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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

Compounds that selectively inhibit specific NOX isoforms, such as S17834 or GKT137831, may be particularly effective

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