Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms

Prion diseases are natural transmissible neurodegenerative disorders in humans and animals. They are characterized by the accumulation of a protease-resistant scrapie-associated prion protein (PrP(Sc)) of the host-encoded cellular prion protein (PrP(C)) mainly in the central nervous system. Polymorp...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Bossers, Alex, Belt, Peter B. G. M., Raymond, Gregory J., Caughey, Byron, de Vries, Ruth, Smits, Mari A.
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences of the USA 1997
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC24608/
https://ncbi.nlm.nih.gov/pubmed/9144167
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky