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Related Blog: The Role of GCP in Ensuring Clinical Trial Integrity Importance of Adverse Event Reporting Adverse events (AEs) are unexpected or harmful effects experienced by participants during clinical trials

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The recent observations from rodent studies by Fu and colleagues (105) highlight the need to better understand the coordinated action of the gut-liver axis on alcohol detoxification and ingestive behavior in humans

doi: 10.1085/jgp.200910388 51 DuJ.XieJ.YueL

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