Software Flaw Casts Doubt on Past Task fMRI Studies
In a validation study, three common software packages produced excessive false positives, but initial stories about previous suspect data might have been overblown.
6566 RESULTS
Sort By:
In a validation study, three common software packages produced excessive false positives, but initial stories about previous suspect data might have been overblown.
AD-linked mutations in presenilin 1 increase the enzyme’s cleavage of STIM1a endoplasmic reticulum calcium receptor, reducing Ca2+ influx into neurons and destabilizing dendritic spines. Researchers proposed targeting the pathway as a therapy.
ApoE2 enhances, while ApoE4 reduces, astrocytes’ ability to gobble up synapses. Researchers propose this is one way the apolipoprotein modulates AD risk.
The kinase prevents tau degradation, raising levels and kicking off hyperphosphorylation.
The largest brain-imaging project in history has sliced and diced data from the first 5 percent of its cohort. Neurodegeneration scientists deplore the lack of AD biomarkers.
In aging rats, the presence of bacterial amyloid in the gut accelerated the formation of α-synuclein aggregates in brain.
When the brain is starved of BIN1, endocytosis goes into overdrive. Vesicles gulp more tau aggregates into neurons, feeding their spread.
Drawing on longitudinal ADNI data, a new study suggests that the degeneration of cholinergic neurons in the basal forebrain kicks off the neurodegenerative cascade of AD.
PET scans detect activated glial cells in current and recently retired professional football players up to 21 years after their last concussion.
Less aquaporin-4 in astrocytes surrounding blood vessels suggests impaired clearance of Aβ in people with AD.
Researchers at SfN 2016 proposed dialing up the immune response in Alzheimer’s brains to enhance phagocytosis.
Parkinsonian symptoms in welders exposed to manganese-laden fumes worsen with continued exposure.
Among older adults living in Ontario, Canada, dementia incidence crept up the closer people lived to busy roads.
ApoE isoforms switch on APP expression in human neurons with a potency commensurate with their propensity to increase risk for Alzheimer’s disease, but some researchers question the relevance of this pathway in the human brain.
An NIA-sponsored initiative will generate and characterize numerous models carrying late-onset AD genes, advancing the best for preclinical drug testing.
No filters selected