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Dickinson DA, Levonen AL, Moellering DR, Arnold EK, Zhang H, Darley-Usmar VM, Forman HJ: Human glutamate cysteine ligase gene regulation through the electrophile response element
Homozygous loss-of-function mutations in the SLC2A9 (encoding the transporter protein GLUT9) and SLC22A12 (encoding the transporter protein URAT1) genes lead to hereditary renal hypouricemia type 1 and 2, respectively [21]
However, HMOX1 plays a dual role in ferroptosis
L.et al (2009)
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Czupryna J
