The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist

This publication has 41 references indexed in Scilit:

• Iatrogenic Creutzfeldt‐Jakob disease
  Australian and New Zealand Journal of Medicine, 1990
• Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome
  Experimental Neurology, 1990
• Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
  Experimental Neurology, 1989
• Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
  Biochemical and Biophysical Research Communications, 1989
• Linkage of the gene for the scrapie-associated fibril protein (PrP) to the Sip gene in Cheviot sheep
  Veterinary Record, 1989
• Localization of a human gene homologous to the PrP gene on the p ARM of chromosome 20 and detection of PrP-related antigens in normal human brain
  Biochemical and Biophysical Research Communications, 1986
• Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
  Cell, 1986
• Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
  New England Journal of Medicine, 1986
• Novel Proteinaceous Infectious Particles Cause Scrapie
  Science, 1982
• Nature of the Scrapie Agent
  Nature, 1967