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Journal Abstract Search

145 related items for PubMed ID: 638266

  • 1. Abnormal binding of spectrin to the membrane of erythrocytes in some cases of hereditary spherocytosis.
    Sheehy R, Ralston GB.
    Blut; 1978 Mar 15; 36(3):145-8. PubMed ID: 638266
    [Abstract] [Full Text] [Related]

  • 2. Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
    Hill JS, Sawyer WH, Howlett GJ, Wiley JS.
    Biochem J; 1982 Feb 01; 201(2):259-66. PubMed ID: 7082289
    [Abstract] [Full Text] [Related]

  • 3. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.
    Marík T, Kselíková M, Bíbr B, Brabec V, Lener J.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1983 Feb 01; 110(1):81-5. PubMed ID: 6192057
    [Abstract] [Full Text] [Related]

  • 4. A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.
    Wolfe LC, John KM, Falcone JC, Byrne AM, Lux SE.
    N Engl J Med; 1982 Nov 25; 307(22):1367-74. PubMed ID: 6215583
    [Abstract] [Full Text] [Related]

  • 5. Phosphorylation in erythrocyte membranes from abnormally shaped cells.
    Greenquist AC, Shohet SB.
    Blood; 1976 Dec 25; 48(6):877-86. PubMed ID: 187264
    [Abstract] [Full Text] [Related]

  • 6. The abnormal phosphorylation of spectrin in human hereditary spherocytosis.
    Thompson S, Maddy AH.
    Biochim Biophys Acta; 1981 Nov 20; 649(1):31-7. PubMed ID: 6272858
    [Abstract] [Full Text] [Related]

  • 7. Altered erythrocyte membrane protein phosphorylation in an unusual case of hereditary spherocytosis.
    Boivin P, Delaunay J, Galand C.
    Scand J Haematol; 1979 Sep 20; 23(3):251-5. PubMed ID: 228388
    [Abstract] [Full Text] [Related]

  • 8. Binding of spectrin to hereditary spherocyte membranes.
    Goodman SR, Weidner SA, Eyster ME, Kesselring JJ.
    J Mol Cell Cardiol; 1982 Sep 20; 14 Suppl 3():91-7. PubMed ID: 7143456
    [No Abstract] [Full Text] [Related]

  • 9. The molecular basis of the defect in phosphorylation of spectrin in human hereditary spherocytosis.
    Thompson S, Maddy AH.
    Biochim Biophys Acta; 1981 Nov 20; 649(1):38-44. PubMed ID: 6796120
    [Abstract] [Full Text] [Related]

  • 10. Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis.
    Burke BE, Shotton DM.
    Br J Haematol; 1983 Jun 20; 54(2):173-87. PubMed ID: 6849841
    [Abstract] [Full Text] [Related]

  • 11. Hereditary spherocytosis of man. Defective cytoskeletal interactions in the erythrocyte membrane.
    Sawyer WH, Hill JS, Howlett GJ, Wiley JS.
    Biochem J; 1983 May 01; 211(2):349-56. PubMed ID: 6870835
    [Abstract] [Full Text] [Related]

  • 12. Detection of erythrocyte membrane protein alterations in hereditary spherocytosis through the use of thermal stress: a spin label study.
    Fung LW, Ostrowski MS, Meena WA, Sarnaik S.
    Life Sci; 1981 Nov 16; 29(20):2071-9. PubMed ID: 6273682
    [No Abstract] [Full Text] [Related]

  • 13. Spectrin oligomers of the red cell membrane extracts in hereditary spherocytosis.
    Marík T, Kodícek M, Brabec V.
    Biomed Biochim Acta; 1983 Nov 16; 42(11-12):S32-7. PubMed ID: 6675711
    [Abstract] [Full Text] [Related]

  • 14. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
    Goodman SR, Shiffer KA, Casoria LA, Eyster ME.
    Blood; 1982 Sep 16; 60(3):772-84. PubMed ID: 7104494
    [Abstract] [Full Text] [Related]

  • 15. Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.
    Liu SC, Palek J, Prchal J, Castleberry RP.
    J Clin Invest; 1981 Sep 16; 68(3):597-605. PubMed ID: 7276161
    [Abstract] [Full Text] [Related]

  • 16. Membrane protein phosphorylation in intact normal and hereditary spherocytic human erythrocytes.
    Nakao M, Fujii Y, Hara Y, Nomura T, Nakao T, Komatsu Y.
    J Biochem; 1980 Aug 16; 88(2):327-35. PubMed ID: 7419497
    [No Abstract] [Full Text] [Related]

  • 17. Study of spectrin phosphorylation and polymerization in normal and spherocytic red blood-cells [proceedings].
    Devogel M, Vincentelli J, Polastro E, Schnek G, Léonis J.
    Arch Int Physiol Biochim; 1979 Oct 16; 87(4):805-7. PubMed ID: 93915
    [No Abstract] [Full Text] [Related]

  • 18. Oxidative erythrocyte membrane damage in hereditary spherocytosis.
    Caprari P, Bozzi A, Ferroni L, Strom R, Salvati AM.
    Biochem Int; 1992 Feb 16; 26(2):265-74. PubMed ID: 1558539
    [Abstract] [Full Text] [Related]

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