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The limited results indicated no measurable adverse acute effects on hepatic, renal, cardiac, or thyroid biomarkers, suggesting basic short-term tolerability

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The data presented here suggest that Nle1-AngIV and Dihexa increase miniature synaptic activity by increasing dendritic spine densities and altering the morphological phenotype of postsynaptic spines in-vitro and may represent the mechanism that underlies facilitated learning observed AngIV analogues (Wright, Stubley et al