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Our group demonstrated the efficacy of a highly specific small molecular inhibitor (PHA665752) in the treatment of medulloblastoma cell lines by reducing cell proliferation, migration and anchorage-independent growth (Kongkham et al

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(2016) described BPC-157 in the context of the brain-gut axis (gut-brain axis) with the NO pathway (nitric oxide) regulation of vascular flow complementary to angiogenesis