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Unraveling Prion Protein Interactions with Aptamers and Other PrP-Binding Nucleic Acids

Transmissible spongiform encephalopathies (TSEs) are a group of neurodegenerative disorders that affect humans and other mammals. The etiologic agents common to these diseases are misfolded conformations of the prion protein (PrP). The molecular mechanisms that trigger the structural conversion of t...

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Bibliografiska uppgifter
I publikationen:Int J Mol Sci
Huvudupphovsmän: Macedo, Bruno, Cordeiro, Yraima
Materialtyp: Artigo
Språk:Inglês
Publicerad: MDPI 2017
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5454936/
https://ncbi.nlm.nih.gov/pubmed/28513534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18051023
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