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5. Structural and mechanistic implications of incorporating naturally occurring aberrant mutations of human dihydropteridine reductase into a rat model. Varughese KI; Xuong NH; Whiteley JM Int J Pept Protein Res; 1994 Sep; 44(3):278-87. PubMed ID: 7822105 [TBL] [Abstract][Full Text] [Related]
6. Human dihydropteridine reductase: characterisation of a cDNA clone and its use in analysis of patients with dihydropteridine reductase deficiency. Dahl HH; Hutchison W; McAdam W; Wake S; Morgan FJ; Cotton RG Nucleic Acids Res; 1987 Mar; 15(5):1921-32. PubMed ID: 3031582 [TBL] [Abstract][Full Text] [Related]
7. Heterogeneity of the molecular defect in human dihydropteridine reductase deficiency. Firgaira FA; Choo KH; Cotton RG; Danks DM Biochem J; 1981 Sep; 198(3):677-82. PubMed ID: 7326033 [TBL] [Abstract][Full Text] [Related]
8. [Dihydropteridine reductase activity in leukocytes and cultured fibroblasts of health individuals and of patients with the classical form of phenylketonuria]. Gromov PS; Val'iano NM; Akhunov VS; Annenkov GA Vopr Med Khim; 1983; 29(5):66-9. PubMed ID: 6649535 [TBL] [Abstract][Full Text] [Related]
9. Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiency. Howells DW; Forrest SM; Dahl HH; Cotton RG Am J Hum Genet; 1990 Aug; 47(2):279-85. PubMed ID: 2116088 [TBL] [Abstract][Full Text] [Related]
10. Role of aspartate-37 in determining cofactor specificity and binding in rat liver dihydropteridine reductase. Matthews DA; Varughese KI; Skinner M; Xuong NH; Hoch J; Trach K; Schneider M; Bray T; Whiteley JM Arch Biochem Biophys; 1991 Jun; 287(2):234-9. PubMed ID: 1898002 [TBL] [Abstract][Full Text] [Related]