Disease: Red cell phospholipid defect with hemolysis
- A mechanism of erythrocyte lysis by lysophosphatidylcholine
- A semisynthetic 5-n-alkylresorcinol derivative and its effect upon biomembrane properties
- A sodium-specific membrane permeability defect induced by phospholipid vesicle treatment of erythrocytes
- Abnormality of erythrocyte membrane n-3 long chain polyunsaturated fatty acids in sickle cell haemoglobin C (HbSC) disease is not as remarkable as in sickle cell anaemia (HbSS)
- Acoustophoretic Orientation of Red Blood Cells for Diagnosis of Red Cell Health and Pathology
- Adenylate cyclase toxin from Bordetella pertussis produces ion conductance across artificial lipid bilayers in a calcium- and polarity-dependent manner
- Alterations to plasma membrane lipid contents affect the biophysical properties of erythrocytes from individuals with hypertension
- Anemia with spur cells: a red cell defect acquired in serum and modified in the circulation
- Band 3 and glycophorin are progressively aggregated in density-fractionated sickle and normal red blood cells. Evidence from rotational and lateral mobility studies
- Biochemical and ultrastructural alterations in platelets, reticulocytes, and lymphocytes from rats fed vitamin E-deficient diets
- Biochemical background of paroxysmal nocturnal hemoglobinuria
- Characteristics of the membrane defect in the hereditary stomatocytosis syndrome
- Comparative analysis of RBC membrane lipids in thalassemia, and iron deficiency anemia in relation to hypochromia and oxidant injury
- Congenital haemolytic anaemia in a low birth weight infant due to congenital stomatocytosis
- Correction of the PNH defect by GPI-anchored protein transfer
- Critical role of phosphatidylserine in hemolysis due to red blood cell enzyme/membrane defects
- Defects in peroxidation of erythrocyte phospholipids in sickle cell trait
- Deficiency of glycosyl phosphatidylinositol-anchored proteins in polymorphonuclear leukocytes from patients with paroxysmal nocturnal hemoglobinuria with low-grade hemolysis
- Deficiency of red cell bound CD55 and CD59 in patients with systemic lupus erythematosus
- Eculizumab treatment modifies the immune profile of PNH patients
- Enhanced suicidal death of erythrocytes from gene-targeted mice lacking the Cl-/HCO(3)(-) exchanger AE1
- Eryptosis: Ally or Enemy
- Erythrocyte glutathione depletion impairs resistance to haemolysis in women consuming alcohol
- Erythrocyte programmed cell death
- Erythrocyte pyruvate kinase deficiency in non-spherocytic hemolytic anemia: a system of multiple genetic markers?
- Five cases of hereditary high red cell membrane phosphatidylcholine hemolytic anemia in three families
- Hemolysis in primary lipoprotein lipase deficiency
- Hemolytic anemia associated with leptospirosis. Morphologic and lipid studies
- Hemolytic syndromes and red cell membrane abnormalities in liver disease
- Hereditary high red cell membrane phosphatidylcholine hemolytic anemia (HPCHA)
- INCUBATION HEMOLYSIS AND RED CELL METABOLISM IN ACANTHOCYTOSIS
- Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling
- Low-pH association of proteins with the membranes of intact red blood cells. II. Studies of the mechanism
- Mechanism of erythrocyte death in human population exposed to arsenic through drinking water
- Mechanisms and significance of eryptosis
- Mechanisms of hemolysis in liver disease
- Mechanisms of suicidal erythrocyte death
- Membrane structure and its relation to haemolysis
- Paroxysmal nocturnal hemoglobinuria: from physiopathology to treatment
- Pathogenesis of paroxysmal nocturnal hemoglobinuria
- Physical determinants of intermembrane protein transfer
- Physiology and pathophysiology of eryptosis
- Preliminary characterization of the acetylcholine receptor in human erythrocytes
- Red blood cell membrane microviscosity correlates with posttransfusion survival
- Red cell membrane phospholipid abnormalities in the hemolytic uremic syndrome
- Rheological Abnormalities in Human Erythrocytes Subjected to Oxidative Inflammation
- Selective accumulation of cytosol CDP-choline as an isolated erythrocyte defect in chronic hemolysis
- Sensitivity of RBC membrane Ca2+-adenosine triphosphatase to calmodulin stimulation. Variations in patients with bipolar affective disorders
- Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria
- Studies on dodecyl betainate in combination with its degradation products or with phosphatidyl choline-phase behavior and hemolytic activity
- Temporal sequence of major biochemical events during blood bank storage of packed red blood cells
- The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry
- The effect of myeloperoxidase isoforms on biophysical properties of red blood cells
- The glycosylphosphatidylinositol anchor and paroxysmal nocturnal haemoglobinuria/aplasia model
- The hemolytic activity of chrysotile asbestos fibers: a freeze-fracture study
- The PIG-anchoring defect in NK lymphocytes of PNH patients
- The role of membrane lipids in the survival of red cells in hereditary spherocytosis
- Transient holes in the erythrocyte membrane during hypotonic hemolysis and stable holes in the membrane after lysis by saponin and lysolecithin