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Additionally, the mortality rate in the peptide subjects appeared to significantly decrease, with a 2-fold decrease in the Thymalin subjects, a 1.8-fold decrease in the Epithalon subjects, and 2.5-fold decrease in the subjects presented with both peptides

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We have previously characterized the antagonistic properties of SSTR2a used for this study, which turned out to be less specific than first anticipated, i.e., antagonizing also SSTR1, SSTR3, and SSTR4 to a variable degree (17)

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