All Stories

  1. Pharmacogenetics of Anticoagulation and Clinical Events in Warfarin-Treated Patients: A Register-Based Cohort Study with Biobank Data and National Health Registries in Finland
  2. Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrients
  3. UGT1A3 and Sex Are Major Determinants of Telmisartan Pharmacokinetics—A Comprehensive Pharmacogenomic Study
  4. Itraconazole Increases Ibrutinib Exposure 10‐Fold and Reduces Interindividual Variation—A Potentially Beneficial Drug‐Drug Interaction
  5. Enantiospecific Pharmacogenomics of Fluvastatin
  6. Clopidogrel and Gemfibrozil Strongly Inhibit the CYP2C8-Dependent Formation of 3-Hydroxydesloratadine and Increase Desloratadine Exposure In Humans
  7. Clopidogrel Increases Dasabuvir Exposure With or Without Ritonavir, and Ritonavir Inhibits the Bioactivation of Clopidogrel
  8. Ketamine and norketamine attenuate oxycodone tolerance markedly less than that of morphine: from behaviour to drug availability
  9. Transporter-Mediated Alterations in Patients With NASH Increase Systemic and Hepatic Exposure to an OATP and MRP2 Substrate
  10. Safety of Single-Dose Primaquine in G6PD-Deficient and G6PD-Normal Males in Mali Without Malaria: An Open-Label, Phase 1, Dose-Adjustment Trial
  11. Safety of single low-dose primaquine in glucose-6-phosphate dehydrogenase deficient falciparum-infected African males: Two open-label, randomized, safety trials
  12. Interactions of (2S,6S;2R,6R)-Hydroxynorketamine, a Secondary Metabolite of (R,S)-Ketamine, with Morphine
  13. Clopidogrel but Not Prasugrel Significantly Inhibits the CYP2C8-Mediated Metabolism of Montelukast in Humans
  14. Effects of Genetic Variants on Carboxylesterase 1 Gene Expression, and Clopidogrel Pharmacokinetics and Antiplatelet Effects
  15. Clopidogrel Carboxylic Acid Glucuronidation is Mediated Mainly by UGT2B7, UGT2B4, and UGT2B17: Implications for Pharmacogenetics and Drug-Drug Interactions
  16. Comprehensive Pharmacogenomic Study Reveals an Important Role of UGT1A3 in Montelukast Pharmacokinetics
  17. Novel copy-number variations in pharmacogenes contribute to interindividual differences in drug pharmacokinetics
  18. Analgesic Plasma Concentrations of Oxycodone After Surgery for Breast Cancer—Which Factors Matter?
  19. Age, Weight, and CYP2D6 Genotype Are Major Determinants of Primaquine Pharmacokinetics in African Children
  20. Do Diuretics have Antinociceptive Actions: Studies of Spironolactone, Eplerenone, Furosemide and Chlorothiazide, Individually and with Oxycodone and Morphine
  21. Primaquine to reduce transmission of Plasmodium falciparum malaria in Mali: a single-blind, dose-ranging, adaptive randomised phase 2 trial
  22. Role of Cytochrome P450 2C8 in Drug Metabolism and Interactions
  23. Clopidogrel Has No Clinically Meaningful Effect on the Pharmacokinetics of the Organic Anion Transporting Polypeptide 1B1 and Cytochrome P450 3A4 Substrate Simvastatin
  24. SLCO1B1 polymorphism markedly affects the pharmacokinetics of lovastatin acid
  25. Drug-Related Inadvertent Deaths in a University Hospital - A Declining Trend
  26. Effect of carboxylesterase 1 c.428G > A single nucleotide variation on the pharmacokinetics of quinapril and enalapril
  27. Effect of grapefruit juice on the bioactivation of prasugrel
  28. Pregabalin enhances the antinociceptive effect of oxycodone and morphine in thermal models of nociception in the rat without any pharmacokinetic interactions
  29. Ketamine coadministration attenuates morphine tolerance and leads to increased brain concentrations of both drugs in the rat
  30. Carboxylesterase 1 c.428G>A single nucleotide variation increases the antiplatelet effects of clopidogrel by reducing its hydrolysis in humans
  31. Paroxetine Markedly Increases Plasma Concentrations of Ophthalmic Timolol; CYP2D6 Inhibitors May Increase the Risk of Cardiovascular Adverse Effects of 0.5% Timolol Eye Drops
  32. Glucuronidation Converts Clopidogrel to a Strong Time-Dependent Inhibitor of CYP2C8: A Phase II Metabolite as a Perpetrator of Drug–Drug Interactions
  33. The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update
  34. Pharmacogenetically based dosing of thiopurines in childhood acute lymphoblastic leukemia: Influence on cure rates and risk of second cancer
  35. PharmGKB summary
  36. Grapefruit Juice Inhibits the Metabolic Activation of Clopidogrel
  37. The mineralocorticoid receptor antagonist spironolactone enhances morphine antinociception
  38. International Transporter Consortium Commentary on Clinically Important Transporter Polymorphisms
  39. Grapefruit juice markedly increases the plasma concentrations and antiplatelet effects of ticagrelor in healthy subjects
  40. Gemfibrozil Impairs Imatinib Absorption and Inhibits the CYP2C8-Mediated Formation of Its Main Metabolite
  41. Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification
  42. SLCO2B1 c.935G>A single nucleotide polymorphism has no effect on the pharmacokinetics of montelukast and aliskiren
  43. A Mechanistic, Model-Based Approach to Safety Assessment in Clinical Development
  44. Drug interactions with oral antidiabetic agents: pharmacokinetic mechanisms and clinical implications
  45. The Clinical Pharmacogenomics Implementation Consortium: CPIC Guideline for SLCO1B1 and Simvastatin-Induced Myopathy
  46. Carboxylesterase 1 Polymorphism Impairs Oseltamivir Bioactivation in Humans
  47. PPARA: A Novel Genetic Determinant of CYP3A4 In Vitro and In Vivo
  48. Gemfibrozil Is a Strong Inactivator of CYP2C8 in Very Small Multiple Doses
  49. Fluconazole but not the CYP3A4 inhibitor, itraconazole, increases zafirlukast plasma concentrations
  50. Gender, but not CYP7A1 or SLCO1B1 Polymorphism, Affects the Fasting Plasma Concentrations of Bile Acids in Human Beings
  51. Transfer of repaglinide in the dually perfused human placenta and the role of organic anion transporting polypeptides (OATPs)
  52. Dose-Dependent Interaction between Gemfibrozil and Repaglinide in Humans: Strong Inhibition of CYP2C8 with Subtherapeutic Gemfibrozil Doses
  53. No significant effect of the SLCO1B1 polymorphism on the pharmacokinetics of ursodeoxycholic acid
  54. Orange and apple juice greatly reduce the plasma concentrations of the OATP2B1 substrate aliskiren
  55. Mechanism-Based Inactivation of CYP2C8 by Gemfibrozil Occurs Rapidly in Humans
  56. Itraconazole, a P-Glycoprotein and CYP3A4 Inhibitor, Markedly Raises the Plasma Concentrations and Enhances the Renin-Inhibiting Effect of Aliskiren
  57. Pharmacokinetics of Intravenous Paracetamol in Elderly Patients
  58. Organic Anion Transporting Polypeptide 1B1: a Genetically Polymorphic Transporter of Major Importance for Hepatic Drug Uptake
  59. Practical recommendations for pharmacogenomics-based prescription: 2010 ESF–UB Conference on Pharmacogenetics and Pharmacogenomics
  60. Frequencies of Single-Nucleotide Polymorphisms of SLCO1A2, SLCO1B3 and SLCO2B1 Genes in a Finnish Population
  61. SLCO1B1 Polymorphism and Oral Antidiabetic Drugs
  62. Grapefruit Juice Greatly Reduces the Plasma Concentrations of the OATP2B1 and CYP3A4 Substrate Aliskiren
  63. Gemfibrozil Markedly Increases the Plasma Concentrations of Montelukast: A Previously Unrecognized Role for CYP2C8 in the Metabolism of Montelukast
  64. Effect of ABCB1 haplotypes on the pharmacokinetics and renin-inhibiting effect of aliskiren
  65. Long-Term Changes in Cyclosporine Pharmacokinetics After Renal Transplantation in Children: Evidence for Saturable Presystemic Metabolism and Effect ofNR1I2Polymorphism
  66. Membrane transporters in drug development
  67. Rifampicin reduces the plasma concentrations and the renin-inhibiting effect of aliskiren
  68. High performance liquid chromatography–tandem mass spectrometry for the determination of bile acid concentrations in human plasma
  69. Transporter Pharmacogenetics and Statin Toxicity
  70. Different effects of the ABCG2 c.421C>A SNP on the pharmacokinetics of fluvastatin, pravastatin and simvastatin
  71. UDP-Glucuronosyltransferase (UGT) Polymorphisms Affect Atorvastatin Lactonization In Vitro and In Vivo
  72. Impact of OATP transporters on pharmacokinetics
  73. CYP2C8 Activity Recovers within 96 Hours after Gemfibrozil Dosing: Estimation of CYP2C8 Half-Life Using Repaglinide as an in Vivo Probe
  74. No significant effect ofABCB1haplotypes on the pharmacokinetics of fluvastatin, pravastatin, lovastatin, and rosuvastatin
  75. Effect of SLCO1B1 polymorphism on the plasma concentrations of bile acids and bile acid synthesis marker in humans
  76. ABCG2 Polymorphism Markedly Affects the Pharmacokinetics of Atorvastatin and Rosuvastatin
  77. The effect ofSLCO1B1polymorphism on repaglinide pharmacokinetics persists over a wide dose range
  78. Effects of the SLCO1B1*1B haplotype on the pharmacokinetics and pharmacodynamics of repaglinide and nateglinide
  79. Polymorphism of the hepatic influx transporter organic anion transporting polypeptide 1B1 is associated with increased cholesterol synthesis rate
  80. Effects of Gemfibrozil and Atorvastatin on the Pharmacokinetics of Repaglinide in Relation to SLCO1B1 Polymorphism
  81. ABCB1 Haplotypes Differentially Affect the Pharmacokinetics of the Acid and Lactone Forms of Simvastatin and Atorvastatin
  82. The Effect of Gemfibrozil on Repaglinide Pharmacokinetics Persists for at Least 12 h After the Dose: Evidence for Mechanism-based Inhibition of CYP2C8 In Vivo
  83. Different Effects ofSLCO1B1Polymorphism on the Pharmacokinetics and Pharmacodynamics of Repaglinide and Nateglinide
  84. Pharmacogenetics of cyclosporine in children suggests an age-dependent influence of ABCB1 polymorphisms
  85. Global analysis of genetic variation in SLCO1B1
  86. No significant effect ofSLCO1B1polymorphism on the pharmacokinetics of rosiglitazone and pioglitazone
  87. Pharmacokinetic Comparison of the Potential Over-the-Counter Statins Simvastatin, Lovastatin, Fluvastatin and Pravastatin
  88. Characterization of novel CYP2C8 haplotypes and their contribution to paclitaxel and repaglinide metabolism
  89. Trimethoprim and the CYP2C8*3 Allele Have Opposite Effects on the Pharmacokinetics of Pioglitazone
  90. Role of OATP transporters in the disposition of drugs
  91. Effects of clarithromycin and grapefruit juice on the pharmacokinetics of glibenclamide
  92. Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin
  93. Stereoselective interaction between the CYP2C8 inhibitor gemfibrozil and racemic ibuprofen
  94. Influence of Drug Transporter Polymorphisms on Pravastatin Pharmacokinetics in Humans
  95. Drug interactions with lipid-lowering drugs: Mechanisms and clinical relevance
  96. SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid
  97. Association of genetic polymorphism in ABCC2 with hepatic multidrug resistance-associated protein 2 expression and pravastatin pharmacokinetics
  98. SLCO1B1 polymorphism and sex affect the pharmacokinetics of pravastatin but not fluvastatin
  99. Cyclosporine A Increases Plasma Concentrations and Effects of Repaglinide
  100. Effect of SLCO1B1 polymorphism on induction of CYP3A4 by rifampicin
  101. Pharmacokinetics and response to pravastatin in paediatric patients with familial hypercholesterolaemia and in paediatric cardiac transplant recipients in relation to polymorphisms of the SLCO1B1 and ABCB1 genes
  102. Montelukast and zafirlukast do not affect the pharmacokinetics of the CYP2C8 substrate pioglitazone
  103. Impact of the SLCO1B1 polymorphism on the pharmacokinetics and lipid-lowering efficacy of multiple-dose pravastatin
  104. Itraconazole, gemfibrozil and their combination markedly raise the plasma concentrations of loperamide
  105. Frequencies of single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide 1B1 SLCO1B1 gene in a Finnish population
  106. Telithromycin, but not montelukast, increases the plasma concentrations and effects of the cytochrome P450 3A4 and 2C8 substrate repaglinide
  107. Muscle Symptoms Associated with Statins: A Series of Twenty Patients
  108. Cyclosporine markedly raises the plasma concentrations of repaglinide
  109. Coadministration of gemfibrozil and itraconazole has only a minor effect on the pharmacokinetics of the CYP2C9 and CYP3A4 substrate nateglinide
  110. Polymorphic organic anion transporting polypeptide 1B1 is a major determinant of repaglinide pharmacokinetics
  111. Acute effects of pravastatin on cholesterol synthesis are associated with SLCO1B1 (encoding OATP1B1) haplotype *17
  112. Fexofenadine pharmacokinetics are associated with a polymorphism of the SLCO1B1 gene (encoding OATP1B1)
  113. CYP3A5 Genotype is Associated with Diagnosis of Hypertension in Elderly Patients
  114. Functional interaction of intestinal CYP3A4 and P-glycoprotein
  115. Effects of trimethoprim and rifampin on the pharmacokinetics of the cytochrome P450 2C8 substrate rosiglitazone
  116. Lipid-lowering response to statins is affected by CYP3A5 polymorphism
  117. Characterisation of cerivastatin as a P-glycoprotein substrate: studies in P-glycoprotein-expressing cell monolayers and mdr1a/b knock-out mice
  118. High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)
  119. The CYP2C8 inhibitor trimethoprim increases the plasma concentrations of repaglinide in healthy subjects
  120. Rifampicin reduces plasma concentrations of celiprolol
  121. Gemfibrozil considerably increases the plasma concentrations of rosiglitazone
  122. Polymorphism in CYP2C8 is associated with reduced plasma concentrations of repaglinide
  123. Effect of rifampicin on the pharmacokinetics and pharmacodynamics of nateglinide in healthy subjects
  124. Effect of fluconazole on the pharmacokinetics and pharmacodynamics of nateglinide
  125. Pharmacokinetic Interactions with Rifampicin
  126. Plasma concentrations of inhaled budesonide and its effects on plasma cortisol are increased by the cytochrome P4503A4 inhibitor itraconazole
  127. Glyburide and glimepiride pharmacokinetics in subjects with different CYP2C9 genotypes*
  128. Effect of gemfibrozil on the pharmacokinetics and pharmacodynamics of glimepiride
  129. The cytochrome P4503A4 inhibitor clarithromycin increases the plasma concentrations and effects of repaglinide
  130. Effects of rifampin on the pharmacokinetics and pharmacodynamics of glyburide and glipizide
  131. Effects of fluconazole and fluvoxamine on the pharmacokinetics and pharmacodynamics of glimepiride
  132. Effect of rifampicin on the pharmacokinetics and pharmacodynamics of glimepiride
  133. Rifampin decreases the plasma concentrations and effects of repaglinide
  134. Effect of fluconazole on plasma fluvastatin and pravastatin concentrations