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was regarded as ideal HO-1 expression promoter, which has better efficacy than sulfasalazine drugs for preventing UC recurrence (Han et al., 2017)

10.7759/cureus.23009 Cureus

Therefore, we chose to use the medial malleolus as our designated placement site

The first reported GPX4 inhibitor RSL3 covalently interacts with selenocysteine, the active site of GPX4, to inhibit enzymatic activity of GPX4, thus inducing ferroptosis

Similarly, whilst data was initially collected on antenatal and household smoking, overall rates in the preterm-born cohort were low suggesting high recall bias, and therefore were not included in our analyses