Disease: Urocanase deficiency
- 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)