On the public citation graph
Neurons expressing pathological Tau protein trigger dramatic changes in microglial morphology and dynamics
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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/(sici)1098-1136(199601)16:1<81::aid-glia9>3.0.co;2-eopenalex-snapshot
Phagocytozing ameboid microglial cells studied in a mouse corpus callosum slice preparation
inferredcites →https://doi.org/10.1002/cne.21888openalex-snapshot
Prokineticin receptor 2 expression identifies migrating neuroblasts and their subventricular zone transient‐amplifying progenitors in adult mice
inferredcites →https://doi.org/10.1002/glia.10161openalex-snapshot
Microglia as a source and target of cytokines
inferredcites →https://doi.org/10.1002/glia.440060106openalex-snapshot
Amoeboid and ramified microglia: Their interrelationship and response to brain injury
inferredcites →https://doi.org/10.1002/glia.440070105openalex-snapshot
The origin and nature of ramified and amoeboid microglia: A historical review and current concepts
inferredcites →https://doi.org/10.1007/s11481-013-9434-zopenalex-snapshot
Microglia: Key Elements in Neural Development, Plasticity, and Pathology
inferredcites →https://doi.org/10.1016/j.bj.2018.01.003openalex-snapshot
Tau and neuroinflammation: What impact for Alzheimer's Disease and Tauopathies?
inferredcites →https://doi.org/10.1016/j.cell.2008.04.037openalex-snapshot
Live Imaging of Neuronal Degradation by Microglia Reveals a Role for v0-ATPase a1 in Phagosomal Fusion In Vivo
inferredcites →https://doi.org/10.1016/j.celrep.2013.11.004openalex-snapshot
An Anti-inflammatory NOD-like Receptor Is Required for Microglia Development
inferredcites →https://doi.org/10.1016/j.celrep.2018.02.004openalex-snapshot
Noninflammatory Changes of Microglia Are Sufficient to Cause Epilepsy
inferredcites →https://doi.org/10.1016/j.devcel.2004.11.014openalex-snapshot
Interplay of Pu.1 and Gata1 Determines Myelo-Erythroid Progenitor Cell Fate in Zebrafish
inferredcites →https://doi.org/10.1016/j.jchemneu.2017.08.007openalex-snapshot
The in situ morphology of microglia is highly sensitive to the mode of tissue fixation
inferredcites →https://doi.org/10.1016/j.neuron.2010.08.023openalex-snapshot
Regulation of Tau Pathology by the Microglial Fractalkine Receptor
inferredcites →https://doi.org/10.1016/j.tins.2012.11.007openalex-snapshot
Microglia: actively surveying and shaping neuronal circuit structure and function
inferredcites →https://doi.org/10.1016/s1474-4422(13)70090-5openalex-snapshot
Tau pathology and neurodegeneration
inferredcites →https://doi.org/10.1038/31508openalex-snapshot
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
inferredcites →https://doi.org/10.1038/nn.3554openalex-snapshot
The microglial sensome revealed by direct RNA sequencing
inferredcites →https://doi.org/10.1038/nn1997openalex-snapshot
Microglia: active sensor and versatile effector cells in the normal and pathologic brain
inferredcites →https://doi.org/10.1038/nrc.2016.112openalex-snapshot
The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia
inferredcites →https://doi.org/10.1038/nrneurol.2014.207openalex-snapshot
Microglial and macrophage polarization—new prospects for brain repair
inferredcites →https://doi.org/10.1038/s41583-018-0057-5openalex-snapshot
Microglial signatures and their role in health and disease
inferredcites →https://doi.org/10.1083/jcb.201709069openalex-snapshot
Microglia in Alzheimer’s disease
inferredcites →https://doi.org/10.1084/jem.20151000openalex-snapshot
A neuroprotective role for microglia in prion diseases
inferredcites →https://doi.org/10.1084/jem.20172158openalex-snapshot
TFEB enhances astroglial uptake of extracellular tau species and reduces tau spreading
inferredcites →https://doi.org/10.1093/brain/awv081openalex-snapshot
Reactive microglia drive tau pathology and contribute to the spreading of pathological tau in the brain
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a002969openalex-snapshot
Microglia: Activation and Their Significance in the Central Nervous System
inferredcites →https://doi.org/10.1126/science.1110647openalex-snapshot
Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo
inferredcites →https://doi.org/10.1155/2015/151979openalex-snapshot
Tau Hyperphosphorylation and Oxidative Stress, a Critical Vicious Circle in Neurodegenerative Tauopathies?
inferredcites →https://doi.org/10.1172/jci37537openalex-snapshot
A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation
inferredcites →https://doi.org/10.1186/s12974-018-1195-4openalex-snapshot
RNA sequencing analysis reveals quiescent microglia isolation methods from postnatal mouse brains and limitations of BV2 cells
inferredcites →https://doi.org/10.1186/s13024-017-0216-6openalex-snapshot
TREM2 deficiency exacerbates tau pathology through dysregulated kinase signaling in a mouse model of tauopathy
inferredcites →https://doi.org/10.1186/s13024-018-0277-1openalex-snapshot
PU.1 regulates Alzheimer’s disease-associated genes in primary human microglia
inferredcites →https://doi.org/10.1186/s40035-018-0111-2openalex-snapshot
Surfen and oxalyl surfen decrease tau hyperphosphorylation and mitigate neuron deficits in vivo in a zebrafish model of tauopathy
inferredcites →https://doi.org/10.1186/s40478-017-0478-9openalex-snapshot
Astrocytes in mouse models of tauopathies acquire early deficits and lose neurosupportive functions
inferredcites →https://doi.org/10.15252/embr.201846171openalex-snapshot
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
inferredcites →https://doi.org/10.2174/092986707780597961openalex-snapshot
Microglial Activation and its Implications in the Brain Diseases
inferredcites →https://doi.org/10.3389/fncel.2018.00172openalex-snapshot
The Role of Microglia in the Spread of Tau: Relevance for Tauopathies
inferredcites →https://doi.org/10.3389/fnins.2015.00414openalex-snapshot
I'll take the low road: the evolutionary underpinnings of visually triggered fear
inferredcites →https://doi.org/10.3389/fnins.2019.00421openalex-snapshot
In vivo Two-Photon Imaging of Anesthesia-Specific Alterations in Microglial Surveillance and Photodamage-Directed Motility in Mouse Cortex
inferredcites →https://doi.org/10.3389/fnins.2019.00442openalex-snapshot
Extracellular Monomeric Tau Is Internalized by Astrocytes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2024.01.28.577642openalex-snapshot
Astrocytic tau inclusions lead to microglial abnormalities, but leave neuronal networks intact
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