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Keywords: prion protein (PrP)
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Biochem Soc Trans (2010) 38 (2): 482–487.
Published: 22 March 2010
... To whom correspondence should be addressed (email grm7@le.ac.uk ). 30 10 2009 © The Authors Journal compilation © 2010 Biochemical Society 2010 behaviour neurodegeneration neurophysiology prion protein (PrP) synaptic dysfunction Compromised synaptic function is thought...
Biochem Soc Trans (2006) 34 (6): 1155–1158.
Published: 25 October 2006
... The Biochemical Society 2006 bovine spongiform encephalopathy (BSE) chronic wasting disease (CWD) Creutzfeldt–Jakob disease (CJD) prion protein (PrP) scrapie transmissible spongiform encephalopathy (TSE) The TSEs (transmissible spongiform encephalopathies) are neurodegenerative diseases which...
Biochem Soc Trans (2005) 33 (5): 1123–1125.
Published: 26 October 2005
... prion protein (PrP) proteolysis reactive oxygen species (ROS) Prion diseases occur when a conformational conversion in the normal PrP C [cellular isoform of PrP (prion protein)] produces a proteinase-resistant form PrP Sc (scrapie isoform of PrP). Examples of such neurodegenerative disorders...