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Transmissible spongiform encephalopathies: transmission, mechanism of disease, and persistence
1Institute for Animal Health Biotechnology and Biological Sciences, Neuropathogenesis Unit, Ogston Building, West Mains Road, Edinburgh EH93JF, UK. Jim.Foster@bbsrc.ac.uk
Current Opinion in Microbiology
|March 6, 1999
Abstract:
Prion protein is central to the control of development of all transmissible spongiform encephalopathies. Controversy exists as to whether the protein itself is responsible for disease manifestation, in one of perhaps several isoforms, or whether an additional informational molecule must be involved in conjunction with the protein. Recent studies have been trying to resolve these issues.