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Article

Assignment of the Human Dihydropyrimidine Dehydrogenase Gene (DPYD) to Chromosome Region 1p22 by Fluorescence in Situ Hybridization

1 Dec 1994

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7713523
DOI: 10.1006/geno.1994.1680

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Assignment of the Human Dihydropyrimidine Dehydrogenase Gene (DPYD) to Chromosome Region 1p22 by Fluorescence in Situ HybridizationPMID 7713523Read ↗

Characterization of the human dihydropyrimidine dehydrogenase gene.Semantic proximity Read ↗

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Regional mapping of the gene encoding dihydroorotate dehydrogenase, an enzyme involved in UMP synthesis, electron transport, and superoxide generation, to human chromosome region 16q22Semantic proximity Read ↗

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1→q11.2Semantic proximity Read ↗

Lack of large intragenic rearrangements in dihydropyrimidine dehydrogenase (DPYD) gene in fluoropyrimidine-treated patients with high-grade toxicity.Semantic proximity Read ↗

Molecular Cloning and Characterization of the Human Xanthine Dehydrogenase Gene (XDH)Semantic proximity Read ↗

A comparative analysis of translated dihydropyrimidine dehydrogenase cDNA; conservation of functional domains and relevance to genetic polymorphismsSemantic proximity Read ↗

Reassignment of pEFD70.3 (D18S23) to human chromosome band 21q22.2 (D21S412) by physical mapping.Semantic proximity Read ↗

Identification of three novel mutations in the dihydropyrimidine dehydrogenase gene associated with altered pre-mRNA splicing or protein function.Semantic proximity Read ↗

Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase GeneSemantic proximity Read ↗

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