• A lipotrope-dependent increase of histidase and urocanase in the livers of choline-deficient rats and in the Reuber H-35 transplanted hepatoma
• A liver urocanase deficiency
• Biochemical study of malnutrition. Part VI: Histidine and its metabolites
• Diagnosis of histidinemia through using the determination of urocanic acid in the sweat by an enzymatic method
• Disturbances in histidine metabolism in children with speech abnormalities
• Effect of the mouse mutants testicular feminization and sex reversal on hormone-mediated induction and repression of enzymes
• Effect of zinc deficiency on histidine metabolism in rats
• Folate deficiency and formiminoglutamic acid excretion during chronic diethylnitrosamine administration to rats
• Formation and operation of the histidine-degrading pathway in Pseudomonas aeruginosa
• Mutations in the urocanase gene UROC1 are associated with urocanic aciduria
• Proteomic and functional analyses reveal a unique lifestyle for Acinetobacter baumannii biofilms and a key role for histidine metabolism
• Quantification of the carbon flow through the folate-dependent one-carbon pool using radiolabeled histidine: effect of altered thyroid and folate status
• Significance of formiminoglutamic acid analysis in clinical tests
• Studies on the production and assessment of experimental histidinemia in the rat
• The effects of vitamin A deficiency on hepatic folate metabolism in rats
• Untargeted metabolomics identifies unique though benign biochemical changes in patients with pathogenic variants in <em>UROC1</em>
• Urocanic aciduria (urocanase deficiency)