S. Mimasu

Full-length in meso structure and mechanism of rat kynurenine 3-monooxygenase inhibition

S. Kubo, Julie Liu, C. Hupp, 2021, Communications biology.

Crystallographic study of a site-specifically cross-linked protein complex with a genetically incorporated photoreactive amino acid.

T. Umehara, S. Yokoyama, K. Sakamoto, 2011, Biochemistry.

FAD-dependent lysine-specific demethylase-1 regulates cellular energy expenditure

M. Nakao, T. Umehara, S. Yokoyama, 2012, Nature Communications.

Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 .

T. Umehara, S. Yokoyama, T. Higuchi, 2010, Biochemistry.

Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25 A.

T. Umehara, S. Yokoyama, S. Fukuzawa, 2008, Biochemical and biophysical research communications.

Pharmacological and Structural Characterizations of Naquotinib, a Novel Third-Generation EGFR Tyrosine Kinase Inhibitor, in EGFR-Mutated Non–Small Cell Lung Cancer

T. Betsuyaku, K. Soejima, K. Naoki, 2018, Molecular Cancer Therapeutics.

Full-length in meso structure and mechanism of rat kynurenine 3-monooxygenase inhibition

S. Kubo, Julie Liu, C. Hupp, 2021, Communications Biology.

Abstract 2586: ASP8273 selectively inhibits mutant EGFR signal pathway and induces tumor shrinkage in EGFR mutated tumor models

S. Kuromitsu, Masaaki Hirano, Hiroko Yamamoto, 2015 .

Discovery and Biological Evaluation of Potent and Orally Active Human 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors for the Treatment of Type 2 Diabetes Mellitus.

Ayako Moritomo, S. Yoshimura, R. Shiraki, 2019, Chemical and pharmaceutical bulletin.