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Dynamic Diagnosis of Familial Prion Diseases Supports the β2-α2 Loop as a Universal Interference Target

BACKGROUND: Mutations in the cellular prion protein associated to familial prion disorders severely increase the likelihood of its misfolding into pathogenic conformers. Despite their postulation as incompatible elements with the native fold, these mutations rarely modify the native state structure....

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Detalhes bibliográficos
Main Authors: Meli, Massimiliano, Gasset, Maria, Colombo, Giorgio
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3084259/
https://ncbi.nlm.nih.gov/pubmed/21552571
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0019093
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