Prion Diseases
Author:
Affiliation:
1. Department of Neuropathology, Neurological Institute, Faculty of Medicine; Kyushu University; 3-1-1 Maidashi Higashi-ku, Fukuoka Fukuoka 812-82 Japan
Publisher
Wiley
Subject
Virology,Immunology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1348-0421.1995.tb03288.x/fullpdf
Reference44 articles.
1. Non-genetic propagation of strain-specific properties of scrapie prion protein;Bessen;Nature,1995
2. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease;Brown;Ann. Neurol.,1994
3. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein;Büeler;Nature,1992
4. Mice devoid of PrP are resistant to scrapie;Büeler;Cell,1993
5. Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy;Caughey;Biochemistry,1991
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Unraveling the Controversy of Human Prion Protein Diseases;Handbook of the Aging Brain;1998
2. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms;Proceedings of the National Academy of Sciences;1997-05-13
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