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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S. Faucheux BA, et al. Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x. Neuropathol Appl Neurobiol. 2011. PMID: 21450052
The N-terminal cleavage of cellular prion protein in the human brain.
Laffont-Proust I, Faucheux BA, Hässig R, Sazdovitch V, Simon S, Grassi J, Hauw JJ, Moya KL, Haïk S. Laffont-Proust I, et al. Among authors: faucheux ba. FEBS Lett. 2005 Nov 21;579(28):6333-7. doi: 10.1016/j.febslet.2005.10.013. Epub 2005 Oct 19. FEBS Lett. 2005. PMID: 16263114 Free article.
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