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PUBMED FOR HANDHELDS

Journal Abstract Search


165 related items for PubMed ID: 2917191

  • 1. Viscoelastic properties of red cell membrane in hereditary elliptocytosis.
    Chabanel A, Sung KL, Rapiejko J, Prchal JT, Palek J, Liu SC, Chien S.
    Blood; 1989 Feb; 73(2):592-5. PubMed ID: 2917191
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  • 3. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
    Waugh RE, Agre P.
    J Clin Invest; 1988 Jan; 81(1):133-41. PubMed ID: 3335631
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  • 4. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
    Coetzer T, Palek J, Lawler J, Liu SC, Jarolim P, Lahav M, Prchal JT, Wang W, Alter BP, Schewitz G.
    Blood; 1990 Jun 01; 75(11):2235-44. PubMed ID: 2346784
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  • 5. 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 01; 65(5):1208-17. PubMed ID: 3922449
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  • 9. Influence of network topology on the elasticity of the red blood cell membrane skeleton.
    Hansen JC, Skalak R, Chien S, Hoger A.
    Biophys J; 1997 May 01; 72(5):2369-81. PubMed ID: 9129841
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  • 10. Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins.
    Palek J.
    Blood Rev; 1987 Sep 01; 1(3):147-68. PubMed ID: 3332099
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  • 12. Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin.
    Dhermy D, Feo C, Garbarz M, Lecomte MC, Bournier O, Chaveroche I, Gautero H, Boivin P, Daffos F, Forestier F.
    Prenat Diagn; 1987 Sep 01; 7(7):471-83. PubMed ID: 3671334
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  • 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 Sep 01; 203(4):284-95. PubMed ID: 1942935
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  • 16. Defective membrane skeleton assembly in hereditary elliptocytosis.
    Liu SC, Palek J, Prchal J.
    Prog Clin Biol Res; 1981 Sep 01; 56():157-69. PubMed ID: 7330008
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  • 20. Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.
    Marchesi SL, Conboy J, Agre P, Letsinger JT, Marchesi VT, Speicher DW, Mohandas N.
    J Clin Invest; 1990 Aug 01; 86(2):516-23. PubMed ID: 2384597
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