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Cited by 954

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Prion Diseases and the BSE Crisis

Prusiner, Stanley B.·1997·Science

Abstract

Bovine spongiform encephalopathy (BSE) and human Creutzfeldt-Jakob disease (CJD) are among the most notable central nervous system degenerative disorders caused by prions. CJD may present as a sporadic, genetic, or infectious illness. Prions are transmissible particles that are devoid of nucleic acid and seem to be composed exclusively of a modified protein (PrP Sc ). The normal, cellular prion protein (PrP C ) is converted into PrP Sc through a posttranslational process during which it acquires a high β-sheet content. It is thought that BSE is a result of cannibalism in which faulty industrial practices produced prion-contaminated feed for cattle. There is now considerable concern that bovine prions may have been passed to humans, resulting in a new form of CJD.

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Metadata

Authors
Prusiner, S. B.
Venue
Science
Published
1997-10-10
Volume
278
Issue
5336
Pages
245-251
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2167564565
Cited by
954
References
1
FWCI
21.71
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Prion Diseases and the BSE Crisis. https://app.cochat.ai/papers/10.1126/science.278.5336.245
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Prusiner, S. B. (1997). Prion Diseases and the BSE Crisis. Science. https://doi.org/10.1126/science.278.5336.245

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