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Investigating catechin-mediated effects on drug solubility as a mechanism underlying a green tea-raloxifene pharmcokinetic interaction

Drug metabolism and pharmacokinetics, 2024-04, Vol.55, p.100843, Article 100843

2024

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Rifampin- and silymarin-mediated pharmcokinetic interactions of pitavastatin, pravastatin, coproporphyrin I, and coproporphyrin III in a transgenic OATP1B mouse model

Drug metabolism and pharmacokinetics, 2024-04, Vol.55, p.100980, Article 100980

2024

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Green Tea Catechins Decrease Solubility of Raloxifene In Vitro and Its Systemic Exposure in Mice

Pharmaceutical research, 2024-03, Vol.41 (3), p.557-566

2024

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Pharmacokinetic Effects of Different Models of Nonalcoholic Fatty Liver Disease in Transgenic Humanized OATP1B Mice

Drug metabolism and disposition, 2024-05, Vol.52 (5), p.355-367

2024

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Rifampin- and Silymarin-Mediated Pharmacokinetic Interactions of Exogenous and Endogenous Substrates in a Transgenic OATP1B Mouse Model

Molecular pharmaceutics, 2024-05, Vol.21 (5), p.2284-2297

2024

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Goldenseal-mediated inhibition of intestinal uptake transporters decreases metformin systemic exposure in mice

Drug metabolism and disposition, 2023-11, Vol.51 (11), p.1483-1489

2023

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Hepatic organic anion transporting polypeptides mediate disposition of milk thistle flavonolignans and pharmacokinetic silymarin‐drug interactions

Phytotherapy research, 2021-06, Vol.35 (6), p.3286-3297

2021

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Multi-factorial pharmacokinetic interactions: unraveling complexities in precision drug therapy

Expert opinion on drug metabolism & toxicology, 2021-04, Vol.17 (4), p.397-412

2021

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Silymarin‐mediated Natural Product–Drug Interactions involving Enteric Organic Anion Transporting Polypeptides

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Abstract 2064: CHRM1-mediated acetylcholine signaling protects prostate cancer cells from the chemotherapy agent docetaxel

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.2064-2064

2019

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Disease-, Natural Product-, and Drug-Mediated Pharmacokinetic Interactions of Hepatic Organic Anion Transporting Polypeptides 1B1 and 1B3 Using Transgenic Humanized OATP1B Mice

Bechtold, Baron J

2024

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Cholinergic signaling via muscarinic M1 receptor confers resistance to docetaxel in prostate cancer

Cell reports. Medicine, 2024-02, Vol.5 (2), p.101388-101388, Article 101388

2024

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GAD-treatment of children and adolescents with recent-onset type 1 diabetes preserves residual insulin secretion after 30 months

Diabetes/metabolism research and reviews, 2014-07, Vol.30 (5), p.405-414

2014

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Investigating catechin-mediated effects on drug solubility as a mechanism underlying a green tea-raloxifene pharmcokinetic interaction

Rifampin- and silymarin-mediated pharmcokinetic interactions of pitavastatin, pravastatin, coproporphyrin I, and coproporphyrin III in a transgenic OATP1B mouse model

Green Tea Catechins Decrease Solubility of Raloxifene In Vitro and Its Systemic Exposure in Mice

Pharmacokinetic Effects of Different Models of Nonalcoholic Fatty Liver Disease in Transgenic Humanized OATP1B Mice

Rifampin- and Silymarin-Mediated Pharmacokinetic Interactions of Exogenous and Endogenous Substrates in a Transgenic OATP1B Mouse Model

Goldenseal-mediated inhibition of intestinal uptake transporters decreases metformin systemic exposure in mice

Hepatic organic anion transporting polypeptides mediate disposition of milk thistle flavonolignans and pharmacokinetic silymarin‐drug interactions

Multi-factorial pharmacokinetic interactions: unraveling complexities in precision drug therapy

Silymarin‐mediated Natural Product–Drug Interactions involving Enteric Organic Anion Transporting Polypeptides

Abstract 2064: CHRM1-mediated acetylcholine signaling protects prostate cancer cells from the chemotherapy agent docetaxel

Disease-, Natural Product-, and Drug-Mediated Pharmacokinetic Interactions of Hepatic Organic Anion Transporting Polypeptides 1B1 and 1B3 Using Transgenic Humanized OATP1B Mice

Cholinergic signaling via muscarinic M1 receptor confers resistance to docetaxel in prostate cancer

GAD-treatment of children and adolescents with recent-onset type 1 diabetes preserves residual insulin secretion after 30 months

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