References
- Ghaemmaghami S, Phuan PW, Perkins B, Ullman J, May BC, Cohen FE, Prusiner SB. Cell division modulates prion accumulation in cultured cells. Proc Natl Acad Sci U S A 2007; 104:17971 - 6; http://dx.doi.org/10.1073/pnas.0708372104; PMID: 17989223
- Herbst A, Banser P, Velasquez CD, Mays CE, Sim VL, Westaway D, Aiken JM, McKenzie D. Infectious prions accumulate to high levels in non proliferative C2C12 myotubes. PLoS Pathog 2013; 9:e1003755; http://dx.doi.org/10.1371/journal.ppat.1003755; PMID: 24244171
- Dlakic WM, Grigg E, Bessen RA. Prion infection of muscle cells in vitro. J Virol 2007; 81:4615 - 24; http://dx.doi.org/10.1128/JVI.02628-06; PMID: 17314174
- Bosque PJ, Ryou C, Telling G, Peretz D, Legname G, DeArmond SJ, Prusiner SB. Prions in skeletal muscle. Proc Natl Acad Sci U S A 2002; 99:3812 - 7; http://dx.doi.org/10.1073/pnas.052707499; PMID: 11904434
- Rubenstein R, Carp RI, Callahan SM. In vitro replication of scrapie agent in a neuronal model: infection of PC12 cells. J Gen Virol 1984; 65:2191 - 8; http://dx.doi.org/10.1099/0022-1317-65-12-2191; PMID: 6439820
- Herva ME, Relano-Gines A, Villa A, Torres JM. Prion infection of differentiated neurospheres. Journal of neuroscience methods. 2010; 188:270 - 5
- Birkett CR, Hennion RM, Bembridge DA, Clarke MC, Chree A, Bruce ME, Bostock CJ. Scrapie strains maintain biological phenotypes on propagation in a cell line in culture. EMBO J 2001; 20:3351 - 8; http://dx.doi.org/10.1093/emboj/20.13.3351; PMID: 11432823
- Hwang D, Lee IY, Yoo H, Gehlenborg N, Cho JH, Petritis B, Baxter D, Pitstick R, Young R, Spicer D, et al. A systems approach to prion disease. Mol Syst Biol 2009; 5:252; http://dx.doi.org/10.1038/msb.2009.10; PMID: 19308092
- Caughey B, Raymond GJ. Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells. J Virol 1993; 67:643 - 50; PMID: 7678300