Scrapie agent: prions or virinos? 1982

R H Kimberlin

UI MeSH Term Description Entries
D011328 Prions Small proteinaceous infectious particles which resist inactivation by procedures that modify NUCLEIC ACIDS and contain an abnormal isoform of a cellular protein which is a major and necessary component. The abnormal (scrapie) isoform is PrPSc (PRPSC PROTEINS) and the cellular isoform PrPC (PRPC PROTEINS). The primary amino acid sequence of the two isoforms is identical. Human diseases caused by prions include CREUTZFELDT-JAKOB SYNDROME; GERSTMANN-STRAUSSLER SYNDROME; and INSOMNIA, FATAL FAMILIAL. Mink Encephalopathy Virus,Prion,Encephalopathy Virus, Mink

Related Publications

R H Kimberlin
January 1989, Annual review of microbiology,
R H Kimberlin
October 1999, Molecular medicine (Cambridge, Mass.),
R H Kimberlin
January 1985, Nature,
R H Kimberlin
November 2010, Journal of virology,
R H Kimberlin
January 2004, Medical hypotheses,
R H Kimberlin
January 1989, Alzheimer disease and associated disorders,
R H Kimberlin
January 1986, International review of neurobiology,
R H Kimberlin
January 1985, Microbiological sciences,
R H Kimberlin
February 2010, Heredity,
R H Kimberlin
January 1989, Progress in clinical and biological research,
Copied contents to your clipboard!