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De novo prions

Prions are responsible for a heterogeneous group of fatal neurodegenerative diseases. They occur in three forms - sporadic, genetic, or acquired - and involve non-covalent post-translational modifications of the cellular prion protein (PrP(C)). Prions (PrP(Sc)) are characterized by their infectious...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Benetti, Federico, Geschwind, Michael D, Legname, Giuseppe
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Faculty of 1000 Ltd 2010
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2950034/
https://ncbi.nlm.nih.gov/pubmed/20948787
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3410/B2-46
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