YEAST PRION PROTEIN Ure2p - A USEFUL MODEL FOR HUMAN PRION DISEASES.

• Auteurs principaux: Tatina T. Todorova (Auteur), Gabriela St. Tsankova (Auteur), Neli M. Ermenlieva (Auteur)
• Format: Livre
• Publié: Peytchinski Publishing, 2015-03-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Mammalian transmissible spongiform encephalopathies are uncommon and irreversible diseases caused by prions. Prions lack nucleic acid and can self-propagate by converting normal cell protein to isomeric prion form. In the pathogenesis of these diseases a long variable incubation period occurs, follo...