In Vitro Approach To Identify Key Amino Acids in Low Susceptibility of Rabbit Prion Protein to Misfolding

Prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of rare progressive neurodegenerative disorders caused by an abnormally folded prion protein (PrP(Sc)). This is capable of transforming the normal cellular prion protein (PrP(C)) into new infectious PrP(Sc). Interspecie...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:J Virol
Autori principali: Eraña, Hasier, Fernández-Borges, Natalia, Elezgarai, Saioa R., Harrathi, Chafik, Charco, Jorge M., Chianini, Francesca, Dagleish, Mark P., Ortega, Gabriel, Millet, Óscar, Castilla, Joaquín
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Microbiology 2017
Soggetti:
Prions
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5709604/
https://ncbi.nlm.nih.gov/pubmed/28978705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.01543-17
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi