Hypoxia affects neprilysin expression through caspase activation and an APP intracellular domain-dependent mechanism
While gene mutations in the amyloid precursor protein (APP) and the presenilins lead to an accumulation of the amyloid β-peptide (Aβ) in the brain causing neurodegeneration and familial Alzheimer’s disease (AD), over 95% of all AD cases are sporadic. Despite the pathologies being indistinguishable,...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2015-11-01
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Series: | Frontiers in Neuroscience |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fnins.2015.00426/full |