Spongiform encephalopathy in transgenic mice expressing a point mutation in the β2-α2 loop of the prion protein.

Autor:in

Sigurdson, Christina J; Joshi-Barr, Shivanjali; Bett, Cyrus; Winson, Olivia; Manco, Giuseppe; Schwarz, Petra; Rülicke, Thomas; Nilsson, K Peter R; Margalith, Ilan; Raeber, Alex; Peretz, David; Hornemann, Simone; Wüthrich, Kurt; Aguzzi, Adriano;

Schlagwörter

Amino Acid Substitution/genetics; Animals; Female; Male; Mice; Mice, Knockout; Mice, Transgenic; Point Mutation/genetics*; PrPC Proteins/biosynthesis*; PrPC Proteins/genetics*; PrPC Proteins/physiology; Prion Diseases/diagnosis; Prion Diseases/genetics*; Prion Diseases/metabolism*; Protein Structure, Secondary/genetics;

ISSN/eISSN

0270-6474 -

WoS ID

WOS:000295363800016