(Q80068795)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

Rapid detection of the DPYD IVS14+1G>A mutation for screening patients to prevent fluorouracil-related toxicity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

6

Jos H Beijnen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

3

Jan H M Schellens

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

author name string

Tessa M Bosch

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Remko Bakker

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Annemieke Cats

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Paul H M Smits

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

publication date

1 January 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

Molecular Diagnosis and Therapy

28 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

volume

11

1 reference

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28 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

page(s)

105-108

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17397246%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf03256229

28 December 2019

exact match

0 references

cites work

Human polymorphism in drug metabolism: mutation in the dihydropyrimidine dehydrogenase gene results in exon skipping and thymine uracilurea.

1 reference

12 December 2020

Clinical pharmacology of 5-fluorouracil

1 reference

12 December 2020

Pharmacogenetic screening for polymorphisms in drug-metabolizing enzymes and drug transporters in a Dutch population

1 reference

12 December 2020

Population study of dihydropyrimidine dehydrogenase in cancer patients

1 reference

12 December 2020

Prevalence of a common point mutation in the dihydropyrimidine dehydrogenase (DPD) gene within the 5'-splice donor site of intron 14 in patients with severe 5-fluorouracil (5-FU)- related toxicity compared with controls.

1 reference

12 December 2020

Dihydropyrimidine dehydrogenase and the efficacy and toxicity of 5-fluorouracil

1 reference

12 December 2020

Implications of dihydropyrimidine dehydrogenase on 5-fluorouracil pharmacogenetics and pharmacogenomics.

1 reference

12 December 2020

Characterization of the human dihydropyrimidine dehydrogenase gene

1 reference

12 December 2020

Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: frequency of the common IVS14+1G>A mutation causing DPD deficiency.

1 reference

12 December 2020

High prevalence of the IVS14 + 1G>A mutation in the dihydropyrimidine dehydrogenase gene of patients with severe 5-fluorouracil-associated toxicity

1 reference

12 December 2020

Application of pharmacogenomics in the individualization of chemotherapy for gastrointestinal malignancies

1 reference

12 December 2020

Metabolism of pyrimidine analogues and their nucleosides

1 reference

12 December 2020

Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency

1 reference

12 December 2020