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Drepanocyte (cell)

Known as: drepanocytes, cells sickle, Sickle cells 
National Institutes of Health

Related topics

Related topics

3 relations
Erythrocyte morphology finding:Prid:Pt:Bld:NomHemoglobin S:PrThr:Pt:Bld:Ord:Solubility testSickle Cell Count

Papers overview

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1998
1998
Two distinct pathways mediate the formation of intermediate density cells and hyperdense cells from normal density sickle red blood cells.
In sickle cell anemia (SS), some red blood cells dehydrate, forming a hyperdense (HD) cell fraction (>1.114 g/mL; mean… 
Highly Cited
1989
Highly Cited
1989
Inhibition of K+ efflux and dehydration of sickle cells by [(dihydroindenyl)oxy]alkanoic acid: an inhibitor of the K+ Cl- cotransport system.
[(Dihydroindenyl)oxy]alkanoic acid (DIOA) was recently introduced as a potent inhibitor of the K+Cl- cotransport system without… 
1984
1984
Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.
Levels of fetal hemoglobin (HbF) bearing reticulocytes (F reticulocytes) range from 2% to 50% in patients with sickle cell (SS… 
1976
1976
Water proton magnetic resonance studies of normal and sickle erythrocytes. Temperature and volume dependence.
1969
1969
Hematuria in sickle cell trait. The effect of intravenous administration of distilled water, urinary alkalinizatíon, and diuresis.
Hematuria in patients with sickle cell trait might be related to sickling in the medullary vessels of the kidney. In vitro… 
Highly Cited
1968
Highly Cited
1968
The fine structure of sickled hemoglobin in situ.
The sickling of susceptible erythrocytes from patients with sickle cell anemia has been related in previous studies to the… 
1960
1960
THE RELATIONSHIP OF SERUM GAMMA-GLOBULIN CONCENTRATION TO MALARIA AND SICKLING
The serum protein patterns of groups of Nigerians including 98 children partially protected by “daraprim” against malaria, and… 
Highly Cited
1958
Highly Cited
1958
Studies on the destruction of red blood cells. XIII. Observations on the role of pH in the pathogenesis and treatment of painful crisis in sickle-cell disease.
The chief clinical features of sickle-cell anemia are chronic hemolytic anemia and episodic painful crises; the underlying defect… 
1954
1954
Splenic infarction following air travel and associated with the sickling phenomenon.
Cooley, Peterson, Engel, and Jernigan recently reported six cases in which the triad of splenic infarction, sicklemia trait, and… 
1937
1937
SICKLE CELL ANEMIA IN THE WHITE RACE: IMPROVEMENT IN TWO CASES FOLLOWING SPLENECTOMY
Sickle cell anemia until recently has been thought to be limited to the Negro race. Even in this race it is relatively uncommon… 
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