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Microglial control of neuronal development via somatic purinergic junctions

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.24604openalex-snapshot
Periventricular microglial cells interact with dividing precursor cells in the nonhuman primate and rodent prenatal cerebral cortex
inferredcites →https://doi.org/10.1002/dvdy.163openalex-snapshot
Microglia in the developing retina couple phagocytosis with the progression of apoptosis via P2RY12 signaling
inferredcites →https://doi.org/10.1002/dvdy.24538openalex-snapshot
Mitochondrial dynamics in the regulation of neurogenesis: From development to the adult brain
inferredcites →https://doi.org/10.1002/glia.20419openalex-snapshot
Microglia instruct subventricular zone neurogenesis
inferredcites →https://doi.org/10.1002/glia.22858openalex-snapshot
Effects of Microglia on Neurogenesis
inferredcites →https://doi.org/10.1002/glia.23097openalex-snapshot
P2Y12receptor is expressed on human microglia under physiological conditions throughout development and is sensitive to neuroinflammatory diseases
inferredcites →https://doi.org/10.1002/glia.23204openalex-snapshot
Siglec‐H is a microglia‐specific marker that discriminates microglia from CNS‐associated macrophages and CNS‐infiltrating monocytes
inferredcites →https://doi.org/10.1002/jnr.20480openalex-snapshot
Visualization of microglia in living tissues using Iba1‐EGFP transgenic mice
inferredcites →https://doi.org/10.1007/s10571-011-9670-9openalex-snapshot
Time Course of Postnatal Distribution of Doublecortin Immunoreactive Developing/Maturing Neurons in the Somatosensory Cortex and Hippocampal CA1 Region of C57BL/6 Mice
inferredcites →https://doi.org/10.1007/s12640-018-9942-yopenalex-snapshot
Mitochondria in Developmental and Adult Neurogenesis
inferredcites →https://doi.org/10.1016/j.bbagen.2017.06.017openalex-snapshot
Extracellular cytochrome c as an intercellular signaling molecule regulating microglial functions
inferredcites →https://doi.org/10.1016/j.bbi.2015.11.001openalex-snapshot
Microglia regulate hippocampal neurogenesis during chronic neurodegeneration
inferredcites →https://doi.org/10.1016/j.brainres.2014.11.032openalex-snapshot
Microglia function during brain development: New insights from animal models
inferredcites →https://doi.org/10.1016/j.brainresbull.2018.12.013openalex-snapshot
Purinergic receptors in neurogenic processes
inferredcites →https://doi.org/10.1016/j.ceb.2017.12.004openalex-snapshot
Mitochondrial metabolism in early neural fate and its relevance for neuronal disease modeling
inferredcites →https://doi.org/10.1016/j.cell.2013.11.030openalex-snapshot
Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor
inferredcites →https://doi.org/10.1016/j.celrep.2014.07.042openalex-snapshot
Microglia Modulate Wiring of the Embryonic Forebrain
inferredcites →https://doi.org/10.1016/j.celrep.2017.07.004openalex-snapshot
The Lifespan and Turnover of Microglia in the Human Brain
inferredcites →https://doi.org/10.1016/j.celrep.2018.06.110openalex-snapshot
Ki67 is a Graded Rather than a Binary Marker of Proliferation versus Quiescence
inferredcites →https://doi.org/10.1016/j.conb.2017.10.004openalex-snapshot
On place and time: microglia in embryonic and perinatal brain development
inferredcites →https://doi.org/10.1016/j.cub.2011.11.057openalex-snapshot
A Vesicular Transport Pathway Shuttles Cargo from Mitochondria to Lysosomes
inferredcites →https://doi.org/10.1016/j.devcel.2015.01.019openalex-snapshot
Programmed Cell Death in Neurodevelopment
inferredcites →https://doi.org/10.1016/j.immuni.2018.11.004openalex-snapshot
Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes
inferredcites →https://doi.org/10.1016/j.jri.2018.01.004openalex-snapshot
Microglia, the missing link in maternal immune activation and fetal neurodevelopment; and a possible link in preeclampsia and disturbed neurodevelopment?
inferredcites →https://doi.org/10.1016/j.mcn.2005.10.006openalex-snapshot
Microglia activated by IL-4 or IFN-γ differentially induce neurogenesis and oligodendrogenesis from adult stem/progenitor cells
inferredcites →https://doi.org/10.1016/j.molcel.2016.02.019openalex-snapshot
Mitochondria—Judges and Executioners of Cell Death Sentences
inferredcites →https://doi.org/10.1016/j.neuron.2011.05.001openalex-snapshot
Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.026openalex-snapshot
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
inferredcites →https://doi.org/10.1016/j.neuron.2015.12.008openalex-snapshot
The Cellular and Molecular Landscapes of the Developing Human Central Nervous System
inferredcites →https://doi.org/10.1016/j.neuron.2017.10.015openalex-snapshot
Compartmentalized Signaling in Neurons: From Cell Biology to Neuroscience
inferredcites →https://doi.org/10.1016/j.neuron.2019.02.006openalex-snapshot
Microglial Phagocytosis of Newborn Cells Is Induced by Endocannabinoids and Sculpts Sex Differences in Juvenile Rat Social Play
inferredcites →https://doi.org/10.1016/j.neuron.2020.11.007openalex-snapshot
Shaping Neuronal Fate: Functional Heterogeneity of Direct Microglia-Neuron Interactions
inferredcites →https://doi.org/10.1016/j.pneurobio.2017.01.002openalex-snapshot
Microglia in CNS development: Shaping the brain for the future
inferredcites →https://doi.org/10.1016/j.semcdb.2018.12.001openalex-snapshot
Purinergic signalling and brain development
inferredcites →https://doi.org/10.1016/j.stem.2010.08.014openalex-snapshot
Microglia Shape Adult Hippocampal Neurogenesis through Apoptosis-Coupled Phagocytosis
inferredcites →https://doi.org/10.1016/j.tins.2010.05.006openalex-snapshot
The molecular and gene regulatory signature of a neuron
inferredcites →https://doi.org/10.1016/s0896-6273(00)80778-3openalex-snapshot
Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons
inferredcites →https://doi.org/10.1016/s0896-6273(04)00069-8openalex-snapshot
Microglia Promote the Death of Developing Purkinje Cells
inferredcites →https://doi.org/10.1016/s1474-4422(13)70261-8openalex-snapshot
Mitochondria: hub of injury responses in the developing brain
inferredcites →https://doi.org/10.1038/jcbfm.2008.64openalex-snapshot
Role of CX3CR1 (Fractalkine Receptor) in Brain Damage and Inflammation Induced by Focal Cerebral Ischemia in Mouse
inferredcites →https://doi.org/10.1038/ncomms12540openalex-snapshot
Microglia contact induces synapse formation in developing somatosensory cortex
inferredcites →https://doi.org/10.1038/nm.4397openalex-snapshot
Microglia emerge as central players in brain disease
inferredcites →https://doi.org/10.1038/nn.3358openalex-snapshot
Layer V cortical neurons require microglial support for survival during postnatal development
inferredcites →https://doi.org/10.1038/nn.4631openalex-snapshot
Microglia turnover with aging and in an Alzheimer's model via long-term in vivo single-cell imaging
inferredcites →https://doi.org/10.1038/nn1472openalex-snapshot
ATP mediates rapid microglial response to local brain injury in vivo
inferredcites →https://doi.org/10.1038/nn1805openalex-snapshot
The P2Y12 receptor regulates microglial activation by extracellular nucleotides
inferredcites →https://doi.org/10.1038/nri.2017.125openalex-snapshot
Microglia and macrophages in brain homeostasis and disease
inferredcites →https://doi.org/10.1038/nrn3819openalex-snapshot
Cation-chloride cotransporters in neuronal development, plasticity and disease
inferredcites →https://doi.org/10.1038/s41467-018-03566-5openalex-snapshot
Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
inferredcites →https://doi.org/10.1038/s41467-020-15409-3openalex-snapshot
Transient microglial absence assists postmigratory cortical neurons in proper differentiation
inferredcites →https://doi.org/10.1038/s41467-020-15530-3openalex-snapshot
Elevated protein synthesis in microglia causes autism-like synaptic and behavioral aberrations
inferredcites →https://doi.org/10.1038/s41467-020-18175-4openalex-snapshot
ABHD4-dependent developmental anoikis safeguards the embryonic brain
inferredcites →https://doi.org/10.1038/s41593-019-0419-yopenalex-snapshot
Sensory lesioning induces microglial synapse elimination via ADAM10 and fractalkine signaling
inferredcites →https://doi.org/10.1038/s41593-020-00724-1openalex-snapshot
Activated microglia cause metabolic disruptions in developmental cortical interneurons that persist in interneurons from individuals with schizophrenia
inferredcites →https://doi.org/10.1038/s41598-019-54684-zopenalex-snapshot
Analysis of proliferating neuronal progenitors and immature neurons in the human hippocampus surgically removed from control and epileptic patients
inferredcites →https://doi.org/10.1073/pnas.2237050100openalex-snapshot
Migration and differentiation of neural precursor cells can be directed by microglia
inferredcites →https://doi.org/10.1083/jcb.201709064openalex-snapshot
Spatiotemporal organization of exocytosis emerges during neuronal shape change
inferredcites →https://doi.org/10.1093/cercor/bhaa351openalex-snapshot
Development of the Neuro-Immune-Vascular Plexus in the Ventricular Zone of the Prenatal Rat Neocortex
inferredcites →https://doi.org/10.1096/fj.202002419rropenalex-snapshot
P2Y 2 deficiency impacts adult neurogenesis and related forebrain functions
inferredcites →https://doi.org/10.1101/cshperspect.a008359openalex-snapshot
Molecular Control of Neurogenesis: A View from the Mammalian Cerebral Cortex
inferredcites →https://doi.org/10.1111/brv.12487openalex-snapshot
Neuronal sub‐compartmentalization: a strategy to optimize neuronal function
inferredcites →https://doi.org/10.1111/ejn.12508openalex-snapshot
Microglia shape corpus callosum axon tract fasciculation: functional impact of prenatal inflammation
inferredcites →https://doi.org/10.1111/ejn.14969openalex-snapshot
The effects of microglia‐ and astrocyte‐derived factors on neurogenesis in health and disease
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04539.xopenalex-snapshot
Neurogenic niche modulation by activated microglia: transforming growth factor β increases neurogenesis in the adult dentate gyrus
inferredcites →https://doi.org/10.1111/j.1469-7580.2010.01245.xopenalex-snapshot
Early microglial colonization of the human forebrain and possible involvement in periventricular white‐matter injury of preterm infants
inferredcites →https://doi.org/10.1126/sciadv.add5220openalex-snapshot
Mitochondrial pyruvate metabolism regulates the activation of quiescent adult neural stem cells
inferredcites →https://doi.org/10.1126/science.1194637openalex-snapshot
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
inferredcites →https://doi.org/10.1126/science.1202529openalex-snapshot
Synaptic Pruning by Microglia Is Necessary for Normal Brain Development
inferredcites →https://doi.org/10.1126/science.aad8670openalex-snapshot
Microglia development follows a stepwise program to regulate brain homeostasis
inferredcites →https://doi.org/10.1126/science.aat0474openalex-snapshot
Microglia and early brain development: An intimate journey
inferredcites →https://doi.org/10.1126/science.aax6752openalex-snapshot
Microglia monitor and protect neuronal function through specialized somatic purinergic junctions
inferredcites →https://doi.org/10.1126/science.aba9760openalex-snapshot
Mitochondrial dynamics in postmitotic cells regulate neurogenesis
inferredcites →https://doi.org/10.1126/stke.3932007pe37openalex-snapshot
The Surprising Catch of a Voltage-Gated Potassium Channel in a Neuronal SNARE
inferredcites →https://doi.org/10.1155/2013/351613openalex-snapshot
Mitochondrial Signaling: Forwards, Backwards, and In Between
inferredcites →https://doi.org/10.1155/2019/4050796openalex-snapshot
The Role of Mitochondrial Damage-Associated Molecular Patterns in Chronic Neuroinflammation
inferredcites →https://doi.org/10.1159/000337115openalex-snapshot
Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity
inferredcites →https://doi.org/10.1172/jci90602openalex-snapshot
Microglia in steady state
inferredcites →https://doi.org/10.1186/1741-7007-12-34openalex-snapshot
Mitochondria as signaling organelles
inferredcites →https://doi.org/10.1186/s40478-016-0374-8openalex-snapshot
Microglial CX3CR1 promotes adult neurogenesis by inhibiting Sirt 1/p65 signaling independent of CX3CL1
inferredcites →https://doi.org/10.1242/dev.152306openalex-snapshot
Two distinct ontogenies confer heterogeneity to mouse brain microglia
inferredcites →https://doi.org/10.1371/journal.pone.0025234openalex-snapshot
Activated Microglia Inhibit Axonal Growth through RGMa
inferredcites →https://doi.org/10.1371/journal.pone.0026317openalex-snapshot
Absence of Colony Stimulation Factor-1 Receptor Results in Loss of Microglia, Disrupted Brain Development and Olfactory Deficits
inferredcites →https://doi.org/10.1523/jneurosci.0487-19.2019openalex-snapshot
Microglial P2Y12 Receptor Regulates Seizure-Induced Neurogenesis and Immature Neuronal Projections
inferredcites →https://doi.org/10.1523/jneurosci.0993-19.2019openalex-snapshot
Microglia Actively Remodel Adult Hippocampal Neurogenesis through the Phagocytosis Secretome
inferredcites →https://doi.org/10.1523/jneurosci.1157-19.2019openalex-snapshot
Pleiotropic Mitochondria: The Influence of Mitochondria on Neuronal Development and Disease
inferredcites →https://doi.org/10.1523/jneurosci.1619-13.2014openalex-snapshot
Microglia Enhance Neurogenesis and Oligodendrogenesis in the Early Postnatal Subventricular Zone
inferredcites →https://doi.org/10.1523/jneurosci.18-21-08900.1998openalex-snapshot
Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1
inferredcites →https://doi.org/10.1523/jneurosci.1897-15.2015openalex-snapshot
Distinct Cell- and Layer-Specific Expression Patterns and Independent Regulation of Kv2 Channel Subtypes in Cortical Pyramidal Neurons
inferredcites →https://doi.org/10.1523/jneurosci.19-23-10372.1999openalex-snapshot
The Establishment of GABAergic and Glutamatergic Synapses on CA1 Pyramidal Neurons is Sequential and Correlates with the Development of the Apical Dendrite
inferredcites →https://doi.org/10.1523/jneurosci.21-24-09770.2001openalex-snapshot
Early Development of Neuronal Activity in the Primate HippocampusIn Utero
inferredcites →https://doi.org/10.1523/jneurosci.3441-12.2013openalex-snapshot
Microglia Regulate the Number of Neural Precursor Cells in the Developing Cerebral Cortex
inferredcites →https://doi.org/10.1523/jneurosci.3751-14.2015openalex-snapshot
Axon Initial Segment–Associated Microglia
inferredcites →https://doi.org/10.1523/jneurosci.4001-11.2012openalex-snapshot
Purinergic Signaling Promotes Proliferation of Adult Mouse Subventricular Zone Cells
inferredcites →https://doi.org/10.1523/jneurosci.5095-13.2014openalex-snapshot
Evidence That Dendritic Mitochondria Negatively Regulate Dendritic Branching in Pyramidal Neurons in the Neocortex
inferredcites →https://doi.org/10.15252/embj.201488104openalex-snapshot
A new pathway for mitochondrial quality control: mitochondrial‐derived vesicles
inferredcites →https://doi.org/10.3233/bpl-150014openalex-snapshot
Interactions Between Microglia and Newly Formed Hippocampal Neurons in Physiological and Seizure-Induced Inflammatory Environment
inferredcites →https://doi.org/10.3233/bpl-170044openalex-snapshot
Mitochondrial Metabolism-Mediated Regulation of Adult Neurogenesis
inferredcites →https://doi.org/10.3389/fcell.2019.00024openalex-snapshot
Rewiring of Memory Circuits: Connecting Adult Newborn Neurons With the Help of Microglia
inferredcites →https://doi.org/10.3389/fimmu.2018.00698openalex-snapshot
Microglia and Beyond: Innate Immune Cells As Regulators of Brain Development and Behavioral Function
inferredcites →https://doi.org/10.3389/fncel.2012.00035openalex-snapshot
Refuting the challenges of the developmental shift of polarity of GABA actions: GABA more exciting than ever!
inferredcites →https://doi.org/10.3389/fncel.2014.00396openalex-snapshot
Neurogenesis in the embryonic and adult brain: same regulators, different roles
inferredcites →https://doi.org/10.3389/fncel.2018.00134openalex-snapshot
Disruption of the Microglial ADP Receptor P2Y13 Enhances Adult Hippocampal Neurogenesis
inferredcites →https://doi.org/10.3389/fnins.2015.00248openalex-snapshot
Neuronal and microglial regulators of cortical wiring: usual and novel guideposts
inferredcites →https://doi.org/10.3389/fnmol.2020.00133openalex-snapshot
SNARE-Mediated Exocytosis in Neuronal Development
inferredcites →https://doi.org/10.3389/fnsyn.2017.00009openalex-snapshot
Function and Dysfunction of Microglia during Brain Development: Consequences for Synapses and Neural Circuits
inferredcites →https://doi.org/10.3389/fphar.2017.00951openalex-snapshot
Specific Temporal Distribution and Subcellular Localization of a Functional Vesicular Nucleotide Transporter (VNUT) in Cerebellar Granule Neurons

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Systemic LPS-Induced RACK1 Downregulation Contributes to Neuronal Necroptosis in the Limbic System in Mice: A Mechanism of Sepsis-Associated Encephalopathy and a Potential Target of Tanshinone IIA
inferred← citeshttps://doi.org/10.1002/advs.202505779openalex-snapshot
Identifying Tipping Points during Healthy Brain Aging through Single‐Nucleus Transcriptomic Analysis
inferred← citeshttps://doi.org/10.1002/cmdc.202400672openalex-snapshot
Inflammaging and Immunosenescence in the Post‐COVID Era: Small Molecules, Big Challenges
inferred← citeshttps://doi.org/10.1002/cns.70687openalex-snapshot
Cellular Communication Networks Mediated by Microglia in Ischemic Stroke
inferred← citeshttps://doi.org/10.1002/eji.202250232openalex-snapshot
Microglial tissue surveillance: The never‐resting gardener in the developing and adult CNS
inferred← citeshttps://doi.org/10.1002/glia.24574openalex-snapshot
The role of microglial TREM2 in development: A path toward neurodegeneration?
inferred← citeshttps://doi.org/10.1002/glia.24650openalex-snapshot
Microglia and Astrocytes in Postnatal Neural Circuit Formation
inferred← citeshttps://doi.org/10.1002/glia.70196openalex-snapshot
Microglial P2ry12 in the Basolateral Amygdala Underlies Neuropathic Pain‐Induced Anxiety
inferred← citeshttps://doi.org/10.1007/978-3-031-55529-9_8openalex-snapshot
Contactomics of Microglia and Intercellular Communication
inferred← citeshttps://doi.org/10.1007/978-3-031-65944-7_1openalex-snapshot
Homeostatic Functions of Tissue-Resident Macrophages and Their Role in Tissue Maintenance
inferred← citeshttps://doi.org/10.1007/s12975-024-01286-1openalex-snapshot
Changes in Neuroimmunological Synapses During Cerebral Ischemia
inferred← citeshttps://doi.org/10.1016/j.cell.2024.01.012openalex-snapshot
Microglia maintain structural integrity during fetal brain morphogenesis
inferred← citeshttps://doi.org/10.1016/j.conb.2025.103062openalex-snapshot
Microglia in early brain development: A window of opportunity
inferred← citeshttps://doi.org/10.1016/j.ejcb.2024.151441openalex-snapshot
The role of integrins in brain health and neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.immuni.2023.12.002openalex-snapshot
Trem2 expression in microglia is required to maintain normal neuronal bioenergetics during development
inferred← citeshttps://doi.org/10.1016/j.immuni.2025.04.022openalex-snapshot
Microglial and TREM2 dialogues in the developing brain
inferred← citeshttps://doi.org/10.1016/j.nbd.2024.106743openalex-snapshot
The effect of a dominant kinase-dead Csf1r mutation associated with adult-onset leukoencephalopathy on brain development and neuropathology
inferred← citeshttps://doi.org/10.1016/j.neuron.2025.12.028openalex-snapshot
Astrocyte-microglia crosstalk through Hevin and Toll-like receptor signaling controls developmental thalamocortical synapse refinement
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2025.07.019openalex-snapshot
Microglia-neuron crosstalk in Alzheimer’s disease: an exploration of molecular mechanisms and pathological implications
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2026.102911openalex-snapshot
Microglial P2Y12 signaling phase-shifts glymphatic circadian rhythms and alters sleep architecture in mice
inferred← citeshttps://doi.org/10.1016/j.stemcr.2024.06.009openalex-snapshot
Human microglia-derived proinflammatory cytokines facilitate human retinal ganglion cell development and regeneration
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Lessons from ex vivo and in vitro models in microglia research
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Microglia contribute to neuronal synchrony despite endogenous ATP-related phenotypic transformation in acute mouse brain slices
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Inhibition of TGF-β signaling in microglia stimulates hippocampal adult neurogenesis and reduces anxiety-like behavior in adult mice
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Therapeutic targeting of neuroimmune mechanisms in neurodegeneration
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Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
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SARS-CoV-2 vaccination during pregnancy enhances offspring hippocampal neurogenesis and working memory via IFN-γ–responsive microglia
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Blocking microglial reactivity via purinergic receptors prevents subacute cognitive deficits after TIA
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Regulation
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SARS-CoV-2 vaccination during pregnancy enhances hippocampal neurogenesis and working memory in offspring via IFN-gamma responsive microglia
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GPCR-targeted imaging and manipulation of homeostatic microglia in living systems
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Knockout of P2Y12 receptor facilitates microglia-neuron body-to-body interactions and accelerates prion disease
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Forecasting of Cyclone Severity using Intelligent NeuralNets subjecting to Infrared Imaging
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Astrocytes and microglia in the coordination of CNS development and homeostasis
inferred← citeshttps://doi.org/10.1136/svn-2025-004465openalex-snapshot
RIC-specific cytoprotective profile mediated by microglia in a mouse model of acute ischaemic stroke
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From Blur to Brilliance: The Ascendance of Advanced Microscopy in Neuronal Cell Biology
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A P2RY12 deficiency results in sex-specific cellular perturbations and sexually dimorphic behavioral anomalies
inferred← citeshttps://doi.org/10.1186/s12974-025-03542-zopenalex-snapshot
Knockout of P2Y12 receptor facilitates neuronal envelopment by reactive microglia and accelerates prion disease
inferred← citeshttps://doi.org/10.1186/s13024-024-00714-yopenalex-snapshot
APOE4 genotype and aging impair injury-induced microglial behavior in brain slices, including toward Aβ, through P2RY12
inferred← citeshttps://doi.org/10.1523/jneurosci.0941-25.2026openalex-snapshot
Microglia Modulate Information Processing in the Mouse Barrel Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.1377-25.2025openalex-snapshot
Adenosine in the Brain: Recent Progress on Detection, Function, and Translation
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SARS-CoV-2 vaccination during pregnancy enhances hippocampal neurogenesis and working memory in offspring through IFN-gamma and CX3CR1-dependent mechanisms
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3997803/v1openalex-snapshot
A P2RY12 Deficiency Results in Sex-specific Cellular Perturbations and Sexually Dimorphic Behavioral Anomalies
inferred← citeshttps://doi.org/10.32657/10356/172964openalex-snapshot
Pancreatic macrophages: from ontogeny to phenotype and function
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Pathogenesis and therapeutic applications of microglia receptors in Alzheimer’s disease
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Microglial CX3CR1 signaling mediates stress-induced pain behavior in mice
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Dual immune modulation of microglia in viral encephalitis: current understanding and future perspectives
inferred← citeshttps://doi.org/10.3389/fnagi.2026.1847223openalex-snapshot
Age-associated microglial heterogeneity includes emergence of mobile microglial states
inferred← citeshttps://doi.org/10.3389/fncel.2023.988952openalex-snapshot
The multifaceted roles of embryonic microglia in the developing brain
inferred← citeshttps://doi.org/10.3389/fncel.2025.1552241openalex-snapshot
Physiological roles of embryonic microglia and their perturbation by maternal inflammation
inferred← citeshttps://doi.org/10.3389/fncel.2026.1936860openalex-snapshot
Microglia and immune signaling as architects of the brain
inferred← citeshttps://doi.org/10.3389/fnhum.2026.1777687openalex-snapshot
The irreplaceable role of sleep in building long-term memories: offline integration of free cortical units and its possible implication in autism
inferred← citeshttps://doi.org/10.3389/fnins.2023.1125729openalex-snapshot
Multifaceted microglia during brain development: Models and tools
inferred← citeshttps://doi.org/10.3389/fnmol.2023.1148219openalex-snapshot
Denervated mouse CA1 pyramidal neurons express homeostatic synaptic plasticity following entorhinal cortex lesion
inferred← citeshttps://doi.org/10.3389/fphar.2023.1179028openalex-snapshot
Diagnostic and therapeutic value of P2Y12R in epilepsy
inferred← citeshttps://doi.org/10.3390/biom13050856openalex-snapshot
Altered Purinergic Signaling in Neurodevelopmental Disorders: Focus on P2 Receptors
inferred← citeshttps://doi.org/10.3390/ijms24076709openalex-snapshot
The Signaling Pathway of the ADP Receptor P2Y12 in the Immune System: Recent Discoveries and New Challenges
inferred← citeshttps://doi.org/10.5204/thesis.eprints.244721openalex-snapshot
The effects of long-term sucrose consumption on olfactory neurogenesis and neuroinflammation
inferred← citeshttps://doi.org/10.5582/bst.2025.01148openalex-snapshot
APOE4 reprograms microglial lipid metabolism in Alzheimer's disease: Mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26691931openalex-snapshot
Additional file 1 of APOE4 genotype and aging impair injury-induced microglial behavior in brain slices, including toward Aβ, through P2RY12
inferred← citeshttps://doi.org/10.6084/m9.figshare.26691934openalex-snapshot
Additional file 2 of APOE4 genotype and aging impair injury-induced microglial behavior in brain slices, including toward Aβ, through P2RY12
inferred← citeshttps://doi.org/10.6084/m9.figshare.26691937openalex-snapshot
Additional file 3 of APOE4 genotype and aging impair injury-induced microglial behavior in brain slices, including toward Aβ, through P2RY12
inferred← citeshttps://doi.org/10.70675/5879aa36z8649z48f9zb359zf349ce3cb429openalex-snapshot
Mechanisms controlling microglial colonization of the forebrain
inferred← citeshttps://doi.org/10.70675/de2fa338z7aecz4991za94eze8b7694a0d22openalex-snapshot
Étude de la forme sporadique de la maladie d'Alzheimer à partir de modèles in vivo et de neurones humains reprogrammés
inferred← citeshttps://doi.org/10.70675/f339157ez1688z4acaz87fcz0ecae062a7ccopenalex-snapshot
Caractérisation du récepteur Smoothened en tant que régulateur majeur des états fonctionnels des cellules microgliales
inferred← citeshttps://doi.org/10.7554/elife.107650openalex-snapshot
Dissecting surveying behavior of reactive microglia under chronic neurodegeneration
inferred← citeshttps://doi.org/10.7554/elife.107650.1openalex-snapshot
Dissecting surveying behavior of reactive microglia under chronic neurodegeneration
inferred← citeshttps://doi.org/10.7554/elife.107650.2openalex-snapshot
Dissecting surveying behavior of reactive microglia under chronic neurodegeneration
inferred← citeshttps://doi.org/10.7554/elife.107650.3openalex-snapshot
Dissecting surveying behavior of reactive microglia under chronic neurodegeneration
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