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PUBMED FOR HANDHELDS

Journal Abstract Search


411 related items for PubMed ID: 8794769

  • 1. Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains.
    Liu R, Sharom FJ.
    Biochemistry; 1996 Sep 10; 35(36):11865-73. PubMed ID: 8794769
    [Abstract] [Full Text] [Related]

  • 2. Fluorescence studies on the nucleotide binding domains of the P-glycoprotein multidrug transporter.
    Liu R, Sharom FJ.
    Biochemistry; 1997 Mar 11; 36(10):2836-43. PubMed ID: 9062112
    [Abstract] [Full Text] [Related]

  • 3. Proximity of the nucleotide binding domains of the P-glycoprotein multidrug transporter to the membrane surface: a resonance energy transfer study.
    Liu R, Sharom FJ.
    Biochemistry; 1998 May 05; 37(18):6503-12. PubMed ID: 9572868
    [Abstract] [Full Text] [Related]

  • 4. The membrane lipid environment modulates drug interactions with the P-glycoprotein multidrug transporter.
    Romsicki Y, Sharom FJ.
    Biochemistry; 1999 May 25; 38(21):6887-96. PubMed ID: 10346910
    [Abstract] [Full Text] [Related]

  • 5. Stoichiometry and affinity of nucleotide binding to P-glycoprotein during the catalytic cycle.
    Qu Q, Russell PL, Sharom FJ.
    Biochemistry; 2003 Feb 04; 42(4):1170-7. PubMed ID: 12549939
    [Abstract] [Full Text] [Related]

  • 6. Human P-glycoprotein exhibits reduced affinity for substrates during a catalytic transition state.
    Ramachandra M, Ambudkar SV, Chen D, Hrycyna CA, Dey S, Gottesman MM, Pastan I.
    Biochemistry; 1998 Apr 07; 37(14):5010-9. PubMed ID: 9538020
    [Abstract] [Full Text] [Related]

  • 7. Structural flexibility of the linker region of human P-glycoprotein permits ATP hydrolysis and drug transport.
    Hrycyna CA, Airan LE, Germann UA, Ambudkar SV, Pastan I, Gottesman MM.
    Biochemistry; 1998 Sep 29; 37(39):13660-73. PubMed ID: 9753453
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  • 8. Fluorescence of native single-Trp mutants in the lactose permease from Escherichia coli: structural properties and evidence for a substrate-induced conformational change.
    Weitzman C, Consler TG, Kaback HR.
    Protein Sci; 1995 Nov 29; 4(11):2310-8. PubMed ID: 8563627
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  • 12. Drug binding and nucleotide hydrolyzability are essential requirements in the vanadate-induced inhibition of the human P-glycoprotein ATPase.
    Rao US.
    Biochemistry; 1998 Oct 20; 37(42):14981-8. PubMed ID: 9778376
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  • 15. The relationship between MRP1 activities and its NBD conformational changes.
    Huang Z, Huang Y.
    Sci China C Life Sci; 2004 Oct 20; 47(5):425-33. PubMed ID: 15623154
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  • 18. Modulator-induced interference in functional cross talk between the substrate and the ATP sites of human P-glycoprotein.
    Maki N, Moitra K, Silver C, Ghosh P, Chattopadhyay A, Dey S.
    Biochemistry; 2006 Feb 28; 45(8):2739-51. PubMed ID: 16489767
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  • 19. P glycoprotein and the mechanism of multidrug resistance.
    Váradi A, Szakács G, Bakos E, Sarkadi B.
    Novartis Found Symp; 2002 Feb 28; 243():54-65; discussion 65-8, 180-5. PubMed ID: 11990782
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  • 20. Involvement of the "occluded nucleotide conformation" of P-glycoprotein in the catalytic pathway.
    Tombline G, Muharemagić A, White LB, Senior AE.
    Biochemistry; 2005 Sep 27; 44(38):12879-86. PubMed ID: 16171403
    [Abstract] [Full Text] [Related]


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