Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Influence of βS allele in the lipid peroxidation and antioxidant capacity parameters.

International journal of laboratory hematology - 1 Apr 2014

Shimauti E L T, Belini Junior E, Baracioli L M da S V, Souza E M de, Granzotto D, Almeida E A de, Silva D G H, Ricci Junior O, Bonini-Domingos C R

Abstract excerpt

INTRODUCTION: The oxidative process plays a fundamental role in the pathophysiology of sickle cell anemia (SCA), and population and environmental characteristics may influence redox balance. The aim of this study was to evaluate lipid peroxidation and antioxidant capacity in Brazilian Hb S carriers undergoing different therapies. METHODS: Blood samples from 270 individuals were analyzed (Hb SS, n = 68; Hb AS,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Oxidative Stress
Share to Anemia, Sickle Cell

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Antioxidants

Share to Blood Transfusion

Share to Brazil

Share to Erythrocyte Indices

Share to Hemoglobin, Sickle

Share to Lipid Peroxidation

Source

Identifiers

PMID: 24118969
DOI: 10.1111/ijlh.12154

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Influence of βS allele in the lipid peroxidation and antioxidant capacity parameters.PMID 24118969Read ↗

Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia.Semantic proximity Read ↗

Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients.Semantic proximity Read ↗

The influence of hydroxyurea on oxidative stress in sickle cell anemiaSemantic proximity Read ↗

Relationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemia.Semantic proximity Read ↗

Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate RelationshipSemantic proximity Read ↗

Sickle Cell Disease: Role of Oxidative Stress and Antioxidant TherapySemantic proximity Read ↗

Impact of genetic polymorphisms in key enzymes of homocysteine metabolism on the pathophysiology of sickle cell anemia.Semantic proximity Read ↗

Oxidative stress status, clinical outcome, and β‐globin gene cluster haplotypes in pediatric patients with sickle cell diseaseSemantic proximity Read ↗

Oxidative stress in β-thalassaemia and sickle cell diseaseSemantic proximity Read ↗

Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide.Semantic proximity Read ↗

Influence of human haptoglobin polymorphism on oxidative stress induced by free hemoglobin on red blood cells.Semantic proximity Read ↗

Resveratrol: Antioxidant activity and induction of fetal hemoglobin in erythroid cells from normal donors and β-thalassemia patientsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.