BSE und variante CJK

Literatur

• 1 Prusiner S B. Genetic and infectious prion diseases.  Arch Neurol. 1993;  50 1129-1153
• 2 Brown P, Preece M A, Will R G. Friendly fire in medicine. Hormones, homografts, and Creutzfeldt-Jakob disease.  Lancet. 1992;  340 24-27
• 3 Gajdusek D C, Gibbs C J, Alpers M. Experimental transmission of a kuru-like syndrome to chimpanzees.  Nature. 1966;  209 794-796
• 4 Tateishi J, Kitamoto T. Inherited prion diseases and transmission to rodents.  Brain Pathol. 1995;  5 53-59
• 5 Bolton D C, McKinley M P, Prusiner S B. Identification of a protein that purifies with the scrapie prion.  Science. 1982;  218 1309-1311
• 6 Brown P, Gibbs C J, Amyx H L, Kingsbury D T, Rohwer R, Sulima M. et al . Chemical disinfection of Creutzfeldt-Jakob disease virus.  NEJM. 1982;  306 1279-1282
• 7 Brown P, Liberski P P, Wolff A, Gajdusek D C. Resistance of scrapie infectivity to steam autoclaving after formaldehyde fixation and limited survival after ashing at 360 ˚C: practical and theoretical implications.  J Infect Dis. 1990;  161 467-472
• 8 Gibbs C J, Gajdusek D C, Latarjet R. Unusual resistance to ionizing radiation of the viruses of kuru, Creutzfeldt-Jakob disease, and scrapie.  Proc Natl Acad Sci USA. 1978;  75 6268-6270
• 9 Tateishi J, Koga M, Sato Y, Mori R. Properties of the transmissible agent derived from chronic spongiform encephalopathy.  Ann Neurol. 1980;  7 390-391
• 10 Aiken J M, Marsh R F. The search for scrapie agent nucleic acid.  Microbiol Rev. 1990;  54 242-246
• 11 Alper T. The scrapie enigma - insights from radiation experiments.  Radiat Res. 1993;  135 283-292
• 12 Diringer H, Beekes M, Oberdieck U. The nature of the scrapie agent: the virus theory.  Ann New York Acad Sci. 1994;  724 246-258
• 13 Pan K M, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D. et al . Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins.  Proc Natl Acad Sci USA. 1993;  90 10 962-10 966
• 14 Weissmann C. A »unified theory« of prion propagation.  Nature. 1991;  352 679-683
• 15 Prusiner S B. Novel proteinaceous infectious particles cause scrapie.  Science. 1982;  216 136-144
• 16 Büeler H, Aguzzi A, Sailer A, Greiner R A, Autenried P, Aguet M. et al . Mice devoid of PrP are resistant to scrapie.  Cell. 1993;  73 1339-1348
• 17 Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arend S. et al . Molecular genetics of human prion diseases in Germany.  Hum Genetics. 1999;  105 244-252
• 18 Pattison I H. Experiments with scrapie with special reference to the nature of the agent and the pathology of the disease. Washington: US Government Printing Office In: Gajdusek DC, Gibbs CJ, Alpers M, editors. Slow, Latent, and Temperate Virus Infections, NINDB Monograph 2 1965: 249-257
• 19 Gajdusek D C, Gibbs C J Jr, Asher D M, Brown P, Diwan A, Hoffman P. et al . Precautions in medical care of, and in handling materials from, patients with transmissible virus dementia (Creutzfeldt-Jakob disease).  NEJM. 1977;  297 1253-1258
• 20 Kimberlin R H, Walker C A. Pathogenesis of mouse scrapie: dynamics of agent replication in spleen, spinal cord and brain after infection by different routes.  J Comp Pathol. 1979;  89 551-562
• 21 Prusiner S B, Groth D F, Cochran S P, Masiarz F R, McKinley M P, Martinez H M. Molecular properties, partial purification and assay by incubation period measurements of the hamster scrapie agent.  Biochemistry. 1980;  19 4883-4891
• 22 Beekes M, McBride P A. Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie [In Process Citation].  Neurosci Lett. 2000;  278 181-184
• 23 McBride P A, Schulz-Schaeffer W J, Donaldson M, Bruce M, Diringer H, Kretzschmar H A. et al . Early spread of scrapie from the gastrointestinal tract to the central nervous system involves autonomic fibers of the splanchnic and vagus nerves.  J Virol JID - 0 113 724. 2001;  75 9320-9327
• 24 van Keulen L JM, Schreuder B EC, Vromans M EV, Langeveld J PM, Smits M A. Pathogenesis of natural scrapie in sheep.  Arch Virol. 2000;  16 S57-S71
• 25 Schulz-Schaeffer W, Fatzer R, Vandevelde M, Kretzschmar H A. Detection of PrP(Sc) in subclinical BSE with the paraffin-embedded tissue (PET) blot.  Arch Virol Suppl. 2000;  16 173-180
• 26 Lasm& eacute;zas C I, Deslys J -P, Demalmay R, Adjou K T, Lamoury F, Dormont D. et al . BSE transmission to macaques.  Nature. 1996;  381 743-744
• 27 Bruce M E, Will R G, Ironside J W, McConnell I, Drummond D, Suttie A. et al . Transmissions to mice indicate that »new variant« CJD is caused by the BSE agent.  Nature. 1997;  398 489-501
• 28 Scott M R, Will R, Ironside J, Nguyen H O, Tremblay P, DeArmond S J. et al . Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans (In Process Citation).  Proc Natl Acad Sci USA. 1999;  96 15 137-15 142
• 29 Beekes M, Baldauf E, Diringer H. Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie.  J Gen Virol. 1996;  77 1925-1934
• 30 Wijeratne W V. A study of the inheritance of susceptibility to bovine spongiform encephalopathy.  Vet Rec. 1990;  126 5-8
• 31 Andrews N J, Farrington C P, Cousens S, Smith P G, Ward H, Knight R S. et al . Incidence of variant Creutzfeldt-Jakob disease in the UK.  Lancet. 2000;  356 481-482