Search Results - "BALAZS, TANIA"

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  1. 1

    Human and mouse hemoglobin association with the transgenic mouse erythrocyte membrane by Chen, Qiuying, Balazs, Tania C., Nagel, Ronald L., Hirsch, Rhoda Elison

    Published in FEBS letters (07-08-2006)
    “…Transgenic mouse models of hemoglobinopathies unravel pathophysiological mechanisms; yet the validity of the red blood cell (RBC) model of human hemoglobin…”
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    Journal Article
  2. 2

    Polymer Structure and Solubility of Deoxyhemoglobin S in the Presence of High Concentrations of Volume-excluding 70-kDa Dextran by Bookchin, Robert M., Balazs, Tania, Wang, Zhiping, Josephs, Robert, Lew, Virgilio L.

    Published in The Journal of biological chemistry (05-03-1999)
    “…Earlier observations indicated that volume exclusion by admixed non-hemoglobin macromolecules lowered the polymer solubility (“ C sat ”) of deoxyhemoglobin…”
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  3. 3

    Polymer structure and solubility of deoxyhemoglobin S in the presence of high concentrations of volume-excluding 70-kDa dextran. Effects of non-s hemoglobins and inhibitors by Bookchin, R M, Balazs, T, Wang, Z, Josephs, R, Lew, V L

    Published in The Journal of biological chemistry (05-03-1999)
    “…Earlier observations indicated that volume exclusion by admixed non-hemoglobin macromolecules lowered the polymer solubility ("Csat") of deoxyhemoglobin (Hb)…”
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    Journal Article
  4. 4

    Measurement of the hemoglobin concentration in deoxyhemoglobin S polymers and characterization of the polymer water compartment by Bookchin, R M, Balazs, T, Lew, V L

    Published in Journal of molecular biology (18-11-1994)
    “…Biological polymers contain freely exchangeable water within intermolecular crevices with restricted access to large extrapolymer solutes. Our recent studies…”
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    Ionic Strength Dependence of the Polymer Solubilities of Deoxyhemoglobin S + C and S + A Mixtures by Bookchin, Robert M., Balazs, Tania

    Published in Blood (01-04-1986)
    “…Factors contributing to the clinical differences between sickle cell-hemoglobin C disease (SC) and the benign sickle cell trait (AS) include the higher…”
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    Hemoglobin Crete (0129 Ala → Pro): A New High-Affinity Variant Interacting With β°-and β°-Thalassemia by Maniatis, Alice, Bousios, Thalia, Nagel, Ronald L., Balazs, Tania, Ueda, Yoshihiro, Bookchin, Robert M., Maniatis, George M.

    Published in Blood (01-07-1979)
    “…Hemoglobin Crete, β129 (H7) ala —► pro, is a new mutant bemoglobin (Hb) with high oxygen affinity that was discovered in a Greek family in various combinations…”
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  11. 11

    Determinants of red cell sickling. Effects of varying pH and of increasing intracellular hemoglobin concentration by osmotic shrinkage by Bookchin, R M, Balazs, T, Landau, L C

    “…The effects of varying pH and of increasing intracellular hemoglobin (Hb) concentration on red cell sickling and oxygen affinity were studied in whole blood…”
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  12. 12

    Dehydration and delayed proton equilibria of red blood cells suspended in isosmotic phosphate buffers. Implications for studies of sickled cells by Bookchin, R M, Lew, D J, Balazs, T, Ueda, Y, Lew, V L

    “…PO4 buffers isosmotic with plasma or phosphate-buffered saline solution with a substantial proportion of PO4 are often used to wash and suspend red blood cells…”
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