Modeling the Cell Biology of Prions
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4614-5305-5_13.pdf
Reference71 articles.
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2. Bate C, Williams A (2012) Neurodegeneration induced by clustering of sialylated glycosylphosphatidylinositols of prion proteins. J Biol Chem 287(11):7935–7944. doi: 10.1074/jbc.M111.275743
3. Beringue V, Vilette D, Mallinson G, Archer F, Kaisar M, Tayebi M, Jackson GS, Clarke AR, Laude H, Collinge J, Hawke S (2004) PrPSc binding antibodies are potent inhibitors of prion replication in cell lines. J Biol Chem 279(38):39671–39676. doi: 10.1074/jbc.M402270200
4. Birkett CR, Hennion RM, Bembridge DA, Clarke MC, Chree A, Bruce ME, Bostock CJ (2001) Scrapie strains maintain biological phenotypes on propagation in a cell line in culture. EMBO J 20(13):3351–3358. doi: 10.1093/emboj/20.13.3351
5. Borchelt DR, Scott M, Taraboulos A, Stahl N, Prusiner SB (1990) Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells. J Cell Biol 110(3):743–752
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