2007 (v1)
Publication
The conversion of the prion protein (PrP) into a protease-resistant isoform (Prp(Res)) is considered the pathogenic event responsible for prion encephalopathies. Microglia activation accompanies PrPRes deposition representing an early event in the progression of these diseases. It is now believed that microglial cells play a worsening, if not...
Uploaded on: March 25, 2023