PrPSc Proteins
Abnormal isoform of PRION PROTEINS resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).
Year introduced: 1995
Date introduced: April 16, 1994
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Subheadings:
Tree Number(s): D12.776.785.340.750
MeSH Unique ID: D018620
Entry Terms:
- Scrapie PrP
- Scrapie PrP 33-35
- PrP 33-35
- PrP-res
- PrP res
- Sp 33-35
- Scrapie Agent
- Scrapie Virus
- Scrapie HaSp33-37 Protein
- HaSp 33-37
- PrP (CJD)
- PrP (GSS)
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