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Comparative Hepatic and Intestinal Metabolism and Pharmacodynamics of Statins

Drug metabolism and disposition, 2021-08, Vol.49 (8), p.658-667

2021

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Systemic hypertonic saline enhances glymphatic spinal cord delivery of lumbar intrathecal morphine

Journal of controlled release, 2022-04, Vol.344, p.214-224

2022

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The UDP-glucuronosyltransferases as oligomeric enzymes

Current drug metabolism, 2008-01, Vol.9 (1), p.70

2008

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Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases

Drug metabolism and disposition, 2010-03, Vol.38 (3), p.386

2010

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Kinetic characterization of the 1A subfamily of recombinant human UDP-glucuronosyltransferases

Drug metabolism and disposition, 2005-07, Vol.33 (7), p.1017

2005

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Glucuronidation of racemic O-desmethyltramadol, the active metabolite of tramadol

European journal of pharmaceutical sciences, 2010-11, Vol.41 (3), p.523-530

2010

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Glucuronidation of anabolic androgenic steroids by recombinant human UDP-glucuronosyltransferases

Drug metabolism and disposition, 2003-09, Vol.31 (9), p.1117

2003

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The interactions between the N-terminal and C-terminal domains of the human UDP-glucuronosyltransferases are partly isoform-specific, and may involve both monomers

Biochemical pharmacology, 2004-12, Vol.68 (12), p.2443-2450

2004

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The Human UDP-Glucuronosyltransferase: Identification of Key Residues within the Nucleotide-Sugar Binding Site

Molecular pharmacology, 2007-09, Vol.72 (3), p.604-611

2007

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Hydroxychloroquine is Metabolized by Cytochrome P450 2D6, 3A4, and 2C8, and Inhibits Cytochrome P450 2D6, while its Metabolites also Inhibit Cytochrome P450 3A in vitro

Drug metabolism and disposition, 2023-03, Vol.51 (3), p.293-305

2023

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Ticagrelor Increases Exposure to the Breast Cancer Resistance Protein Substrate Rosuvastatin

Clinical pharmacology and therapeutics, 2024-01, Vol.115 (1), p.71-79

2024

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Introduction of an electrochemical point‐of‐care assay for quantitative determination of paracetamol in finger‐prick capillary whole blood samples

British journal of clinical pharmacology, 2023-09, Vol.89 (9), p.2933-2938

2023

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Relationship of Edoxaban Plasma Concentration and Blood Coagulation in Healthy Volunteers Using Standard Laboratory Tests and Viscoelastic Analysis

Journal of clinical pharmacology, 2021-04, Vol.61 (4), p.522-530

2021

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Fluorescence-based high-throughput screening assay for drug interactions with UGT1A6

Assay and drug development technologies, 2011-10, Vol.9 (5), p.496

2011

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Interactions with other human UDP-glucuronosyltransferases attenuate the consequences of the Y485D mutation on the activity and substrate affinity of UGT1A6

Pharmacogenetics and genomics, 2007-02, Vol.17 (2), p.115-126

2007

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Isoform-Selective Inhibition of the Human UDP-glucuronosyltransferase 2B7 by Isolongifolol Derivatives

Journal of medicinal chemistry, 2007-05, Vol.50 (11), p.2655-2664

2007

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Potent Inhibitors of the Human UDP-Glucuronosyltransferase 2B7 Derived from the Sesquiterpenoid Alcohol Longifolol

ChemMedChem, 2007-06, Vol.2 (6), p.881-889

2007

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Comparative Hepatic and Intestinal Metabolism and Pharmacodynamics of Statins

Systemic hypertonic saline enhances glymphatic spinal cord delivery of lumbar intrathecal morphine

The UDP-glucuronosyltransferases as oligomeric enzymes

Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases

Kinetic characterization of the 1A subfamily of recombinant human UDP-glucuronosyltransferases

Glucuronidation of racemic O-desmethyltramadol, the active metabolite of tramadol

Glucuronidation of anabolic androgenic steroids by recombinant human UDP-glucuronosyltransferases

The interactions between the N-terminal and C-terminal domains of the human UDP-glucuronosyltransferases are partly isoform-specific, and may involve both monomers

The Human UDP-Glucuronosyltransferase: Identification of Key Residues within the Nucleotide-Sugar Binding Site

Hydroxychloroquine is Metabolized by Cytochrome P450 2D6, 3A4, and 2C8, and Inhibits Cytochrome P450 2D6, while its Metabolites also Inhibit Cytochrome P450 3A in vitro

Ticagrelor Increases Exposure to the Breast Cancer Resistance Protein Substrate Rosuvastatin

Introduction of an electrochemical point‐of‐care assay for quantitative determination of paracetamol in finger‐prick capillary whole blood samples

Relationship of Edoxaban Plasma Concentration and Blood Coagulation in Healthy Volunteers Using Standard Laboratory Tests and Viscoelastic Analysis

Fluorescence-based high-throughput screening assay for drug interactions with UGT1A6

Interactions with other human UDP-glucuronosyltransferases attenuate the consequences of the Y485D mutation on the activity and substrate affinity of UGT1A6

Isoform-Selective Inhibition of the Human UDP-glucuronosyltransferase 2B7 by Isolongifolol Derivatives

Potent Inhibitors of the Human UDP-Glucuronosyltransferase 2B7 Derived from the Sesquiterpenoid Alcohol Longifolol

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