All Stories

  1. Pharmacokinetics of fixed-dose combination of atorvastatin and metformin compared with individual tablets
  2. Pharmacokinetic comparison of a fixed-dose combination versus concomitant administration of amlodipine, olmesartan, and rosuvastatin in healthy adult subjects
  3. Inhibition of Cytochrome P450 Activities by Sophora flavescens Extract and Its Prenylated Flavonoids in Human Liver Microsomes
  4. Effect of Cilostazol on the Pharmacokinetics of Simvastatin in Healthy Subjects
  5. Comprehensive Substrate Characterization of 22 Antituberculosis Drugs for Multiple Solute Carrier (SLC) Uptake TransportersIn Vitro
  6. Development of a Physiologically Based Pharmacokinetic Model of Ethionamide in the Pediatric Population by Integrating Flavin-Containing Monooxygenase 3 Maturational Changes Over Time
  7. Pharmacokinetics of Perampanel in Healthy Korean, White, and Japanese Adult Subjects
  8. Pharmacokinetic comparison of a fixed-dose combination versus concomitant administration of fimasartan, amlodipine, and rosuvastatin using partial replicated design in healthy adult subjects
  9. Comparative pharmacokinetics of a fixed-dose combination vs concomitant administration of telmisartan and S-amlodipine in healthy adult volunteers
  10. Evaluation of para-Aminosalicylic Acid as a Substrate of Multiple Solute Carrier Uptake Transporters and Possible Drug Interactions with Nonsteroidal Anti-inflammatory Drugs In Vitro
  11. Functional characterization and genetic effects on ethambutol uptake by organic cation transporter 2 (OCT2)
  12. Allopurinol-induced severe cutaneous adverse reactions: A report of three cases with the HLA-B*58:01 allele who underwent lymphocyte activation test
  13. The Effect of Age on the Pharmacokinetics of Udenafil in Healthy Subjects
  14. Inhibitory Interaction Potential of 22 Antituberculosis Drugs on Organic Anion and Cation Transporters of the SLC22A Family
  15. Population pharmacokinetics of levofloxacin in Korean patients
  16. Characterization of 22 Antituberculosis Drugs for Inhibitory Interaction Potential on Organic Anionic Transporter Polypeptide (OATP)-Mediated Uptake
  17. The pharmacokinetic and pharmacodynamic interaction of clopidogrel and cilostazol in relation toCYP2C19andCYP3A5genotypes
  18. Absolute bioavailability and pharmacokinetics of the angiotensin II receptor antagonist fimasartan in healthy subjects
  19. The effect ofGinkgo bilobaextracts on the pharmacokinetics and pharmacodynamics of cilostazol and its active metabolites in healthy Korean subjects
  20. Effect of renal impairment and haemodialysis on the pharmacokinetics of gemigliptin (LC15-0444)
  21. The Pharmacogenomics of Cytochrome P450s: From Molecular to Clinical Application
  22. The effect of CYP2C19 genotype on the time course of platelet aggregation inhibition after clopidogrel administration
  23. The Tyrosine Kinase Inhibitor Nilotinib Selectively Inhibits CYP2C8 Activities in Human Liver Microsomes
  24. Effect of CYP2C19 Genetic Polymorphism on Pharmacokinetics and Pharmacodynamics and Pharmacodynamics of a New Proton Pump Inhibitor, Ilaprazole
  25. Enantioselective carbonyl reduction of eperisone in human liver microsomes
  26. Research Highlights
  27. Potent inhibition of CYP2D6 by haloperidol metabolites: stereoselective inhibition by reduced haloperidol
  28. Duplex pyrosequencing assay of the 388A>G and 521T>C SLCO1B1 polymorphisms in three Asian populations
  29. Severe Leukopenia after Intravenous Cyclophosphamide Pulse Therapy in a Patient Having Cytochrome P450 2A6*1B
  30. Sequence-based CYP2D6 Genotyping in the Korean Population
  31. Effects of CYP2C19 and CYP2C9 genetic polymorphisms on the disposition of and blood glucose lowering response to tolbutamide in humans
  32. Clinical Significance of the Cytochrome P450 2C19 Genetic Polymorphism
  33. Drug Interaction on Metabolism : Induction of Metabolism
  34. Kinetics of isoniazid transfer into cerebrospinal fluid in patients with tuberculous meningitis
  35. Comparative Study of Captopril Tablets on the Bioavailability and the Time Course of Plasma Angiotensin-Converting Enzyme Inhibition