Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. [electronic resource]
Producer: 20140422Description: 4870-81 p. digitalISSN:- 1083-351X
- Animals
- Antibodies -- metabolism
- Creutzfeldt-Jakob Syndrome -- metabolism
- Electrophoresis, Gel, Two-Dimensional
- Endopeptidase K -- metabolism
- Epitope Mapping
- Gerstmann-Straussler-Scheinker Disease -- metabolism
- Humans
- Mice
- Mice, Inbred C57BL
- Mice, Transgenic
- Molecular Weight
- Mutant Proteins -- metabolism
- PrPSc Proteins -- metabolism
- Prions -- chemistry
- Protein Conformation
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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