Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes.

Prion-related encephalopathies are characterized by the intracerebral accumulation of an abnormal isoform of the cellular prion protein (PrPC) named scrapie prion protein (PrPSc). The pathological forms of this protein and its cellular precursor are not only expressed in the brain but also, at lower...

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Hlavní autoři: Diomede, L, Sozzani, S, Luini, W, Algeri, M, De Gioia, L, Chiesa, R, Lievens, P M, Bugiani, O, Forloni, G, Tagliavini, F, Salmona, M
Médium: Artigo
Jazyk:Inglês
Vydáno: 1996
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1217966/
https://ncbi.nlm.nih.gov/pubmed/8973567
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