Prion Strain Interference
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4614-5305-5_14.pdf
Reference58 articles.
1. Bartz JC, Bessen R, McKenzie D, Marsh R, Aiken JM (2000) Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy. J Virol 74:5542–5547
2. Bartz JC, Aiken JM, Bessen RA (2004) Delay in onset of prion disease for the HY strain of transmissible mink encephalopathy as a result of prior peripheral inoculation with the replication-deficient DY strain. J Gen Virol 85:265–273
3. Bartz JC, Dejoia C, Tucker T, Kincaid AE, Bessen RA (2005) Extraneural prion neuroinvasion without lymphoreticular system infection. J Virol 79:11858–11863
4. Bartz JC, Kramer ML, Sheehan MH, Hutter JAL, Ayers JI, Bessen RA, Kincaid AE (2007) Prion interference is due to a reduction in strain-specific PrPSc levels. J Virol 81:689–697
5. Basler K, Oesch B, Scott M, Westaway D, Walchli M, Groth D, McKinley M, Prusiner S, Weissmann C (1986) Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell 46:417–428
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