The state of the prion
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Immunology and Microbiology,Microbiology,Infectious Diseases
Link
http://www.nature.com/articles/nrmicro1025.pdf
Reference124 articles.
1. Prusiner, S. B. Novel proteinaceous infectious particles cause scrapie. Science 216, 136–144 (1982). A historically important paper providing a major breakthrough in the understanding of spongiform encephalopathies.
2. Oesch, B. et al. A cellular gene encodes scrapie PrP 27-30 protein. Cell 40, 735–746 (1985). A historically important paper showing that the gene encoding what is believed to be the infectious molecule is encoded by the host.
3. Chesebro, B. et al. Identification of scrapie prion protein-specific messenger RNA in scrapie-infected and uninfected brain. Nature 315, 331–333 (1985).
4. Basler, K. et al. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell 46, 417–428 (1986).
5. Stahl, N. et al. Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing. Biochemistry 32, 1991–2002 (1993).
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