Comparative proteomics of HepG2 cells reveals NGLY1 as an important regulator of ferroptosis resistance and iron uptake
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DOI: 10.1371/journal.pone.0328166
Abstract: NGLY1 deficiency is a rare genetic disorder caused by mutations in the NGLY1 gene. This disorder presents a wide range of clinical symptoms, and its severity varies among affected individuals. Previous studies have focused on… read more here.
Keywords: iron uptake; comparative proteomics; proteomics hepg2; ferroptosis ... See more keywords