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Division Of Drug Metabolism And Molecular Toxicology Graduate School Of Pharmaceutical Sciences Toho | 論文
- C-14-2 Development of Radio on Free Space Optics System for Ubiquitous Wireless Services : (2) Evaluation of Performance Degradation due to Scintillation in IEEE 802.1 la
- C-14-13 統合型光無線システムの研究開発(C-14.マイクロ波フォトニクス,一般セッション)
- Involvement of thioredoxin-binding protein 2 in the antitumor activity of CD437
- C-14-4 統合型光無線システムの研究開発(C-14. マイクロ波フォトニクス,一般セッション)
- ヒトP450分子種の HepG2 細胞における複数同時発現 : 組換えアデノウイルスを用いたP450再構成系
- ヒト薬物動態関連遺伝子の発現に対するHNF4αの寄与をsiRNA発現アデノウイルスを用いて解析する
- MACROMOLECULAR BINDING OF CARCINOGENIC/MUTAGENIC N- HYDROXYARYLAMINES THROUGH O-ACETYLATION PATHWAY
- C-14-10 Development of Radio on Free Space Optics System for Ubiquitous Wireless Services : (4) A New Analytical Approach for Scintillation Model
- C-14-2 Development of Radio on Free Space Optics System for Ubiquitous Wireless Services : (2)Time-Correlated Optical Intensity Fluctuation Model for RoFSO Link Evaluation
- Genetic analysis of expression profile involved in retinoid metabolism in non-alcoholic fatty liver disease
- Tumor Necrosis Factor-Alpha–Nuclear Factor-Kappa B-Signaling Enhances St2b2 Expression during 12-O-Tetradecanoylphorbol-13-acetate-Induced Epidermal Hyperplasia
- C-14-9 統合型光無線システムの研究開発(C-14.マイクロ波フォトニクス,一般講演)
- Molecular Cloning and Characterization of Rat ST1B1 and Human ST1B2 cDNAs, Encoding Thyroid Hormone Sulfotransferases
- Formation of 2-Amino-3-methylimidazo[4,5-f]quinoline- and 2-Amino-3, 8-dimethylimidazo[4,5-f]quinoxaline-sulfamates by cDNA-expressed Mammalian Phenol Sulfotransferases
- 327 Isolation and expression of hamster acetyltransferase genes, AT-A and AT-B
- CLONING, EXPRESSION, AND FUNCTIONAL CHARACTERIZATION OF RAT AND HUMAN PHENOL SULFOTRANSFERASES
- RAT LIVER SULFOTRANSFERASE ACTIVATING CARCINOGENIC HYDROXYMETHYL-ARENES : ITS PROPERTIES AND SEQUENCE ANALYSIS OF cDNA
- Bile Acid-Induced Elevated Oxidative Stress in the Absence of Farnesoid X Receptor(Biochemistry)
- Hydroxysteroid sulfotransferase (SULT2A) の発現はFXRにより抑制的に調節される
- Bile acid sulfates as a possible early marker of liver toxicity(Drug metabolism, Proceedings of the 32nd Annual Meeting)
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