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Update on human prion disease
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A Sakudo et al.
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Biological and biochemical characteristics of prion strains conserved in persistently infected cell cultures
K Arima et al.
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Separation of native prion protein (PrP) glycoforms by copper-binding using immobilized metal affinity chromatography (IMAC)
H Müller et al.
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The scrapie prion protein is present in flotillin-1-positive vesicles in central- but not peripheral-derived neuronal cell lines
F Pimpinelli et al.
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C Féraudet et al.
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HK Hayashi et al.
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Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type
T Pan et al.
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M Moudjou et al.
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S Cronier et al.
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A Arjona et al.
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F Archer et al.
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Calpain-dependent endoproteolytic cleavage of PrPSc modulates scrapie prion propagation
R Yadavalli et al.
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Regional heterogeneity of cellular prion protein isoforms in the mouse brain
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