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show
6 studies tagged show, dated 2001-08-01 to 2023-12-13. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Longitudinal cerebrospinal fluid measurements show glial hypo- and hyperactivation in predementia Alzheimer's disease 2023-12-13
- Human microglia show unique transcriptional changes in Alzheimer's disease 2023-05-29
- Immune cells lacking Y chromosome show dysregulation of autosomal gene expression 2021-04-10
Studies
6 studies carry this tag.
Date range
2001 to 2023
Top journals
- Cellular and molecular life sciences : CMLS 1
- Experimental neurology 1
- Journal of neuroinflammation 1
- Nature aging 1
- The American journal of pathology 1
6 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Cross-sectionally, CSF sTREM2, YKL-40, clusterin and fractalkine were higher only in groups with tau pathology, independent of amyloidosis (p < 0.001, A+/T+ or N+ and A-/T+ or N+, compared to A-/T-/N-).
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Microglia, the innate immune cells of the brain, influence Alzheimer's disease (AD) progression and are potential therapeutic targets.
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Epidemiological investigations show that mosaic loss of chromosome Y (LOY) in leukocytes is associated with earlier mortality and morbidity from many diseases in men.
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Different neurodegenerative disorders often show similar lesions, such as the presence of amyloid plaques, TAU-neurotangles and synuclein inclusions.
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Microglia accumulation at the site of amyloid plaques is a strong indication that microglia play a major role in Alzheimer's disease pathogenesis.
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For the purpose of studying the potential neurobehavioral effects of different human apolipoprotein E (apoE) isoforms produced within the brain, transgenic (TG) mice were generated in which human apoE3 or apoE4 isoforms were under control of an astrocyte-specific, glial fibrillary acidic protein promoter and these TG mice were bred back to apoE knockout (KO) mice.