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Treatment With Antipsychotics in Pregnancy: Changes in Drug Disposition

Clinical pharmacology and therapeutics, 2018-03, Vol.103 (3), p.477-484

2018

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Effects of Pregnancy on CYP3A and P-glycoprotein Activities as Measured by Disposition of Midazolam and Digoxin: A University of Washington Specialized Center of Research Study

Clinical pharmacology and therapeutics, 2008-08, Vol.84 (2), p.248-253

2008

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Use of Real‐World Data and Physiologically‐Based Pharmacokinetic Modeling to Characterize Enoxaparin Disposition in Children With Obesity

Clinical pharmacology and therapeutics, 2022-08, Vol.112 (2), p.391-403

2022

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Food Effect on Rosuvastatin Disposition and Low‐Density Lipoprotein Cholesterol

Clinical pharmacology and therapeutics, 2018-09, Vol.104 (3), p.525-533

2018

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Imatinib Disposition and ABCB1 (MDR1, P‐Glycoprotein) Genotype

Clinical pharmacology and therapeutics, 2007-07, Vol.82 (1), p.33-40

2007

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Common Polymorphisms of CYP2B6 Influence Stereoselective Bupropion Disposition

Clinical pharmacology and therapeutics, 2019-01, Vol.105 (1), p.142-152

2019

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Influence of OATPs on Hepatic Disposition of Erlotinib Measured With Positron Emission Tomography

Clinical pharmacology and therapeutics, 2018-07, Vol.104 (1), p.139-147

2018

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Altered morphine glucuronide and bile acid disposition in patients with nonalcoholic steatohepatitis

Clinical pharmacology and therapeutics, 2015-04, Vol.97 (4), p.419-427

2015

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Use of Physiologically Based Pharmacokinetic Modeling to Evaluate the Effect of Chronic Kidney Disease on the Disposition of Hepatic CYP2C8 and OATP1B Drug Substrates

Clinical pharmacology and therapeutics, 2019-03, Vol.105 (3), p.719-729

2019

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CYP2A6 genotype and the metabolism and disposition kinetics of nicotine

Clinical pharmacology and therapeutics, 2006-11, Vol.80 (5), p.457-467

2006

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CYP3A5 and CYP3A4 but not MDR1 Single‐nucleotide Polymorphisms Determine Long‐term Tacrolimus Disposition and Drug‐related Nephrotoxicity in Renal Recipients

Clinical pharmacology and therapeutics, 2007-12, Vol.82 (6), p.711-725

2007

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Disposition of Acetaminophen at 4, 6, and 8 g day for 3 Days in Healthy Young Adults

Clinical pharmacology and therapeutics, 2007-06, Vol.81 (6), p.840-848

2007

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Assessment of Placental Disposition of Infliximab and Etanercept in Women With Autoimmune Diseases and in the Ex Vivo Perfused Placenta

Clinical pharmacology and therapeutics, 2020-07, Vol.108 (1), p.99-106

2020

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Population Modeling Highlights Drug Disposition Differences Between Tenofovir Alafenamide and Tenofovir Disoproxil Fumarate in the Blood and Semen

Clinical pharmacology and therapeutics, 2019-10, Vol.106 (4), p.821-830

2019

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Pharmacogenetic Characterization of Sulfasalazine Disposition Based on NAT2 and ABCG2 (BCRP) Gene Polymorphisms in Humans

Clinical pharmacology and therapeutics, 2008-07, Vol.84 (1), p.95-103

2008

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OATP1B1 Polymorphism as a Determinant of Erythromycin Disposition

Clinical pharmacology and therapeutics, 2012-11, Vol.92 (5), p.642-650

2012

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Bergamottin contribution to the grapefruit juice-felodipine interaction and disposition in humans

Clinical pharmacology and therapeutics, 2004-12, Vol.76 (6), p.607-617

2004

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Carbamazepine regulates intestinal P-glycoprotein and multidrug resistance protein MRP2 and influences disposition of talinolol in humans

Clinical pharmacology and therapeutics, 2004-09, Vol.76 (3), p.192-200

2004

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Measurement and Compartmental Modeling of the Effect of CYP3A5 Gene Variation on Systemic and Intrarenal Tacrolimus Disposition

Clinical pharmacology and therapeutics, 2012-12, Vol.92 (6), p.737-745

2012

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Role of hepatic and intestinal cytochrome P450 3A and 2B6 in the metabolism, disposition, and miotic effects of methadone

Clinical pharmacology and therapeutics, 2004-09, Vol.76 (3), p.250-269

2004

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6′,7′-Dihydroxybergamottin in grapefruit juice and Seville orange juice: Effects on cyclosporine disposition, enterocyte CYP3A4, and P-glycoprotein

Clinical pharmacology and therapeutics, 1999-03, Vol.65 (3), p.237-244

1999

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Effect of verapamil on pharmacokinetics and pharmacodynamics of risperidone: In vivo evidence of involvement of P-glycoprotein in risperidone disposition

Clinical pharmacology and therapeutics, 2005-07, Vol.78 (1), p.43-51

2005

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The effect of rifampin administration on the disposition of fexofenadine

Clinical pharmacology and therapeutics, 2001-03, Vol.69 (3), p.114-121

2001

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The pharmacokinetics and metabolic disposition of tacrolimus: A comparison across ethnic groups

Clinical pharmacology and therapeutics, 2001-01, Vol.69 (1), p.24-31

2001

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The effects of the human MDR1 genotype on the expression of duodenal P‐glycoprotein and disposition of the probe drug talinolol

Clinical pharmacology and therapeutics, 2002-11, Vol.72 (5), p.572-583

2002

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Zeitschrift / SerieThe American Journal Of Emergency Medicine

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Treatment With Antipsychotics in Pregnancy: Changes in Drug Disposition

Effects of Pregnancy on CYP3A and P-glycoprotein Activities as Measured by Disposition of Midazolam and Digoxin: A University of Washington Specialized Center of Research Study

Use of Real‐World Data and Physiologically‐Based Pharmacokinetic Modeling to Characterize Enoxaparin Disposition in Children With Obesity

Food Effect on Rosuvastatin Disposition and Low‐Density Lipoprotein Cholesterol

Imatinib Disposition and ABCB1 (MDR1, P‐Glycoprotein) Genotype

Common Polymorphisms of CYP2B6 Influence Stereoselective Bupropion Disposition

Influence of OATPs on Hepatic Disposition of Erlotinib Measured With Positron Emission Tomography

Altered morphine glucuronide and bile acid disposition in patients with nonalcoholic steatohepatitis

Use of Physiologically Based Pharmacokinetic Modeling to Evaluate the Effect of Chronic Kidney Disease on the Disposition of Hepatic CYP2C8 and OATP1B Drug Substrates

CYP2A6 genotype and the metabolism and disposition kinetics of nicotine

CYP3A5 and CYP3A4 but not MDR1 Single‐nucleotide Polymorphisms Determine Long‐term Tacrolimus Disposition and Drug‐related Nephrotoxicity in Renal Recipients

Disposition of Acetaminophen at 4, 6, and 8 g day for 3 Days in Healthy Young Adults

Assessment of Placental Disposition of Infliximab and Etanercept in Women With Autoimmune Diseases and in the Ex Vivo Perfused Placenta

Population Modeling Highlights Drug Disposition Differences Between Tenofovir Alafenamide and Tenofovir Disoproxil Fumarate in the Blood and Semen

Pharmacogenetic Characterization of Sulfasalazine Disposition Based on NAT2 and ABCG2 (BCRP) Gene Polymorphisms in Humans

OATP1B1 Polymorphism as a Determinant of Erythromycin Disposition

Bergamottin contribution to the grapefruit juice-felodipine interaction and disposition in humans

Carbamazepine regulates intestinal P-glycoprotein and multidrug resistance protein MRP2 and influences disposition of talinolol in humans

Measurement and Compartmental Modeling of the Effect of CYP3A5 Gene Variation on Systemic and Intrarenal Tacrolimus Disposition

Role of hepatic and intestinal cytochrome P450 3A and 2B6 in the metabolism, disposition, and miotic effects of methadone

6′,7′-Dihydroxybergamottin in grapefruit juice and Seville orange juice: Effects on cyclosporine disposition, enterocyte CYP3A4, and P-glycoprotein

Effect of verapamil on pharmacokinetics and pharmacodynamics of risperidone: In vivo evidence of involvement of P-glycoprotein in risperidone disposition

The effect of rifampin administration on the disposition of fexofenadine

The pharmacokinetics and metabolic disposition of tacrolimus: A comparison across ethnic groups

The effects of the human MDR1 genotype on the expression of duodenal P‐glycoprotein and disposition of the probe drug talinolol

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