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Journal of Pharmaceutical Sciences|January 29, 2022
Multiple Transport Mechanisms Involved in the Intestinal Absorption of Metformin: Impact on the Nonlinear Absorption KineticsYoshiyuki Shirasaka, Maria Seki, Marie Hatakeyama, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 4, 2025
The role of FLVCR1 and FLVCR2 in choline transport in the Caco-2 intestinal epithelial cell model and rat small intestineTomoya Yasujima, Chitaka Namba, Yosuke Azuma, et al.
Drug Metabolism and Pharmacokinetics|January 7, 2014
Evaluation of the potency of telaprevir and its metabolites as inhibitors of renal organic cation transporters, a potential mechanism for the elevation of serum creatinineTomohisa Nakada, Tomoko Kito, Katsuhisa Inoue, et al.
Pharmaceutical Research|August 3, 2013
Investigation of endogenous compounds for assessing the drug interactions in the urinary excretion involving multidrug and toxin extrusion proteinsKoji Kato, Haruyuki Mori, Tomoko Kito, et al.
Human Cell|August 31, 2013
Common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibilityAkiyoshi Nakayama, Hirotaka Matsuo, Takuya Shimizu, et al.
The Journal of Biological Chemistry|February 27, 2026
SLC52A1 Is a Neofunctionalized Primate Urate Transporter Enabling Intestinal Urate SecretionSyunsuke Yamamoto, Katsuhisa Inoue, Tomoya Yasujima, et al.
Annals of the Rheumatic Diseases|February 4, 2015
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypesHirotaka Matsuo, Ken Yamamoto, Hirofumi Nakaoka, et al.
Annals of the Rheumatic Diseases|December 1, 2016
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genesAkiyoshi Nakayama, Hirofumi Nakaoka, Ken Yamamoto, et al.
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