Leqembi Maintenance Dosing Approved in the U.S.
The nod will allow people who have completed 18 months of biweekly IV dosing to transition to monthly IVs. An application for subcutaneous dosing is still pending.
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The nod will allow people who have completed 18 months of biweekly IV dosing to transition to monthly IVs. An application for subcutaneous dosing is still pending.
Triggered by oxidative stress, this degradation signal may protect neurons.
By tracking how mutations influence the incorporation of monomers, scientists pinpoint which residues shape tau fibrils.
In female mice, the silencing of several cognitive genes on maternally inherited X chromosomes correlated with poor memory; re-expressing the genes improved memory.
In people with PD and other Lewy body diseases, α-synuclein accumulates in the kidneys, scientists say. In mice, it spreads from there to the brain.
New 3D model shows how a tau kinase and Apoe4 astrocytes kill neurons through oxidative stress.
Hyperconnectivity ushers tangles from temporal lobe to posterior cortex. Study could revive interest in trialing anti-convulsants with tau biomarkers as an outcome.
Cell survival factor EBP1 binds the enzyme’s presenilin subunit, interfering with APP binding and lowering Aβ output. EBP1 drops with age and in AD brains.
In mice, lactylation of APP reduces amyloid deposits and slows disease progression.
Recent genetic and mechanistic studies on SORL1 place the endolysosomal system, in both neurons and microglia, front and center in the pathogenesis of AD.
In models of amyloidosis and tauopathy, the noble gas curbed inflammation and made microglia more phagocytic, resulting in fewer aggregates and healthier neurons.
Survey of post-translationally modified and noncoding RNA identified more than 25,000 differences between AD and control brain.
In AD brain, cells ramp up expression of herpes virus proteins. In cultured neurons, these proteins boost p-tau, which then suppresses viral proteins.
In mice, eliminating the NPC1 gene from microglia recapitulated aspects of the lysosomal storage disorder.
In lab animals, lithocholic acid replicates life-extending benefits of caloric restriction.
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