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Journal Abstract Search

150 related items for PubMed ID: 7530501

  • 1. Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis.
    Jarolim P, Rubin HL, Brabec V, Chrobak L, Zolotarev AS, Alper SL, Brugnara C, Wichterle H, Palek J.
    Blood; 1995 Feb 01; 85(3):634-40. PubMed ID: 7530501
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  • 2. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
    Jarolim P, Murray JL, Rubin HL, Taylor WM, Prchal JT, Ballas SK, Snyder LM, Chrobak L, Melrose WD, Brabec V, Palek J.
    Blood; 1996 Dec 01; 88(11):4366-74. PubMed ID: 8943874
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  • 4. Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
    Jarolim P, Rubin HL, Liu SC, Cho MR, Brabec V, Derick LH, Yi SJ, Saad ST, Alper S, Brugnara C.
    J Clin Invest; 1994 Jan 01; 93(1):121-30. PubMed ID: 8282779
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  • 5. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
    Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG.
    J Clin Invest; 1996 Jan 15; 97(2):373-80. PubMed ID: 8567957
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  • 6. Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.
    Jarolim P, Palek J, Rubin HL, Prchal JT, Korsgren C, Cohen CM.
    Blood; 1992 Jul 15; 80(2):523-9. PubMed ID: 1378323
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  • 7. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.
    Inaba M, Yawata A, Koshino I, Sato K, Takeuchi M, Takakuwa Y, Manno S, Yawata Y, Kanzaki A, Sakai J, Ban A, Ono K, Maede Y.
    J Clin Invest; 1996 Apr 15; 97(8):1804-17. PubMed ID: 8621763
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  • 12. Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis.
    Kanzaki A, Hayette S, Morlé L, Inoue F, Matsuyama R, Inoue T, Yawata A, Wada H, Vallier A, Alloisio N, Yawata Y, Delaunay J.
    Br J Haematol; 1997 Dec 15; 99(3):522-30. PubMed ID: 9401060
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  • 14. The red blood cell band 3 variant (band 3Biceêtrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect.
    Dhermy D, Burnier O, Bourgeois M, Grandchamp B.
    Mol Membr Biol; 1999 Dec 15; 16(4):305-12. PubMed ID: 10766130
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  • 17. 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 15; 71(2):118-35. PubMed ID: 10745622
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