These in vitro observations not only provide an initial basis for in vivo treatment regimens focusing on the stimulation of endogenous hepatic glutathione levels, but could also contribute to an optimization of treatment intervals to limit the risk of adverse effects when NFT is administered as an antibiotic
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All relevant evidence remains at the preclinical stage, including studies based on in vitro cell lines, patient-derived organoids, and mouse xenograft models
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Il2rgc / (FRG) mice, facilitating the investigation of tumor-promoting gene-environment interactions pertinent to metabolic liver diseases
