Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments

Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-related proteinase K-resistant prion protein (resPrP(D)) assoc...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Acta Neuropathol Commun
Main Authors: Cracco, Laura, Xiao, Xiangzhu, Nemani, Satish K., Lavrich, Jody, Cali, Ignazio, Ghetti, Bernardino, Notari, Silvio, Surewicz, Witold K., Gambetti, Pierluigi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6540574/
https://ncbi.nlm.nih.gov/pubmed/31142381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-019-0734-2
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados