Abstract
To assess interspecies barriers to transmission of transmissible spongiform encephalopathies (TSEs), we investigated the ability of disease-associated prion proteins (PrPd) to initiate conversion of the human normal cellular form of prion protein of the 3 major PRNP polymorphic variants in vitro. Protein misfolding cyclic amplification showed that conformation of PrPd partly determines host susceptibility.
| Original language | English |
|---|---|
| Pages (from-to) | 2013-6 |
| Number of pages | 4 |
| Journal | Emerging Infectious Diseases |
| Volume | 15 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - Dec 2009 |