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In vitro studies with human hepatocytes showed that phenytoin and phenobarbital inhibit acetaminophen glucuronidation, suggesting that other pathways of the drug metabolism, like oxidation to toxic NAPQI, may be potentiated [17,18]

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Anitens A class of small-molecule inhibitors that target the N-terminal domain of the androgen receptor (AR), currently being tested in the treatment for prostate cancer

Gap junction dysfunction reduces acetaminophen hepatotoxicity with impact on apoptotic signaling and connexin 43 protein induction in rat

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