Autocatalytic Conversion of Recombinant Prion Proteins Displays a Species Barrier

This publication has 40 references indexed in Scilit:

• Isolation of Isoforms of Mouse Prion Protein with PrP^SC-like Structural Properties
  Biochemistry, 2001
• Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
  Nature, 2001
• Neurodegenerative Diseases and Prions
  New England Journal of Medicine, 2001
• Folding of Prion Protein to Its Native α-Helical Conformation Is under Kinetic Control
  Journal of Biological Chemistry, 2001
• Aggregation and Fibrillization of the Recombinant Human Prion Protein huPrP90−231
  Biochemistry, 1999
• Protease-resistant prion protein produced in vitro lacks detectable infectivity.
  Journal of General Virology, 1999
• PATHOLOGIC CONFORMATIONS OF PRION PROTEINS
  Annual Review of Biochemistry, 1998
• Prion Diseases and the BSE Crisis
  Science, 1997
• Non-genetic propagation of strain-specific properties of scrapie prion protein
  Nature, 1995
• Creutzfeldt‐Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
  Annals of Neurology, 1979