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Synaptic pruning by microglia is necessary for normal brain development.
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Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes.
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Microglia sculpt postnatal neural circuits in an activity and complement-dependent manner.
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Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor.
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Host microbiota constantly control maturation and function of microglia in the CNS.
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Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing.
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Microglia modulate wiring of the embryonic forebrain.
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Microglia regulate the number of neural precursor cells in the developing cerebral cortex.
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Microglia contact induces synapse formation in developing somatosensory cortex.
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The classical complement cascade mediates CNS synapse elimination.
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Microglia contribute to normal myelinogenesis and to oligodendrocyte progenitor maintenance during adulthood.
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Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors.
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An environment-dependent transcriptional network specifies human microglia identity.
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A Combination of Ontogeny and CNS Environment Establishes Microglial Identity.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.