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New insights into structural determinants of prion protein folding and stability

Prions are the etiological agent of fatal neurodegenerative diseases called prion diseases or transmissible spongiform encephalopathies. These maladies can be sporadic, genetic or infectious disorders. Prions are due to post-translational modifications of the cellular prion protein leading to the fo...

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Dades bibliogràfiques
Publicat a:Prion
Autors principals: Benetti, Federico, Legname, Giuseppe
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4601514/
https://ncbi.nlm.nih.gov/pubmed/25746597
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2015.1022023
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