Disease: Orotidylic decarboxylase deficiency
- A reporter gene construct for studying the regulation of manganese peroxidase gene expression
- Altered erythrocyte pyrimidine activity in vitamin B12 or folate deficiency
- Hereditary Orotic Aciduria and the Excretion of Orotidine
- Hereditary orotic aciduria: results of a screening survey
- Hereditary orotic aciduria. II. A urinary screening test
- Hypoxanthine-guanine phosphoribosyltransferase. Characterization of a mutant in a patient with gout
- Identification of a small genetic region that encodes orotate phosphoribosylatransferase and orotidylate decarboxylase in Droxophila melanogaster
- Inhibition of orotidylate decarboxylase by 4(5H)-oxo-1-beta-D-ribofuranosylpyrazolo[3,4-d] pyrimidine-3-thiocarboxamide (APR-TC) in B lymphoblasts. Activation by adenosine kinase
- Isolated Orotic Aciduria in an 11-Year-Old Boy
- Isolation and transformation of uracil auxotrophs of the lignin-degrading basidiomycete Phanerochaete chrysosporium
- Orotic aciduria and uridine monophosphate synthase: a reappraisal
- Regulation of orotidylic acid pyrophosphorylase in Saccharomyces cerevisiae
- Studies on the coordinate activity and liability of orotidylate phosphoribosyltransferase and decarboxylase in human erythrocytes, and the effects of allopurinol administration
- Subunit structure of the orotate phosphoribosyltransferase--orotidylate decarboxylase complex from human erythrocytes
- UMP synthase activity expressed in deficient hamster cells by separate transferase and decarboxylase proteins or by linker-deleted bifunctional protein