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- W1597028963 abstract "Publisher Summary Prions are transmissible pathogens that cause fatal neurodegenerative diseases of the central nervous system in humans and animals. In humans, prion diseases have been subdivided into four classes and are referred to as kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker disease (GSS), and fatal familial insomnia (FFI). These diseases can be sporadic, inherited, or infectious (or iatrogenic) disorders. They differ from other infectious diseases, in that the pathogen is a proteinaceous particle, termed a “prion,” and the essential component of prions is the scrapie prion protein (PrP Sc )." @default.
- W1597028963 created "2016-06-24" @default.
- W1597028963 creator A5021239442 @default.
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- W1597028963 date "2001-01-01" @default.
- W1597028963 modified "2023-09-27" @default.
- W1597028963 title "Simulations and computational analyses of prion protein conformations" @default.
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- W1597028963 doi "https://doi.org/10.1016/s0065-3233(01)57020-5" @default.
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