Structured Summary
Abstract
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.
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Synonyms
3 entry terms
- Prion
- Mink Encephalopathy Virus
- Encephalopathy Virus, Mink
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Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pathogenicity, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
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History Note
86; MINK ENCEPHALOPATHY VIRUS was heading 1991-92, was see under VERTEBRATE VIRUSES, UNCLASSIFIED (now VIRUSES, UNCLASSIFIED) 1975-90; TRANSMISSIBLE ENCEPHALOPATHY VIRUS OF MINK was see MINK ENCEPHALOPATHY VIRUS 1975-92
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Previous Indexing
- PrPSc Proteins (1966-1985)
- Viral Proteins (1966-1985)
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QU 55
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References
- National Library of Medicine. Prions. Medical Subject Headings (MeSH). 2026. Unique ID D011328. http://id.nlm.nih.gov/mesh/2026/D011328
- Prions. In: Wikipedia. https://en.wikipedia.org/wiki/Prion
- Prions. In: Wikidata. https://www.wikidata.org/wiki/Q47051