T. Naito

发表

Pioglitazone, a peroxisome proliferator-activated receptor gamma agonist, reduces the progression of experimental osteoarthritis in guinea pigs.

J. Pelletier, J. Martel-Pelletier, Tetsuya Kobayashi, 2005, Arthritis and rheumatism.

Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1″ binding site.

H. Oki, Kenjiro Sato, O. Uchikawa, 2014, Bioorganic & medicinal chemistry.

Improvement of pulmonary arterial hypertension, inflammatory response, and epithelium injury by dual activation of cAMP/cGMP pathway in a rat model of monocrotaline-induced pulmonary hypertension

T. Matsuo, K. Tohyama, Yo Muraki, 2019, Bioscience, biotechnology, and biochemistry.

Effects of prostaglandins on ornithine decarboxylase activity in rat small intestine

H. Kuwayama, T. Naito, 1993, Digestive Diseases and Sciences.

Discovery of novel, highly potent, and selective quinazoline-2-carboxamide-based matrix metalloproteinase (MMP)-13 inhibitors without a zinc binding group using a structure-based design approach.

H. Oki, Kenjiro Sato, O. Uchikawa, 2014, Journal of medicinal chemistry.

Antiproliferative activity of mammalian lignan derivatives against the human breast carcinoma cell line, ZR-75-1.

K. Oka, T. Naito, T. Hirano, 1990, Cancer investigation.

Differential Contribution of Insulin and Amino Acids to the mTORC1-Autophagy Pathway in the Liver and Muscle*

N. Mizushima, Akiko Kuma, T. Naito, 2013, The Journal of Biological Chemistry.

Ring1B promotes hepatic stem/progenitor cell expansion through simultaneous suppression of Cdkn1a and Cdkn2a in mice

Susumu Nakata, K. Sekine, H. Taniguchi, 2014, Hepatology.

Role of Polycomb group proteins in the hepatic stem cell self-renewal

H. Taniguchi, Y. Ueno, T. Naito, 2009 .

Discovery of Novel, Highly Potent, and Selective Matrix Metalloproteinase (MMP)-13 Inhibitors with a 1,2,4-Triazol-3-yl Moiety as a Zinc Binding Group Using a Structure-Based Design Approach.

H. Oki, Kenjiro Sato, A. Kaieda, 2017, Journal of medicinal chemistry.

Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1″ binding site.

H. Oki, Kenjiro Sato, O. Uchikawa, 2014, Bioorganic & medicinal chemistry.

Ion-sparing diuresis by 2,3-dibenzylbutane-1,4-diol, a synthetic mammalian-lignan derivative.

K. Oka, M. Homma, T. Hirano, 1991, Life sciences.