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Journal Abstract Search

729 related items for PubMed ID: 7082289

  • 1. 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]

  • 2. 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]

  • 3. Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis.
    Burke BE, Shotton DM.
    Br J Haematol; 1983 Jun 01; 54(2):173-87. PubMed ID: 6849841
    [Abstract] [Full Text] [Related]

  • 4. The role of band 4.1 in the association of actin with erythrocyte membranes.
    Cohen CM, Foley SF.
    Biochim Biophys Acta; 1982 Jun 28; 688(3):691-701. PubMed ID: 6889438
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Selective association of spectrin with the cytoplasmic surface of human erythrocyte plasma membranes. Quantitative determination with purified (32P)spectrin.
    Bennett V, Branton D.
    J Biol Chem; 1977 Apr 25; 252(8):2753-63. PubMed ID: 15998
    [Abstract] [Full Text] [Related]

  • 7. Ultracentrifugal analysis of the junction complexes of the red cell membrane cytoskeletal network: application to hereditary spherocytosis and metabolically depleted cells.
    Morris SA, Kaufman M.
    Blut; 1989 Oct 25; 59(4):385-9. PubMed ID: 2790221
    [Abstract] [Full Text] [Related]

  • 8. 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 25; 60(3):772-84. PubMed ID: 7104494
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
    De Franceschi L, Olivieri O, Miraglia del Giudice E, Perrotta S, Sabato V, Corrocher R, Iolascon A.
    Am J Hematol; 1997 Jul 15; 55(3):121-8. PubMed ID: 9256290
    [Abstract] [Full Text] [Related]

  • 11. A phenomenological difference between membrane skeletal protein complexes isolated from normal and hereditary spherocytosis erythrocytes.
    Pinder JC, Dhermy D, Baines AJ, Lux SE, Gratzer WB.
    Br J Haematol; 1983 Nov 15; 55(3):455-63. PubMed ID: 6639887
    [Abstract] [Full Text] [Related]

  • 12. Binding of spectrin to hereditary spherocyte membranes.
    Goodman SR, Weidner SA, Eyster ME, Kesselring JJ.
    J Mol Cell Cardiol; 1982 Sep 15; 14 Suppl 3():91-7. PubMed ID: 7143456
    [No Abstract] [Full Text] [Related]

  • 13. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
    Liu SC, Derick LH, Agre P, Palek J.
    Blood; 1990 Jul 01; 76(1):198-205. PubMed ID: 2364170
    [Abstract] [Full Text] [Related]

  • 14. Vesicle release from rat red cell ghosts and increased association of cell membrane proteins with cytoskeletons induced by cadmium.
    Kunimoto M, Miura T.
    Biochim Biophys Acta; 1985 Jun 11; 816(1):37-45. PubMed ID: 4039948
    [Abstract] [Full Text] [Related]

  • 15. Spectrin-dependent and -independent association of F-actin with the erythrocyte membrane.
    Cohen CM, Foley SF.
    J Cell Biol; 1980 Aug 11; 86(2):694-8. PubMed ID: 6893203
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H.
    Rinsho Byori; 1990 Apr 20; 38(4):360-4. PubMed ID: 2195190
    [Abstract] [Full Text] [Related]

  • 18. Phosphorylation in erythrocyte membranes from abnormally shaped cells.
    Greenquist AC, Shohet SB.
    Blood; 1976 Dec 20; 48(6):877-86. PubMed ID: 187264
    [Abstract] [Full Text] [Related]

  • 19. 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 Dec 20; 110(1):81-5. PubMed ID: 6192057
    [Abstract] [Full Text] [Related]

  • 20. Shape and volume changes in erythrocyte ghosts and spectrin-actin networks.
    Johnson RM, Taylor G, Meyer DB.
    J Cell Biol; 1980 Aug 20; 86(2):371-6. PubMed ID: 6893198
    [Abstract] [Full Text] [Related]

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