BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

437 related articles for article (PubMed ID: 6236232)

  • 1. Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
    Zail SS; Coetzer TL
    J Clin Invest; 1984 Sep; 74(3):753-62. PubMed ID: 6236232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
    Eber SW
    Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
    Giorgi M; Cianci CD; Gallagher PG; Morrow JS
    Exp Mol Pathol; 2001 Jun; 70(3):215-30. PubMed ID: 11418000
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
    Eber SW; Morris SA; Schröter W; Gratzer WB
    J Clin Invest; 1988 Feb; 81(2):523-30. PubMed ID: 3276733
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Defective spectrin dimer-dimer association in a family with transfusion dependent homozygous hereditary elliptocytosis.
    Evans JP; Baines AJ; Hann IM; Al-Hakim I; Knowles SM; Hoffbrand AV
    Br J Haematol; 1983 Jun; 54(2):163-72. PubMed ID: 6849840
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Abnormalities of beta spectrin with hereditary elliptocytosis in mother and child].
    Iyori H; Kobayashi N; Fujisawa K; Akatsuka J; Nakamura H; Mishima K; Kanzaki A; Wada H; Ata K; Yamada O
    Rinsho Ketsueki; 1992 Feb; 33(2):167-72. PubMed ID: 1635163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
    Kanzaki A; Wada H; Yawata Y
    Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
    Lane PA; Shew RL; Iarocci TA; Mohandas N; Hays T; Mentzer WC
    J Clin Invest; 1987 Mar; 79(3):989-96. PubMed ID: 3818958
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis.
    Garbarz M; Dhermy D; Lecomte MC; Féo C; Chaveroche I; Galand C; Bournier O; Bertrand O; Boivin P
    Blood; 1984 Nov; 64(5):1006-15. PubMed ID: 6487803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular heterogeneity of hereditary elliptocytosis in Italy.
    Miraglia del Giudice E; Perrotta S; Sannino E; De Angelis F; Nobili B; Iolascon A
    Haematologica; 1994; 79(5):400-5. PubMed ID: 7843625
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reduced spectrin-ankyrin binding in a South African hereditary elliptocytosis kindred homozygous for spectrin St Claude.
    Burke JP; Van Zyl D; Zail SS; Coetzer TL
    Blood; 1998 Oct; 92(7):2591-2. PubMed ID: 9746802
    [No Abstract]   [Full Text] [Related]  

  • 12. Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane.
    Rybicki AC; Heath R; Wolf JL; Lubin B; Schwartz RS
    J Clin Invest; 1988 Mar; 81(3):893-901. PubMed ID: 2963832
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 307(22):1367-74. PubMed ID: 6215583
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.
    Lecomte MC; Dhermy D; Solis C; Ester A; Féo C; Gautero H; Bournier O; Boivin P
    Blood; 1985 May; 65(5):1208-17. PubMed ID: 3922449
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectrin tetramer-dimer equilibrium in hereditary elliptocytosis.
    Coetzer T; Zail S
    Blood; 1982 May; 59(5):900-5. PubMed ID: 7074218
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
    Lawler J; Liu SC; Palek J; Prchal J
    J Clin Invest; 1984 Jun; 73(6):1688-95. PubMed ID: 6725555
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tryptic digestion of spectrin in variants of hereditary elliptocytosis.
    Coetzer T; Zail SS
    J Clin Invest; 1981 May; 67(5):1241-8. PubMed ID: 7229027
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ankyrin and synapsin: spectrin-binding proteins associated with brain membranes.
    Bennett V; Baines AJ; Davis JQ
    J Cell Biochem; 1985; 29(2):157-69. PubMed ID: 2933418
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phosphorylation of ankyrin down-regulates its cooperative interaction with spectrin and protein 3.
    Cianci CD; Giorgi M; Morrow JS
    J Cell Biochem; 1988 Jul; 37(3):301-15. PubMed ID: 2970468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.
    Palek J; Coetzer T
    Blood Cells; 1987; 13(1-2):237-50. PubMed ID: 3311220
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.