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A pregnancy physiologically based pharmacokinetic (p‐PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4

British journal of clinical pharmacology, 2012-11, Vol.74 (5), p.873-885

2012

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A novel simple disposition index (SPINA‐DI) from fasting insulin and glucose concentration as a robust measure of carbohydrate homeostasis

Journal of diabetes, 2024-09, Vol.16 (9), p.e13525-n/a

2024

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Pharmacogenetics of artemether‐lumefantrine influence on nevirapine disposition: Clinically significant drug–drug interaction?

British journal of clinical pharmacology, 2019-03, Vol.85 (3), p.540-550

2019

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Metabolic disposition of the EGFR covalent inhibitor furmonertinib in humans

Acta pharmacologica Sinica, 2022-02, Vol.43 (2), p.494-503

2022

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Metabolism and disposition of pyrotinib in healthy male volunteers: covalent binding with human plasma protein

Acta pharmacologica Sinica, 2019-07, Vol.40 (7), p.980-988

2019

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Nonelective hospital admissions, discharge disposition, and health services utilization in epilepsy patients: A population‐based study

Epilepsia (Copenhagen), 2020-09, Vol.61 (9), p.1969-1978

2020

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Drug disposition and modelling before and after gastric bypass: immediate and controlled‐release metoprolol formulations

British journal of clinical pharmacology, 2015-11, Vol.80 (5), p.1021-1030

2015

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Effect of rifampin on enantioselective disposition and anti‐hypertensive effect of benidipine

British journal of clinical pharmacology, 2019-04, Vol.85 (4), p.737-745

2019

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Human disposition, metabolism and excretion of etamicastat, a reversible, peripherally selective dopamine β‐hydroxylase inhibitor

British journal of clinical pharmacology, 2014-06, Vol.77 (6), p.1017-1026

2014

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Interaction between ABCG2 421C>A polymorphism and valproate in their effects on steady‐state disposition of lamotrigine in adults with epilepsy

British journal of clinical pharmacology, 2018-09, Vol.84 (9), p.2106-2119

2018

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Development of a risk prediction nomogram for disposition of acute toxic exposure patients to intensive care unit

Basic & clinical pharmacology & toxicology, 2021-09, Vol.129 (3), p.256-267

2021

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Target‐Mediated Drug Disposition Pharmacokinetic/Pharmacodynamic Model‐Informed Dose Selection for the First‐in‐Human Study of AVB‐S6‐500

Clinical and translational science, 2020-01, Vol.13 (1), p.204-211

2020

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Disposition of orally administered atuliflapon, a novel 5-lipoxygenase-activating protein inhibitor in healthy participants

Pharmacology research & perspectives, 2024-10, Vol.12 (5), p.e70029

2024

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Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage

Journal of the American Heart Association, 2023-05, Vol.12 (10), p.e027403-e027403

2023

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Stereoselective disposition of fluoxetine and norfluoxetine during pregnancy and breast‐feeding

British journal of clinical pharmacology, 2006-02, Vol.61 (2), p.155-163

2006

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Effects of proton pump inhibitors, esomeprazole and vonoprazan, on the disposition of proguanil, a CYP2C19 substrate, in healthy volunteers

British journal of clinical pharmacology, 2019-07, Vol.85 (7), p.1454-1463

2019

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Influence of SLCO1B3 haplotype‐tag SNPs on docetaxel disposition in Chinese nasopharyngeal cancer patients

British journal of clinical pharmacology, 2012-04, Vol.73 (4), p.606-618

2012

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Viral Nucleic Acid Testing (NAT) and OPO‐Level Disposition of High‐Risk Donor Organs

American journal of transplantation, 2009-03, Vol.9 (3), p.620-628

2009

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A target‐mediated drug disposition population pharmacokinetic model of GC1118, a novel anti‐EGFR antibody, in patients with solid tumors

Clinical and translational science, 2021-05, Vol.14 (3), p.990-1001

2021

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Trans‐3′‐hydroxycotinine: Disposition kinetics, effects and plasma levels during cigarette smoking

British journal of clinical pharmacology, 2001-01, Vol.51 (1), p.53-59

2001

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Relationship of CYP3A5 genotype and ABCB1 diplotype to tacrolimus disposition in Brazilian kidney transplant patients

British journal of clinical pharmacology, 2014-08, Vol.78 (2), p.364-372

2014

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Physiologically Based Pharmacokinetic Models for Adults and Children Reveal a Role of Intracellular Tubulin Binding in Vincristine Disposition

CPT: pharmacometrics and systems pharmacology, 2019-10, Vol.8 (10), p.759-768

2019

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Doxazosin treatment of phaeochromocytoma during pregnancy: placental transfer and disposition in breast milk

British journal of clinical pharmacology, 2016-08, Vol.82 (2), p.568-569

2016

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Bioavailability and disposition of azelastine and fluticasone propionate when delivered by MP29‐02, a novel aqueous nasal spray

British journal of clinical pharmacology, 2012-07, Vol.74 (1), p.125-133

2012

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Pharmacokinetics, disposition, and biotransformation of the cardiac myosin inhibitor aficamten in humans

Pharmacology research & perspectives, 2024-10, Vol.12 (5), p.e70006

2024

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A pregnancy physiologically based pharmacokinetic (p‐PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4

A novel simple disposition index (SPINA‐DI) from fasting insulin and glucose concentration as a robust measure of carbohydrate homeostasis

Pharmacogenetics of artemether‐lumefantrine influence on nevirapine disposition: Clinically significant drug–drug interaction?

Metabolic disposition of the EGFR covalent inhibitor furmonertinib in humans

Metabolism and disposition of pyrotinib in healthy male volunteers: covalent binding with human plasma protein

Nonelective hospital admissions, discharge disposition, and health services utilization in epilepsy patients: A population‐based study

Drug disposition and modelling before and after gastric bypass: immediate and controlled‐release metoprolol formulations

Effect of rifampin on enantioselective disposition and anti‐hypertensive effect of benidipine

Human disposition, metabolism and excretion of etamicastat, a reversible, peripherally selective dopamine β‐hydroxylase inhibitor

Interaction between ABCG2 421C>A polymorphism and valproate in their effects on steady‐state disposition of lamotrigine in adults with epilepsy

Development of a risk prediction nomogram for disposition of acute toxic exposure patients to intensive care unit

Target‐Mediated Drug Disposition Pharmacokinetic/Pharmacodynamic Model‐Informed Dose Selection for the First‐in‐Human Study of AVB‐S6‐500

Disposition of orally administered atuliflapon, a novel 5-lipoxygenase-activating protein inhibitor in healthy participants

Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage

Stereoselective disposition of fluoxetine and norfluoxetine during pregnancy and breast‐feeding

Effects of proton pump inhibitors, esomeprazole and vonoprazan, on the disposition of proguanil, a CYP2C19 substrate, in healthy volunteers

Influence of SLCO1B3 haplotype‐tag SNPs on docetaxel disposition in Chinese nasopharyngeal cancer patients

Viral Nucleic Acid Testing (NAT) and OPO‐Level Disposition of High‐Risk Donor Organs

A target‐mediated drug disposition population pharmacokinetic model of GC1118, a novel anti‐EGFR antibody, in patients with solid tumors

Trans‐3′‐hydroxycotinine: Disposition kinetics, effects and plasma levels during cigarette smoking

Relationship of CYP3A5 genotype and ABCB1 diplotype to tacrolimus disposition in Brazilian kidney transplant patients

Physiologically Based Pharmacokinetic Models for Adults and Children Reveal a Role of Intracellular Tubulin Binding in Vincristine Disposition

Doxazosin treatment of phaeochromocytoma during pregnancy: placental transfer and disposition in breast milk

Bioavailability and disposition of azelastine and fluticasone propionate when delivered by MP29‐02, a novel aqueous nasal spray

Pharmacokinetics, disposition, and biotransformation of the cardiac myosin inhibitor aficamten in humans

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