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In the present study, we have investigated, for the first time, the prevalence of three single nucleotide polymorphisms in GPx genes ( GPX1 rs1050450, GPX3 rs2070593 and GPX4 rs713041), and the association between these genetic polymorphisms and CS risk in patients with EH

Individuals carrying filaggrin gene mutations are not only at a higher risk of developing skin dryness on the trunk and extensor surfaces of the limbs in infants aged 36 months, but they also face an increased risk of developing eczema and AD (16)

Intracellular delivery of redox cycler-doxorubicin to the mitochondria of cancer cell by folate receptor targeted mitocancerotropic liposomes