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Geneva: WHO

The first part of the study began by randomly dividing the test subjects in four groups including: wild type, APP/PS1, APP/PS1 + Dihexa administered at a dose of 1.44 mg/kg, and APP/PS1 + Dihexa administered at a dose of 2.88 mg/kg [1]

10 l of 150S fractions, derived from both BSO-treated and untreated infections, were titered by plaque assay (Materials and Methods)