrat, R., Vicente‐Gutiérrez, C., Ioannidou, C., Gómez-Sotres, P., López-Fabuel, I., Resch-Beusher, M., Resel, E., et al. (2020) · Nature · doi:10.1038/s41586-020-2470-y · Cited by 272 · see citing works

Emerging roles of exosomes in neuron-glia communication

Frühbeis, C., Fröhlich, D., & Krämer-Albers, E.-M. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00119 · Cited by 275 · see citing works

Astrocytes as a Source for Extracellular Matrix Molecules and Cytokines

Wiese, S., Karus, M., & Faissner, A. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2012.00120 · Cited by 262 · see citing works

The neurobiology of depression in later-life: Clinical, neuropsychological, neuroimaging and pathophysiological features

Naismith, S. L., Norrie, L. M., Mowszowski, L., & Hickie, I. B. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.05.009 · Cited by 269 · see citing works

Bioenergetics and redox adaptations of astrocytes to neuronal activity

Bolaños, J. P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13486 · Cited by 262 · see citing works

Organic electrode coatings for next-generation neural interfaces

Robles, U. A. A., Woolley, A. J., Poole-Warren, L. A., Lovell, N. H., & Green, R. A. (2014) · Frontiers in Neuroengineering · doi:10.3389/fneng.2014.00015 · Cited by 255 · see citing works

The Neuron-Astrocyte-Microglia Triad in Normal Brain Ageing and in a Model of Neuroinflammation in the Rat Hippocampus

Cerbai, F., Lana, D., Nosi, D., Petkova-Kirova, P., Zecchi, S., Brothers, H. M., Wenk, G. L., & Giovannini, M. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045250 · Cited by 251 · see citing works

Ultrasonic Neuromodulation via Astrocytic TRPA1

Oh, S., Lee, J. M., Kim, H., Lee, J., Han, S., Bae, J. Y., Hong, G., Koh, W., Kwon, J., Hwang, E., et al. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.021 · Cited by 251 · see citing works

Myelination, oligodendrocytes, and serious mental illness

Haroutunian, V. H., Katsel, P., Roussos, P., Davis, K. L., Altshuler, L. L., & Bartzokis, G. (2014) · Glia · doi:10.1002/glia.22716 · Cited by 247 · see citing works

Progression in translational research on spinal cord injury based on microenvironment imbalance

Fan, B., Wei, Z., & Feng, S. (2022) · Bone Research · doi:10.1038/s41413-022-00199-9 · Cited by 248 · see citing works

Scientist Spotlight Homework Assignments Shift Students’ Stereotypes of Scientists and Enhance Science Identity in a Diverse Introductory Science Class

Schinske, J. N., Perkins, H., Snyder, A., & Wyer, M. (2016) · CBE—Life Sciences Education · doi:10.1187/cbe.16-01-0002 · Cited by 247 · see citing works

Neuroprotective Effects of Marine Algae

Pangestuti, R., & Kim, S. (2011) · Marine Drugs · doi:10.3390/md9050803 · Cited by 245 · see citing works

Glia: The many ways to modulate synaptic plasticity

Achour, S. B., & Pascual, O. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.02.013 · Cited by 232 · see citing works

The role(s) of astrocytes and astrocyte activity in neurometabolism, neurovascular coupling, and the production of functional neuroimaging signals

Figley, C. R., & Stroman, P. W. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07584.x · Cited by 232 · see citing works

Contrasting the Glial Response to Axon Injury in the Central and Peripheral Nervous Systems

Lutz, A. B., & Barres, B. A. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.002 · Cited by 229 · see citing works

Reactive Astrocytes Protect Melanoma Cells from Chemotherapy by Sequestering Intracellular Calcium through Gap Junction Communication Channels

Lin, Q., Balasubramanian, K., Fan, D., Kim, S., Guo, L., Wang, H., Bar‐Eli, M., Aldape, K., & Fidler, I. J. (2010) · Neoplasia · doi:10.1593/neo.10602 · Cited by 228 · see citing works

Blood-Brain Barrier Dysfunction in CNS Disorders and Putative Therapeutic Targets: An Overview

Archie, S. R., Shoyaib, A. A., & Cucullo, L. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13111779 · Cited by 232 · see citing works

Parkinson’s disease as a result of aging

Rodriguez, M., Rodriguez‐Sabate, C., Morales, I., Sanchez, A., & Sabate, M. (2015) · Aging Cell · doi:10.1111/acel.12312 · Cited by 214 · see citing works

Astrocyte molecular signatures in Huntington’s disease

Diaz-Castro, B., Gangwani, M. R., Yu, X., Coppola, G., & Khakh, B. S. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aaw8546 · Cited by 255 · see citing works

Dimethyl Sulfoxide Damages Mitochondrial Integrity and Membrane Potential in Cultured Astrocytes

Chan, Y., Gao, J., Guo, J., Bai, L., Marshall, C., Cai, Z., Wang, L., & Xiao, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107447 · Cited by 220 · see citing works

Effects of Lithium on Inflammation

Nassar, A., & Azab, A. N. (2014) · ACS Chemical Neuroscience · doi:10.1021/cn500038f · Cited by 218 · see citing works

The role of the organ microenvironment in brain metastasis

Fidler, I. J. (2010) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.12.009 · Cited by 217 · see citing works

The effects of microglia‐ and astrocyte‐derived factors on neurogenesis in health and disease

Araki, T., Ikegaya, Y., & Koyama, R. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14969 · Cited by 208 · see citing works

Optogenetic Countering of Glial Acidosis Suppresses Glial Glutamate Release and Ischemic Brain Damage

Beppu, K., Sasaki, T., Tanaka, K. F., Yamanaka, A., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.011 · Cited by 195 · see citing works

Do stars govern our actions? Astrocyte involvement in rodent behavior

Oliveira, J. F., Sardinha, V. M., Guerra-Gomes, S., Araque, A., & Sousa, N. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.006 · Cited by 189 · see citing works

A cytokine network involving brain-borne IL-1β, IL-1ra, IL-18, IL-6, and TNFα operates during long-term potentiation and learning

del Rey, A., Balschun, D., Wetzel, W., Randolf, A., & Besedovsky, H. O. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.05.011 · Cited by 182 · see citing works

Neuroprotective Properties of Chitosan and Its Derivatives

Pangestuti, R., & Kim, S. (2010) · Marine Drugs · doi:10.3390/md8072117 · Cited by 173 · see citing works

The cytosolic redox state of astrocytes: Maintenance, regulation and functional implications for metabolite trafficking

Hirrlinger, J., & Dringen, R. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.10.003 · Cited by 171 · see citing works

Cocaine Self-Administration and Extinction Leads to Reduced Glial Fibrillary Acidic Protein Expression and Morphometric Features of Astrocytes in the Nucleus Accumbens Core

Scofield, M. D., Li, H., Siemsen, B. M., Healey, K. L., Tran, P. K., Woronoff, N., Boger, H. A., Kalivas, P. W., & Reissner, K. J. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.022 · Cited by 171 · see citing works

Pathophysiology, Diagnosis, and Treatment of Radiation Necrosis in the Brain

Miyatake, S., Nonoguchi, N., Furuse, M., Yoritsune, E., Miyata, T., Kawabata, S., & Kuroiwa, T. (2014) · Neurologia medico-chirurgica · doi:10.2176/nmc.ra.2014-0188 · Cited by 171 · see citing works

Cell‐specific blood–brain barrier regulation in health and disease: a focus on hypoxia

Engelhardt, S., Patkar, S., & Ogunshola, O. O. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12489 · Cited by 165 · see citing works

Environmental stress, ageing and glial cell senescence: a novel mechanistic link to Parkinson's disease?

Chinta, S. J., Lieu, C. A., DeMaria, M., Laberge, R. ‐., Campisi, J., & Andersen, J. K. (2013) · Journal of Internal Medicine · doi:10.1111/joim.12029 · Cited by 165 · see citing works

Heat shock proteins in neurodegenerative disorders and aging

Leak, R. K. (2014) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-014-0243-9 · Cited by 170 · see citing works

Extracellular Vesicle-Mediated Cell–Cell Communication in the Nervous System: Focus on Neurological Diseases

Bavisotto, C. C., Scalia, F., Marino, A., Carlisi, D., Bucchieri, F., de Macario, E. C., Macario, A. J. L., Cappello, F., & Campanella, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20020434 · Cited by 166 · see citing works

Application of an optogenetic byway for perturbing neuronal activity via glial photostimulation

Sasaki, T., Beppu, K., Tanaka, K. F., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213458109 · Cited by 156 · see citing works

IL-17 Enhancement of the IL-6 Signaling Cascade in Astrocytes

Ma, X., Reynolds, S. L., Baker, B. J., Li, X., Benveniste, E. N., & Qin, H. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000142 · Cited by 155 · see citing works

The role of tissue microstructure and water exchange in biophysical modelling of diffusion in white matter

Nilsson, M., van Westen, D., Ståhlberg, F., Sundgren, P. C., & Lätt, J. (2013) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-013-0371-x · Cited by 151 · see citing works

Gait alterations in healthy carriers of the LRRK2 G2019S mutation

Mirelman, A., Gurevich, T., Giladi, N., Bar‐Shira, A., Orr‐Urtreger, A., & Hausdorff, J. M. (2011) · Annals of Neurology · doi:10.1002/ana.22165 · Cited by 149 · see citing works

Neuroimmunomodulatory and Neuroprotective Effects of the Flavonoid Apigenin in in vitro Models of Neuroinflammation Associated With Alzheimer’s Disease

Dourado, N. S., Souza, C. D. S., de Almeida, M. M. A., da Silva, A. B., dos Santos, B. L., da Silva, V. D. A., de Assis, A. M., da Silva, J. S., Souza, D. O., Costa, M. D. F. D., et al. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00119 · Cited by 150 · see citing works

tDCS possibly stimulates glial cells

Ruohonen, J., & Karhu, J. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2012.02.082 · Cited by 145 · see citing works

Antibody therapies in CNS diseases

Freskgård, P., & Urich, E. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.014 · Cited by 139 · see citing works

What is microglia neurotoxicity (Not)?

Biber, K. P. H., Owens, T., & Boddeke, E. (2014) · Glia · doi:10.1002/glia.22654 · Cited by 141 · see citing works

Astroglial correlates of neuropsychiatric disease: From astrocytopathy to astrogliosis

Kim, R., Healey, K. L., Sepulveda-Orengo, M. T., & Reissner, K. J. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.10.002 · Cited by 141 · see citing works

Dynamics of electric activities in neuron and neurons of network induced by autapses

Qin, H., Ma, J., Jin, W., & Wang, C. (2014) · Science China Technological Sciences · doi:10.1007/s11431-014-5534-0 · Cited by 140 · see citing works

Neuron-Glia Interactions in Neural Plasticity: Contributions of Neural Extracellular Matrix and Perineuronal Nets

Dzyubenko, E., Gottschling, C., & Faissner, A. (2016) · Neural Plasticity · doi:10.1155/2016/5214961 · Cited by 134 · see citing works

Pharmacological and genetic approaches to study connexin-mediated channels in glial cells of the central nervous system

Giaume, C., & Theis, M. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.11.005 · Cited by 135 · see citing works

Three-Dimensional Neural Spheroid Culture: An In Vitro Model for Cortical Studies

Dingle, Y. L., Boutin, M. E., Chirila, A. M., Livi, L. L., Labriola, N. R., Jakubek, L. M., Morgan, J. R., Darling, E. M., Kauer, J. A., & Hoffman–Kim, D. (2015) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2015.0135 · Cited by 132 · see citing works

Dysfunction of homeostatic control of dopamine by astrocytes in the developing prefrontal cortex leads to cognitive impairments

Petrelli, F., Dallérac, G. M., Pucci, L., Calì, C., Zehnder, T., Sultan, S., Lecca, S., Chicca, A., Ivanov, A. D., Asensio, C. S., et al. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0226-y · Cited by 127 · see citing works

Astrocyte Depletion Impairs Redox Homeostasis and Triggers Neuronal Loss in the Adult CNS

Schreiner, B., Romanelli, E., Liberski, P. P., Ingold‐Heppner, B., Sobottka, B., Hartwig, T., Chandrasekar, V., Johannssen, H. C., Zeilhofer, H. U., Aguzzi, A., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.07.051 · Cited by 129 · see citing works

Omega-3 Polyunsaturated Fatty Acid Supplementation Improves Neurologic Recovery and Attenuates White Matter Injury after Experimental Traumatic Brain Injury

Pu, H., Guo, Y., Zhang, W., Huang, L., Wang, G., Liou, A. K. F., Zhang, J., Zhang, P., Leak, R. K., Wang, Y., et al. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.108 · Cited by 126 · see citing works

A Critical Review of Microelectrode Arrays and Strategies for Improving Neural Interfaces

Ferguson, M., Sharma, D., Ross, D., & Zhao, F. (2019) · Advanced Healthcare Materials · doi:10.1002/adhm.201900558 · Cited by 124 · see citing works

Emerging roles for cholesterol in Huntington's disease

Valenza, M., & Cattaneo, E. F. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.06.005 · Cited by 123 · see citing works

Astrocytes influence the severity of spinal muscular atrophy

Rindt, H., Feng, Z., Mazzasette, C., Glascock, J., Valdivia, D. O., Pyles, N. J., Crawford, T. O., Swoboda, K. J., Patitucci, T. N., Ebert, A. D., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv148 · Cited by 123 · see citing works

Kir4.1-Dependent Astrocyte-Fast Motor Neuron Interactions Are Required for Peak Strength

Kelley, K. W., Haim, L. B., Schirmer, L., Tyzack, G. E., Tolman, M., Miller, J. G., Tsai, H., Chang, S., Molofsky, A. V., Yang, Y., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.010 · Cited by 118 · see citing works

Host Cell Preference of Toxoplasma gondii Cysts in Murine Brain: A Confocal Study

Melzer, T. C., Cranston, H., Weiss, L. M., & Halonen, S. K. (2010) · Journal of Neuroparasitology · doi:10.4303/jnp/n100505 · Cited by 122 · see citing works

Müller glia provide essential tensile strength to the developing retina

MacDonald, R. B., Randlett, O., Oswald, J., Yoshimatsu, T., Franze, K., & Harris, W. A. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201503115 · Cited by 122 · see citing works

From Synapses to Circuits, Astrocytes Regulate Behavior

Lyon, K. A., & Allen, N. J. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.786293 · Cited by 117 · see citing works

Positively correlated miRNA-mRNA regulatory networks in mouse frontal cortex during early stages of alcohol dependence

Núnez, Y. O., Truitt, J., Gorini, G., Ponomareva, O. N., Blednov, Y. A., Harris, R. A., & Mayfield, R. D. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-725 · Cited by 120 · see citing works

Neuroprotective Function of High Glycolytic Activity in Astrocytes: Common Roles in Stroke and Neurodegenerative Diseases

Takahashi, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126568 · Cited by 119 · see citing works

Cross-talk between energy and redox metabolism in astrocyte-neuron functional cooperation

Almeida, Á., Jiménez-Blasco, D., & Bolaños, J. P. (2023) · Essays in Biochemistry · doi:10.1042/ebc20220075 · Cited by 115 · see citing works

Cell Surface-Anchored Fluorescent Aptamer Sensor Enables Imaging of Chemical Transmitter Dynamics

Tokunaga, T., Namiki, S., Yamada, K., Imaishi, T., Nonaka, H., Hirose, K., & Sando, S. (2012) · Journal of the American Chemical Society · doi:10.1021/ja302551p · Cited by 117 · see citing works

Gap junction communication in myelinating glia

Nualart-Marti, A., Solsona, C., & Fields, R. D. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.01.024 · Cited by 116 · see citing works

Amyloid-β oligomers in cellular models of Alzheimer’s disease

Fontana, I. C., Zimmer, A. R., Rocha, A. S., Gosmann, G., Souza, D. O., Lourenco, M. V., Ferreira, S. T., & Zimmer, E. R. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15030 · Cited by 115 · see citing works

Astrocytes and neuroinflammation in Alzheimer's disease

Phillips, E. C., Croft, C. L., Crane, K., O’Neill, M. J., Hutton, M. L., Hanger, D. P., Garwood, C. J., & Noble, W. J. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140155 · Cited by 114 · see citing works

Acrylamide induces mitochondrial dysfunction and apoptosis in BV-2 microglial cells

Liu, Z., Song, G., Zou, C., Liu, G., Wu, W., Yuan, T., & Liu, X. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.03.013 · Cited by 114 · see citing works

Direct modulation of GFAP-expressing glia in the arcuate nucleus bi-directionally regulates feeding

Chen, N., 杉原, 弘., Kim, J., Fu, Z., Barak, B., Sur, M., Feng, G., & Han, W. (2016) · eLife · doi:10.7554/elife.18716 · Cited by 105 · see citing works

Nonlinear Gap Junctions Enable Long-Distance Propagation of Pulsating Calcium Waves in Astrocyte Networks

Goldberg, M., Pittà, M. D., Volman, V., Berry, H., & Ben‐Jacob, E. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000909 · Cited by 113 · see citing works

High Systolic Blood Pressure Induces Cerebral Microvascular Endothelial Dysfunction, Neurovascular Unit Damage, and Cognitive Decline in Mice

de Montgolfier, O., Pinçon, A., Pouliot, P., Gillis, M., Bishop, J. E., Sled, J. G., Villeneuve, L. R., Ferland, G., Levy, B. I., Lesage, F., et al. (2018) · Hypertension · doi:10.1161/hypertensionaha.118.12048 · Cited by 112 · see citing works

Activation of astrocytes in hippocampus decreases fear memory through adenosine A1 receptors

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Developmental Origins of Astrocyte Heterogeneity: The Final Frontier of CNS Development

Chaboub, L. S., & Deneen, B. (2012) · Developmental Neuroscience · doi:10.1159/000343723 · Cited by 111 · see citing works

Central and Peripheral Cytokines Mediate Immune-Brain Connectivity

Besedovsky, H. O., & del Rey, A. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0252-x · Cited by 111 · see citing works

Extracellular Vesicles in neural cell interaction and CNS homeostasis

Schnatz, A., Müller, C., Brahmer, A., & Krämer‐Albers, E. (2021) · FASEB BioAdvances · doi:10.1096/fba.2021-00035 · Cited by 110 · see citing works

Deep Artificial Neural Networks and Neuromorphic Chips for Big Data Analysis: Pharmaceutical and Bioinformatics Applications

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Hypothalamic microinflammation: a common basis of metabolic syndrome and aging

Tang, Y., Purkayastha, S., & Cai, D. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.10.002 · Cited by 109 · see citing works

Fragile X astrocytes induce developmental delays in dendrite maturation and synaptic protein expression

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Anti-TNF-α Compounds as a Treatment for Depression

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Glia make up most of the cells in the brain, yet until recently they were believed to have only a passive, supporting role. It is now becoming increasingly clear that these cells have other functions: they make crucial contributions to the formation, operation and adaptation of neural circuitry.

Allen, N. J., & Barres, B. A. (2009)

New functions for glia in the brain

Temburni, M. K., & Jacob, M. H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081073198 · Cited by 57 · see citing works

Glee for Glia

Stern, P. (2010) · Science · doi:10.1126/science.330.6005.773 · Cited by 9 · see citing works

The Biology of GliaPreprint

Stevens, B., Monk, K. R., & Freeman, M. R. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041809

Introductory Speaker:

Diseases, G. (2013)