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Endothelial-leukocyte adhesive interactions in inflammatory diseases

The stomach contains powerful enzymes designed to break down proteins

The extent to which drugs cross the placenta is also modulated by the actions of placental phase I and II drug-metabolising enzymes, which are present at levels that fluctuate throughout gestation

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The results show that by disrupting metabolites and gut flora in mice, co-exposure to PS and BaP leads to ferroptosis in the kidneys