| Literature DB >> 9358067 |
S Kaluz1, M Kaluzova, A P Flint.
Abstract
An abnormal isoform of the prion protein (PrP) appears to be the agent responsible for transmissible spongiform encephalopathies (TSE). The normal isoform of PrP is host-encoded and expressed in the central nervous system. The recent bovine spongiform encephalopathy (BSE) epidemic in the UK and the incidence of prion-related diseases in other animals could indicate that ruminants are highly susceptible to infection via ingestion of prion-contaminated food. Sequence analysis of PrP gene open reading frames from red deer and camel was carried out to investigate sequence variability of these genes among ruminants.Entities:
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Year: 1997 PMID: 9358067 DOI: 10.1016/s0378-1119(97)00382-x
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688