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Mechanistically, autoantibodies and interferon- present in the serum induce neutrophil ferroptosis through enhanced binding of the transcriptional repressor CREM to the glutathione peroxidase 4 ( Gpx4 , the key ferroptosis regulator) promoter, which leads to suppressed expression of Gpx4 and subsequent elevation of lipid-reactive oxygen species

Cerebrospinalfluid apolipo protein E, calcium and cerebral vasospasm after subarachnoid hemorrhage

Oxidative stress with an activation of the reninangiotensin system in human vascular endothelial cells as a novel mechanism of uric acid-induced endothelial dysfunction

Identification of the bladder dose and volume constraints to control late urinary toxicity after external beam radiotherapy for prostate cancer