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Used alone, it produces GH pulses, but without the additive GHRH signal, those pulses are smaller than the combination produces

Its primary pharmacological characterization was published in European Journal of Endocrinology (PMID 9849822), where the authors identified it as the first growth-hormone-secretagogue receptor (GHSR-1a) agonist achieving GH-release selectivity comparable to GHRH in animal models

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Radioprotection by glutathione ester: transport of glutathione ester into human lymphoid cells and fibroblasts

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