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218 related items for PubMed ID: 16455806
1. In vitro p-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: a recommendation for probe substrates. Rautio J, Humphreys JE, Webster LO, Balakrishnan A, Keogh JP, Kunta JR, Serabjit-Singh CJ, Polli JW. Drug Metab Dispos; 2006 May; 34(5):786-92. PubMed ID: 16455806 [Abstract] [Full Text] [Related]
2. Chalcogenopyrylium dyes as inhibitors/modulators of P-glycoprotein in multidrug-resistant cells. Sawada GA, Raub TJ, William Higgins J, Brennan NK, Moore TM, Tombline G, Detty MR. Bioorg Med Chem; 2008 Nov 15; 16(22):9745-56. PubMed ID: 18849167 [Abstract] [Full Text] [Related]
3. Development, validation and utility of an in vitro technique for assessment of potential clinical drug-drug interactions involving P-glycoprotein. Keogh JP, Kunta JR. Eur J Pharm Sci; 2006 Apr 15; 27(5):543-54. PubMed ID: 16406207 [Abstract] [Full Text] [Related]
4. Rational use of in vitro P-glycoprotein assays in drug discovery. Polli JW, Wring SA, Humphreys JE, Huang L, Morgan JB, Webster LO, Serabjit-Singh CS. J Pharmacol Exp Ther; 2001 Nov 15; 299(2):620-8. PubMed ID: 11602674 [Abstract] [Full Text] [Related]
5. In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system. Feng B, Mills JB, Davidson RE, Mireles RJ, Janiszewski JS, Troutman MD, de Morais SM. Drug Metab Dispos; 2008 Feb 15; 36(2):268-75. PubMed ID: 17962372 [Abstract] [Full Text] [Related]
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 15; 303(1):323-32. PubMed ID: 12235267 [Abstract] [Full Text] [Related]
9. Gomisin A alters substrate interaction and reverses P-glycoprotein-mediated multidrug resistance in HepG2-DR cells. Wan CK, Zhu GY, Shen XL, Chattopadhyay A, Dey S, Fong WF. Biochem Pharmacol; 2006 Sep 28; 72(7):824-37. PubMed ID: 16889754 [Abstract] [Full Text] [Related]
10. Functional role of P-glycoprotein in limiting intestinal absorption of drugs: contribution of passive permeability to P-glycoprotein mediated efflux transport. Varma MV, Sateesh K, Panchagnula R. Mol Pharm; 2005 Sep 28; 2(1):12-21. PubMed ID: 15804173 [Abstract] [Full Text] [Related]
11. Kinetic profiling of P-glycoprotein-mediated drug efflux in rat and human intestinal epithelia. Stephens RH, O'Neill CA, Warhurst A, Carlson GL, Rowland M, Warhurst G. J Pharmacol Exp Ther; 2001 Feb 28; 296(2):584-91. PubMed ID: 11160647 [Abstract] [Full Text] [Related]
13. If the KI is defined by the free energy of binding to P-glycoprotein, which kinetic parameters define the IC50 for the Madin-Darby canine kidney II cell line overexpressing human multidrug resistance 1 confluent cell monolayer? Lumen AA, Acharya P, Polli JW, Ayrton A, Ellens H, Bentz J. Drug Metab Dispos; 2010 Feb 28; 38(2):260-9. PubMed ID: 19889884 [Abstract] [Full Text] [Related]
14. Calcein assay: a high-throughput method to assess P-gp inhibition. Glavinas H, von Richter O, Vojnits K, Mehn D, Wilhelm I, Nagy T, Janossy J, Krizbai I, Couraud P, Krajcsi P. Xenobiotica; 2011 Aug 28; 41(8):712-9. PubMed ID: 21657832 [Abstract] [Full Text] [Related]
15. Comparison of 3 assay systems using a common probe substrate, calcein AM, for studying P-gp using a selected set of compounds. Szerémy P, Pál A, Méhn D, Tóth B, Fülöp F, Krajcsi P, Herédi-Szabó K. J Biomol Screen; 2011 Jan 28; 16(1):112-9. PubMed ID: 21057029 [Abstract] [Full Text] [Related]
17. Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug. Fenner KS, Troutman MD, Kempshall S, Cook JA, Ware JA, Smith DA, Lee CA. Clin Pharmacol Ther; 2009 Feb 28; 85(2):173-81. PubMed ID: 18987624 [Abstract] [Full Text] [Related]
18. Comparison of drug efflux transport kinetics in various blood-brain barrier models. Bachmeier CJ, Trickler WJ, Miller DW. Drug Metab Dispos; 2006 Jun 28; 34(6):998-1003. PubMed ID: 16554372 [Abstract] [Full Text] [Related]
19. From bench to bedside: utilization of an in vitro model to predict potential drug-drug interactions in the kidney: the digoxin-mifepristone example. Woodland C, Koren G, Ito S. J Clin Pharmacol; 2003 Jul 28; 43(7):743-50. PubMed ID: 12856388 [Abstract] [Full Text] [Related]
20. Comparison of in vitro P-glycoprotein screening assays: recommendations for their use in drug discovery. Schwab D, Fischer H, Tabatabaei A, Poli S, Huwyler J. J Med Chem; 2003 Apr 24; 46(9):1716-25. PubMed ID: 12699389 [Abstract] [Full Text] [Related] Page: [Next] [New Search]