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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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Detalles Bibliográficos
Autores principales: Meli, Massimiliano, Gasset, Maria, Colombo, Giorgio
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084259/
https://www.ncbi.nlm.nih.gov/pubmed/21552571
http://dx.doi.org/10.1371/journal.pone.0019093