Review
doi: 10.1016/s0065-3233(01)57016-3.
Prion protein diversity and disease in the transmissible spongiform encephalopathies
Affiliations
- PMID: 11447687
- DOI: 10.1016/s0065-3233(01)57016-3
Item in Clipboard
Review
Prion protein diversity and disease in the transmissible spongiform encephalopathies
Adv Protein Chem.
2001.
No abstract available
Similar articles
-
Prion propagation and molecular chaperones.Q Rev Biophys. 1999 Nov;32(4):309-70. doi: 10.1017/s0033583500003553. Q Rev Biophys. 1999. PMID: 11194568 Review. No abstract available.
-
The state of the prion.Nat Rev Microbiol. 2004 Nov;2(11):861-71. doi: 10.1038/nrmicro1025. Nat Rev Microbiol. 2004. PMID: 15494743 Review.
-
Structuring the puzzle of prion propagation.Curr Opin Struct Biol. 2005 Dec;15(6):724-30. doi: 10.1016/j.sbi.2005.10.011. Epub 2005 Nov 2. Curr Opin Struct Biol. 2005. PMID: 16263262 Review.
-
Non-genetic propagation of strain-specific properties of scrapie prion protein.Nature. 1995 Jun 22;375(6533):698-700. doi: 10.1038/375698a0. Nature. 1995. PMID: 7791905
-
Human and animal spongiform encephalopathies are the result of chronic autoimmune attack in the CNS: a novel medical theory supported by overwhelming experimental evidence.Histol Histopathol. 2005 Apr;20(2):575-92. doi: 10.14670/HH-20.575. Histol Histopathol. 2005. PMID: 15736062 Review.
Cited by
-
Co-infection with the friend retrovirus and mouse scrapie does not alter prion disease pathogenesis in susceptible mice.PLoS One. 2012;7(1):e30872. doi: 10.1371/journal.pone.0030872. Epub 2012 Jan 25. PLoS One. 2012. PMID: 22295118 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources