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However, the latter mechanism is not supported by our experimental findings for two reasons: first, only didepsipeptides and a multiple thereof were found by means of UPLC-TOF MS and not even traces of depsipeptide intermediates showing uneven numbers of monomers were detectable

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Integrin-associated FAK is selectively activated in BRAF V600E-mutated CRC cells in response to pharmacologic BRAF inhibition

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