In addition, recent experiments have indicated that addition of arachidonic acid, the physiolog- ical substrate for PGS, produces only a minimal increase irn hydroquinone binding in human and rodent bone mar- row in vitro, whereas H202 produces highly significant increases in the amount of hydroquinone equivalents bound (D.
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Peroxidase-dependent metabolism of benzene's phenolic metabolites and its potential role in benzene toxicity and carcinogenicity.
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