Tetsuya Mitsui

The reconstituted 'humanized liver' in TK-NOG mice is mature and functional.

M. Suematsu, H. Suemizu, Masato Nakamura, 2011, Biochemical and biophysical research communications.

In vitro model for the prediction of clinical CYP3A4 induction using HepaRG cells

K. Takeda, Y. Aso, N. Sekiguchi, 2009, Xenobiotica; the fate of foreign compounds in biological systems.

Nonlinear intestinal pharmacokinetics of mitemcinal, the first acid-resistant non-peptide motilin receptor agonist, in rats

S. Ōmura, T. Kawanishi, Y. Aso, 2007, Xenobiotica; the fate of foreign compounds in biological systems.

Method for predicting the risk of drug–drug interactions involving inhibition of intestinal CYP3A4 and P-glycoprotein

Y. Sugiyama, T. Tachibana, T Tachibana, 2009, Xenobiotica; the fate of foreign compounds in biological systems.

Structure-permeability relationship analysis of the permeation barrier properties of the stratum corneum and viable epidermis/dermis of rat skin.

K. Sugibayashi, Y. Aso, Yoshinori Aso, 2008, Journal of pharmaceutical sciences.

Selective SGLT2 inhibition by tofogliflozin reduces renal glucose reabsorption under hyperglycemic but not under hypo- or euglycemic conditions in rats.

Y. Kawabe, Kiyofumi Honda, Mio Kawai, 2013, American journal of physiology. Endocrinology and metabolism.

Quantitative Prediction of Mechanism-Based Inhibition Caused by Mibefradil in Rats

Motohiro Kato, Y. Aso, M. Ishigai, 2011, Drug Metabolism and Disposition.

A Useful Model Capable of Predicting the Clearance of Cytochrome P450 3A4 (CYP3A4) Substrates in Humans: Validity of CYP3A4 Transgenic Mice Lacking Their Own Cyp3a Enzymes

M. Ishigai, T. Miyake, H. Yamada, 2014, Drug Metabolism and Disposition.