Yüklüyor......

Alternative fates of newly formed PrP(Sc) upon prion conversion on the plasma membrane

Prion diseases are fatal neurodegenerative diseases characterised by the accumulation of misfolded prion protein (PrP(Sc)) in the brain. They are caused by the templated misfolding of normal cellular protein, PrP(C), by PrP(Sc). We have recently generated a unique cell system in which epitope-tagged...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Goold, Rob, McKinnon, Chris, Rabbanian, Samira, Collinge, John, Schiavo, Giampietro, Tabrizi, Sarah J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Company of Biologists 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3744024/
https://ncbi.nlm.nih.gov/pubmed/23813960
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.120477
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!