Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell disease.
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Reflecting on 80 years of excellenceL-glutamine therapy reduces endothelial adhesion of sickle red blood cells to human umbilical vein endothelial cellsSickle cell disease biochip: a functional red blood cell adhesion assay for monitoring sickle cell disease."Do-it-yourself in vitro vasculature that recapitulates in vivo geometries for investigating endothelial-blood cell interactions"Activation of sickle red blood cell adhesion via integrin-associated protein/CD47-induced signal transductionPrimary role for adherent leukocytes in sickle cell vascular occlusion: a new paradigmEpinephrine-induced activation of LW-mediated sickle cell adhesion and vaso-occlusion in vivo.The rate of hemolysis in sickle cell disease correlates with the quantity of active von Willebrand factor in the plasma.High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia.Altered membrane structure and surface potential in homozygous hemoglobin C erythrocytesPlasma or serum from patients with systemic sclerosis alters behaviour of normal erythrocytes.Hydroxycarbamide decreases sickle reticulocyte adhesion to resting endothelium by inhibiting endothelial lutheran/basal cell adhesion molecule (Lu/BCAM) through phosphodiesterase 4A activationPotential therapeutic action of nitrite in sickle cell diseaseTreating sickle cell disease by targeting HbS polymerizationMicrovascular sites and characteristics of sickle cell adhesion to vascular endothelium in shear flow conditions: pathophysiological implications.Modeling sickle cell vasoocclusion in the rat leg: quantification of trapped sickle cells and correlation with 31P metabolic and 1H magnetic resonance imaging changes.A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis.Aggregation of mononuclear and red blood cells through an {alpha}4{beta}1-Lu/basal cell adhesion molecule interaction in sickle cell diseaseShape and Biomechanical Characteristics of Human Red Blood Cells in Health and DiseaseSpecific binding of red blood cells to endothelial cells is regulated by nonadsorbing macromolecules.Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesiclesHeinz bodies induce clustering of band 3, glycophorin, and ankyrin in sickle cell erythrocytesThrombin stimulates the adherence of neutrophils to human endothelial cells in vitroConcurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytesIncreased adherence of sickled and phosphatidylserine-enriched human erythrocytes to cultured human peripheral blood monocytes.Sickle red cell-endothelium interactions.Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion.The role of rib infarcts in the acute chest syndrome of sickle cell diseases.Sickle cell disease in the Sudan. Clinical and biochemical aspects. Minireview based on a doctoral thesis.Interaction of sickle cell hemoglobin with erythrocyte membranesCytokines in sickle cell disease.Intravital microscopy of capillary hemodynamics in sickle cell disease.Unusually large von Willebrand factor multimers increase adhesion of sickle erythrocytes to human endothelial cells under controlled flow.Potentiated adherence of sickle erythrocytes to endothelium infected by virus.Membrane phospholipid asymmetry as a determinant of erythrocyte recognition by macrophagesMicrofluidic study of enhanced deposition of sickle cells at acute corners.Sickle cell disease: old discoveries, new concepts, and future promise.Sickle erythrocytes, after sickling, regulate the expression of the endothelin-1 gene and protein in human endothelial cells in culture.In vivo demonstration of red cell-endothelial interaction, sickling and altered microvascular response to oxygen in the sickle transgenic mouseBand 3 and glycophorin are progressively aggregated in density-fractionated sickle and normal red blood cells. Evidence from rotational and lateral mobility studies.
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P2860
Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell disease.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1980
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@en
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@nl
type
label
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@en
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@nl
prefLabel
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@en
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@nl
P2093
P2860
P356
P1476
Abnormal adherence of sickle e ...... lusion in sickle cell disease.
@en
P2093
P2860
P304
P356
10.1172/JCI109646
P407
P577
1980-01-01T00:00:00Z