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Journal Abstract Search

292 related items for PubMed ID: 24305879

  • 1. MDR1 synonymous polymorphisms alter transporter specificity and protein stability in a stable epithelial monolayer.
    Fung KL, Pan J, Ohnuma S, Lund PE, Pixley JN, Kimchi-Sarfaty C, Ambudkar SV, Gottesman MM.
    Cancer Res; 2014 Jan 15; 74(2):598-608. PubMed ID: 24305879
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  • 2. Effects of MDR1 1236C > T-2677G > T-3435C > T polymorphisms on the intracellular accumulation of tacrolimus, cyclosporine A, sirolimus and everolimus.
    Wang R, Sun X, Deng YS, Qiu XW.
    Xenobiotica; 2019 Nov 15; 49(11):1373-1378. PubMed ID: 30587068
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  • 3. Specificity of doxorubicin versus rhodamine-123 in assessing P-glycoprotein functionality in the LLC-PK1, LLC-PK1:MDR1 and Caco-2 cell lines.
    van der Sandt IC, Blom-Roosemalen MC, de Boer AG, Breimer DD.
    Eur J Pharm Sci; 2000 Sep 15; 11(3):207-14. PubMed ID: 11042226
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  • 4. Structure, function and regulation of P-glycoprotein and its clinical relevance in drug disposition.
    Zhou SF.
    Xenobiotica; 2008 Jul 15; 38(7-8):802-32. PubMed ID: 18668431
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  • 5. Differences in the expression of endogenous efflux transporters in MDR1-transfected versus wildtype cell lines affect P-glycoprotein mediated drug transport.
    Kuteykin-Teplyakov K, Luna-Tortós C, Ambroziak K, Löscher W.
    Br J Pharmacol; 2010 Jul 15; 160(6):1453-63. PubMed ID: 20590635
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  • 7. Functional characterization of a glycine 185-to-valine substitution in human P-glycoprotein by using a vaccinia-based transient expression system.
    Ramachandra M, Ambudkar SV, Gottesman MM, Pastan I, Hrycyna CA.
    Mol Biol Cell; 1996 Oct 15; 7(10):1485-98. PubMed ID: 8898356
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  • 12. Functional characterization of coding polymorphisms in the human MDR1 gene using a vaccinia virus expression system.
    Kimchi-Sarfaty C, Gribar JJ, Gottesman MM.
    Mol Pharmacol; 2002 Jul 15; 62(1):1-6. PubMed ID: 12065748
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  • 14. Cinnamophilin overcomes cancer multi-drug resistance via allosterically modulating human P-glycoprotein on both drug binding sites and ATPase binding sites.
    Teng YN, Huang BH, Huang SY, Wu IT, Wu TS, Lee TE, Hung CC.
    Biomed Pharmacother; 2021 Dec 15; 144():112379. PubMed ID: 34794239
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  • 17. Selection of an Optimal In Vitro Model to Assess P-gp Inhibition: Comparison of Vesicular and Bidirectional Transcellular Transport Inhibition Assays.
    Yabut J, Houle R, Wang S, Liaw A, Katwaru R, Collier H, Hittle L, Chu X.
    Drug Metab Dispos; 2022 Jul 15; 50(7):909-922. PubMed ID: 35489778
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  • 18. Screening novel CNS drug candidates for P-glycoprotein interactions using the cell line iP-gp: In vitro efflux ratios from iP-gp and MDCK-MDR1 monolayers compared to brain distribution data from mice.
    Ozgür B, Saaby L, Janfelt C, Langthaler K, Eneberg E, Jacobsen AM, Badolo L, Montanari D, Brodin B.
    Eur J Pharm Biopharm; 2021 Dec 15; 169():211-219. PubMed ID: 34756975
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  • 20. The molecular interaction of a copper chelate with human P-glycoprotein.
    Ghosh RD, Chakraborty P, Banerjee K, Adhikary A, Sarkar A, Chatterjee M, Das T, Choudhuri SK.
    Mol Cell Biochem; 2012 May 15; 364(1-2):309-20. PubMed ID: 22258826
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