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We aimed to research the consequence of an FGF21 analogue (LY2405319) from the development of atherosclerosis and its own associated parameters. ApoE-/- mice had been provided an atherogenic diet for 14 months and were randomly assigned to control (saline) or FGF21 (0.1 mg/kg) therapy group (n = 10/group) for 5 days. Plaque size in the aortic arch/valve areas and cardiovascular threat markers were evaluated in bloodstream and tissues. The effects of FGF21 on numerous ath
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