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Journal Abstract Search

168 related items for PubMed ID: 531038

  • 1. Lipid loss in spectrin deficient mouse erythrocytes.
    Shohet SB.
    Prog Clin Biol Res; 1979; 30():471-4. PubMed ID: 531038
    [No Abstract] [Full Text] [Related]

  • 2. Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes.
    Shohet SB.
    J Clin Invest; 1979 Aug; 64(2):483-94. PubMed ID: 379045
    [Abstract] [Full Text] [Related]

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  • 4. Spectrin and spherocytosis.
    Shohet SB.
    N Engl J Med; 1982 May 13; 306(19):1170-1. PubMed ID: 7070421
    [No Abstract] [Full Text] [Related]

  • 5. 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 May 13; 110(1):81-5. PubMed ID: 6192057
    [Abstract] [Full Text] [Related]

  • 6. [Measurement of phospholipids in erythrocytes, plasma and platelets in a patient with hereditary spherocytosis].
    César JM, Fernández I, Navarro JL.
    Sangre (Barc); 1989 Aug 13; 34(4):300-2. PubMed ID: 2772783
    [Abstract] [Full Text] [Related]

  • 7. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
    Coetzer TL, Lawler J, Liu SC, Prchal JT, Gualtieri RJ, Brain MC, Dacie JV, Palek J.
    N Engl J Med; 1988 Jan 28; 318(4):230-4. PubMed ID: 2961992
    [No Abstract] [Full Text] [Related]

  • 8. Erythrocyte membrane phosphorylation in hereditary spherocytosis.
    Boivin P, Galand C.
    Biomedicine; 1977 Jan 31; 27(1):34-6. PubMed ID: 192356
    [Abstract] [Full Text] [Related]

  • 9. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
    Agre P, Asimos A, Casella JF, McMillan C.
    N Engl J Med; 1986 Dec 18; 315(25):1579-83. PubMed ID: 3785322
    [Abstract] [Full Text] [Related]

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  • 11. Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin.
    Gauthier E, El Nemer W, Wautier MP, Renaud O, Tchernia G, Delaunay J, Le Van Kim C, Colin Y.
    Br J Haematol; 2010 Feb 18; 148(3):456-65. PubMed ID: 20092464
    [Abstract] [Full Text] [Related]

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  • 13. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
    Brabec V, Palek J, Petrtýlová K, Cermák J, Jarolím P.
    Vnitr Lek; 1997 Feb 18; 43(2):91-4. PubMed ID: 9245075
    [Abstract] [Full Text] [Related]

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

  • 15. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
    Ferrándiz F, Ródenas S, Villegas A.
    Sangre (Barc); 1993 Oct 18; 38(5):393-7. PubMed ID: 8140503
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  • 17. [Current theories on the etiopathogenesis of congenital spherocytosis].
    Zelenay E, Ochocka M.
    Pediatr Pol; 1985 Jan 18; 60(1):91-4. PubMed ID: 3898003
    [No Abstract] [Full Text] [Related]

  • 18.
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  • 19. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
    Agre P, Casella JF, Zinkham WH, McMillan C, Bennett V.
    Nature; 1985 Jan 18; 314(6009):380-3. PubMed ID: 3982506
    [Abstract] [Full Text] [Related]

  • 20. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
    Margetis P, Antonelou M, Karababa F, Loutradi A, Margaritis L, Papassideri I.
    Blood Cells Mol Dis; 2007 Jan 18; 38(3):210-20. PubMed ID: 17208471
    [Abstract] [Full Text] [Related]

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