Blood‐based biomarkers are essential for early detection, monitoring, and therapeutic development in Alzheimer's disease (AD) and related dementia (ADRD), but current assays lack brain cell specificity and sensitivity to low‐abundant proteins.
Using human induced pluripotent stem cells (hiPSCs)‐derived neurons, human induced pluripotent stem cells were assayed how reducing gene expression of MSN and CD44 affected amyloid beta secretion, tau phosphorylation, and transcriptional state.
Eiden H. Brewer, Charles A. Williams, Gregory A. Cary et al.· Alzheimer's & Dementia· 0 citations
Alzheimer's disease (AD) features amyloid beta (Aβ) plaques and tau tangles, yet how their coexistence reshapes brain transcriptomic programs remains unclear.
Jung Hyun Park, Byungwook Kim, Mamun Md Al‐Amin et al.· Alzheimer's & Dementia· 0 citations
Astrocyte dysfunction is central to Alzheimer's disease (AD), yet expression patterns of astrocytic markers remain poorly defined. We measured Aquaporin‐4 (AQP4) and glial fibrillary acidic protein (GFAP) in post‐mortem frontal cortex of AD patients and controls across BrainNet Europe (BNE) stages.
Harry Alexopoulos, X. Louka, E. D. de Natale et al.· Alzheimer's & Dementia· 0 citations
We recently identified a plasma‐based seven‐protein model with strong performance for Alzheimer's disease (AD) classification. Here, we evaluated whether these proteins, alone or combined with plasma phosphorylated tau 217 (p‐tau217), predict progression from cognitively unimpaired to symptomatic AD.
We read with interest the Viewpoint by Percetti and colleagues proposing the concept of a biologically de fi ned mitochondrial subtype of Parkinson ’ s disease (PD) ( “ MitoPD
Julia C Fitzgerald, P. May, A. Grünewald· Movement Disorders· 0 citations