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Journal Abstract Search

74 related items for PubMed ID: 9765504

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  • 5. Tissue distribution of the human MDR3 P-glycoprotein.
    Smit JJ, Schinkel AH, Mol CA, Majoor D, Mooi WJ, Jongsma AP, Lincke CR, Borst P.
    Lab Invest; 1994 Nov; 71(5):638-49. PubMed ID: 7734012
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  • 6. Interaction of cytochrome P450 3A inhibitors with P-glycoprotein.
    Yasuda K, Lan LB, Sanglard D, Furuya K, Schuetz JD, Schuetz EG.
    J Pharmacol Exp Ther; 2002 Oct; 303(1):323-32. PubMed ID: 12235267
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  • 7. Altered expression of hepatic cytochromes P-450 in mice deficient in one or more mdr1 genes.
    Schuetz EG, Umbenhauer DR, Yasuda K, Brimer C, Nguyen L, Relling MV, Schuetz JD, Schinkel AH.
    Mol Pharmacol; 2000 Jan; 57(1):188-97. PubMed ID: 10617694
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  • 8. HIV-1 protease inhibitors are substrates for the MDR1 multidrug transporter.
    Lee CG, Gottesman MM, Cardarelli CO, Ramachandra M, Jeang KT, Ambudkar SV, Pastan I, Dey S.
    Biochemistry; 1998 Mar 17; 37(11):3594-601. PubMed ID: 9530286
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  • 9. Establishment and characterization of new cellular lymphoma model expressing transgenic human MDR1.
    Findling-Kagan S, Sivan H, Ostrovsky O, Nagler A, Galski H.
    Leuk Res; 2005 Apr 17; 29(4):407-14. PubMed ID: 15725475
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  • 10. Downregulation of JNK/SAPK activity is associated with the cross-resistance to P-glycoprotein-unrelated drugs in multidrug-resistant FM3A/M cells overexpressing P-glycoprotein.
    Kang CD, Ahn BK, Jeong CS, Kim KW, Lee HJ, Yoo SD, Chung BS, Kim SH.
    Exp Cell Res; 2000 Apr 10; 256(1):300-7. PubMed ID: 10739677
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  • 11. Synthesis, molecular structure, and validation of metalloprobes for assessment of MDR1 P-glycoprotein-mediated functional transport.
    Sivapackiam J, Harpstrite SE, Prior JL, Gu H, Rath NP, Sharma V.
    Dalton Trans; 2010 Jul 07; 39(25):5842-50. PubMed ID: 20505882
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  • 12. Structural and functional characterization of the mouse multidrug resistance gene family.
    Dhir R, Buschman E, Gros P.
    Bull Cancer; 1990 Jul 07; 77(11):1125-9. PubMed ID: 1980424
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  • 13. In vivo RNA interference-mediated ablation of MDR1 P-glycoprotein.
    Pichler A, Zelcer N, Prior JL, Kuil AJ, Piwnica-Worms D.
    Clin Cancer Res; 2005 Jun 15; 11(12):4487-94. PubMed ID: 15958634
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  • 14. 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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  • 15. The inability of the mouse mdr2 gene to confer multidrug resistance is linked to reduced drug binding to the protein.
    Buschman E, Gros P.
    Cancer Res; 1994 Sep 15; 54(18):4892-8. PubMed ID: 7915194
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  • 16. Modulation of P-glycoprotein expression and function by curcumin in multidrug-resistant human KB cells.
    Anuchapreeda S, Leechanachai P, Smith MM, Ambudkar SV, Limtrakul PN.
    Biochem Pharmacol; 2002 Aug 15; 64(4):573-82. PubMed ID: 12167476
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  • 17. Biochemical basis of polyvalency as a strategy for enhancing the efficacy of P-glycoprotein (ABCB1) modulators: stipiamide homodimers separated with defined-length spacers reverse drug efflux with greater efficacy.
    Sauna ZE, Andrus MB, Turner TM, Ambudkar SV.
    Biochemistry; 2004 Mar 02; 43(8):2262-71. PubMed ID: 14979722
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  • 18. Conferone from Ferula schtschurowskiana enhances vinblastine cytotoxicity in MDCK-MDR1 cells by competitively inhibiting P-glycoprotein transport.
    Barthomeuf C, Demeule M, Grassi J, Saidkhodjaev A, Beliveau R.
    Planta Med; 2006 Jun 02; 72(7):634-9. PubMed ID: 16739070
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  • 19. Inhibition of P-glycoprotein transport function and reversion of MDR1 multidrug resistance by cnidiadin.
    Barthomeuf C, Grassi J, Demeule M, Fournier C, Boivin D, Béliveau R.
    Cancer Chemother Pharmacol; 2005 Aug 02; 56(2):173-81. PubMed ID: 15824923
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