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

• Asıl Yazarlar: Tatina T. Todorova (Yazar), Gabriela St. Tsankova (Yazar), Neli M. Ermenlieva (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Peytchinski Publishing, 2015-03-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...