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Failure of Prion Protein Oxidative Folding Guides the Formation of Toxic Transmembrane Forms

The mechanism by which pathogenic mutations in the globular domain of the cellular prion protein (PrP(C)) increase the likelihood of misfolding and predispose to diseases is not yet known. Differences in the evidences provided by structural and metabolic studies of these mutants suggest that in vivo...

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Detalhes bibliográficos
Main Authors: Lisa, Silvia, Domingo, Beatriz, Martínez, Javier, Gilch, Sabine, Llopis, Juan F., Schätzl, Hermann M., Gasset, María
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3481273/
https://ncbi.nlm.nih.gov/pubmed/22955286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M112.398776
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