Changes in the properties of normal human red blood cells during in vivo aging
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Philip S Low | Clinton H Joiner | P. Low | R. Cohen | Robert M Cohen | M. Palascak | C. Joiner | R. Franco | Robert S Franco | Mary B Palascak | M Estela Puchulu-Campanella | Latorya A Barber | M. E. Puchulu-Campanella | L. A. Barber | Robert M. Cohen | M. Estela Puchulu‐Campanella
[1] S. Urbaniak,et al. ADCC (K‐Cell) Lysis of Human Erythrocytes Sensitized with Rhesus Alloantibodies III. COMPARISON OF IgG ANTI‐D AGGLUTINATING AND LYTIC (ADCC) ACTIVITY AND THE ROLE OF IgG SUBCLASSES , 1980, British journal of haematology.
[2] D. Brooks,et al. Physiological shear stresses enhance the Ca2+ permeability of human erythrocytes , 1981, Nature.
[3] M. Kay. Localization of senescent cell antigen on band 3. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[4] P. Low,et al. The role of hemoglobin denaturation and band 3 clustering in red blood cell aging. , 1985, Science.
[5] P. Low,et al. Heinz bodies induce clustering of band 3, glycophorin, and ankyrin in sickle cell erythrocytes. , 1986, The Journal of clinical investigation.
[6] U. Galili,et al. The natural anti-alpha-galactosyl IgG on human normal senescent red blood cells. , 1986, British journal of haematology.
[7] U. Galili,et al. The natural anti‐α‐galactosyl IgG on human normal senescent red blood cells , 1986 .
[8] T. Suzuki,et al. Biotinylated erythrocytes: in vivo survival and in vitro recovery. , 1987, Blood.
[9] T. Suzuki,et al. Senescent erythrocytes: isolation of in vivo aged cells and their biochemical characteristics. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[10] M. R. Clark,et al. Senescence of red blood cells: progress and problems. , 1988, Physiological reviews.
[11] T. Suzuki,et al. Membrane proteins in senescent erythrocytes. , 1989, The Biochemical journal.
[12] J. Marchalonis,et al. Definition of a physiologic aging autoantigen by using synthetic peptides of membrane protein band 3: localization of the active antigenic sites. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[13] L. Forman,et al. In vivo aging of red cell enzymes: Study of biotinylated red blood cells in rabbits , 1990, American journal of hematology.
[14] G. Dale,et al. Density fractionation of erythrocytes by Percoll/hypaque results in only a slight enrichment for aged cells. , 1990, Biochimica et biophysica acta.
[15] R. Daniels,et al. Characterization of senescent red cells from the rabbit. , 1991, Advances in experimental medicine and biology.
[16] R. Daniels,et al. Quantitation of immunoglobulin associated with senescent erythrocytes from the rabbit. , 1991, Blood.
[17] P. Low,et al. Clustering of integral membrane proteins of the human erythrocyte membrane stimulates autologous IgG binding, complement deposition, and phagocytosis. , 1991, The Journal of biological chemistry.
[18] U. Galili,et al. Comparison of serum anti-band 3 and anti-Gal antibody binding to density-separated human red blood cells. , 1991, Blood.
[19] M. R. Halie,et al. Characteristics of red blood cell populations fractionated with a combination of counterflow centrifugation and Percoll separation. , 1992, Blood.
[20] R. Johnson,et al. Induction of a Ca(2+)-activated K+ channel in human erythrocytes by mechanical stress. , 1992, Biochimica et biophysica acta.
[21] T Suzuki,et al. Rheologic properties of senescent erythrocytes: loss of surface area and volume with red blood cell age. , 1992, Blood.
[22] P. Low,et al. Senescence of canine biotinylated erythrocytes: increased autologous immunoglobulin binding occurs on erythrocytes aged in vivo for 104 to 110 days. , 1993, Blood.
[23] P. Low,et al. Methodologic considerations for the use of canine in vivo aged biotinylated erythrocytes to study RBC senescence. , 1996, Experimental hematology.
[24] D. Gibson,et al. Increased erythrocyte phosphatidylserine exposure in sickle cell disease: flow-cytometric measurement and clinical associations. , 1996, Blood.
[25] E. Silberstein,et al. Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells. , 1998, The Journal of clinical investigation.
[26] F. Boas,et al. Phosphatidylserine exposure and red cell viability in red cell aging and in hemolytic anemia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[27] P. Low,et al. How old are dense red blood Cells? The dog's tale. , 1998, Blood.
[28] J. A. Gimm,et al. Evaluation of biochemical changes during in vivo erythrocyte senescence in the dog. , 1999, Blood.
[29] V. Lew,et al. Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[30] V. Lew,et al. low-density sickle and normal red cells , 2000 .
[31] M. Weiner,et al. The survival characteristics of dense sickle cells. , 2000, Blood.
[32] G. Küllertz,et al. Separation of Erythrocytes into Age-Related Fractions by Density or Size? Counterflow Centrifugation , 2000, Clinical chemistry and laboratory medicine.
[33] F. Kuypers,et al. Characterization of the phosphatidylserine-exposing subpopulation of sickle cells. , 2001, Blood.
[34] J. D. Holtzclaw,et al. Rehydration of high-density sickle erythrocytes in vitro. , 2002, Blood.
[35] Clinton H Joiner,et al. Phosphatidylserine externalization in sickle red blood cells: associations with cell age, density, and hemoglobin F. , 2003, Blood.
[36] A. Hall,et al. Effects of high hydrostatic pressure on ‘passive’ monovalent cation transport in human red cells , 2005, The Journal of Membrane Biology.
[37] Sergey S Shevkoplyas,et al. A high‐resolution, double‐labeling method for the study of in vivo red blood cell aging , 2006, Transfusion.
[38] Sergey S Shevkoplyas,et al. A detailed study of time‐dependent changes in human red blood cells: from reticulocyte maturation to erythrocyte senescence , 2006, British journal of haematology.
[39] F. Kuypers,et al. Flippase Activity Decreases throughout Erythrocyte Life-Span in Normal and Sickle Mice. , 2006 .
[40] T. Tiffert,et al. Effects of age-dependent membrane transport changes on the homeostasis of senescent human red blood cells , 2007, Blood.
[41] M. Jiang,et al. Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes. , 2007, Blood.
[42] C. Lindsell,et al. Red cell life span heterogeneity in hematologically normal people is sufficient to alter HbA1c. , 2008, Blood.
[43] B. D. de Pauw,et al. Erythrocyte vesiculation: a self‐protective mechanism? , 2008, British journal of haematology.
[44] C. Lindsell,et al. A method for the continuous calculation of the age of labeled red blood cells , 2008, American journal of hematology.
[45] M. Palascak,et al. Aminophospholipid translocase and phospholipid scramblase activities in sickle erythrocyte subpopulations , 2009, British journal of haematology.
[46] H. Lutz,et al. A pair of naturally occurring antibodies may dampen complement‐dependent phagocytosis of red cells with a positive antiglobulin test in healthy blood donors , 2009, Vox sanguinis.
[47] M. Davenport,et al. A novel fluorescent-based assay reveals that thrombopoietin signaling and Bcl-X(L) influence, respectively, platelet and erythrocyte lifespans. , 2010, Experimental hematology.
[48] V. Lew,et al. Local Membrane Deformations Activate Ca2+-Dependent K+ and Anionic Currents in Intact Human Red Blood Cells , 2010, PloS one.