Detection of the GPI-anchorless prion protein fragment PrP226* in human brain

BACKGROUND: The accumulation of the misfolded forms of cellular prion protein, i.e. prions (PrP(Sc)), in the brain is one of the crucial characteristics of fatal neurodegenerative disorders, called transmissible spongiform encephalopathies (TSEs). Cellular prion protein is normally linked to the cel...

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Detalhes bibliográficos
Main Authors: Dvorakova, Eva, Vranac, Tanja, Janouskova, Olga, Černilec, Maja, Koren, Simon, Lukan, Anja, Nováková, Jana, Matej, Radoslav, Holada, Karel, Čurin Šerbec, Vladka
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3849060/
https://ncbi.nlm.nih.gov/pubmed/24063733
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-13-126
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