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GPR35 agonists (YE120, zaprinast, and pamoic acid) promoted wound maintenance in the focus-dependent manner independently of cell proliferation, While a certain GPR35 antagonist CID2745687, forskolin, and pertussis toxin reversed the YE120-induced outcome. YE120 increased the mRNA expression of fibronectin and its receptor integrin αfive, and ERK1

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