Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.

Gerstmann-Sträussler-Scheinker disease (GSS) is a prion-related encephalopathy pathologically characterized by massive deposition of prion protein (PrP) amyloid in the central nervous system. The major component of amyloid fibrils isolated from patients of the Indiana kindred of GSS (GSS-Ik) is an 1...

Descripció completa

Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Tagliavini, F, Prelli, F, Verga, L, Giaccone, G, Sarma, R, Gorevic, P, Ghetti, B, Passerini, F, Ghibaudi, E, Forloni, G
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1993
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC47633/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8105481/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.90.20.9678
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!