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Prion protein biosynthesis and its emerging role in neurodegeneration

Various fatal neurodegenerative disorders are caused by altered metabolism of the prion protein (PrP). These diseases are typically transmissible by an unusual ‘protein-only’ mechanism in which a misfolded isomer, PrP(Sc), confers its aberrant conformation onto normal cellular PrP. An impressive ran...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Chakrabarti, Oishee, Ashok, Aarthi, Hegde, Ramanujan S.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3132587/
https://ncbi.nlm.nih.gov/pubmed/19447626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tibs.2009.03.001
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