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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

http://www.wikidata.org/entity/Q33822227

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Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait Kinetic assay shows that increasing red cell volume could be a treatment for sickle cell disease.Kinetics of increased deformability of deoxygenated sickle cells upon oxygenation.Conjunctival sign in sickle cell anaemia: an in-vivo correlate of the extent of red cell heterogeneity.Treating sickle cell disease by targeting HbS polymerization Modeling sickle cell vasoocclusion in the rat leg: quantification of trapped sickle cells and correlation with 31P metabolic and 1H magnetic resonance imaging changes.Effects of deoxygenation on active and passive Ca2+ transport and on the cytoplasmic Ca2+ levels of sickle cell anemia red cells.Polymerization in erythrocytes containing S and non-S hemoglobins Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.Light-scattering study of depolymerization kinetics of sickle hemoglobin polymers inside single erythrocytes.Polymerization of sickle cell hemoglobin at arterial oxygen saturation impairs erythrocyte deformability.Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations.Universality of supersaturation in protein-fiber formation.Intravascular hemolysis and the pathophysiology of sickle cell disease.Macromolecular crowding and confinement in cells exposed to hypertonicity.Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration.Oxpentifylline and cetiedil citrate improve deformability of dehydrated sickle cells.Sodium metabisulfite-induced polymerization of sickle cell hemoglobin incubated in the extracts of three medicinal plants (Anacardium occidentale, Psidium guajava, and Terminalia catappa).Simultaneous determination of low free Mg2+ and pH in human sickle cells using 31P NMR spectroscopy.Influence of βS allele in the lipid peroxidation and antioxidant capacity parameters.Effect of hemoglobin concentration on nucleation and polymer formation in sickle red blood cells.Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.Sickle cell disease: new opportunities and challenges in Africa.

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P2860

Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

http://www.wikidata.org/entity/Q33822227

description

1983 nî lūn-bûn

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1983 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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1983 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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1983年の論文

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1983年論文

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1983年論文

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1983年論文

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1983年論文

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1983年論文

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1983年论文

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

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Journal of Clinical Investigation

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

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Noguchi CT

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Schechter AN

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Torchia DA

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P2860

Kinetic studies on photolysis-induced gelation of sickle cell hemoglobin suggest a new mechanism

Molecular and cellular pathogenesis of hemoglobin SC disease.

Determination of deoxyhemoglobin S polymer in sickle erythrocytes upon deoxygenation.

Kinetics of sickle haemoglobin polymerization in single red cells.

Deformability of oxygenated irreversibly sickled cells.

SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequences.

Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins.

Relationship of density distribution and pyruvate kinase electrophoretic pattern of erythrocytes in sickle cell diseases and other disorders.

The intracellular polymerization of sickle hemoglobin and its relevance to sickle cell disease.

Stabilization of the shape of sickled cells by calcium and A23187.

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scholarly article

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10.1172/JCI111055

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sickle-cell disease

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