M. Hobbs

Cyclosporine Inhibition of Hepatic and Intestinal CYP3A4, Uptake and Efflux Transporters: Application of PBPK Modeling in the Assessment of Drug-Drug Interaction Potential

Malcolm Rowland, Michael Gertz, Aleksandra Galetin, 2012, Pharmaceutical Research.

Elevation of cysteine and replenishment of glutathione in rat lung slices by cysteine isopropylester and other cysteine precursors.

M. Butterworth, G. Cohen, M. Hobbs, 1993, Biochemical pharmacology.

Murine Oatp1a/1b Uptake Transporters Control Rosuvastatin Systemic Exposure Without Affecting Its Apparent Liver Exposure

E. van de Steeg, A. Schinkel, E. Wagenaar, 2013, Molecular Pharmacology.

Structure-activity relationships of cysteine esters and their effects on thiol levels in rat lung in vitro.

M. Butterworth, G. Cohen, M. Hobbs, 1993, Biochemical pharmacology.

Controlled Delivery of Dutasteride Using Dissolvable Microarrays: Initial Formulation and In-vivo Evaluation.

M. Hobbs, M. D. Burke, K. Brackenborough, 2019, Journal of pharmaceutical sciences.

Elevation of endogenous nucleophiles in rat lung by cysteine and glutathione esters in vitro.

S. K. Patel, M. Hobbs, D. G. Upshall, 1998, Biochemical pharmacology.

Organic anion-transporting polypeptides 1a/1b control the hepatic uptake of pravastatin in mice.

J. Beijnen, E. van de Steeg, A. Schinkel, 2012, Molecular pharmaceutics.

Cyclosporine Inhibition of Hepatic and Intestinal CYP3A4, Uptake and Efflux Transporters: Application of PBPK Modeling in the Assessment of Drug-Drug Interaction Potential

A. Galetin, J. Houston, M. Rowland, 2013, Pharmaceutical Research.

Understanding the interplay of drug transporters involved in the disposition of rosuvastatin in the isolated perfused rat liver using a physiologically-based pharmacokinetic model

Kathryn E. Kenworthy, M. Hobbs, C. Parker, 2012, Xenobiotica; the fate of foreign compounds in biological systems.