Varaico: Literature-Extracted Genetic Variants

Gene:GSTA2
Variant:p.S112T
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GSTA2

NM_000846.5:p.S112T

Associated Papers

Single-Nucleotide Polymorphisms Associated with Mercury Levels and Neurological Symptoms: An Overview.

Perini JA et al.

Toxics, 2024

38535959 (PubMed )
Supplement: toxics-12-00226-s001.zip › toxics-2905208-supplementary.pdf

Population pharmacokinetic analysis of intravenous busulfan: GSTA1 genotype is not a predictive factor of initial dose in Chinese adult patients undergoing hematopoietic stem cell transplantation.

Sun Y et al.

Cancer Chemotherapy and Pharmacology, 2020

An exploratory study by DMET array identifies a germline signature associated with imatinib response in gastrointestinal stromal tumor.

Ravegnini G et al.

The Pharmacogenomics Journal, 2019

Use of Germline Genetic Variability for Prediction of Chemoresistance and Prognosis of Breast Cancer Patients.

Hlavac V et al.

Cancers, 2018

The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine.

Broekman MMTJ et al.

The Pharmacogenomics Journal, 2018

Candidate Gene Association Studies of Anthracycline-induced Cardiotoxicity: A Systematic Review and Meta-analysis.

Leong SL et al.

Scientific Reports, 2017

28232737 (PubMed )
Supplement: 41598_2017_75_MOESM1_ESM.pdf

The Association between Gene-Environment Interactions and Diseases Involving the Human GST Superfamily with SNP Variants.

Hollman AL et al.

International Journal of Environmental Research and Public Health, 2016

Role of Pharmacogenetics in Hematopoietic Stem Cell Transplantation Outcome in Children.

Franca R et al.

International Journal of Molecular Sciences, 2015

The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.

Tang X et al.

Nucleic Acids Research, 2014

25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Y-01A.domain

Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq data.

Reimann E et al.

Human Genomics, 2014

25496518 (PubMed )
Supplement: 40246_2014_20_MOESM1_ESM.xlsx › Sheet1

Glutathione transferase-A2 S112T polymorphism predicts survival, transplant-related mortality, busulfan and bilirubin blood levels after allogeneic stem cell transplantation.

Bonifazi F et al.

Haematologica, 2014

Induction of sister chromatid exchange by acrylamide and glycidamide in human lymphocytes: role of polymorphisms in detoxification and DNA-repair genes in the genotoxicity of glycidamide.

Pingarilho M et al.

Mutation Research, 2013

Genetic polymorphisms in detoxification and DNA repair genes and susceptibility to glycidamide-induced DNA damage.

Pingarilho M et al.

Journal of Toxicology and Environmental Health. Part A, 2012

Differences among allelic variants of human glutathione transferase A2-2 in the activation of azathioprine.

Zhang W et al.

Chemico-biological Interactions, 2010

The role of GSTA2 polymorphisms and haplotypes in breast cancer susceptibility: a case-control study in the Portuguese population.

Silva SN et al.

Oncology Reports, 2009

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.

Harris SE et al.

Bmc Genetics, 2007

17601350 (PubMed )
Supplement: 1471-2156-8-43-S1.doc

Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.

Gemignani F et al.

Carcinogenesis, 2007

The relationship between the pharmacology of antiepileptic drugs and human gene variation: an overview.

Ferraro TN et al.

Epilepsy & Behavior : E&b, 2005

Human alpha class glutathione S-transferases: genetic polymorphism, expression, and susceptibility to disease.

Coles BF et al.

Methods in Enzymology, 2005

Human glutathione S-transferase A2 polymorphisms: variant expression, distribution in prostate cancer cases/controls and a novel form.

Ning B et al.

Pharmacogenetics, 2004

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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."