Pitfalls in the determination of mutant alleles of the thiopurine methyltransferase gene
- 1 November 2001
- journal article
- Published by Springer Nature in Leukemia
- Vol. 15 (11) , 1792-1793
- https://doi.org/10.1038/sj.leu.2402285
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Genotyping of Eight Thiopurine Methyltransferase Mutations: Three-Color Multiplexing, “Two-Color/Shared” Anchor, and Fluorescence-quenching Hybridization Probe Assays Based on Thermodynamic Nearest-Neighbor Probe DesignClinical Chemistry, 2000
- Allelic variants of the thiopurine s-methyltranferase deficiency in patients with ulcerative colitis and in healthy controlsAmerican Journal of Gastroenterology, 2000
- Thiopurine methyltransferase polymorphic tandem repeat: Genotype-phenotype correlation analysisClinical Pharmacology & Therapeutics, 2000
- Screening for azathioprine toxicity: A pharmacoeconomic analysis based on a target caseJournal of the American Academy of Dermatology, 2000
- Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemiaLeukemia, 2000
- Human thiopurine methyltransferase pharmacogenetics: Gene sequence polymorphisms*Clinical Pharmacology & Therapeutics, 1997
- Enhanced proteolysis of thiopurine S -methyltransferase (TPMT) encoded by mutant alleles in humans ( TPMT ∗ 3 A , TPMT ∗ 2 ): Mechanisms for the genetic polymorphism of TPMT activityProceedings of the National Academy of Sciences, 1997
- Molecular Diagnosis of Thiopurine S-Methyltransferase Deficiency: Genetic Basis for Azathioprine and Mercaptopurine IntoleranceAnnals of Internal Medicine, 1997