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Asymmetric-flow field-flow fractionation of prions reveals a strain-specific continuum of quaternary structures with protease resistance developing at a hydrodynamic radius of 15 nm
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J. C. Espinosa et al.
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Emmanuel A. Asante et al.
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Drug resistance confounding prion therapeutics
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Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays
Jason M. Wilham et al.
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The POM Monoclonals: A Comprehensive Set of Antibodies to Non-Overlapping Prion Protein Epitopes
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Prion strain discrimination in cell culture: The cell panel assay
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A general model of prion strains and their pathogenicity
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JG Safar et al.
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Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
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Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
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Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein
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