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Polar substitutions in helix 3 of the prion protein produce transmembrane isoforms that disturb vesicle trafficking

Prion diseases encompass a diverse group of neurodegenerative conditions characterized by the accumulation of misfolded prion protein (PrP) isoforms. Other conformational variants of PrP have also been proposed to contribute to neurotoxicity in prion diseases, including misfolded intermediates as we...

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Detalhes bibliográficos
Main Authors: Sanchez-Garcia, Jonatan, Arbelaez, Daniela, Jensen, Kurt, Rincon-Limas, Diego E., Fernandez-Funez, Pedro
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3792687/
https://ncbi.nlm.nih.gov/pubmed/23771030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt276
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