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Importantly, results also demonstrated that the enhancement effect of LASSS on the c-met binding-affinity of HGF is consistently maintained, even after the removal of un-reacted free LASSS (and any degradation products of LASSS), by an interaction between HGF and LASSS or potentially by specific chemical modification of HGF at a high molar ratio of 1:8000 to HGF (over 1:4000)

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2) (30), indicating that BRD4 is likely to activate SLC7A11 transcription through epigenetic mechanisms