Characterization of the Human Dihydropyrimidine Dehydrogenase Gene

This publication has 29 references indexed in Scilit:

• Partial epilepsy in a girl with a symptom-free sister: First two Finnish patients with dihydropyrimidine dehydrogenase deficiency
  Journal of Inherited Metabolic Disease, 1997
• Lack of correlation between phenotype and genotype for the polymorphically expressed dihydropyrimidine dehydrogenase in a family of Pakistani origin
  Pharmacogenetics, 1997
• An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis
  Pharmacogenetics, 1995
• Diagnostic analysis, clinical importance and molecular basis of dihydropyrimidine dehydrogenase deficiency
  Trends in Pharmacological Sciences, 1995
• Human Polymorphism in Drug Metabolism: Mutation in the Dihydropyrimidine Dehydrogenase Gene Results in Exon Skipping and Thymine Uracilurea
  DNA and Cell Biology, 1995
• Dihydropyrimidine dehydrogenase activity and fluorouracil chemotherapy.
  Journal of Clinical Oncology, 1994
• Deaths bring clinical trials under scrutiny in Japan
  Nature, 1994
• Severe 5-fluorouracil toxicity secondary to dihydropyrimidine dehydrogenase deficiency. A potentially more common pharmacogenetic syndrome
  Cancer, 1991
• Isolation of Single-Copy Human Genes from a Library of Yeast Artificial Chromosome Clones
  Science, 1989
• Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1984