Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 130

1.

cDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria.

Yokota H, Fernandez-Salguero P, Furuya H, Lin K, McBride OW, Podschun B, Schnackerz KD, Gonzalez FJ.

J Biol Chem. 1994 Sep 16;269(37):23192-6.

2.

Porcine recombinant dihydropyrimidine dehydrogenase: comparison of the spectroscopic and catalytic properties of the wild-type and C671A mutant enzymes.

Rosenbaum K, Jahnke K, Curti B, Hagen WR, Schnackerz KD, Vanoni MA.

Biochemistry. 1998 Dec 15;37(50):17598-609.

PMID:
9860876
3.
4.

Lack of correlation between phenotype and genotype for the polymorphically expressed dihydropyrimidine dehydrogenase in a family of Pakistani origin.

Fernandez-Salguero PM, Sapone A, Wei X, Holt JR, Jones S, Idle JR, Gonzalez FJ.

Pharmacogenetics. 1997 Apr;7(2):161-3.

PMID:
9170156
5.

Characterization of the human dihydropyrimidine dehydrogenase gene.

Wei X, Elizondo G, Sapone A, McLeod HL, Raunio H, Fernandez-Salguero P, Gonzalez FJ.

Genomics. 1998 Aug 1;51(3):391-400.

PMID:
9721209
6.

Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria.

Au KM, Lai CK, Yuen YP, Shek CC, Lam CW, Chan AY.

Hong Kong Med J. 2003 Apr;9(2):130-2.

7.

Rapid detection of a common dihydropyrimidine dehydrogenase mutation associated with 5-fluorouracil toxicity and congenital thymine uraciluria using fluorogenic hybridization probes.

Nauck M, Gierens H, März W, Wieland H.

Clin Biochem. 2001 Mar;34(2):103-5. No abstract available. Erratum in: Clin Biochem 2002 Feb;35(1):85.

PMID:
11311218
8.

On the iron-sulfur clusters in the complex redox enzyme dihydropyrimidine dehydrogenase.

Hagen WR, Vanoni MA, Rosenbaum K, Schnackerz KD.

Eur J Biochem. 2000 Jun;267(12):3640-6.

9.

Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure.

van Kuilenburg AB, Dobritzsch D, Meinsma R, Haasjes J, Waterham HR, Nowaczyk MJ, Maropoulos GD, Hein G, Kalhoff H, Kirk JM, Baaske H, Aukett A, Duley JA, Ward KP, Lindqvist Y, van Gennip AH.

Biochem J. 2002 May 15;364(Pt 1):157-63.

10.

FRA1E common fragile site breaks map within a 370kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD).

Hormozian F, Schmitt JG, Sagulenko E, Schwab M, Savelyeva L.

Cancer Lett. 2007 Feb 8;246(1-2):82-91. Epub 2006 Mar 23.

PMID:
16556484
12.

Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism.

Berger R, Stoker-de Vries SA, Wadman SK, Duran M, Beemer FA, de Bree PK, Weits-Binnerts JJ, Penders TJ, van der Woude JK.

Clin Chim Acta. 1984 Aug 31;141(2-3):227-34.

PMID:
6488556
13.

Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism.

Wadman SK, Berger R, Duran M, de Bree PK, Stoker-de Vries SA, Beemer FA, Weits-Binnerts JJ, Penders TJ, van der Woude JK.

J Inherit Metab Dis. 1985;8 Suppl 2:113-4. No abstract available.

PMID:
3930854
14.

Dihydropyrimidine dehydrogenase (DPD) deficiency: identification and expression of missense mutations C29R, R886H and R235W.

Vreken P, Van Kuilenburg AB, Meinsma R, van Gennip AH.

Hum Genet. 1997 Dec;101(3):333-8.

PMID:
9439663
15.

Molecular basis of the human dihydropyrimidine dehydrogenase deficiency and 5-fluorouracil toxicity.

Wei X, McLeod HL, McMurrough J, Gonzalez FJ, Fernandez-Salguero P.

J Clin Invest. 1996 Aug 1;98(3):610-5.

16.

cDNA cloning of bovine liver dihydropyrimidine dehydrogenase.

Albin N, Johnson MR, Diasio RB.

DNA Seq. 1996;6(4):243-50.

PMID:
8912928
17.

Assignment of the human dihydropyrimidine dehydrogenase gene (DPYD) to chromosome region 1p22 by fluorescence in situ hybridization.

Takai S, Fernandez-Salguero P, Kimura S, Gonzalez FJ, Yamada K.

Genomics. 1994 Dec;24(3):613-4. No abstract available.

PMID:
7713523
18.
19.

Combined deficiencies of NADPH- and NADH-dependent dihydropyrimidine dehydrogenases, a new finding in a family with thymine-uraciluria.

van Gennip AH, van Lenthe H, Abeling NG, Bakker HD, van Kuilenburg AB.

J Inherit Metab Dis. 1995;18(2):185-8. No abstract available.

PMID:
7564242
20.

Dihydropyrimidine dehydrogenase deficiency presenting at birth.

Al-Sanna'a NA, Van Kuilenburg AB, Atrak TM, Abdul-Jabbar MA, Van Gennip AH.

J Inherit Metab Dis. 2005;28(5):793-6.

PMID:
16151913
Items per page

Supplemental Content

Write to the Help Desk