References:
Gabizon R, Telling G, Meiner Z, Halimi M, Kahana I, Prusiner SB. Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease. Nat Med. 1996 Jan;2(1):59-64.
Friedman-Levi Y, Mizrahi M, Frid K, Binyamin O, Gabizon R (2013) PRP(St), a soluble, protease resistant and truncated PRP form features in the pathogenesis of a genetic prion disease. PloS one 8(7):e69583
Rosenmann H, Grigoriadis N, Eldar-Levy H, Avital A, Rozenstein L, Touloumi O, Behar L, Ben-Hur T, Avraham Y, Berry E (2008) A novel transgenic mouse expressing double mutant tau driven by its natural promoter exhibits tauopathy characteristics. Exp Neurol 212(1):71-84