Westergard, Laura <br/><br/>
A naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formation.  [electronic resource] 

 -  The Journal of biological chemistry  Dec 2011 
 - 44234-44242 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1083-351X 
<br/><br/><label>Standard No.: </label>10.1074/jbc.M111.286195  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Brain--metabolism<br/>Genes, Dominant<br/>Genotype<br/>Mice<br/>Mice, Transgenic<br/>Models, Genetic<br/>Neurodegenerative Diseases--genetics<br/>PrPSc Proteins--chemistry<br/>Protein Structure, Tertiary<br/>Scrapie--genetics<br/>Time Factors