The role of transporters in drug interactions.
暂无分享,去创建一个
Christopher J Endres | Jashvant D Unadkat | C. Endres | J. Unadkat | P. Hsiao | Peng Hsiao | Francisco S Chung | Peng Hsiao | Francisco S. Chung
[1] Masahiro Okuda,et al. Metformin Transport by Renal Basolateral Organic Cation Transporter hOCT2 , 2005, Pharmaceutical Research.
[2] T. Cihlar,et al. The antiviral nucleotide analogs cidofovir and adefovir are novel substrates for human and rat renal organic anion transporter 1. , 1999, Molecular pharmacology.
[3] S. Cole,et al. The MRP-related and BCRP/ABCG2 multidrug resistance proteins: biology, substrate specificity and regulation. , 2004, Current drug metabolism.
[4] I. Tamai,et al. Competitive interaction of cyclosporins with the Vinca alkaloid-binding site of P-glycoprotein in multidrug-resistant cells. , 1990, The Journal of biological chemistry.
[5] P. Meier,et al. St John's Wort induces intestinal P‐glycoprotein/MDR1 and intestinal and hepatic CYP3A4 , 2000, Clinical pharmacology and therapeutics.
[6] B. Angelin,et al. Interactions in the renal and biliary elimination of digoxin: Stereoselective difference between quinine and quinidine , 1990, Clinical pharmacology and therapeutics.
[7] Y. Lai,et al. Simultaneous Expression of hCNT1-CFP and hENT1-YFP in Madin-Darby Canine Kidney Cells , 2002, The Journal of Biological Chemistry.
[8] M. Melamed,et al. Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[9] Jashvant D Unadkat,et al. Placental drug transporters. , 2004, Current drug metabolism.
[10] J. Unadkat,et al. The effect of clarithromycin, fluconazole, and rifabutin on sulfamethoxazole hydroxylamine formation in individuals with human immunodeficiency virus infection (AACTG 283) , 2004, Clinical pharmacology and therapeutics.
[11] H. Saito,et al. Molecular cloning and tissue distribution of rat peptide transporter PEPT2. , 1996, Biochimica et biophysica acta.
[12] P. Sinko,et al. P-Glycoprotein and Mutlidrug Resistance-Associated Proteins Limit the Brain Uptake of Saquinavir in Mice , 2005, Journal of Pharmacology and Experimental Therapeutics.
[13] Y. Sugiyama,et al. Inhibition of biliary excretion of methotrexate by probenecid in rats: quantitative prediction of interaction from in vitro data. , 2001, The Journal of pharmacology and experimental therapeutics.
[14] A. Somogyi,et al. Reduction of metformin renal tubular secretion by cimetidine in man. , 1987, British journal of clinical pharmacology.
[15] B. Beermann,et al. Non-linear elimination and protein binding of probenecid , 2004, European Journal of Clinical Pharmacology.
[16] Peijin Zhang,et al. CHARACTERIZATION OF TRANSPORT PROTEIN EXPRESSION IN MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN (MRP) 2-DEFICIENT RATS , 2006, Drug Metabolism and Disposition.
[17] T. Cihlar,et al. Cytotoxicity of antiviral nucleotides adefovir and cidofovir is induced by the expression of human renal organic anion transporter 1. , 2000, Journal of the American Society of Nephrology : JASN.
[18] G. Mudge,et al. On the mechanism of action of probenecid on renal tubular secretion. , 1960, Bulletin of the Johns Hopkins Hospital.
[19] A. Schinkel,et al. P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs. , 1996, The Journal of clinical investigation.
[20] Cuiping Chen,et al. P-glycoprotein limits the brain penetration of nonsedating but not sedating H1-antagonists. , 2003, Drug metabolism and disposition: the biological fate of chemicals.
[21] G. Szakács,et al. MDR3 P-glycoprotein, a Phosphatidylcholine Translocase, Transports Several Cytotoxic Drugs and Directly Interacts with Drugs as Judged by Interference with Nucleotide Trapping* , 2000, The Journal of Biological Chemistry.
[22] R H Levy,et al. Influence of stiripentol on cytochrome P450‐mediated metabolic pathways in humans: In vitro and in vivo comparison and calculation of in vivo inhibition constants , 1997, Clinical pharmacology and therapeutics.
[23] Kari Laine,et al. Functional role of P‐glycoprotein in the human blood‐placental barrier , 2005, Clinical pharmacology and therapeutics.
[24] Joanne Wang,et al. (Section A: Molecular, Structural, and Cellular Biology of Drug Transporters) Mammalian Nucleoside Transporters , 2004 .
[25] W. Jaross,et al. Pharmacokinetics and Pharmacodynamics of Fluvastatin in Heart Transplant Recipients Taking Cyclosporine A , 2001, Journal of cardiovascular pharmacology and therapeutics.
[26] M. Breen,et al. pABC11 (Also Known as MOAT-C and MRP5), a Member of the ABC Family of Proteins, Has Anion Transporter Activity but Does Not Confer Multidrug Resistance When Overexpressed in Human Embryonic Kidney 293 Cells* , 1999, The Journal of Biological Chemistry.
[27] G. Kruh,et al. The MRP family of drug efflux pumps , 2003, Oncogene.
[28] D. Markovich,et al. Expression cloning of a cDNA from rabbit small intestine related to proton-coupled transport of peptides, ßlactam antibiotics and ACE-inhibitors , 1994, Pflügers Archiv.
[29] P. Neuvonen,et al. Plasma concentrations of active simvastatin acid are increased by gemfibrozil , 2000, Clinical pharmacology and therapeutics.
[30] Peter J. Meier,et al. Organic anion transporting polypeptides of the OATP/SLC21 family: phylogenetic classification as OATP/SLCO superfamily, new nomenclature and molecular/functional properties , 2004, Pflügers Archiv.
[31] D. Drayer,et al. Age and renal clearance of cimetidine , 1982, Clinical pharmacology and therapeutics.
[32] T. Abe,et al. Human liver-specific organic anion transporter, LST-1, mediates uptake of pravastatin by human hepatocytes. , 2001, The Journal of pharmacology and experimental therapeutics.
[33] J. Verweij,et al. Development of Multidrug-Resistance Convertors: Sense or Nonsense? , 2000, Investigational New Drugs.
[34] T. Abe,et al. Transcellular Transport of Organic Anions Across a Double-transfected Madin-Darby Canine Kidney II Cell Monolayer Expressing Both Human Organic Anion-transporting Polypeptide (OATP2/SLC21A6) and Multidrug Resistance-associated Protein 2 (MRP2/ABCC2)* , 2002, The Journal of Biological Chemistry.
[35] L. Moore,et al. The Pregnane X Receptor: A Promiscuous Xenobiotic Receptor That Has Diverged during Evolution , 2000 .
[36] M. Hediger,et al. Molecular cloning of PEPT 2, a new member of the H+/peptide cotransporter family, from human kidney. , 1995, Biochimica et biophysica acta.
[37] P. Meier,et al. The Sister of P-glycoprotein Represents the Canalicular Bile Salt Export Pump of Mammalian Liver* , 1998, The Journal of Biological Chemistry.
[38] A. Seelig,et al. A method to determine the ability of drugs to diffuse through the blood-brain barrier. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[39] K. Giacomini,et al. Cloning and functional expression of a human liver organic cation transporter. , 1997, Molecular pharmacology.
[40] S. Adibi. The oligopeptide transporter (Pept-1) in human intestine: biology and function. , 1997, Gastroenterology.
[41] M. Hediger,et al. Human Intestinal H+/Peptide Cotransporter , 1995, The Journal of Biological Chemistry.
[42] T. Litman,et al. Overexpression of the ATP-binding cassette half-transporter, ABCG2 (Mxr/BCrp/ABCP1), in flavopiridol-resistant human breast cancer cells. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[43] L. Doyle,et al. A multidrug resistance transporter from human MCF-7 breast cancer cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[44] Paul D. Martin,et al. Lack of effect of ketoconazole on the pharmacokinetics of rosuvastatin in healthy subjects. , 2003, British journal of clinical pharmacology.
[45] Y. Pommier,et al. Camptothecin resistance: role of the ATP-binding cassette (ABC), mitoxantrone-resistance half-transporter (MXR), and potential for glucuronidation in MXR-expressing cells. , 1999, Cancer research.
[46] O. van Tellingen,et al. Absence or pharmacological blocking of placental P-glycoprotein profoundly increases fetal drug exposure. , 1999, The Journal of clinical investigation.
[47] J. C. Martin,et al. (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]cytosine (cidofovir): results of a phase I/II study of a novel antiviral nucleotide analogue. , 1995, The Journal of infectious diseases.
[48] M. J. van de Vijver,et al. Subcellular localization and distribution of the breast cancer resistance protein transporter in normal human tissues. , 2001, Cancer research.
[49] S. Wright,et al. Molecular and cellular physiology of renal organic cation and anion transport. , 2004, Physiological reviews.
[50] B. M. Forman,et al. The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux , 2001, Nature Medicine.
[51] D. Mankoff,et al. Imaging P‐glycoprotein Transport Activity at the Human Blood‐brain Barrier with Positron Emission Tomography , 2005, Clinical pharmacology and therapeutics.
[52] J. Beijnen,et al. Improved penetration of docetaxel into the brain by co-administration of inhibitors of P-glycoprotein. , 2004, European journal of cancer.
[53] Y. Sugiyama,et al. The potential for an interaction between MRP2 (ABCC2) and various therapeutic agents: probenecid as a candidate inhibitor of the biliary excretion of irinotecan metabolites. , 2002, Drug metabolism and pharmacokinetics.
[54] G. Koren,et al. A model for the prediction of digoxin-drug interactions at the renal tubular cell level. , 1998, Therapeutic drug monitoring.
[55] John D. Allen,et al. A mutation hot spot in the Bcrp1 (Abcg2) multidrug transporter in mouse cell lines selected for Doxorubicin resistance. , 2002, Cancer research.
[56] L. Mangravite,et al. Nucleoside transporters in the disposition and targeting of nucleoside analogs in the kidney. , 2003, European journal of pharmacology.
[57] U. Christians,et al. Accumulation of lovastatin, but not pravastatin, in the blood of cyclosporine‐treated kidney graft patients after multiple doses , 1997, Clinical pharmacology and therapeutics.
[58] M. Kool,et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin‐Johnson syndrome , 1997, Hepatology.
[59] W. Haefeli,et al. Substantial pharmacokinetic interaction between digoxin and ritonavir in healthy volunteers , 2004, Clinical pharmacology and therapeutics.
[60] R. Béliveau,et al. Inhibition of P-glycoprotein by cyclosporin A analogues and metabolites. , 1999, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[61] M C Willingham,et al. Immunohistochemical localization in normal tissues of different epitopes in the multidrug transport protein P170: evidence for localization in brain capillaries and crossreactivity of one antibody with a muscle protein. , 1989, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[62] C. Funk,et al. Cholestatic potential of troglitazone as a possible factor contributing to troglitazone-induced hepatotoxicity: in vivo and in vitro interaction at the canalicular bile salt export pump (Bsep) in the rat. , 2001, Molecular pharmacology.
[63] Leslie Z. Benet,et al. Ex Situ Inhibition of Hepatic Uptake and Efflux Significantly Changes Metabolism: Hepatic Enzyme-Transporter Interplay , 2004, Journal of Pharmacology and Experimental Therapeutics.
[64] P. Hinderling,et al. Pharmacokinetics of Digoxin and Main Metabolites/Derivatives in Healthy Humans , 1991, Therapeutic drug monitoring.
[65] S. Cole,et al. Characterization of vincristine transport by the M(r) 190,000 multidrug resistance protein (MRP): evidence for cotransport with reduced glutathione. , 1998, Cancer research.
[66] L. Moore,et al. St. John's wort induces hepatic drug metabolism through activation of the pregnane X receptor. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[67] J. Nezu,et al. Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family. , 2000, Biochemical and biophysical research communications.
[68] H. Saito,et al. Interaction of β-Lactam Antibiotics with Histidine Residue of Rat H+/Peptide Cotransporters, PEPT1 and PEPT2* , 1998, The Journal of Biological Chemistry.
[69] F. Russel,et al. Molecular aspects of renal anionic drug transport. , 2002, Annual review of physiology.
[70] B. Kuppermann,et al. Intravenous Cidofovir for Peripheral Cytomegalovirus Retinitis in Patients with AIDS , 1997, Annals of Internal Medicine.
[71] P. A. Rea,et al. MRP Subfamily Transporters and Resistance to Anticancer Agents , 2001, Journal of bioenergetics and biomembranes.
[72] R. Traber,et al. Cyclosporins: structure-activity relationships for the inhibition of the human MDR1 P-glycoprotein ABC transporter. , 2002, Journal of medicinal chemistry.
[73] N. Klitgaard,et al. Effect of quinidine on digoxin bioavailability , 2004, European Journal of Clinical Pharmacology.
[74] H K Kroemer,et al. The role of intestinal P-glycoprotein in the interaction of digoxin and rifampin. , 1999, The Journal of clinical investigation.
[75] J. D. Karkas,et al. Plasma concentration profiles of simvastatin 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase inhibitory activity in kidney transplant recipients with and without ciclosporin. , 1993, Nephron.
[76] P. Neuvonen,et al. Gemfibrozil inhibits CYP2C8-mediated cerivastatin metabolism in human liver microsomes. , 2002, Drug metabolism and disposition: the biological fate of chemicals.
[77] M C Willingham,et al. Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[78] C Roland Wolf,et al. Directional trans-epithelial transport of organic anions in porcine LLC-PK1 cells that co-express human OATP1B1 (OATP-C) and MRP2. , 2005, Biochemical pharmacology.
[79] E. L. Volk,et al. Wild-type breast cancer resistance protein (BCRP/ABCG2) is a methotrexate polyglutamate transporter. , 2003, Cancer research.
[80] S. Mirski,et al. Multidrug resistance in a human small cell lung cancer cell line selected in adriamycin. , 1987, Cancer research.
[81] K. Audus,et al. Controlling drug delivery across the placenta. , 1999, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[82] H Nakano,et al. Basal membrane localization of MRP1 in human placental trophoblast. , 2003, Placenta.
[83] Oliver Burk,et al. Nuclear Receptor Response Elements Mediate Induction of Intestinal MDR1 by Rifampin* , 2001, The Journal of Biological Chemistry.
[84] L. Goodman,et al. The Pharmacological Basis of Therapeutics , 1941 .
[85] Y. Sawada,et al. Functional characterization of mouse cation transporter mOCT2 compared with mOCT1. , 2002, Biochemical and biophysical research communications.
[86] Richard J. Thompson,et al. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis , 1998, Nature Genetics.
[87] C. Beglinger,et al. Relevance of p‐glycoprotein for the enteral absorption of cyclosporin A: in vitro‐in vivo correlation , 1996, British journal of pharmacology.
[88] D. Meijer,et al. Hepatobiliary secretion of organic compounds; molecular mechanisms of membrane transport. , 1995, Biochimica et biophysica acta.
[89] Yuichi Sugiyama,et al. Comparative Studies on in Vitro Methods for Evaluating in Vivo Function of MDR1 P-Glycoprotein , 2001, Pharmaceutical Research.
[90] Paul D. Martin,et al. The effect of gemfibrozil on the pharmacokinetics of rosuvastatin , 2004, Clinical pharmacology and therapeutics.
[91] R. Flavell,et al. Double knockout of the MRP gene leads to increased drug sensitivity in vitro. , 1996, Cancer research.
[92] F. Marchlinski,et al. Adenosine as an antiarrhythmic agent. , 1997, The American journal of cardiology.
[93] L. Mangravite,et al. Localization of human equilibrative nucleoside transporters, hENT1 and hENT2, in renal epithelial cells. , 2003, American journal of physiology. Renal physiology.
[94] William A. Lee,et al. Effect of oral probenecid coadministration on the chronic toxicity and pharmacokinetics of intravenous cidofovir in cynomolgus monkeys. , 1998, Toxicological sciences : an official journal of the Society of Toxicology.
[95] F. Loor,et al. The potent immunosuppressive cyclosporin FR901459 inhibits the human P-glycoprotein and formyl peptide receptor functions. , 2000, The Journal of antibiotics.
[96] Ling He,et al. Interaction of multidrug resistance reversal agents with P-glycoprotein ATPase activity on blood-brain barrier. , 2002, Acta pharmacologica Sinica.
[97] R. Kim,et al. Human Organic Anion Transporting Polypeptide-C (SLC21A6) Is a Major Determinant of Rifampin-Mediated Pregnane X Receptor Activation , 2003, Journal of Pharmacology and Experimental Therapeutics.
[98] Hiroshi Suzuki,et al. Characterization of the Transport Properties of Cloned Rat Multidrug Resistance-associated Protein 3 (MRP3)* , 1999, The Journal of Biological Chemistry.
[99] K. Cundy. Clinical Pharmacokinetics of the Antiviral Nucleotide Analogues Cidofovir and Adefovir , 1999, Clinical pharmacokinetics.
[100] G R Lankas,et al. Placental P-glycoprotein deficiency enhances susceptibility to chemically induced birth defects in mice. , 1998, Reproductive toxicology.
[101] D. Drayer,et al. Aging and renal clearance of procainamide and acetylprocainamide , 1980, Clinical pharmacology and therapeutics.
[102] W. Sadee,et al. An oligopeptide transporter is expressed at high levels in the pancreatic carcinoma cell lines AsPc-1 and Capan-2. , 1998, Cancer research.
[103] A. Hartmann,et al. Bilateral Pharmacokinetic Interaction Between Cyclosporine A and Atorvastatin in Renal Transplant Recipients , 2001, American Journal of Transplantation.
[104] R. Davidson,et al. Preclinical and clinical pharmacology of Rosuvastatin, a new 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor. , 2001, The American journal of cardiology.
[105] K. Schenck-Gustafsson,et al. Digoxin‐verapamil interaction: Reduction of biliary but not renal digoxin clearance in humans , 1991, Clinical pharmacology and therapeutics.
[106] P. Neuvonen,et al. Gemfibrozil greatly increases plasma concentrations of cerivastatin , 2002, Clinical pharmacology and therapeutics.
[107] V. Ganapathy,et al. Interaction of anionic cephalosporins with the intestinal and renal peptide transporters PEPT 1 and PEPT 2. , 1997, Biochimica et biophysica acta.
[108] G R Wilkinson,et al. Pharmacological inhibition of P-glycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes. , 2000, Drug metabolism and disposition: the biological fate of chemicals.
[109] W. Sabbagh,et al. SXR, a novel steroid and xenobiotic-sensing nuclear receptor. , 1998, Genes & development.
[110] L Fritsche,et al. Increase in cerivastatin systemic exposure after single and multiple dosing in cyclosporine‐treated kidney transplant recipients , 1999, Clinical pharmacology and therapeutics.
[111] P. Borst,et al. Normal viability and altered pharmacokinetics in mice lacking mdr1-type (drug-transporting) P-glycoproteins. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[112] Vincenzo,et al. A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance. , 1998, Cancer research.
[113] J. Schellens,et al. Overexpression of the BCRP/MXR/ABCP gene in a topotecan-selected ovarian tumor cell line. , 1999, Cancer research.
[114] V. Natarajan,et al. Ritonavir Decreases the Nonrenal Clearance of Digoxin in Healthy Volunteers with Known MDR1 Genotypes , 2004, Therapeutic drug monitoring.
[115] D. Johnston,et al. Semi quantitative expression analysis of MDR3, FIC1, BSEP, OATP-A, OATP-C,OATP-D, OATP-E and NTCP gene transcripts in 1st and 3rd trimester human placenta. , 2003, Placenta.
[116] S. Bates,et al. Transport of methotrexate, methotrexate polyglutamates, and 17beta-estradiol 17-(beta-D-glucuronide) by ABCG2: effects of acquired mutations at R482 on methotrexate transport. , 2003, Cancer research.
[117] D. Piwnica-Worms,et al. Effects of MDR1 and MDR3 P-glycoproteins, MRP1, and BCRP/MXR/ABCP on the transport of (99m)Tc-tetrofosmin. , 2000, Biochemical pharmacology.
[118] Sean Ekins,et al. Three-Dimensional Quantitative Structure-Permeability Relationship Analysis for a Series of Inhibitors of Rhinovirus Replication , 2001, J. Chem. Inf. Comput. Sci..
[119] P. Welling,et al. Pharmacokinetics of cephradine given intravenously with and without probenecid. , 1981, British Journal of Clinical Pharmacology.
[120] Tsuyoshi Mikkaichi,et al. The organic anion transporter (OATP) family. , 2004, Drug metabolism and pharmacokinetics.
[121] M. Melamed,et al. Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[122] V A Levin,et al. Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeability. , 1980, Journal of medicinal chemistry.
[123] J. Schellens,et al. Role of breast cancer resistance protein in the bioavailability and fetal penetration of topotecan. , 2000, Journal of the National Cancer Institute.
[124] D. Keppler,et al. Differential inhibition by cyclosporins of primary‐active ATP‐dependent transporters in the hepatocyte canalicular membrane , 1993, FEBS letters.
[125] P. Neuvonen,et al. Itraconazole decreases renal clearance of digoxin. , 1997, Therapeutic drug monitoring.
[126] C. Sibley,et al. Role of MDR1 and MRP1 in trophoblast cells, elucidated using retroviral gene transfer. , 2003, American journal of physiology. Cell physiology.
[127] S. Bates,et al. Single-Nucleotide Polymorphism (SNP) Analysis in the ABC Half-Transporter ABCG2 (MXR/BCRP/ABCP1) , 2002, Cancer biology & therapy.
[128] A. Gavazzi,et al. Altered disposition of pravastatin following concomitant drug therapy with cyclosporin A in transplant recipients. , 1993, Transplantation proceedings.
[129] T. Litman,et al. Acquired mutations in the MXR/BCRP/ABCP gene alter substrate specificity in MXR/BCRP/ABCP-overexpressing cells. , 2001, Cancer research.
[130] J. S. Wang,et al. Gemfibrozil is a potent inhibitor of human cytochrome P450 2C9. , 2001, Drug metabolism and disposition: the biological fate of chemicals.
[131] D. Keppler,et al. Transport of glutathione, glucuronate, and sulfate conjugates by the MRP gene-encoded conjugate export pump. , 1996, Cancer research.
[132] V. Sasseville,et al. A Novel Human Hepatic Organic Anion Transporting Polypeptide (OATP2) , 1999, The Journal of Biological Chemistry.
[133] H. Kotani,et al. Single nucleotide polymorphisms result in impaired membrane localization and reduced atpase activity in multidrug transporter ABCG2 , 2004, International journal of cancer.
[134] S. Herrine,et al. Severe hepatotoxicity associated with troglitazone. , 1999, Annals of internal medicine.
[135] H. Yawo,et al. Identification of a Novel Gene Family Encoding Human Liver-specific Organic Anion Transporter LST-1* , 1999, The Journal of Biological Chemistry.
[136] M. Polis,et al. Clinical pharmacokinetics of cidofovir in human immunodeficiency virus-infected patients , 1995, Antimicrobial agents and chemotherapy.
[137] K. Maeda,et al. Bile Salt Export Pump (BSEP/ABCB11) Can Transport a Nonbile Acid Substrate, Pravastatin , 2005, Journal of Pharmacology and Experimental Therapeutics.
[138] T. Voskoglou-Nomikos,et al. Expression of multidrug resistance protein-related genes in lung cancer: correlation with drug response. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.
[139] M Zschiesche,et al. Oral bioavailability of digoxin is enhanced by talinolol: Evidence for involvement of intestinal P‐glycoprotein , 2000, Clinical pharmacology and therapeutics.
[140] S. Cole,et al. Patterns of cross-resistance in a multidrug-resistant small-cell lung carcinoma cell line , 2008, Cancer Chemotherapy and Pharmacology.
[141] J. Hitti,et al. P-glycoprotein and breast cancer resistance protein expression in human placentae of various gestational ages. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.
[142] E. Schuetz,et al. Natural allelic variants of breast cancer resistance protein (BCRP) and their relationship to BCRP expression in human intestine. , 2003, Pharmacogenetics.
[143] H. Krum,et al. Cytochrome P450 Drug Interactions Within the HMG-CoA Reductase Inhibitor Class , 2003, Drug safety.
[144] J. Beijnen,et al. The functional role of P-glycoprotein in the blood-brain barrier. , 1997, Journal of pharmaceutical sciences.
[145] D. Roden,et al. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. , 1998, The Journal of clinical investigation.
[146] G. Bodemar,et al. Oral absorption of cimetidine and its clearance in patients with renal failure , 1979, European Journal of Clinical Pharmacology.
[147] E. Randinitis,et al. Clinical Pharmacokinetics of Troglitazone , 1999, Clinical pharmacokinetics.
[148] J. Wijnholds,et al. The mouse Bcrp1/Mxr/Abcp gene: amplification and overexpression in cell lines selected for resistance to topotecan, mitoxantrone, or doxorubicin. , 1999, Cancer research.
[149] P. Neuvonen,et al. Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate , 2001, Clinical pharmacology and therapeutics.
[150] I. Pastan,et al. Biochemistry of multidrug resistance mediated by the multidrug transporter. , 1993, Annual review of biochemistry.
[151] A. Somogyi,et al. Cimetidine-procainamide pharmacokinetic interaction in man: Evidence of competition for tubular secretion of basic drugs , 2004, European Journal of Clinical Pharmacology.
[152] D. Piwnica-Worms,et al. Characterization of a 67Ga/68Ga radiopharmaceutical for SPECT and PET of MDR1 P-glycoprotein transport activity in vivo: validation in multidrug-resistant tumors and at the blood-brain barrier. , 2005, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[153] Paul D. Martin,et al. Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine , 2004, Clinical pharmacology and therapeutics.
[154] Roger L. Nation,et al. Differential Bidirectional Transfer of Indinavir in the Isolated Perfused Human Placenta , 2005, Antimicrobial Agents and Chemotherapy.
[155] A. Somogyi,et al. Pharmacokinetics and Bioavailability of Cimetidine in Gastric and Duodenal Ulcer Patients , 1980, Clinical pharmacokinetics.
[156] J. Schellens,et al. Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[157] Hua Yang,et al. The Binding of Cyclosporin A to Human Plasma: An in Vitro Microdialysis Study , 1996, Pharmaceutical Research.
[158] S. Bates,et al. Mutations at amino-acid 482 in the ABCG2 gene affect substrate and antagonist specificity , 2003, British Journal of Cancer.
[159] K. Ward,et al. Preclinical Pharmacokinetic Properties of the P-Glycoprotein Inhibitor GF120918A (HCl salt of GF120918, 9,10-Dihydro-5-methoxy-9-oxo-N-[4-[2-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolinyl)ethyl]phenyl]-4-acridine-carboxamide) in the Mouse, Rat, Dog, and Monkey , 2004, Journal of Pharmacology and Experimental Therapeutics.
[160] W Vaalburg,et al. Complete in vivo reversal of P‐glycoprotein pump function in the blood‐brain barrier visualized with positron emission tomography , 1998, British journal of pharmacology.
[161] G. Sousa,et al. Metabolism of digoxin, digoxigenin digitoxosides and digoxigenin in human hepatocytes and liver microsomes , 1991, Fundamental & clinical pharmacology.
[162] G. M. Wilson,et al. Pharmacological characterization of multidrug resistant MRP-transfected human tumor cells. , 1994, Cancer research.
[163] Y. Miki,et al. C421A polymorphism in the human breast cancer resistance protein gene is associated with low expression of Q141K protein and low-level drug resistance. , 2002, Molecular cancer therapeutics.
[164] R. Kim,et al. P-glycoprotein and cytochrome P-450 3A inhibition: dissociation of inhibitory potencies. , 1999, Cancer research.