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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Autors principals: Dvorakova, Eva, Vranac, Tanja, Janouskova, Olga, Černilec, Maja, Koren, Simon, Lukan, Anja, Nováková, Jana, Matej, Radoslav, Holada, Karel, Čurin Šerbec, Vladka
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2013
Matèries:
Research Article
Accés en línia: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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