Zanusso, Gianluigi <br/><br/>
Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.  [electronic resource] 

 -  The Journal of biological chemistry  Feb 2014 
 - 4870-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1083-351X 
<br/><br/><label>Standard No.: </label>10.1074/jbc.M113.531335  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Antibodies--metabolism<br/>Creutzfeldt-Jakob Syndrome--metabolism<br/>Electrophoresis, Gel, Two-Dimensional<br/>Endopeptidase K--metabolism<br/>Epitope Mapping<br/>Gerstmann-Straussler-Scheinker Disease--metabolism<br/>Humans<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Transgenic<br/>Molecular Weight<br/>Mutant Proteins--metabolism<br/>PrPSc Proteins--metabolism<br/>Prions--chemistry<br/>Protein Conformation