Molecular Pathology of the Prions - Baker, Harry F.; SpringerLink (Online service) (Totowa, NJ : Humana Press : Imprint: Humana, 2001)
What Would Thomas Henry Huxley Have Made of Prion Diseases? -- Prion Protein as Copper-Binding Protein at the Synapse -- A Function for the Prion Protein? -- Prion Protein Peptide -- Characterization of Bovine Spongiform Encephalopathy and Scrapie Strains/Isolates by Immunochemical Analysis of PrPSc -- Differential Targeting of Neurons by Prion Strains -- Transgenic Studies of Prion Diseases -- Prions: From Neurografts to Neuroinvasion -- Cellular and Transgenic Models of Familial Prion Diseases -- Central Nervous System Inflammation and Prion Disease Pathogenesis -- The Electroneuropathology of Prion Disease -- Transmissible Spongiform Encephalopathy Neurobiology and Ultrastructure Suggests Extracellular PrPSc Conversion Consistent with Classical Amyloidosis -- Conformation as Therapeutic Target in the Prionoses and Other Neurodegenerative Conditions -- Prions of Yeast From Cytoplasmic Genes to Heritable Amyloidosis.
Keywords: Pathology; Pathology