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The researchers used a powerful molecule called bone morphogenetic protein 2 (BMP2) to initiate bone formation after microfracture, but then stopped the process midway with a molecule that blocked another signaling molecule important in bone formation, called vascular endothelial growth factor (VEGF)

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Researchers investigate DSIP in studies involving central nervous system signalling, hypothalamic function, circadian rhythm biology, neuroendocrine regulation, stress physiology, and peptide signalling pathways