M. Ohshima

Probing the Ubiquinone Reduction Site of Mitochondrial Complex I Using Novel Cationic Inhibitors*

H. Iwamura, H. Miyoshi, M. Inoue, 1997, The Journal of Biological Chemistry.

Essential structural factors of annonaceous acetogenins as potent inhibitors of mitochondrial complex I.

H. Iwamura, H. Miyoshi, H. Shimada, 1998, Biochimica et biophysica acta.

Role of the isoprenyl tail of ubiquinone in reaction with respiratory enzymes: studies with bovine heart mitochondrial complex I and Escherichia coli bo-type ubiquinol oxidase.

H. Iwamura, H. Miyoshi, K. Kano, 1998, Biochemistry.

Characterization of the ubiquinone reduction site of mitochondrial complex I using bulky synthetic ubiquinones.

H. Iwamura, T. Yagi, H. Miyoshi, 1998, Biochemistry.

Comparison of the structural features of ubiquinone reduction sites between glucose dehydrogenase in Escherichia coli and bovine heart mitochondrial complex I.

H. Iwamura, H. Miyoshi, K. Matsushita, 1996, European journal of biochemistry.

High oxidizing activity of 3,10-dimethyl-8-azaisoalloxazine (8-azaflavin) and its synthetic application as a turnover redox catalyst under aerobic conditions

A. Kitani, M. Ohshima, K. Sasaki, 1985 .

Flavin mimics posssessing remarkably high oxidizing power: 6,8-diazaflavins

M. Ohshima, Y. Yano, M. Nakazato, 1984 .