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PUBMED FOR HANDHELDS

Journal Abstract Search


153 related items for PubMed ID: 9576864

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  • 6. Co-expressed complementary fragments of the human red cell anion exchanger (band 3, AE1) generate stilbene disulfonate-sensitive anion transport.
    Groves JD, Tanner MJ.
    J Biol Chem; 1995 Apr 21; 270(16):9097-105. PubMed ID: 7721823
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  • 8. Glycophorin A facilitates the expression of human band 3-mediated anion transport in Xenopus oocytes.
    Groves JD, Tanner MJ.
    J Biol Chem; 1992 Nov 05; 267(31):22163-70. PubMed ID: 1385395
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  • 9. Structural studies on the effects of the deletion in the red cell anion exchanger (band 3, AE1) associated with South East Asian ovalocytosis.
    Chambers EJ, Bloomberg GB, Ring SM, Tanner MJ.
    J Mol Biol; 1999 Jan 22; 285(3):1289-307. PubMed ID: 9887277
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  • 11. Distinct regions of human glycophorin A enhance human red cell anion exchanger (band 3; AE1) transport function and surface trafficking.
    Young MT, Tanner MJ.
    J Biol Chem; 2003 Aug 29; 278(35):32954-61. PubMed ID: 12813056
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  • 12. A conductive pathway generated from fragments of the human red cell anion exchanger AE1.
    Parker MD, Young MT, Daly CM, Meech RW, Boron WF, Tanner MJ.
    J Physiol; 2007 May 15; 581(Pt 1):33-50. PubMed ID: 17317744
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  • 13. The N-terminal region of the transmembrane domain of human erythrocyte band 3. Residues critical for membrane insertion and transport activity.
    Kanki T, Young MT, Sakaguchi M, Hamasaki N, Tanner MJ.
    J Biol Chem; 2003 Feb 21; 278(8):5564-73. PubMed ID: 12482865
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  • 15. Functional consequences of mutations in the transmembrane domain and the carboxy-terminus of the murine AE1 anion exchanger.
    Chernova MN, Humphreys BD, Robinson DH, Stuart-Tilley AK, Garcia AM, Brosius FC, Alper SL.
    Biochim Biophys Acta; 1997 Oct 02; 1329(1):111-23. PubMed ID: 9370249
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  • 17. Role of N-glycosylation in the expression of human band 3-mediated anion transport.
    Groves JD, Tanner MJ.
    Mol Membr Biol; 1994 Oct 02; 11(1):31-8. PubMed ID: 8019599
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  • 20. Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A.
    Tanphaichitr VS, Sumboonnanonda A, Ideguchi H, Shayakul C, Brugnara C, Takao M, Veerakul G, Alper SL.
    J Clin Invest; 1998 Dec 15; 102(12):2173-9. PubMed ID: 9854053
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