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In addition, the damaged distal colonic histology (Figure 2C) and the increased mRNA expression of proinflammatory cytokines in the distal colonic tissues, associated with DSS (Figure 2D), were significantly reduced with VIP treatment
Iron quantification by inductively coupled plasmatriple quadrupole mass spectrometer SK-MEL-103 and IMR90 cells were cultured in 15-cm dishes, and senescence was induced for 6 days with etoposide and tozasertib (SK-MEL-103) or etoposide (IMR90) treatment (density and drug concentration are indicated in Supplementary Table 8)
In: SinghSKGulatiMMutalikSDhanasekaranMDuaK, editors
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