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Thus, the drug resistance capabilities of MRP8 resemble those of MRP4 and MRP5, which it topologically resembles, in that the latter pumps also confer resistance to nucleoside-based agents [2729]

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Combined hypothesis of migration synergy: If BPC-157 favors the transcriptional and signaling environment that enables migration and survival, while TB-500 favors actin-associated motility and the physical execution of movement, co-administration could increase both (1) the number of functional cells and (2) the efficiency with which they reach the injury site and organize the repair matrix

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