N. Morita

The renal-specific transporter mediates facilitative transport of organic anions at the brush border membrane of mouse renal tubules.

H. Kusuhara, Y. Sugiyama, H. Endou, 2004, Journal of the American Society of Nephrology : JASN.

Failure to Demonstrate a Major Anti-Inflammatory Effect With Alpha Tocopherol Supplementation (400 IU/Day) in Normal Subjects

K. Kagawa, N. Morita, 2001 .

Activity of a novel carotenoid analog, 4,4′-(3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaen-1,18-diyl) bis(1-ethylpyridinium) dibromide (Y-18598) on mouse leukemia P388

T. Okumoto, M. Yamaguchi, N. Morita, 2004, Journal of Cancer Research and Clinical Oncology.

Functional characterization of rat organic anion transporter 2 in LLC-PK1 cells.

H. Kusuhara, Y. Sugiyama, H. Endou, 2001, The Journal of pharmacology and experimental therapeutics.

Discovery and characterization of a novel potent, selective and orally active inhibitor for mammalian ELOVL6.

R. Yoshimoto, T. Ohe, T. Nagase, 2010, European journal of pharmacology.

5,5-Dimethyl-3-(5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-1-phenyl-3-(trifluoromethyl)-3,5,6,7-tetrahydro-1H-indole-2,4-dione, a Potent Inhibitor for Mammalian Elongase of Long-Chain Fatty Acids Family 6: Examination of Its Potential Utility as a Pharmacological Tool

R. Yoshimoto, T. Ohe, T. Nagase, 2009, Journal of Pharmacology and Experimental Therapeutics.

5,5-dimethyl-3-( 5-methyl-3-oxo-2 -phenyl-2,3-dihy dro-1H-pyrazol-4-yl)-1- phenyl-3-(triflu oromethyl)-3,5,6,7-tetrahydro-1H -indole-2,4-dion e, A Potent Inhibitor for Mammalian ELOVL6: Examination of Its Potential Utility As A Pharmacological Tool

R. Yoshimoto, Y. Miyamoto, Maki Kanesaka, 2009 .

Human MDR1 polymorphism: G2677T/A and C3435T have no effect on MDR1 transport activities.

K. Nakayama, T. Yasumori, N. Morita, 2003, Biochemical pharmacology.

FUNCTIONAL INVOLVEMENT OF RAT ORGANIC ANION TRANSPORTER 2 (SLC22A7) IN THE HEPATIC UPTAKE OF THE NONSTEROIDAL ANTI-INFLAMMATORY DRUG KETOPROFEN

H. Kusuhara, Y. Sugiyama, H. Endou, 2005, Drug Metabolism and Disposition.