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Its recombinant formulation (serelaxin) was proven to decrease infarct size and give a wide berth to excessive scar formation in pet types of cardiac ischemia-reperfusion injury. B7-33, a synthetically designed peptide analogous to B-chain of relaxin-2, invokes signaling at relaxin family peptide receptor 1 (cognate receptor for relaxin-2) by preferentially phosphorylating the mitogen-activated protein kinase extracellular signal-regulated kinase 1/2. We desired to investigate the results of
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