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Nav Persaud, Canada Research Chair in Health Justice and a staff physician at St

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One is that the development of DPP-4 inhibition is a rational drug design based in scientific studies on pathophysiology of type 2 diabetes and that the development shows that it is important to target both the impaired insulin secretion and the high glucagon

M2 macrophage-derived exosomal miR-590-3p attenuates DSS-induced mucosal damage and promotes epithelial repair via the LATS1/YAP/ -catenin signalling axis

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This selective pathway modulation demonstrates context-dependent signaling intelligence, activating growth pathways while suppressing inflammatory cascades