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(1998, Eur J Endocrinol) as a GHS-R1a agonist with GH-release potency comparable to GHRP-6 but without the ACTH, cortisol or prolactin elevation that limits other secretagogues

To monitor the oxidation of roGFP2 WT by the intramolecular disulfide of PfGrx C88S , 1 M reduced roGFP2 WT was mixed with 2 M diamide-oxidized PfGrx C88S at room temperature

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CJC-1295, animal model Alba et al., 2006 (Endocrinology): once-daily CJC-1295 normalized growth in a GHRH-knockout mouse, supporting the GHRH-receptor mechanism

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