Further, pathway-based functional prediction from the Kyoto Encyclopaedia of Genes and Genomes (KEGG) database revealed that steroid biosynthesis, sphingolipid metabolism and tryptophan metabolism were varied between the pre-dose faecal samples in the above-mentioned groups of mice
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[1] At the cellular level, the tendon work is genuinely mechanistic: in cultured rat tendon fibroblasts, BPC-157 accelerated cell outgrowth, improved survival under oxidative stress, and increased migration in a dose-dependent way, apparently through the FAKpaxillin pathway
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10.1016/j.redox.2022.102324 178 RenX.LiY.ZhouY.HuW.YangC.JingQ.et al (2021)