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This compound reduced the inflammatory response and oxidative stress caused by sleep deprivation through the inhibition of Toll-like receptor 4 (TLR4) and activation of the NRF2/HO-1 pathway (Wang et al

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IGF-1 LR3 and the IGFBP Regulatory System Structural analysis confirmed that among the series of N-terminal IGF-1 analogues tested, Long Arg3 IGF-1 demonstrated the greatest growth-promoting potential exceeding shorter analogues such as Arg3 IGF-1, Gly3 IGF-1, and Des(1-3) IGF-1 directly correlating with its superior IGFBP evasion profile