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The thiol group of C32 in PfGrx therefore facilitates the C29-dependent deglutathionylation of roGFP2(SSG) without forming an intramolecular disulfide bond

Both methods bypass the digestive system, providing superior absorption compared to oral supplements

The findings stimulate further studies in large biobank samples to clarify whether such signatures could prove valuable for detecting pathology or follow-up of treatment effect in clinical trials

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