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Journal Abstract Search

156 related items for PubMed ID: 2291540

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  • 2. Mouse beta thalassemia, a model for the membrane defects of erythrocytes in the human disease.
    Rouyer-Fessard P, Leroy-Viard K, Domenget C, Mrad A, Beuzard Y.
    J Biol Chem; 1990 Nov 25; 265(33):20247-51. PubMed ID: 2243088
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  • 3. Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemia.
    Scott MD, Rouyer-Fessard P, Lubin BH, Beuzard Y.
    J Biol Chem; 1990 Oct 15; 265(29):17953-9. PubMed ID: 2211672
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  • 7. Catabolism of hemoglobin by human erythrocyte membranes.
    Ballas SK, Burka ER.
    J Lab Clin Med; 1978 Sep 15; 92(3):387-92. PubMed ID: 681824
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  • 14. Turnover of excess hemoglobin alpha chains in beta-thalassemic cells is ATP-dependent.
    Shaeffer JR.
    J Biol Chem; 1983 Nov 10; 258(21):13172-7. PubMed ID: 6195159
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  • 15. Effect of human beta (s)-globin chains on cellular properties of red cells from beta-thalassemic mice.
    Rubin EM, Kan YW, Mohandas N.
    J Clin Invest; 1988 Sep 10; 82(3):1129-33. PubMed ID: 3417869
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  • 16. A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemia.
    Rouyer-Fessard P, Garel MC, Domenget C, Guetarni D, Bachir D, Colonna P, Beuzard Y.
    J Biol Chem; 1989 Nov 15; 264(32):19092-8. PubMed ID: 2808414
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  • 17. Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.
    Shinar E, Rachmilewitz EA, Lux SE.
    J Clin Invest; 1989 Feb 15; 83(2):404-10. PubMed ID: 2521488
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  • 18. The role of membrane skeletal-associated alpha-globin in the pathophysiology of beta-thalassemia.
    Sorensen S, Rubin E, Polster H, Mohandas N, Schrier S.
    Blood; 1990 Mar 15; 75(6):1333-6. PubMed ID: 1690033
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  • 20. The relationship between in vivo generated hemoglobin skeletal protein complex and increased red cell membrane rigidity.
    Fortier N, Snyder LM, Garver F, Kiefer C, McKenney J, Mohandas N.
    Blood; 1988 May 15; 71(5):1427-31. PubMed ID: 3359048
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