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α2,3 linkage of sialic acid to a GPI anchor and an unpredicted GPI attachment site in human prion protein
Prion diseases are transmissible, lethal neurodegenerative disorders caused by accumulation of the aggregated scrapie form of the prion protein (PrP(Sc)) after conversion of the cellular prion protein (PrP(C)). The glycosylphosphatidylinositol (GPI) anchor of PrP(C) is involved in prion disease path...
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| Publicado no: | J Biol Chem |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7261787/ https://ncbi.nlm.nih.gov/pubmed/32321762 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.013444 |
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