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Perspectives for drug intervention in amyloid diseases
Simon Kolstoe
,
Steve Wood
Institute of Life Sciences and Healthcare
Research output
:
Contribution to journal
›
Article
›
peer-review
Overview
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INIS
drugs
100%
interventions
100%
diseases
100%
tissues
66%
proteins
66%
humans
33%
precursor
33%
design
33%
deposition
33%
damage
33%
range
33%
production
33%
growth
33%
hypothesis
33%
pathology
33%
fibers
33%
removal
33%
pools
33%
plasma
33%
molecules
33%
foundations
33%
clearance
33%
protein structure
33%
polypeptides
33%
Immunology and Microbiology
Serum Amyloid P Component
100%
Cross Linking
50%
Blood Plasma
50%
Precursor
50%
Protein Structure
50%
Tetrameric Protein
50%
Medicine and Dentistry
Diseases
100%
Amyloid Protein
100%
Serum Amyloid P
20%
Precursor
10%
Tissue Injury
10%
Polypeptide
10%
Protein Structure
10%
Transthyretin
10%
Beta Secretase Inhibitor
10%
Beta Secretase
10%
Thyroxine
10%
Guilt
10%
Cross-Link
10%
Biochemistry, Genetics and Molecular Biology
Amyloid Protein
100%
Serum Amyloid P Component
20%
Secretase
20%
Small Molecule
10%
Cross-Link
10%
Tetrameric Protein
10%
Protein Structure
10%
Precursor
10%
Blood Plasma
10%
Transthyretin
10%
Guilt
10%
Neuroscience
Amyloid Protein
100%
Serum Amyloid P
20%
Beta Secretase
20%
Blood Plasma
10%
Polypeptide
10%
Protein Structure
10%
Thyroxine
10%
Transthyretin
10%