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ANNUAL REVIEW OF NEUROSCIENCE (2008)
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Reduced translocation of nascent prion protein during ER stress contributes to neurodegeneration
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Coexpression of wild-type and mutant prion proteins alters their cellular localization and partitioning into detergent-resistant membranes
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Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob disease
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Human prion proteins with pathogenic mutations share common conformational changes resulting in enhanced binding to glycosaminoglycans
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Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathway
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