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Disruption of the X-loop turn of the prion protein linked to scrapie resistance

The prion diseases are a class of neurodegenerative diseases caused by the misfolding and aggregation of the prion protein (PrP(C)) into toxic and infectious oligomers (PrP(Sc)). These oligomers are critical to understanding and combating these diseases. Differences in the sequence of PrP affect dis...

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Détails bibliographiques
Auteurs principaux: Scouras, Alexander D., Daggett, Valerie
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3530274/
https://ncbi.nlm.nih.gov/pubmed/22447804
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/protein/gzs009
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