These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

313 related articles for article (PubMed ID: 1832469)

  • 1. [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]  

  • 2. [Cytoskeleton and membrane anomalies in disorders of red cell membrane proteins].
    Kanzaki A; Yawata Y
    Rinsho Byori; 1991 Sep; Suppl 91():37-46. PubMed ID: 1836821
    [No Abstract]   [Full Text] [Related]  

  • 3. Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.
    Yawata Y; Kanzaki A; Inoue T; Ata K; Wada H; Okamoto N; Higo I; Yawata A; Sugihara T; Yamada O
    Int J Hematol; 1994 Jul; 60(1):23-38. PubMed ID: 7919236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
    Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
    Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
    Lux SE; Tse WT; Menninger JC; John KM; Harris P; Shalev O; Chilcote RR; Marchesi SL; Watkins PC; Bennett V
    Nature; 1990 Jun; 345(6277):736-9. PubMed ID: 2141669
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
    Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
    Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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; 110(1):81-5. PubMed ID: 6192057
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
    C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 38(3):210-20. PubMed ID: 17208471
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 16. 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]  

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

  • 18. [Hereditary elliptocytosis].
    Iyori H; Akatsuka J
    Nihon Rinsho; 1996 Sep; 54(9):2484-91. PubMed ID: 8890583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.
    Iolascon A; Miraglia del Giudice E; Camaschella C
    Haematologica; 1992; 77(1):60-72. PubMed ID: 1356891
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Abnormal changes in erythrocyte membrane proteins in hereditary spherocytosis and their relation to clinical and biological aspects of the disease].
    Ayala S; Besson I; Aymerich M; Berga L; Vives Corrons JL
    Med Clin (Barc); 1995 Jun; 105(2):45-9. PubMed ID: 7603093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.