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DPD Deficiency Foundation | Grafton MA
DPD Deficiency Foundation | Grafton MA

Population-scale predictions of DPD and TPMT phenotypes using a  quantitative pharmacogene-specific ensemble classifier | British Journal of  Cancer
Population-scale predictions of DPD and TPMT phenotypes using a quantitative pharmacogene-specific ensemble classifier | British Journal of Cancer

DPD Biomarker | Colorectal Cancer Alliance
DPD Biomarker | Colorectal Cancer Alliance

Issues and limitations of available biomarkers for fluoropyrimidine-based  chemotherapy toxicity, a narrative review of the literature - ESMO Open
Issues and limitations of available biomarkers for fluoropyrimidine-based chemotherapy toxicity, a narrative review of the literature - ESMO Open

JCM | Free Full-Text | In Vitro Assessment of Fluoropyrimidine-Metabolizing  Enzymes: Dihydropyrimidine Dehydrogenase, Dihydropyrimidinase, and  β-Ureidopropionase
JCM | Free Full-Text | In Vitro Assessment of Fluoropyrimidine-Metabolizing Enzymes: Dihydropyrimidine Dehydrogenase, Dihydropyrimidinase, and β-Ureidopropionase

Dihydrofluorouracil - an overview | ScienceDirect Topics
Dihydrofluorouracil - an overview | ScienceDirect Topics

DPD Gene Mutations (5-FU toxicity) detection test in Alwar
DPD Gene Mutations (5-FU toxicity) detection test in Alwar

TRUPCR® DPYD Mutation Detection Kit | TRUPCR Europe
TRUPCR® DPYD Mutation Detection Kit | TRUPCR Europe

The clinical relevance of multiple DPYD polymorphisms on patients candidate  for fluoropyrimidine based-chemotherapy. An Italian case-control study |  British Journal of Cancer
The clinical relevance of multiple DPYD polymorphisms on patients candidate for fluoropyrimidine based-chemotherapy. An Italian case-control study | British Journal of Cancer

Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single  Center during an 8-Year Period of Time - ScienceDirect
Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time - ScienceDirect

DPD-dependent inactivation of 5-FU and effects of DPD deficiency. For... |  Download Scientific Diagram
DPD-dependent inactivation of 5-FU and effects of DPD deficiency. For... | Download Scientific Diagram

DPYD*2A mutation: the most common mutation associated with DPD deficiency |  SpringerLink
DPYD*2A mutation: the most common mutation associated with DPD deficiency | SpringerLink

Dihydropyrimidine Dehydrogenase - an overview | ScienceDirect Topics
Dihydropyrimidine Dehydrogenase - an overview | ScienceDirect Topics

DPYD genotype-guided dose individualization to improve patient safety of  fluoropyrimidine therapy: call for a drug label update - Annals of Oncology
DPYD genotype-guided dose individualization to improve patient safety of fluoropyrimidine therapy: call for a drug label update - Annals of Oncology

Treating patients with dihydropyrimidine dehydrogenase (DPD) deficiency  with fluoropyrimidine chemotherapy since the onset of routine prospective  testing—The experience of a large oncology center in the United Kingdom -  ScienceDirect
Treating patients with dihydropyrimidine dehydrogenase (DPD) deficiency with fluoropyrimidine chemotherapy since the onset of routine prospective testing—The experience of a large oncology center in the United Kingdom - ScienceDirect

Cancers | Free Full-Text | Testing for Dihydropyrimidine Dehydrogenase  Deficiency to Individualize 5-Fluorouracil Therapy
Cancers | Free Full-Text | Testing for Dihydropyrimidine Dehydrogenase Deficiency to Individualize 5-Fluorouracil Therapy

Pharmaceutics | Free Full-Text | DPYD and Fluorouracil-Based Chemotherapy:  Mini Review and Case Report
Pharmaceutics | Free Full-Text | DPYD and Fluorouracil-Based Chemotherapy: Mini Review and Case Report

Localization of the point mutation sites in the DPD crystal structure |  Download Scientific Diagram
Localization of the point mutation sites in the DPD crystal structure | Download Scientific Diagram

Genome sequencing reveals a novel genetic mechanism underlying  dihydropyrimidine dehydrogenase deficiency: A novel missense variant  c.1700G>A and a large intragenic inversion in DPYD spanning intron 8 to  intron 12 - Kuilenburg -
Genome sequencing reveals a novel genetic mechanism underlying dihydropyrimidine dehydrogenase deficiency: A novel missense variant c.1700G>A and a large intragenic inversion in DPYD spanning intron 8 to intron 12 - Kuilenburg -

Dihydropyrimidine dehydrogenase gene as a major predictor of severe  5-fluorouracil toxicity | Pharmacogenomics
Dihydropyrimidine dehydrogenase gene as a major predictor of severe 5-fluorouracil toxicity | Pharmacogenomics

DPD Biomarker | Colorectal Cancer Alliance
DPD Biomarker | Colorectal Cancer Alliance

Dihydropyrimidine dehydrogenase deficiency: MedlinePlus Genetics
Dihydropyrimidine dehydrogenase deficiency: MedlinePlus Genetics

Regulation of human dihydropyrimidine dehydrogenase: implications in the  pharmacogenetics of 5-FU-based chemotherapy | Pharmacogenomics
Regulation of human dihydropyrimidine dehydrogenase: implications in the pharmacogenetics of 5-FU-based chemotherapy | Pharmacogenomics

Reduced 5-FU clearance in a patient with low DPD activity due to  heterozygosity for a mutant allele of the DPYD gene | British Journal of  Cancer
Reduced 5-FU clearance in a patient with low DPD activity due to heterozygosity for a mutant allele of the DPYD gene | British Journal of Cancer