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10.1093/nar/gkab951 Summary Keywords glutathione synthetase deficiency, 5-oxoprolinuria, glutathione synthetase gene variation, newborn, inherited metabolic disease, case report Citation Wu X, Jiao J, Xia Y, Yan X, Liu Z, Cao Y and Ma L (2023) Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation

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The cyanoenone class of Nrf2 activators has also been shown to be targeting Cys151 in KEAP1, irrespective of their molecular size [308]

[DOI] [PubMed] [Google Scholar] 30.Dimant E, Landsberg E, London IM

At Weeks 4, 8, 12 and 16, cheilitis, xerosis, and dryness of eyes and nose were less frequent in patients who received the concomitant omega-3 supplement, compared to those who received tretinoin alone

4361 71.10.1093/emboj/18.16.4361 Guertl B, Noehammer C, Hoefler G (2000) Metabolic cardiomyopathies Int J Exp Pathol, 81(6): p