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Keywords: Duchenne muscular dystrophy, protandim , mdx mice, dystrophin, dystrophic muscle, paraoxonase, osteopontin, oxidative stress INTRODUCTION Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder that occurs in 1 in 3,500 live male births and is the most common fatal genetic disorder in children (Emery, 1991)

When a compound is not in the database, however, it cannot be identified by this approach

The epigenetic regulation of the expression of GPx1 is therefore a function of the methylation of its coding gene [32]