Increased Prevalence of GSTM<sub>1</sub> Null Genotype in Patients with Myelodysplastic Syndrome: A Case-Control Study-Reference-Cited by-同舟云学术

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Increased Prevalence of GSTM₁ Null Genotype in Patients with Myelodysplastic Syndrome: A Case-Control Study

Published:2000 Issue:4 Volume:104 Page:169-173
ISSN:0001-5792
Container-title:Acta Haematologica
language:en
Short-container-title:Acta Haematol

Author:

Tsabouri S.E.,Georgiou I.,Alamanos I.,Bourantas K.L.

Publisher

S. Karger AG

Subject

Hematology,General Medicine

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypermethylation of GSTM5 and its effect on oxidation in myelodysplastic syndrome;iLABMED;2024-06

2. Investigation of DNA repair gene variants on myelodysplastic syndromes in a Turkish population;Medical Oncology;2014-08-26

3. Association between glutathione S-transferase T1 null genotype and risk of myelodysplastic syndromes: a comprehensive meta-analysis;Tumor Biology;2013-05-22

4. Detoxification and DNA repair genes polymorphisms and susceptibility of primary myelodysplastic syndromes in Chinese population;Leukemia Research;2011-06

5. Susceptibility Susceptibility to MDS: DNA Repai DNA repair r and Detoxification Detoxification Genes;The Myelodysplastic Syndromes;2011

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