Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy

Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease

(2010) Martin Jeffrey et al.   ACTA NEUROPATHOLOGICA

Fatal Transmissible Amyloid Encephalopathy: A New Type of Prion Disease Associated with Lack of Prion Protein Membrane Anchoring

(2010) Bruce Chesebro et al.   PLoS Pathogens

Prion Protein with an Insertional Mutation Accumulates on Axonal and Dendritic Plasmalemma and Is Associated with Distinctive Ultrastructural Changes

(2009) Martin Jeffrey et al.   AMERICAN JOURNAL OF PATHOLOGY

Getting a Grip on Prions: Oligomers, Amyloids, and Pathological Membrane Interactions

(2009) Byron Caughey et al.   Annual Review of Biochemistry

Formation and maintenance of Alzheimer's disease β-amyloid plaques in the absence of microglia

(2009) Stefan A Grathwohl et al.   NATURE NEUROSCIENCE

Strain-Associated Variations in Abnormal PrP Trafficking of Sheep Scrapie

(2008) Martin Jeffrey et al.   BRAIN PATHOLOGY

Abnormal prion protein is associated with changes of plasma membranes and endocytosis in bovine spongiform encephalopathy (BSE)-affected cattle brains

(2008) C. Ersdal et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY