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Stability and Cu(II) Binding of Prion Protein Variants Related to Inherited Human Prion Diseases

All inherited forms of human prion diseases are linked with mutations in the prion protein (PrP) gene. Here we have investigated the stability and Cu(II) binding properties of three recombinant variants of murine full-length PrP(23–231)-containing destabilizing point mutations that are associated wi...

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Detalhes bibliográficos
Main Authors: Cereghetti, Grazia M., Schweiger, Arthur, Glockshuber, Rudi, Van Doorslaer, Sabine
Formato: Artigo
Idioma:Inglês
Publicado em: Biophysical Society 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1302768/
https://ncbi.nlm.nih.gov/pubmed/12609901
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