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

• Principais autores: Tatina T. Todorova (Autor), Gabriela St. Tsankova (Autor), Neli M. Ermenlieva (Autor)
• Formato: Livro
• Publicado em: Peytchinski Publishing, 2015-03-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: 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...