,

Functional roles of wild-type and mutant PrP on prion diseases

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Creutzfeldt-Jakob Disease with the V203I Mutation and M129V Polymorphism of the Prion Protein Gene (PRNP) and a 17 kDa Prion Protein Fragment

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Mitochondrial Dysfunction via Differential Modulation of Mitochondrial Fusion/Fission Proteins in the Brain of Scrapie-Infected Mice

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Subcellular Localization of Peptidylarginine Deiminase 2 and Citrullinated Proteins in Brains of Scrapie-infected Mice: Nuclear Localization of PAD2 and Membrane Fraction-Enriched Citrullinated Proteins

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The Cellular Prion Protein Prevents Oxidative Stress-induced Autophagic Cell Death