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Widening the therapeutic window for redox-targeting drugs Given that SCLC cells are unable to adapt to redox-targeting drugs, such as TXNRD1 inhibitors, we hypothesized that activating the NRF2 pathway would enhance antioxidant defenses specifically in non-cancerous cells, thereby further widening the therapeutic window

Dulude, D., Berchiche, Y

pylori might promote GC tumorigenesis by upregulating THAP9-AS1 levels ( 4.5 SNHG17 A microassay was carried out to examine the lncRNA profiles in H

Arch Biochem Biophys 640:4752 Asahi T, Wu X, Shimoda H, Hisaka S, Harada E, Kanno T, Nakamura Y, Kato Y, Osawa T (2016) A mushroom-derived amino acid, ergothioneine, is a potential inhibitor of inflammation-related DNA halogenation

J.TrostP.GuisezY.et al (2004)

However, a possible confounding factor is that ribose models tend to use a supraphysiological ribose concentration, which may induce an excessive AGE crosslinking profile