Is there more to TSE diseases than PrP? (multiple letters) [3]

Trends in Microbiology

Volumn 8, Issue 4, 2000, Pages 157-158

  Somerville, Robert A ^a  

^a INSTITUTE FOR ANIMAL HEALTH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

BRAIN SPONGIOSIS; CELL VACUOLE; GENOTYPE; HUMAN; LETTER; PRION DISEASE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN ISOLATION; PROTEIN PROTEIN INTERACTION;

EID: 0034176504     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0966-842X(00)01725-X     Document Type: Letter

References (13)

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2. R.I. Carp Scrapie strain-specific interactions with endogenous murine leukaemia virus J. Gen. Virol 80 1999 5 10
3. R.I. Carp An endogenous retrovirus and exogenous scrapie in a mouse model of aging Trends Microbiol 8 2000 39 42
4. C.F. Farquhar Straining the prion hypothesis Nature 391 1998 345 346
5. R.C. Moore Mice with gene targeted prion protein alterations show that Prnp, Sinc and Prni are congruent Nat. Genet 18 1998 118 124
6. J. Manson A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy EMBO J 18 1999 6855 6864
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9. M.E. Bruce PrP in pathology and pathogenesis in scrapie-infected mice Mol. Neurobiol 8 1994 105 112
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11. G.W. Outram The pathogenesis of scrapie in mice Front. Biol 44 1976 325 357
12. M. Bruce Transmission of bovine spongiform encephalopathy and scrapie to mice strain variation and the species barrier Philos. Trans. R. Soc. London Ser. B 343 1994 405 411
13. Fraser, H. (1979) Neuropathology of scrapie: the precision of the lesions and their diversity. In Slow Transmissible Diseases of the Central Nervous System (Vol. 1) (Prusiner, S.B. and Hadlow, W.J., eds), pp. 387–408, Academic Press