Upregulation of the Genes Encoding Lysosomal Hydrolases, a Perforin-Like Protein, and Peroxidases in the Brains of Mice Affected with an Experimental Prion Disease

Lignende værker

• Physiological Expression of the Gene for PrP-Like Protein, PrPLP/Dpl, by Brain Endothelial Cells and its Ectopic Expression in Neurons of PrP-Deficient Mice Ataxic Due to Purkinje Cell Degeneration
  af: Li, Aimin, et al.
  Udgivet: (2000)
• Biological and Biochemical Characteristics of Prion Strains Conserved in Persistently Infected Cell Cultures
  af: Arima, Kazuhiko, et al.
  Udgivet: (2005)
• Abnormal activation of glial cells in the brains of prion protein-deficient mice ectopically expressing prion protein-like protein, PrPLP/Dpl.
  af: Atarashi, R., et al.
  Udgivet: (2001)
• Prion Strain-Dependent Differences in Conversion of Mutant Prion Proteins in Cell Culture
  af: Atarashi, Ryuichiro, et al.
  Udgivet: (2006)
• Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent.
  af: Sakaguchi, S, et al.
  Udgivet: (1995)