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Conserved amyloid core structure of stop mutants of the human prion protein
Prion diseases are associated with misfolding of the natively α-helical prion protein into isoforms that are rich in cross β-structure. However, both the mechanism by which pathological conformations are produced and their structural properties remain unclear. Using a combination of nuclear magnetic...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3783102/ https://ncbi.nlm.nih.gov/pubmed/23406905 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.23956 |
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