Varaico: Literature-Extracted Genetic Variants

Gene:TPMT
Variant:p.V18I
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TPMT

NM_000367.5:p.V18I

Associated Papers

Comparative assessment of anti-cancer drugs against NUDT15 variants to prevent leucopenia side effect in leukemia patients.

V J et al.

Journal, Genetic Engineering & Biotechnology, 2023

ABCC4, ITPA, NUDT15, TPMT and their interaction as genetic predictors of 6-mercaptopurine intolerance in chinese patients with acute lymphoblastic leukemia.

Fan POL et al.

Pediatric Hematology and Oncology, 2022

Pharmacogenetics of Drugs Used in the Treatment of Cancers.

Franczyk B et al.

Genes, 2022

NUDT15 polymorphism in healthy children with Bai nationality in Yunnan of China.

Pu G et al.

Pediatrics International : Official Journal of the Japan Pediatric Society, 2021

Genome wide association studies for treatment-related adverse effects of pediatric acute lymphoblastic leukemia.

Franca R et al.

Wires Mechanisms of Disease, 2021

NUDT15 gene variants and thiopurine-induced leukopenia in patients with inflammatory bowel disease.

Matsuoka K

Intestinal Research, 2020

High-resolution melt analysis enables simple genotyping of complicated polymorphisms of codon 18 rendering the NUDT15 diplotype.

Kakuta Y et al.

Journal of Gastroenterology, 2020

[Significance of NUDT15 gene in individualized treatment with 6-mercaptopurine in children with acute lymphoblastic leukemia].

He J et al.

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics, 2019

Association between the c.415C > T, c.52G > A, and 36_37insGGAGTC polymorphisms of NUDT 15 and thiopurine-induced leukopenia, thiopurine intolerance, and severe hair loss: an updated meta-analysis.

Wang R et al.

Drug Design, Development and Therapy, 2019

NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.

Kakuta Y et al.

Journal of Gastroenterology, 2018

29923122 (PubMed )
Supplement: 535_2018_1486_MOESM1_ESM.pdf

SMAD4 and NF1 mutations as potential biomarkers for poor prognosis to cetuximab-based therapy in Chinese metastatic colorectal cancer patients.

Mei Z et al.

Bmc Cancer, 2018

29703253 (PubMed )
Supplement: 12885_2018_4298_MOESM2_ESM.xlsx › Sheet1

Pharmacogenetics of thiopurines for inflammatory bowel disease in East Asia: prospects for clinical application of NUDT15 genotyping.

Kakuta Y et al.

Journal of Gastroenterology, 2018

Influence of NUDT15 variants on hematological pictures of patients with inflammatory bowel disease treated with thiopurines.

Kojima Y et al.

World Journal of Gastroenterology, 2018

Predictive role of NUDT15 variants on thiopurine-induced myelotoxicity in Asian inflammatory bowel disease patients.

Sutiman N et al.

Pharmacogenomics, 2018

Emerging role of NUDT15 polymorphisms in 6-mercaptopurine metabolism and dose related toxicity in acute lymphoblastic leukaemia.

Singh M et al.

Leukemia Research, 2017

Pharmacogenetic Predictors of Treatment-Related Toxicity Among Children With Acute Lymphoblastic Leukemia.

Maxwell RR et al.

Current Hematologic Malignancy Reports, 2017

Nucleoside diphosphate-linked moiety X-type motif 15 C415T variant as a predictor for thiopurine-induced toxicity in Indian patients.

Shah SA et al.

Journal of Gastroenterology and Hepatology, 2017

Analysis of Thiopurine S-Methyltransferase Deficient Alleles in Acute Lymphoblastic Leukemia Patients in Mexican Patients.

Jiménez-Morales S et al.

Archives of Medical Research, 2016

Genetic polymorphisms of CYP2B6 affect the pharmacokinetics/pharmacodynamics of cyclophosphamide in Japanese cancer patients.

Nakajima M et al.

Pharmacogenetics and Genomics, 2007

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."