The Neurochemistry of Prion Diseases

This publication has 78 references indexed in Scilit:

• Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters.
  Genes & Development, 1992
• Further analysis of nucleic acids in purified scrapie prion preparations by improved return refocusing gel electrophoresis
  Journal of General Virology, 1992
• Creutzfeldt‐Jakob disease cosegregates with the codon 178^AsnPRNP mutation in families of European origin
  Annals of Neurology, 1992
• Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
  New England Journal of Medicine, 1992
• A 'unified theory' of prion propagation
  Nature, 1991
• Mutation of the Prion Protein in Libyan Jews with Creutzfeldt–Jakob Disease
  New England Journal of Medicine, 1991
• Neurite outgrowth in response to transfected N-CAM and N-cadherin reveals fundamental differences in neuronal responsiveness to CAMs
  Neuron, 1991
• Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.
  The Journal of cell biology, 1990
• 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
• Temporary and Permanent Modifications to a Single Strain of Mouse Scrapie on Transmission to Rats and Hamsters
  Journal of General Virology, 1987