Mechanical properties of sickle cell membranes.
暂无分享,去创建一个
R. Messmann | S. Sarnaik | R Messmann | S Gannon | S Sarnaik | R M Johnson | S. Gannon | R. Johnson | Richard Messmann | Sharada A. Sarnaik | Robert M. Johnson
[1] H J Meiselman,et al. Mechanical properties of oxygenated red blood cells in sickle cell (HbSS) disease. , 1984, Blood.
[2] N. Mohandas,et al. Laser Diffraction Patterns of Sickle Cells in Fluid Shear Fields , 1978 .
[3] T. Steck. Preparation of Impermeable Inside-Out and Right-Side-Out Vesicles from Erythrocyte Membranes , 1974 .
[4] T. Coetzer,et al. Spectrin tetramer-dimer equilibrium in hereditary elliptocytosis. , 1982, Blood.
[5] S. Lux,et al. Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias. , 1983, Seminars in hematology.
[6] P. Gillette,et al. Hemolysis in sickle cell disease. , 1974, Archives of internal medicine.
[7] N. Mohandas,et al. Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations , 1986, The Journal of cell biology.
[8] D. Speicher,et al. Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis. , 1983, The Journal of clinical investigation.
[9] D. Wallach,et al. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. , 1971, Biochemistry.
[10] N. Mohandas,et al. Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria , 1984 .
[11] P. Agre,et al. Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis. , 1988, The Journal of clinical investigation.
[12] S. Piomelli,et al. Separation of erythrocytes according to age on a simplified density gradient. , 1974, The Journal of laboratory and clinical medicine.
[13] R. Hebbel,et al. Phagocytosis of sickle erythrocytes: immunologic and oxidative determinants of hemolytic anemia. , 1984, Blood.
[14] S. Jain,et al. Red cell membrane stiffness in iron deficiency. , 1983, Blood.
[15] J. Prchal,et al. Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis. , 1981, Blood.
[16] N. Mohandas,et al. Deformability of isolated red blood cell membranes. , 1982, Biochimica et biophysica acta.
[17] E. Beutler,et al. The removal of leukocytes and platelets from whole blood. , 1976, The Journal of laboratory and clinical medicine.
[18] S. Liu,et al. Detection of hemin release during hemoglobin S denaturation. , 1988, Blood.
[19] T. Steck,et al. Preparation of impermeable ghosts and inside-out vesicles from human erythrocyte membranes. , 1974, Methods in enzymology.
[20] R. Hebbel. Auto-oxidation and a membrane-associated 'Fenton reagent': a possible explanation for development of membrane lesions in sickle erythrocytes. , 1985, Clinics in haematology.
[21] N. Mohandas,et al. A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders. , 1982, Blood.
[22] M. Clark,et al. Mean Corpuscular Hemoglobin Concentration and Cell Deformability a , 1989, Annals of the New York Academy of Sciences.
[23] N. Mohandas,et al. Deformability of oxygenated irreversibly sickled cells. , 1980, The Journal of clinical investigation.
[24] Vann Bennett,et al. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis , 1985, Nature.
[25] A Leung,et al. Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration. , 1984, The Journal of clinical investigation.
[26] S. Shohet,et al. Monovalent cation composition and ATP and lipid content of irreversibly sickled cells. , 1978, Blood.
[27] N. Mohandas,et al. The relationship between in vivo generated hemoglobin skeletal protein complex and increased red cell membrane rigidity. , 1988, Blood.
[28] J. Harris,et al. Studies on the destruction of red blood cells. X. The biophysics and biology of sickle-cell disease. , 1956, A.M.A. archives of internal medicine.
[29] H. Meiselman,et al. Geometric, osmotic, and membrane mechanical properties of density-separated human red cells. , 1982, Blood.
[30] R. Schwartz,et al. Protein 4.1 in sickle erythrocytes. Evidence for oxidative damage. , 1987, The Journal of biological chemistry.
[31] O. Platt,et al. Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesicles. , 1985, The Journal of clinical investigation.
[32] N. Mohandas,et al. Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis. , 1987, The Journal of clinical investigation.
[33] R. Hebbel,et al. Abnormal redox status of membrane-protein thiols in sickle erythrocytes. , 1985, The Journal of clinical investigation.
[34] S. Schrier,et al. Identification of the hereditary pyropoikilocytosis carrier state , 1984 .
[35] Shih-Chun Liu,et al. Defective spectrin dimer-dimer association in hereditary elliptocytosis ( spectrin transformation / membrane skeleton ) , 2022 .
[36] G. Serjeant,et al. The Irreversibly Sickled Cell; a Determinant of Haemolysis in Sickle Cell Anaemia , 1969, British journal of haematology.
[37] C. M. Cohen,et al. The effect of mild diamide oxidation on the structure and function of human erythrocyte spectrin. , 1986, The Journal of biological chemistry.
[38] J. White,et al. Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell disease. , 1980, The Journal of clinical investigation.
[39] M. Karnovsky,et al. Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells. , 1976, The Journal of clinical investigation.