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G., Baker, C

This review focuses on the pharmacological landscape, encompassing single and dual agonist therapies targeting glucagon receptors (GcgRs), glucagon-like peptide-1 receptors (GLP-1Rs), glucose-dependent insulinotropic polypeptide receptors (GIPRs), amylin, triiodothyronine, fibroblast growth factor 21, and peptide tyrosine tyrosine

273 Moreover, GLP-1RAs could decelerate the progression of OA and mitigate pathological damage in a rat OA model

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A higher gauge number means a thinner needle (e.g., 31G is thinner than 29G)

Modeling the extracellular matrix in cell migration and morphogenesis: a guide for the curious biologist