New technologies reveal cross-cutting breakdowns in Alzheimer’s disease
“Single-cell profiling” is helping neuroscientists see how disease affects major brain cell types and identify common, potentially targetable pathways.
“Single-cell profiling” is helping neuroscientists see how disease affects major brain cell types and identify common, potentially targetable pathways.
In people carrying APOE4, a key brain cell mismanages cholesterol needed to insulate neurons properly — another sign APOE4 contributes to disease by disrupting brain lipids.
MIT AgeLab co-hosts 10th anniversary celebration of Boston Bridge, a longtime collaborator offering development, networking, career growth, and mentorship in the field of aging.
Study indicates ailing neurons may instigate an inflammatory response from the brain’s microglia immune cells.
OMEGA scholarships encourage bonds between younger and older adults.
Mel King Community Fellows from MIT's Community Innovators Lab meet in Berlin to examine the German elder care model.
MIT alumni-founded WalkWise uses a motion-detecting device for walkers to allow family members and care professionals to monitor adults with mobility challenges.
Program supports family caregivers with dedicated service coordinators based on learning from MIT's AgeLab.
Targeting these circuits could offer a new way to reverse motor dysfunction and depression in Parkinson’s patients.
Projects from a new MIT urban studies and planning course speak to the impact of increased longevity on systems and markets.
Two types of tau proteins mix together in a nearly random way to generate the tangles seen in the brains of Alzheimer’s patients.
K. Lisa Yang Brain-Body Center to investigate the brain’s complex relationship with other body systems.
This circuit, which weakens with age, could offer a target to help prevent age-related decline in spatial memory.
Competitive seed grants launch yearlong investigations of novel hypotheses about potential causes, biomarkers, treatments of Alzheimer’s and ALS.
Extra chromosome alters chromosomal conformation and DNA accessibility in neural progenitor cells; study establishes senescence as a potentially targetable mechanism for future treatment.