New Role for Tau: Making Lipid Droplets in Glia?
Glia need just the right amount of tau for lipid droplets to bud from the endoplasmic reticulum. These soak up toxic lipids spilled by stressed neurons.
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Glia need just the right amount of tau for lipid droplets to bud from the endoplasmic reticulum. These soak up toxic lipids spilled by stressed neurons.
In a head-to-head comparison with aducanumab, gantenerumab, and donanemab, lecanemab demonstrated the highest affinity, especially for smaller aggregates.
In two hospital systems, people who received heparin were diagnosed with AD a year later than people who never took the anticoagulant.
The NIH removed Masliah from his post after an investigation found two publications with falsified data. At least 130 more papers with 500 co-authors face allegations.
The analysis of nearly 8,000 brains turned up three genes linked to cerebrovascular disease, and one linked to tangles.
A whole-genome sequencing study estimated that people are two to three times more likely to be affected by these mutations than predicted by epidemiology.
In mice with prion disease, microglia shifted from gobbling up misfolded protein to engulfing flagging neurons. This change coincided with symptom onset.
The adaptive nature of the interface between blood and brain led some scientists to envision it more like an actively managed border crossing, not a wall.
With genetic tinkering to their antibody transport vehicle, Denali scientists aim to temper both ARIA and anemia, while maintaining potency against Aβ.
In tauopathy mice, a peptide construct recruited protein phosphatase 1 to tau. Dephosphorylation lowered total tau, restoring synaptic density and memory.
In mouse brain, mRNA methylation distinguishes cell subtypes and changes with age. One standout: APP. It loses its methyls over time.
Three new papers report these myelin-producing cells contribute up to a third of plaque Aβ in transgenic mice.
Plaques rev up neural oscillations, while tangles turn them down, ultimately leading to sluggish synapses. The slowdown foreshadows symptoms.
Transcriptomes of more than 400 postmortem brains reveal microglia and astrocyte subtypes that collaborate to precipitate pathologic changes.
XWAS from three research groups identified a dozen genetic loci that may help explain sex differences in AD.
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