4.7 Review

PrP genetics in ruminant transmissible spongiform encephalopathies

期刊

VETERINARY RESEARCH
卷 39, 期 4, 页码 -

出版社

BMC
DOI: 10.1051/vetres:2008010

关键词

scrapie; transmissible spongiform encephalopathy; PrP; genetics; ruminant

资金

  1. NeuroPrion European Network of Excellence
  2. Biotechnology and Biological Sciences Research Council, UK
  3. Department of the Environment, Food and Rural Affairs, UK

向作者/读者索取更多资源

Scrapie, bovine spongiform encephalopathy (BSE), and chronic wasting disease (CWD) are prion diseases in ruminants with considerable impact on animal health and welfare. They can also pose a risk to human health and control is therefore an important issue. Prion protein (PrP) genetics may be used to control and eventually eradicate animal prion diseases. The PrP gene in sheep and other representatives of the order Artiodactyles has many polymorphisms of which several are crucial determinants of susceptibility to prion diseases, also known as transmissible spongiform encephalopathies (TSE). This review will present the current understanding of PrP genetics in ruminants highlighting similarity and difference between the species in the context of TSE.

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