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Description
6A, Fig S6)
The demonstration that OEA is the most active endogenous ligand for GPR119 is of particular interest since previous work has demonstrated that OEA, when administered to laboratory animals, causes a significant reduction in food intake and body weight gain
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The peptides effects on VEGF expression, FAK-paxillin signalling, and nitric oxide pathways provide mechanistic rationale for its observed effects on tendon, muscle, gastric, and other tissues documented in peer-reviewed studies
