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. 2017 Feb 8;12(2):e0171923. doi: 10.1371/journal.pone.0171923

Table 1. Genetically modified mice used in this study.

Line (abbreviation) Genetic modification Description of mice used Ref.
PrnpΔF (ΔF) Transgenic mice expressing a truncated PrPC (32–134) on a B6129-PrnpZrchI/ZrchI background Adult mice with signs of neurodegeneration [31]
B6-Tg/Thy1APP23Sdz (APP23) Transgenic mice overexpressing the human APP with the Swedish double mutation at 670/671 (KM→NL) 1.5 year-old mice with histologic evidence of astrogliosis, microgliosis and amyloid β plaque [32]
C57BL/6J-PrnpZH3/ZH3 (ZH3) Co-isogenic C57BL/6J mice lacking the cellular prion protein. Adult mice [18]