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The latter result confirms the previous study on the ScGrx1-catalyzed oxidation of rxYFP, although the removal of the second active-site cysteinyl residue had opposite effects on the reactivity of PfGrx and ScGrx1 (Table 1) 31

The rationale is that glucagon also increases energy expenditure and promotes hepatic fat mobilization, so a molecule that combines glucagons metabolic-rate effect with GLP-1/GIPs appetite-and-glucose control can, in principle, drive weight loss from both sides of the energy-balance equation at once

Cryptococcus neoformans also employs an enzymatic defense against NO produced by the host

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