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Article

Characterization of a novel TPMT mutation associated with azathioprine-induced myelosuppression.

British journal of clinical pharmacology - 1 Nov 2009

de Beaumais Tiphaine Adam, Fakhoury May, Pigneur Benedicte, Viola Sheila, Medard Yves, Broly Franck, Jacqz-Aigrain Evelyne

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Topics

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Share to Antimetabolites
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Share to Inflammatory Bowel Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methyltransferases

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Share to Polymorphism, Genetic

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Source

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Identifiers

PMID: 19917002
DOI: 10.1111/j.1365-2125.2009.03439.x
PMCID: PMC2791984

Genes

TPMT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of a novel TPMT mutation associated with azathioprine-induced myelosuppression.PMID 19917002Read ↗

A novel TPMT missense mutation associated with TPMT deficiency in a 5-year-old boy with ALLSemantic proximity Read ↗

Thiopurine S-methyltransferase deficiency associated with a novel mutation.Semantic proximity Read ↗

TPMT*26 (208F-->L), a novel mutation detected in a Chinese.Semantic proximity Read ↗

Point-Counterpoint: TPMT Genotyping for Azathioprine in Adult Medicine.Semantic proximity Read ↗

Azathioprine-induced fatal myelosuppression in a renal-transplant recipient who carried heterozygous TPMT*1/*3C.Semantic proximity Read ↗

Identification of a novel thiopurine S-methyltransferase allele (TPMT*37).Semantic proximity Read ↗

Rare gene variants in a patient with azathioprine-induced lethal myelosuppression.Semantic proximity Read ↗

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance.Semantic proximity Read ↗

Thiopurine Drugs in the Treatment of Ulcerative Colitis: Identification of a Novel Deleterious Mutation in TPMT.Semantic proximity Read ↗

Severe azathioprine-induced myelotoxicity in a kidney transplant patient with thiopurine S-methyltransferase-deficient genotype (TPMT*3A/*3C).Semantic proximity Read ↗

Impact of TP53 mutations in acute myeloid leukemia patients treated with azacitidine.Semantic proximity Read ↗

Nomenclature for alleles of the thiopurine methyltransferase gene.Semantic proximity Read ↗

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