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Besides their enzymatic activity, cytosolic GSTs (such as class Alpha) exhibit an ability to bind various hydrophobic ligands (xenobiotics as well as hormones) and thus contribute to their intracellular transport and disposition

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Alanine mutations of E124 3.33 and R283 6.55 nearly abolished the binding of ghrelin-A2 and the ghrelin-induced receptor activity, indicating the critical role of the salt bridge in maintaining the integrity of the bifurcated binding pockets, and thus affecting ghrelin binding and receptor activation (Supplementary Figs

These are the patients for whom GH secretagogue therapy most reliably addresses the physiological gap between training intention and training outcome

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