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Drug Metabolism & Disposition

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Most cited article(s)

  • You have access
    Regulation of Drug-Metabolizing Enzymes and Transporters in Infection, Inflammation, and Cancer
    Edward T. Morgan, Kerry B. Goralski, Micheline Piquette-Miller, Kenneth W. Renton, Graham R. Robertson, Madhusudana R. Chaluvadi, Kellie A. Charles, Stephen J. Clarke, Marina Kacevska, Christopher Liddle, Terrilyn A. Richardson, Rohini Sharma and Christopher J. Sinal
    Drug Metabolism and Disposition February 2008, 36 (2) 205-216; DOI: https://doi.org/10.1124/dmd.107.018747
  • You have access
    SELECTIVITY OF SUBSTRATE (TRIFLUOPERAZINE) AND INHIBITOR (AMITRIPTYLINE, ANDROSTERONE, CANRENOIC ACID, HECOGENIN, PHENYLBUTAZONE, QUINIDINE, QUININE, AND SULFINPYRAZONE) “PROBES” FOR HUMAN UDP-GLUCURONOSYLTRANSFERASES
    Verawan Uchaipichat, Peter I. Mackenzie, David J. Elliot and John O. Miners
    Drug Metabolism and Disposition March 2006, 34 (3) 449-456; DOI: https://doi.org/10.1124/dmd.105.007369
  • You have access
    Glucuronidation of Amines and Other Xenobiotics Catalyzed by Expressed Human UDP-Glucuronosyltransferase 1A3
    Mitchell D. Green, Christopher D. King, Behnaz Mojarrabi, Peter I. Mackenzie and Thomas R. Tephly
    Drug Metabolism and Disposition June 1998, 26 (6) 507-512;
  • You have access
    Induction of CYP2C Genes in Human Hepatocytes in Primary Culture
    Sabine Gerbal-Chaloin, Jean-Marc Pascussi, Lydiane Pichard-Garcia, Martine Daujat, Felix Waechter, Jean-Michel Fabre, Nicolas Carrère and Patrick Maurel
    Drug Metabolism and Disposition March 2001, 29 (3) 242-251;
  • You have access
    A Combined Model for Predicting CYP3A4 Clinical Net Drug-Drug Interaction Based on CYP3A4 Inhibition, Inactivation, and Induction Determined in Vitro
    Odette A. Fahmi, Tristan S. Maurer, Mary Kish, Edwin Cardenas, Sherri Boldt and David Nettleton
    Drug Metabolism and Disposition August 2008, 36 (8) 1698-1708; DOI: https://doi.org/10.1124/dmd.107.018663
  • You have access
    Evaluation of the Selectivity of In Vitro Probes and Suitability of Organic Solvents for the Measurement of Human Cytochrome P450 Monooxygenase Activities
    Dean Hickman, Ji-Ping Wang, Yi Wang and Jashvant D. Unadkat
    Drug Metabolism and Disposition March 1998, 26 (3) 207-215;
  • You have access
    EVALUATION OF 3′-AZIDO-3′-DEOXYTHYMIDINE, MORPHINE, AND CODEINE AS PROBE SUBSTRATES FOR UDP-GLUCURONOSYLTRANSFERASE 2B7 (UGT2B7) IN HUMAN LIVER MICROSOMES: SPECIFICITY AND INFLUENCE OF THE UGT2B7*2 POLYMORPHISM
    Michael H. Court, Soundarajan Krishnaswamy, Qin Hao, Su X. Duan, Christopher J. Patten, Lisa L. von Moltke and David J. Greenblatt
    Drug Metabolism and Disposition September 2003, 31 (9) 1125-1133; DOI: https://doi.org/10.1124/dmd.31.9.1125
  • You have access
    DRUG-DRUG INTERACTION BETWEEN PITAVASTATIN AND VARIOUS DRUGS VIA OATP1B1
    Masaru Hirano, Kazuya Maeda, Yoshihisa Shitara and Yuichi Sugiyama
    Drug Metabolism and Disposition July 2006, 34 (7) 1229-1236; DOI: https://doi.org/10.1124/dmd.106.009290
  • You have access
    Development of a Substrate-Activity Based Approach To Identify the Major Human Liver P-450 Catalysts of Cyclophosphamide and Ifosfamide Activation Based on cDNA-Expressed Activities and Liver Microsomal P-450 Profiles
    Partha Roy, Li J. Yu, Charles L. Crespi and David J. Waxman
    Drug Metabolism and Disposition June 1999, 27 (6) 655-666;
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    EXPRESSION OF CYTOCHROMES P450, CONJUGATING ENZYMES AND NUCLEAR RECEPTORS IN HUMAN HEPATOMA HepaRG CELLS
    Caroline Aninat, Amélie Piton, Denise Glaise, Typhen Le Charpentier, Sophie Langouët, Fabrice Morel, Christiane Guguen-Guillouzo and André Guillouzo
    Drug Metabolism and Disposition January 2006, 34 (1) 75-83; DOI: https://doi.org/10.1124/dmd.105.006759

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