GSTT1 (rs4025935) null genotype is associated with increased risk of sickle cell disease in the populations of Tabuk—Northwestern region of Saudi Arabia

F Abu-Duhier, R Mir - Hematology, 2017 - Taylor & Francis
Background: Glutathione system plays an important role in the protection of cells and tissue
against damage from oxidative stress. Impairment of the glutathione system due to genetic …

[PDF][PDF] GSTM1 and GSTT1 polymorphism in Egyptian sickle cell anemia patients.

MA Rabab, MH Bothina - UHOD: International Journal of Hematology & …, 2013 - uhod.org
Glutathione S-transferase gene deletions are known detoxification agents and cause
oxidative damage. In different studies, variations in null allele frequency have been …

Relation between glutathione S-transferase genes (GSTM1, GSTT1, and GSTP1) polymorphisms and clinical manifestations of sickle cell disease in Egyptian patients

HN Ellithy, S Yousri, GH Shahin - Hematology, 2015 - Taylor & Francis
Objectives Clinical manifestations of sickle cell disease (SCD) result from sickling of Hb S
due to oxidation, which is augmented by accumulation of oxygen-free radicals. Deficiencies …

Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease

HF Shiba, MK El-Ghamrawy… - Pediatric and …, 2014 - journals.sagepub.com
Sickle cell disease (SCD) complications are associated with oxidative stress. Glutathione S-
transferases (GSTs) are a group of enzymes that protect against oxidative stress. The aims …

[PDF][PDF] Prevalence of Glutathione S Transferase (GSTM1, GSTP1 and GSTT1) Genes Polymorphisms among Pediatric Sudanese Patients with Sickle Cell Anemia

NT Ali, OYM Ahmed, FO Mohammed… - J Blood Disord …, 2020 - academia.edu
Background: Sickle cell disease (SCD) is taken into account as one of the foremost types of
anemia in Sudan, particulary in the western part of the country. The glutathione system plays …

Association between the genetic polymorphisms of glutathione S-transferase (GSTM1 and GSTT1) and the clinical manifestations in sickle cell anemia

RA de Oliveira Filho, GJ Silva… - Blood Cells, Molecules …, 2013 - Elsevier
The hereditary deficiency of antioxidant enzymes when associated with sickle cell anemia
(SCA) further contributes to the oxidation of hemoglobin S, which increases the formation of …

A positive correlation between mutated gene of sickle cell anemia and glucose-6-phosphate dehydrogenase among gond tribes of Chhattisgarh, India

E Singh, LR Shivwanshi, A Kumar - Mutation Research/Fundamental and …, 2024 - Elsevier
Abstract Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most
common enzymopathy affecting millions of individuals worldwide. It is believed that the …

A positive correlation between sickle cell anemia and g6pd deficiency from population of Chhattisgarh, India

LR Shivwanshi, E Singh, A Kumar - Gene, 2019 - Elsevier
Objective Present study was undertaken to study the association between sickle cell anemia
(SCA) and glucose-6-phosphate dehydrogenase (G6PD) deficiency from Sahu and Kurmi …

A cross‐sectional clinic‐based study exploring whether variants within the glutathione S‐transferase, haptoglobin and uridine 5′‐diphospho …

S Howell, K Marshall, M Reid… - European Journal of …, 2018 - Wiley Online Library
Objectives To explore putative associations between specific variants in either the
glutathione S‐transferase (GST), haptoglobin (HP) or uridine 5′‐diphospho …

Influence of genetic polymorphisms of glutathione S-transferase T1 (GSTT1) and M1 (GSTM1) on hematological parameters

I Saadat, M Saadat - Molecular biology reports, 2010 - Springer
To find the influence of genetic polymorphisms of glutathione S-transferases M1 (GSTM1)
and T1 (GSTT1) on hematological parameters in smoker and non-smoker subjects, the …