T Yubisui

Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type).

Komei Shirabe, T Yubisui, Nica Borgese et al. · Journal of Biological Chemistry · 1992 · 62 citations · Full text

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type

Yukio Kobayashi, Y Fukumaki, T Yubisui et al. · Blood · 1990 · 60 citations · Full text

Molecular cloning of cDNAs of human liver and placenta NADH-cytochrome b5 reductase.

T Yubisui, Y. Naitoh, Shuhei Zenno et al. · Proceedings of the National Academy of Sciences · 1987 · 51 citations · Full text

Aldo-keto Reductase, Genetics, Molecular Biology +16

Characterization of the purified NADH-cytochrome b5 reductase of human erythrocytes as a FAD-containing enzyme.

T Yubisui, M Takeshita · Journal of Biological Chemistry · 1980 · 48 citations · Full text

An in-frame deletion of codon 298 of the NADH-cytochrome b5 reductase gene results in hereditary methemoglobinemia type II (generalized type). A functional implication for the role of the COOH-terminal region of the enzyme.

Komei Shirabe, Yoshio Fujimoto, T Yubisui et al. · Journal of Biological Chemistry · 1994 · 45 citations · Full text

Alcohol Dehydrogenases, Biochemistry, Cellular Enzymology +14