Prion diseases are transmissible neurodegenerative disorders that affect humans and
ruminant species consumed by humans. Ruminant prion diseases include bovine …

Scrapie is a naturally occurring transmissible spongiform encephalopathy (TSE) or prion
disease of sheep and goats. Scrapie is a protein misfolding disease where the normal prion …

Transmissible Spongiform Encephalopathies (TSEs) or prion diseases are a fatal group of
infectious, inherited and spontaneous neurodegenerative diseases affecting human and …

Transmissible spongiform encephalopathies are fatal neurodegenerative diseases that
include variant Creutzfeldt-Jakob disease in humans, scrapie in small ruminants, and bovine …

Prion diseases are infectious neurodegenerative disorders characterized by accumulations
of abnormally folded cellular prion protein in affected tissues. Many natural prion diseases …

Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal protein-
misfolding neurodegenerative diseases. TSEs have been described in several species …

Background Chronic wasting disease (CWD) is a prion disease affecting members of the
Cervidae family. PrP C primary structures play a key role in CWD susceptibility resulting in …

Prion disorders are infectious, neurodegenerative diseases that affect humans and animals.
Susceptibility to some prion diseases such as kuru or the new variant of Creutzfeldt‐Jakob …

Prion diseases are sub-acute neurodegenerative diseases that affect humans and some
domestic and free-ranging animals. Infectious prion agents are considered to comprise …

The application of genetic breeding programmes to eradicate transmissible spongiform
encephalopathies in goats is an important aim for reasons of animal welfare as well as …