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Understanding the role of amyloid beta and tau protein in neuronal vulnerability in models of sporadic Alzheimer’s disease

Abstract:

Alzheimer's disease (AD) is a neurodegenerative disease, and it is the most common form of dementia. AD is characterised by two main pathological hallmarks: the accumulation of extracellular plaques, composed mainly of amyloid beta (A$\beta$), and of intracellular neurofibrillary tangles (NFTs) containing mostly hyperphosphorylated tau aggregates. Most animal and cellular models to date have focused on fAD, and recapitulate some key pathological features of AD. However, sporadic AD (sAD) mode...

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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy and Genetics
Research group:
Wade-Martins Group
Oxford college:
New College
Role:
Author
ORCID:
0000-0002-6717-6663

Contributors

Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Centre for Human Genetics
Research group:
Fowler Group
Role:
Contributor
ORCID:
0009-0006-5411-2392
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy and Genetics
Role:
Contributor
Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Role:
Contributor
ORCID:
0000-0003-1536-896X
Institution:
A*STAR Institute of Molecular and Cell Biology
Role:
Contributor
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy and Genetics
Oxford college:
Christ Church
Role:
Supervisor


DOI:
Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford

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