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Simulations of Membrane-bound Diglycosylated Human Prion Protein Reveal Potential Protective Mechanisms against Misfolding

Prion diseases are associated with the misfolding of the prion protein (PrP) from its normal cellular form (PrP(C)) to its infectious scrapie form (PrP(Sc)). Posttranslational modifications of PrP in vivo can play an important role in modulating the process of misfolding. To gain more insight into t...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Neurochem
Egile Nagusiak: Cheng, Chin Jung, Koldsø, Heidi, Van der Kamp, Marc W., Schiøtt, Birgit, Daggett, Valerie
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2017
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5500178/
https://ncbi.nlm.nih.gov/pubmed/28407243
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jnc.14044
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