Protein Folding Activity of the Ribosome (PFAR) –– A Target for Antiprion Compounds
Prion diseases are fatal neurodegenerative diseases affecting mammals. Prions are misfolded amyloid aggregates of the prion protein (PrP), which form when the alpha helical, soluble form of PrP converts to an aggregation-prone, beta sheet form. Thus, prions originate as protein folding problems. The...
שמור ב:
| Principais autores: | , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
MDPI AG
2014-10-01
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| סדרה: | Viruses |
| נושאים: | |
| גישה מקוונת: | http://www.mdpi.com/1999-4915/6/10/3907 |
| תגים: |
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