Morphology of Microglia Across Contexts of Health and Disease

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827 · see citing works

A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease

Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493 · see citing works

The M1 and M2 paradigm of macrophage activation: Time for reassessment

Martinez, F. O., & Gordon, S. (2014) · F1000Prime Reports · doi:10.12703/p6-13 · Cited by 4,689 · see citing works

ATP mediates rapid microglial response to local brain injury in vivo

Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913 · see citing works

jvenn: an interactive Venn diagram viewer

Bardou, P., Mariette, J., Escudié, F., Djemiel, C., & Klopp, C. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-293 · Cited by 2,506 · see citing works

Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain

Lawson, L. J., Perry, V. H., Dri, P., & Gordon, S. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90229-w · Cited by 2,045 · see citing works

How neuroinflammation contributes to neurodegeneration

Ransohoff, R. M. (2016) · Science · doi:10.1126/science.aag2590 · Cited by 1,967 · see citing works

New tools for studying microglia in the mouse and human CNS

Bennett, M. L., Bennett, F. C., Liddelow, S. A., Ajami, B., Zamanian, J. L., Fernhoff, N. B., Mulinyawe, S. B., Bohlen, C. J., Adil, A., Tucker, A., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525528113 · Cited by 1,804 · see citing works

Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease

Zhang, B., Gaiteri, C., Bodea, L.-G., Wang, Z., McElwee, J., Podtelezhnikov, A. A., Zhang, C., Xie, T., Tran, L., Dobrin, R., et al. (2013) · Cell · doi:10.1016/j.cell.2013.03.030 · Cited by 1,657 · see citing works

Microglia Shape Adult Hippocampal Neurogenesis through Apoptosis-Coupled Phagocytosis

Sierra, A., Encinas, J. M., Deudero, J. J. P., Chancey, J. H., Enikolopov, G., Overstreet-Wadiche, L. S., Tsirka, S. E., & Maletic-Savatic, M. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.08.014 · Cited by 1,622 · see citing works

Microglial interactions with synapses are modulated by visual experience

Tremblay, M.-È., Lowery, R. L., & Majewska, A. K. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000527 · Cited by 1,542 · see citing works

Soluble Amyloid β Peptide Concentration as a Predictor of Synaptic Change in Alzheimer's Disease

Lue, L.-F., Kuo, Y.-M., Roher, A. E., Brachova, L., Shen, Y., Sue, L., Beach, T., Kurth, J. H., Rydel, R. E., & Rogers, J. (1999) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)65184-x · Cited by 1,530 · see citing works

Microglial priming in neurodegenerative disease

Perry, V. H., & Holmes, C. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.38 · Cited by 1,127 · see citing works

Cytology & cellular pathology of the nervous system

Penfield, W. G. (1965) · Medical Entomology and Zoology · Cited by 1,035 · see citing works

Alzheimer’s Disease Risk Gene CD33 Inhibits Microglial Uptake of Amyloid Beta

Griciuc, A., Serrano-Pozo, A., Parrado, A. R., Lesinski, A. N., Asselin, C. N., Mullin, K., Hooli, B., Choi, S. H., Hyman, B. T., & Tanzi, R. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.014 · Cited by 1,004 · see citing works

Review: Activation patterns of microglia and their identification in the human brain

Boche, D., Perry, V. H., & Nicoll, J. A. R. (2012) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12011 · Cited by 911 · see citing works

CNS immune privilege: hiding in plain sight

Carson, M. J., Doose, J. M., Melchior, B., Schmid, C. D., & Ploix, C. C. (2006) · Immunological Reviews · doi:10.1111/j.1600-065x.2006.00441.x · Cited by 801 · see citing works

Review: microglia of the aged brain: primed to be activated and resistant to regulation

Norden, D. M., & Godbout, J. P. (2013) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2012.01306.x · Cited by 792 · see citing works

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

Streit, W. J., Braak, H., Xue, Q.-S., & Bechmann, I. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0556-6 · Cited by 727 · see citing works

Changing face of microglia

Graeber, M. B. (2010) · Science · doi:10.1126/science.1190929 · Cited by 608 · see citing works

Age-related myelin degradation burdens the clearance function of microglia during aging

Safaiyan, S., Kannaiyan, N., Snaidero, N., Brioschi, S., Biber, K., Yona, S., Edinger, A. L., Jung, S., Rossner, M. J., & Simons, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4325 · Cited by 604 · see citing works

TAM receptors regulate multiple features of microglial physiology

Fourgeaud, L., Través, P. G., Tufail, Y., Leal-Bailey, H., Lew, E. D., Burrola, P. G., Callaway, P., Zagórska, A., Rothlin, C. V., Nimmerjahn, A., et al. (2016) · Nature · doi:10.1038/nature17630 · Cited by 600 · see citing works

Immune phenotypes of microglia in human neurodegenerative disease: challenges to detecting microglial polarization in human brains

Walker, D. G., & Lue, L.-F. (2015) · Alzheimer's Research & Therapy · doi:10.1186/s13195-015-0139-9 · Cited by 562 · see citing works

Microglia across the lifespan: from origin to function in brain development, plasticity and cognition

Tay, T. L., Savage, J. C., Hui, C. W., Bisht, K., & Tremblay, M. (2017) · The Journal of Physiology · doi:10.1113/jp272134 · Cited by 562 · see citing works

Microglia contribute to normal myelinogenesis and to oligodendrocyte progenitor maintenance during adulthood

Hagemeyer, N., Hanft, K.-M., Akriditou, M.-A., Unger, N., Park, E. S., Stanley, E. R., Staszewski, O., Dimou, L., & Prinz, M. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1747-1 · Cited by 558 · see citing works

Modulating inflammatory monocytes with a unique microRNA gene signature ameliorates murine ALS

Butovsky, O., Siddiqui, S., Gabriely, G., Lanser, A. J., Dake, B., Murugaiyan, G., Doykan, C. E., Wu, P. M., Gali, R. R., Iyer, L. K., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62636 · Cited by 481 · see citing works

Microglial Ramification, Surveillance, and Interleukin-1β Release Are Regulated by the Two-Pore Domain K+ Channel THIK-1

Madry, C., Kyrargyri, V., Arancibia-Cárcamo, I. L., Jolivet, R., Kohsaka, S., Bryan, R. M., & Attwell, D. (2018) · Neuron · doi:10.1016/j.neuron.2017.12.002 · Cited by 464 · see citing works

Dark microglia: A new phenotype predominantly associated with pathological states

Bisht, K., Sharma, K. P., Lecours, C., Gabriela Sánchez, M., El Hajj, H., Milior, G., Olmos‐Alonso, A., Gómez‐Nicola, D., Luheshi, G., Vallières, L., et al. (2016) · Glia · doi:10.1002/glia.22966 · Cited by 421 · see citing works

Chronic Stress Induced Remodeling of the Prefrontal Cortex: Structural Re-Organization of Microglia and the Inhibitory Effect of Minocycline

Hinwood, M., Tynan, R. J., Charnley, J. L., Beynon, S. B., Day, T. A., & Walker, F. R. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs151 · Cited by 325 · see citing works

Evidence for synaptic stripping by cortical microglia

Trapp, B. D., Wujek, J. R., Criste, G. A., Jalabi, W., Yin, X., Kidd, G. J., Stohlman, S. A., & Ransohoff, R. M. (2006) · Glia · doi:10.1002/glia.20462 · Cited by 318 · see citing works

Microglial pathology

Streit, W. J., Xue, Q.-S., Tischer, J., & Bechmann, I. (2014) · Acta Neuropathologica Communications · doi:10.1186/s40478-014-0142-6 · Cited by 317 · see citing works

Effects of aging and sensory loss on glial cells in mouse visual and auditory cortices

Tremblay, M., Zettel, M. L., Ison, J. R., Allen, P. D., & Majewska, A. K. (2012) · Glia · doi:10.1002/glia.22287 · Cited by 309 · see citing works

Neuroprotective function for ramified microglia in hippocampal excitotoxicity

Vinet, J., van Weering, H. R., Heinrich, A., Kälin, R. E., Wegner, A., Brouwer, N., Heppner, F. L., van Rooijen, N., Boddeke, H. W., & Biber, K. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-27 · Cited by 274 · see citing works

The “Big‐Bang” for modern glial biology: Translation and comments on Pío del Río‐Hortega 1919 series of papers on microglia

Sierra, A., de Castro, F., del Río-Hortega, J., Iglesias-Rozas, J. R., Garrosa, M., & Kettenmann, H. (2016) · Glia · doi:10.1002/glia.23046 · Cited by 267 · see citing works

Microglial and Astroglial Reactions to Ischemic and Kainic Acid-Induced Lesions of the Adult Rat Hippocampus

Jørgensen, M. B., Finsen, B. R., Jensen, M. B., Castellano, B., Diemer, N. H., & Zimmer, J. (1993) · Experimental Neurology · doi:10.1006/exnr.1993.1041 · Cited by 264 · see citing works

Disease-related microglia heterogeneity in the hippocampus of Alzheimer’s disease, dementia with Lewy bodies, and hippocampal sclerosis of aging

Bachstetter, A. D., Van Eldik, L. J., Schmitt, F. A., Neltner, J. H., Ighodaro, E. T., Webster, S. J., Patel, E., Abner, E. L., Kryscio, R. J., & Nelson, P. T. (2015) · Acta Neuropathologica Communications · doi:10.1186/s40478-015-0209-z · Cited by 258 · see citing works

Altered microglia morphology and higher resilience to stress-induced depression-like behavior in CX3CR1-deficient mice

Hellwig, S., Brioschi, S., Dieni, S., Frings, L., Masuch, A., Blank, T., & Biber, K. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.11.008 · Cited by 252 · see citing works

Microglia show altered morphology and reduced arborization in human brain during aging and <scp>A</scp>lzheimer's disease

Davies, D. S., Ma, J., Jegathees, T., & Goldsbury, C. (2017) · Brain Pathology · doi:10.1111/bpa.12456 · Cited by 251 · see citing works

Cytology and Cellular Pathology of the Nervous System.

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Insulin‐like growth factor type 1 receptor signaling in the cells of oligodendrocyte lineage is required for normal in vivo oligodendrocyte development and myelination

Zeger, M., Popken, G., Zhang, J., Xuan, S., Lu, Q. R., Schwab, M. H., Nave, K., Rowitch, D. H., D’Ercole, A. J., & Ye, P. (2006) · Glia · doi:10.1002/glia.20469 · Cited by 194 · see citing works

Human-to-mouse prion-like propagation of mutant huntingtin protein

Jeon, I., Cicchetti, F., Cisbani, G., Lee, S., Li, E., Bae, J., Lee, N., Li, L., Im, W., Kim, M., et al. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1582-9 · Cited by 193 · see citing works

Rod microglia: elongation, alignment, and coupling to form trains across the somatosensory cortex after experimental diffuse brain injury

Ziebell, J. M., Taylor, S. E., Cao, T., Harrison, J., & Lifshitz, J. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-247 · Cited by 185 · see citing works

Activation of microglia in the brains of humans with heart disease and hypercholesterolemic rabbits

Streit, W. J., & Sparks, D. L. (1997) · Journal of Molecular Medicine · doi:10.1007/s001090050097 · Cited by 168 · see citing works

Bipolar/rod-shaped microglia are proliferating microglia with distinct M1/M2 phenotypes

Tam, W. Y., & Ma, C. H. E. (2014) · Scientific Reports · doi:10.1038/srep07279 · Cited by 158 · see citing works

Prenatal Immune Challenge in Mice Leads to Partly Sex-Dependent Behavioral, Microglial, and Molecular Abnormalities Associated with Schizophrenia

Hui, C. W., St-Pierre, A., Hajj, H. E., Remy, Y., Hébert, S. S., Luheshi, G. N., Srivastava, L. K., & Tremblay, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00013 · Cited by 158 · see citing works

Transitory macrophages in the white matter of the developing visual cortex. II. Development and relations with axonal pathways

Innocenti, G. M., Clarke, S., & Koppel, H. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90201-8 · Cited by 150 · see citing works

Shape descriptors of the “never resting” microglia in three different acute brain injury models in mice

Zanier, E. R., Fumagalli, S., Perego, C., Pischiutta, F., & De Simoni, M.-G. (2015) · Intensive Care Medicine Experimental · doi:10.1186/s40635-015-0039-0 · Cited by 147 · see citing works

Priming of microglia in a DNA-repair deficient model of accelerated aging

Raj, D. D. A., Jaarsma, D., Holtman, I. R., Olah, M., Ferreira, F. M., Schaafsma, W., Brouwer, N., Meijer, M., de Waard, M. C., van der Pluijm, I., et al. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.03.025 · Cited by 144 · see citing works

Axon Initial Segment–Associated Microglia

Baalman, K. L., Marin, M. A., Ho, T. S., Godoy, M. I., Cherian, L., Robertson, C. S., & Rasband, M. N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3751-14.2015 · Cited by 138 · see citing works

Rod Microglia: A Morphological Definition

Taylor, S. E., Morganti-Kossmann, M. C., Lifshitz, J., & Ziebell, J. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097096 · Cited by 138 · see citing works

Species differences in vasopressin receptor binding are evident early in development: Comparative anatomic studies in prairie and montane voles

Wang, Z., Young, L. J., Liu, Y., & Insel, T. R. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970224)378:4 · Cited by 135 · see citing works

Microglia activation and phagocytosis: relationship with aging and cognitive impairment in the rhesus monkey

Shobin, E., Bowley, M. P., Estrada, L. I., Heyworth, N. C., Orczykowski, M. E., Eldridge, S. A., Calderazzo, S. M., Mortazavi, F., Moore, T. L., & Rosene, D. L. (2017) · GeroScience · doi:10.1007/s11357-017-9965-y · Cited by 121 · see citing works

Transcriptome analysis of amoeboid and ramified microglia isolated from the corpus callosum of rat brain

Rangarajan, P., Jiang, B., Baby, N., Manivannan, J., Jayapal, M., Lu, J., Tay, S. S. W., Ling, E., & Dheen, S. T. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-64 · Cited by 118 · see citing works

Inhomogeneous distribution of Iba‐1 characterizes microglial pathology in Alzheimer's disease

Tischer, J., Krueger, M., Mueller, W. C., Staszewski, O., Prinz, M., Streit, W. J., & Bechmann, I. (2016) · Glia · doi:10.1002/glia.23024 · Cited by 117 · see citing works

Increased expression of the chemokines CXCL1 and MIP-1α by resident brain cells precedes neutrophil infiltration in the brain following prolonged soman-induced status epilepticus in rats

Johnson, E. A., Dao, T. L., Guignet, M. A., Geddes, C. E., Koemeter-Cox, A., & Kan, R. K. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-41 · Cited by 113 · see citing works

High resolution dissection of reactive glial nets in Alzheimer’s disease

Bouvier, D. S., Jones, E. V., Quesseveur, G., Davoli, M. A., A. Ferreira, T., Quirion, R., Mechawar, N., & Murai, K. K. (2016) · Scientific Reports · doi:10.1038/srep24544 · Cited by 111 · see citing works

Fluoxetine treatment affects the inflammatory response and microglial function according to the quality of the living environment

Alboni, S., Poggini, S., Garofalo, S., Milior, G., Hajj, H. E., Lecours, C., Girard, I., Gagnon, S., Boisjoly‐Villeneuve, S., Brunello, N., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.07.155 · Cited by 110 · see citing works

Morphological and Phagocytic Profile of Microglia in the Developing Rat Cerebellum

Perez‐Pouchoulen, M., VanRyzin, J. W., & McCarthy, M. M. (2015) · eNeuro · doi:10.1523/eneuro.0036-15.2015 · Cited by 100 · see citing works

Spatial arrangement of microglia in the mouse hippocampus: A stereological study in comparison with astrocytes

Jinno, S., Fleischer, F., Eckel, S., Schmidt, V., & Kosaka, T. (2007) · Glia · doi:10.1002/glia.20552 · Cited by 98 · see citing works

A Brief History of Microglial Ultrastructure: Distinctive Features, Phenotypes, and Functions Discovered Over the Past 60 Years by Electron Microscopy

Savage, J. C., Picard, K., Ibáñez, F. G., & Tremblay, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00803 · Cited by 93 · see citing works

Formation of multinucleated giant cells and microglial degeneration in rats expressing a mutant Cu/Zn superoxide dismutase gene

Fendrick, S. E., Xue, Q., & Streit, W. J. (2007) · Journal of Neuroinflammation · doi:10.1186/1742-2094-4-9 · Cited by 88 · see citing works

Rod-shaped microglia morphology is associated with aging in 2 human autopsy series

Bachstetter, A. D., Ighodaro, E. T., Hassoun, Y., Aldeiri, D., Neltner, J. H., Patel, E., Abner, E. L., & Nelson, P. T. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.12.028 · Cited by 84 · see citing works

Resting Microglial Motility Is Independent of Synaptic Plasticity in Mammalian Brain

Wu, L., & Zhuo, M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01210.2007 · Cited by 81 · see citing works

An MRI study of age-related white and gray matter volume changes in the rhesus monkey

Wisco, J. J., Killiany, R., Guttmann, C. R. G., Warfield, S. K., Moss, M. B., & Rosene, D. L. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.03.022 · Cited by 79 · see citing works

Increased activation of Iba1+ microglia in pediatric epilepsy patients with Rasmussen's encephalitis compared with cortical dysplasia and tuberous sclerosis complex

Wirenfeldt, M., Clare, R., Tung, S., Bottini, A. R., Mathern, G. W., & Vinters, H. V. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.02.015 · Cited by 76 · see citing works

Age-related changes in the hippocampus (loss of synaptophysin and glial–synaptic interaction) are modified by systemic treatment with an NCAM-derived peptide, FGL

Ojo, B., Rezaie, P., Gabbott, P. L. A., Davies, H. A., Colyer, F. M., Cowley, T. R., Lynch, M. A., & Stewart, M. G. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.09.013 · Cited by 61 · see citing works

Nonfunctional mutant Wrn protein leads to neurological deficits, neuronal stress, microglial alteration, and immune imbalance in a mouse model of Werner syndrome

Hui, C. W., St‐Pierre, M., Detuncq, J., Aumailley, L., Dubois, M.-J., Couture, V., Skuk, D., Marette, A., Tremblay, J. P., Lebel, M., et al. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.06.007 · Cited by 46 · see citing works

A lysosome-specific two-photon phosphorescent binuclear cyclometalated platinum(ii) probe for in vivo imaging of live neurons

Ho, Y., Au, N. P. B., Wong, K., Chan, C. T., Kwok, W., Law, G., Tang, K.-K., Wong, W., Ma, C. H. E., & Lam, M. H. (2014) · Chemical Communications · doi:10.1039/c3cc48934e · Cited by 41 · see citing works

Differences in Origin of Reactive Microglia in Bone Marrow Chimeric Mouse and Rat After Transient Global Ischemia

Lambertsen, K. L., Deierborg, T., Gregersen, R., Clausen, B. H., Wirenfeldt, M., Nielsen, H. H., Dalmau, I., Diemer, N. H., Dagnæs‐Hansen, F., Johansen, F. F., et al. (2011) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31821db3aa · Cited by 39 · see citing works

Microglia: An Intrinsic Component of the Proliferative Zones in the Fetal Rhesus Monkey (Macaca mulatta) Cerebral Cortex

Barger, N., Keiter, J. A., Kreutz, A., Krishnamurthy, A., Weidenthaler, C., Martínez‐Cerdeño, V., Tarantal, A. F., & Noctor, S. C. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy145 · Cited by 38 · see citing works

Microglia: Senescence Impairs Clearance of Myelin Debris

Thériault, P., & Rivest, S. (2016) · Current Biology · doi:10.1016/j.cub.2016.06.066 · Cited by 34 · see citing works

Satellite microglia show spontaneous electrical activity that is uncorrelated with activity of the attached neuron

Wogram, E., Wendt, S., Matyash, M., Pivneva, T. A., Draguhn, A., & Kettenmann, H. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13256 · Cited by 33 · see citing works

Ultrastructure of microglia-synapse interactions in the HIV-1 Tat-injected murine central nervous system

Tremblay, M., Marker, D. F., Puccini, J. M., Muly, E. C., Lu, S., & Gelbard, H. A. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.27670 · Cited by 28 · see citing works

The Importance of Inter-Species Variation in Traumatic Brain Injury-Induced Alterations of Microglial-Axonal Interactions

Gorse, K. M., & Lafrenaye, A. D. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00778 · Cited by 22 · see citing works

Gitter cells and their relationship to macrophages in the developing cerebellum

Das, G. D. (1976) · Virchows Archiv B Cell Pathology Including Molecular Pathology · doi:10.1007/bf02890348 · Cited by 18 · see citing works

Three-Dimensional Nanostructure of an Intact Microglia Cell

Bolasco, G., Weinhard, L., Boissonnet, T., Neujahr, R., & Gross, C. T. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00105 · Cited by 17 · see citing works

Microglial response to murine leukemia virus-induced encephalopathy is a good indicator of neuronal perturbations

Xue, Q., Yang, C., Hoffman, P. M., & Streit, W. J. (2010) · Brain Research · doi:10.1016/j.brainres.2009.12.089 · Cited by 13 · see citing works

Microglia Detection by Enzymatic Histochemistry

Almolda, B., González, B., & Castellano, B. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-520-0_22 · Cited by 7 · see citing works

Microglia states and nomenclature: A field at its crossroads

Paolicelli, R. C., Sierra, A., Stevens, B., Tremblay, M.-E., Aguzzi, A., Ajami, B., Amit, I., Audinat, E., Bechmann, I., Bennett, M., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.020 · Cited by 1,973 · see citing works

Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets

Gao, C., Jiang, J., Tan, Y., & Chen, S. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01588-0 · Cited by 1,616 · see citing works

Neuropathobiology of COVID-19: The Role for Glia

Tremblay, M.-E., Madore, C., Bordeleau, M., Tian, L., & Verkhratsky, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.592214 · Cited by 159 · see citing works

Microglial morphometric analysis: so many options, so little consistency

Reddaway, J., Richardson, P., Bevan, R. J., Stoneman, J., & Palombo, M. (2023) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2023.1211188 · Cited by 119 · see citing works

Plasticity of microglia

Augusto‐Oliveira, M., Arrifano, G. D. P., Delage, C. I., Tremblay, M., Lopez, M. E. C., & Verkhratsky, A. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12797 · Cited by 107 · see citing works

Microglial vesicles improve post-stroke recovery by preventing immune cell senescence and favoring oligodendrogenesis

Raffaele, S., Gelosa, P., Bonfanti, E., Lombardi, M., Castiglioni, L., Cimino, M., Sironi, L., Abbracchio, M. P., Verderio, C., & Fumagalli, M. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.12.009 · Cited by 106 · see citing works

Quantifying microglial morphology: an insight into function

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Novel microglia-mediated mechanisms underlying synaptic loss and cognitive impairment after traumatic brain injury

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The Safeguarding Microglia: Central Role for P2Y12 Receptors

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Microglia in the context of multiple sclerosis

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Epigenetics and Communication Mechanisms in Microglia Activation with a View on Technological Approaches

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Chronic cochlear implantation with and without electric stimulation in a mouse model induces robust cochlear influx of CX3CR1+/GFP macrophages

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Defining Microglial States and Nomenclature: A Roadmap to 2030Preprint

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TREM2 and Microglia Contribute to the Synaptic Plasticity: from Physiology to Pathology

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Adult neurogenesis improves spatial information encoding in the mouse hippocampus

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Age-at-Injury Determines the Extent of Long-Term Neuropathology and Microgliosis After a Diffuse Brain Injury in Male Rats

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Microglia are involved in phagocytosis and extracellular digestion during Zika virus encephalitis in young adult immunodeficient mice

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Microglia Sing the Prelude of Neuroinflammation-Associated Depression

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Mechanisms and Therapeutic Prospects of Microglia-Astrocyte Interactions in Neuropathic Pain Following Spinal Cord Injury

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Imaging the Neuroimmune Dynamics Across Space and Time

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All roads lead to heterogeneity: The complex involvement of astrocytes and microglia in the pathogenesis of Alzheimer’s disease

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Microglial Morphology Across Distantly Related Species: Phylogenetic, Environmental and Age Influences on Microglia Reactivity and Surveillance States

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Assaying Microglia Functions In Vitro

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FKBP51 is involved in LPS-induced microglial activation via NF-κB signaling to mediate neuroinflammation

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Role of Oxidative Stress and Neuroinflammation in the Etiology of Alzheimer’s Disease: Therapeutic Options

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Critical Involvement of Glial Cells in Manganese Neurotoxicity

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Microglia as a Hub for Suicide Neuropathology: Future Investigation and Prevention Targets

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Ultrasound Neuromodulation Reduces Demyelination in a Rat Model of Multiple Sclerosis

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Homeostasis of carbohydrates and reactive oxygen species is critically changed in the brain of middle-aged mice: Molecular mechanisms and functional reasons

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Morphological diversity of microglia: Implications for learning, environmental adaptation, ageing, sex differences and neuropathology

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The Complementary Role of Morphology in Understanding Microglial Functional Heterogeneity

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Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice

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Loss of Function in the Neurodevelopmental Disease and Schizophrenia-Associated Gene CYFIP1 in Human Microglia-like Cells Supports a Functional Role in Synaptic Engulfment

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Neonatal kaempferol exposure attenuates impact of cerebral palsy model on neuromotor development, cell proliferation, microglia activation, and antioxidant enzyme expression in the hippocampus of rats

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Extracellular Nucleosomes Accelerate Microglial Inflammation via C-Type Lectin Receptor 2D and Toll-Like Receptor 9 in mPFC of Mice With Chronic Stress

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The versatile role of TREM2 in regulating of microglia fate in the ischemic stroke

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Reactive morphology of dividing microglia following kainic acid administration

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Using focused ultrasound to modulate microglial structure and function

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Brain Tissue-Derived Extracellular Vesicle Mediated Therapy in the Neonatal Ischemic Brain

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Muse cells decrease the neuroinflammatory response by modulating the proportion of M1 and M2 microglia in vitro

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Sex chromosomes and sex hormones differently shape microglial properties during normal physiological conditions in the adult mouse hippocampus

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The Shape of μ—How Morphological Analyses Shape the Study of Microglia

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Microglia contribute to methamphetamine reinforcement and reflect persistent transcriptional and morphological adaptations to the drug

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Distinct olfactory mucosal macrophage populations mediate neuronal maintenance and pathogen defense

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Rnf-213 Knockout Induces Pericyte Reduction and Blood-Brain Barrier Impairment in Mouse

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