क्यूआर कोड

A role for intermolecular disulfide bonds in prion diseases?

The key event in prion diseases seems to be the conversion of the prion protein PrP from its normal cellular isoform (PrP(C)) to an aberrant “scrapie” isoform (PrP(Sc)). Earlier studies have detected no covalent modification in the scrapie isoform and have concluded that the PrP(C) → PrP(Sc) convers...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Proc Natl Acad Sci U S A
मुख्य लेखकों: Welker, Ervin, Wedemeyer, William J., Scheraga, Harold A.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: National Academy of Sciences 2001
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC31835/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11274354/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.071066598
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