Genes contributing to prion pathogenesis

Prion diseases are caused by conversion of a normally folded, nonpathogenic isoform of the prion protein (PrP(C)) to a misfolded, pathogenic isoform (PrP(Sc)). Prion inoculation experiments in mice expressing homologous PrP(C) molecules on different genetic backgrounds displayed different incubation...

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Detaylı Bibliyografya
Asıl Yazarlar: Tamgüney, Gültekin, Giles, Kurt, Glidden, David V., Lessard, Pierre, Wille, Holger, Tremblay, Patrick, Groth, Darlene F., Yehiely, Fruma, Korth, Carsten, Moore, Richard C., Tatzelt, Jörg, Rubenstein, Eric, Boucheix, Claude, Yang, Xiaoping, Stanley, Pamela, Lisanti, Michael P., Dwek, Raymond A., Rudd, Pauline M., Moskovitz, Jackob, Epstein, Charles J., Cruz, Tracey Dawson, Kuziel, William A., Maeda, Nobuyo, Sap, Jan, Ashe, Karen Hsiao, Carlson, George A., Tesseur, Ina, Wyss-Coray, Tony, Mucke, Lennart, Weisgraber, Karl H., Mahley, Robert W., Cohen, Fred E., Prusiner, Stanley B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2828448/
https://ncbi.nlm.nih.gov/pubmed/18559949
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1099/vir.0.2008/001255-0
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