Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
about
Soft tissue and cellular preservation in vertebrate skeletal elements from the Cretaceous to the presentAged garlic extract therapy for sickle cell anemia patients.Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.Impaired vasodilation by red blood cells in sickle cell disease.Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytesFree heme and the polymerization of sickle cell hemoglobinDrug-loaded sickle cells programmed ex vivo for delayed hemolysis target hypoxic tumor microvessels and augment tumor drug delivery.Naturally occurring anti-band-3 antibodies and complement together mediate phagocytosis of oxidatively stressed human erythrocytes.microRNA miR-144 modulates oxidative stress tolerance and associates with anemia severity in sickle cell disease.Membrane protein lesions in erythrocytes with Heinz bodiesSickle cell disease in the Sudan. Clinical and biochemical aspects. Minireview based on a doctoral thesis.Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytesA posttranslational modification of beta-actin contributes to the slow dissociation of the spectrin-protein 4.1-actin complex of irreversibly sickled cells.Sickle cell disease and malariaErythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease.Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity.Endothelin-1 receptor antagonists regulate cell surface-associated protein disulfide isomerase in sickle cell disease.Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemiaSickle cell anemia with malaria: a rare case report.Pharmacologic interception of heme: a potential therapeutic strategy for the treatment of β thalassemia?Sickle cell membranes and oxidative damageIncreased oxidative stress alters nucleosides metabolite levels in sickle cell anemia.Oral L-glutamine therapy for sickle cell anemia: I. Subjective clinical improvement and favorable change in red cell NAD redox potential.Zinc and antioxidant vitamin deficiency in patients with severe sickle cell anemia.
P2860
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P2860
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
description
1985 nî lūn-bûn
@nan
1985 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@ast
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@en
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@nl
type
label
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@ast
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@en
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@nl
prefLabel
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@ast
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@en
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@nl
P2093
P2860
P356
P1476
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
@en
P2093
P2860
P304
P356
10.1172/JCI111857
P407
P577
1985-05-01T00:00:00Z