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In scientific studies of other receptor tyrosine kinases implicated within the oncogenesis of GIST, nilotinib realized strong and selective inhibition of PDGFRα and PDGFRβ. As is the case with imatinib, nilotinib potently inhibited the autophosphorylation of A31 cells reworked by PDGFRAnilotinib will improve the amount or effect of tucatinib by O