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The Kaleidoscope of Microglial Phenotypes
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“In response to injury, the functional phenotype of microglia switches from quiescent to activated, and activated microglia are further divided into two distinct states, M1 and M2 (Dubbelaar et al. 2018).”
From MiR-124 and MiR-155 as Therapeutic Targets in Microglia-Mediated Inflammation in Multiple Sclerosis (2025) · cites this paper as Dubbelaar et al. 2018
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InfluentialSynaptic Pruning by Microglia Is Necessary for Normal Brain Development
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InfluentialMicroglia development follows a stepwise program to regulate brain homeostasis
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“Consecutive Stages A recent study combining transcriptome with epigenome analysis identified genes and chromatin modulators that regu late different stages of microglia development in mice (19).”
InfluentialHoeffel, G., Chen, J., Lavin, Y., Low, D., Almeida, F. F., See, P., Beaudin, A. E., Lum, J., Low, I., Forsberg, E. C., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.011 · Cited by 1,135 · cited 5×
“5) in the YS, a process dependent on the transcription factors (TFs) Spf1 (Pu.1) and Irf8 (Kierdorf et al. , 2013; Hoeffel et al. , 2015).”
InfluentialYang, J., Zhang, L., Yu, C., Yang, X.-F., & Wang, H. (2014) · Biomarker Research · doi:10.1186/2050-7771-2-1 · Cited by 1,099
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Self-citationAn updated histological classification system for multiple sclerosis lesions
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Local cues establish and maintain region-specific phenotypes of basal ganglia microglia
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Targeting mi R‐155 restores abnormal microglia and attenuates disease in SOD 1 mice
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PU.1 and C/EBPα/β convert fibroblasts into macrophage-like cells
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Single-cell epigenomics: powerful new methods for understanding gene regulation and cell identity
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Microglia Versus Myeloid Cell Nomenclature during Brain Inflammation
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“brain tissue (6, 8), resulting in issues regarding the distinction of microglia and”
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Increased White Matter Inflammation in Aging- and Alzheimer’s Disease Brain
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“In contrast to the general notion that microglia obtain a primed profile (40, 86, 87) and are neurotoxic during aging and age-related diseases (88), Hickman and coworkers identified a neuroprotective gene expression profile of microglia derived from the entire brain in aged mice (24 months) due to upregulation of gene…”
InfluentialSelf-citationTREM2 in CNS homeostasis and neurodegenerative disease
Painter, M. M., Atagi, Y., Liu, C.-C., Rademakers, R., Xu, H., Fryer, J. D., & Bu, G. (2015) · Molecular Neurodegeneration · doi:10.1186/s13024-015-0040-9 · Cited by 169
The transcription factor PU.1 is critical for viability and function of human brain microglia
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Macrophage development from HSCs requires PU.1-coordinated microRNA expression
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A new genetic strategy for targeting microglia in development and disease
McKinsey, G. L., Lizama, C. O., Keown-Lang, A. E., Niu, A., Santander, N., Larpthaveesarp, A., Chee, E., Gonzalez, F. F., & Arnold, T. D. (2020) · eLife · doi:10.7554/elife.54590 · Cited by 176
Abnormal synaptic pruning during adolescence underlying the development of psychotic disorders
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Metadata
- Authors
- Dubbelaar, M. L., Kracht, L., Eggen, B. J. L., & Boddeke, E. W. G. M.
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2018-07-31
- Volume
- 9
- ISSN
- 1664-3224
- PMC
- PMC6079257
- Cited by
- 260
- References
- 47
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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