Prion Diseases - Baker, Harry F.; Ridley, Rosalind M.; SpringerLink (Online service) (Totowa, NJ : Humana Press : Imprint: Humana, 1996)
The Paradox of Prion Disease -- Human Spongiform Encephalopathy -- Neuropathological Diagnosis of Human Prion Disease -- Neuropathological Diagnosis of Human Prion Disease -- The Diagnosis of Bovine Spongiform Encephalopathy and Scrapie by the Detection of Fibrils and the Abnormal Protein lsoform -- Exposure to, and Inactivation of, the Unconventional Agents that Cause Transmissible Degenerative Encephalopathies -- Surveillance of Prion Diseases in Humans -- Environmental Causes of Human Spongiform Encephalopathy -- Bovine Spongiform Encephalopathy -- Handling the BSE Epidemic in Great Britain -- Special Problems of Genetic Counseling in Adult-Onset Diseases -- Genotyping and Susceptibility of Sheep to Scrapie -- Strain Typing Studies of Scrapie and BSE -- PrP-Deficient Mice in the Study of Transmissible Spongiform Encephalopathies -- Transgenic Approaches to Prion "Species-Barrier" Effects -- Methods for Studying Prion Protein Amyloid -- Methods for Studying Prion Protein (PrP) Metabolism and the Formation of Protease-Resistant PrP in Cell Culture and Cell-Free Systems -- Immunohistochemistry of Resinated Tissues for Light and Electron Microscopy.
Keywords: Cell biology; Cell Biology