Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes
about
Oxidative stress in β-thalassaemia and sickle cell diseaseOxidative stress and β-thalassemic erythroid cells behind the molecular defectBlood antioxidant status and urinary levels of catecholamine metabolites in beta-thalassemiaLoss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemiaThe tumor suppressor cybL, a component of the respiratory chain, mediates apoptosis inductionThe role of alpha-hemoglobin stabilizing protein in redox chemistry, denaturation, and hemoglobin assembly.Association of Iron Overload with Oxidative Stress, Hepatic Damage and Dyslipidemia in Transfusion-Dependent β-Thalassemia/HbE Patients.Nutritional deficiencies in iron overloaded patients with hemoglobinopathiesBrain iron accumulation in unexplained fetal and infant death victims with smoker mothers--the possible involvement of maternal methemoglobinemia.Cytoprotective effects of the antioxidant phytochemical indicaxanthin in beta-thalassemia red blood cells.Protection against oxidative stress in beta thalassemia/hemoglobin E erythrocytes by inhibitors of glutathione efflux transporters.The regulation of erythropoiesis by selenium in mice.The utility of iron chelators in the management of inflammatory disorders.A transgenic mouse model expressing exclusively human hemoglobin E: indications of a mild oxidative stress.Insights into hemoglobin assembly through in vivo mutagenesis of α-hemoglobin stabilizing proteinHbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics.Oxidative stress and inflammation in iron-overloaded patients with beta-thalassaemia or sickle cell disease.Deterioration of red blood cell mechanical properties is reduced in anaerobic storageOxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemia.Cyst fluid hemoglobin species in endometriosis and its malignant transformation: The role of metallobiology.α-Hemoglobin-stabilizing protein (AHSP) perturbs the proximal heme pocket of oxy-α-hemoglobin and weakens the iron-oxygen bond.Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemiaBiopreservation of red blood cells--the struggle with hemoglobin oxidation.Berberine-induced haemolysis revisited: safety of Rhizoma coptidis and Cortex phellodendri in chronic haematological diseases.Effects of oxidants and antioxidants evaluated using parinaric acid as a sensitive probe for oxidative stress.Reduction of hydrogen peroxide-induced erythrocyte damage by Carica papaya leaf extract.Glucose homeostasis in Egyptian children and adolescents with β-Thalassemia major: Relationship to oxidative stress.Pharmacologic interception of heme: a potential therapeutic strategy for the treatment of β thalassemia?Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in beta-thalassemia intermedia patients.Lack of correlation between non-labile iron parameters, total carbonyl and malondialdehyde in major thalassemia.Oxidative status and malondialdehyde in beta-thalassaemia patients.Oxidative status and plasma lipid profile in β-thalassemia patients.Microfluidic analysis of cellular deformability of normal and oxidatively damaged red blood cells.Differential regulatory and compensatory responses in hematopoiesis/erythropoiesis in alpha- and beta-globin hemizygous mice.Phospholipid composition and organization in model beta-thalassemic erythrocytes.Structure of oxidized alpha-haemoglobin bound to AHSP reveals a protective mechanism for haem.Plasma homocysteine levels in patients with beta-thalassaemia major.Preliminary in vitro and ex vivo evaluation of afzelin, kaempferitrin and pterogynoside action over free radicals and reactive oxygen species.Influence of cow or goat milk consumption on antioxidant defence and lipid peroxidation during chronic iron repletion.Comparative study of hypocholesterolemic and hypolipidemic effects of conjugated linolenic acid isomers against induced biochemical perturbations and aberration in erythrocyte membrane fluidity.
P2860
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P2860
Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes
description
1993 nî lūn-bûn
@nan
1993 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@ast
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@en
type
label
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@ast
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@en
prefLabel
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@ast
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@en
P2093
P2860
P356
P1476
Effect of excess alpha-hemoglo ...... beta-thalassemic erythrocytes
@en
P2093
J J van den Berg
P Rouyer-Fessard
R P Hebbel
P2860
P304
P356
10.1172/JCI116380
P407
P577
1993-04-01T00:00:00Z