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Frontiers in Bioscience : a Journal and Virtual Library|December 1, 2004
Tissue-distribution of aldehyde dehydrogenase 2 and effects of the ALDH2 gene-disruption on the expression of enzymes involved in alcohol metabolismTsunehiro Oyama, Toyohi Isse, Norio Kagawa, et al.
FEBS Letters|November 10, 2006
The cytochrome P450 gene family CYP157 does not contain EXXR in the K-helix reducing the absolute conserved P450 residues to a single cysteineSanjeewa Rupasinghe, Mary A Schuler, Norio Kagawa, et al.
Frontiers in Bioscience : a Journal and Virtual Library|June 23, 2005
Expression of aldehyde dehydrogenase 2 in the normal esophageal epithelium and alcohol consumption in patients with esophageal cancerMasaru Morita, Tsunehiro Oyama, Norio Kagawa, et al.
Frontiers in Bioscience (Scholar Edition)|June 2, 2012
Cytochrome P450 in non-small cell lung cancer related to exogenous chemical metabolismTsunehiro Oyama, Hidetaka Uramoto, Norio Kagawa, et al.
Frontiers in Bioscience (Landmark Edition)|March 11, 2009
Hazardous environmental factors enhance impairment of liver function in HBV and HCV hepatitisYasunori Yashima, Tsunehiro Oyama, Thi Thu Phuong Pham, et al.
Frontiers in Bioscience (Elite Edition)|June 3, 2010
Effects of acetaldehyde inhalation in mitochondrial aldehyde dehydrogenase deficient mice (Aldh2-/-)Tsunehiro Oyama, Haruna Nagayoshi, Tomonari Matsuda, et al.
Frontiers in Bioscience : a Journal and Virtual Library|May 30, 2008
Expression of cytochrome P450 in non-small cell lung cancerTsunehiro Oyama, Kenji Sugio, Toyohi Isse, et al.
Frontiers in Bioscience : a Journal and Virtual Library|December 1, 2004
Tetracycline protects myocardium against ischemic injuryNorio Kagawa, Taka-aki Senbonmatsu, Kumi Satoh, et al.
Frontiers in Bioscience : a Journal and Virtual Library|February 24, 2004
Expression of cytochrome P450 in tumor tissues and its association with cancer developmentTsunehiro Oyama, Norio Kagawa, Naoki Kunugita, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD PhenotypeShaheena Parween, Mónica Fernández-Cancio, Sara Benito-Sanz, et al.
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