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Organic Process Research & Development, 2015

Wilson Disease levels help separate Wilson disease Wilson disease Wilson disease (hepatolenticular degeneration) is an autosomal recessive disorder caused by various mutations in the ATP7B gene, which regulates copper transport within hepatocytes

Lancet, 1(8435): 965

Livingstone C, Davis J, Review

The role of H 2 O 2 in pathological processes in the thyroid gland Because iron is present in TPO and H 2 O 2 is required for the activity of TPO, under certain conditions the thyroid gland may be exposed to excessive amounts of either ferrous ion (Fe 2+ ) or H 2 O 2 , or both

Mulcahy, Regulation of gamma-glutamylcysteine synthetase subunit gene expression: Insights into transcriptional control of antioxidant defenses