スポンサーリンク
Hospital for Sick Children | 論文
- 9.成人発症II型シトルリン血症疾患モデルマウスの開発
- Substrate Specificity of Human 3(20)α-Hydroxysteroid Dehydrogenase for Neurosteroids and Its Inhibition by Benzodiazepines
- Structure-specific Effcects of Thyroxine Analogs on Human Liver 3α-Hydroxysteroid Dehydrogenase.
- Substrate Specificity of a Mouse Aldo-Keto Reductase (AKR1C12)(Biochemistry)
- Molecular Cloning of a Novel Type of Rat Cytoplasmic 17β-Hydroxysteroid Dehydrogenase Distinct from the Type 5 Isozyme
- Enzymatic Properties of a Member (AKR1C20) of the Aldo-Keto Reductase Family(Biochemistry)
- Enzymatic Properties of a Member (AKR1C19) of the Aldo-Keto Reductase Family(Biochemistry/Molecular Biology)
- Structural and Functional Characterization of Rabbit and Human L-Gulonate 3-Dehydrogenase
- Characterization of Two Isoforms of Mouse 3(17)α-Hydroxysteroid Dehydrogenases of the Aldo-Keto Reductase Family(Biochemistry/Molecular Biology)
- Characterization of a Major Form of Human Isatin Reductase and the Reduced Metabolite.
- Molecular Cloning, Expression and Tissue Distribution of Hamster Diacetyl Reductase. : Identity with L-Xylulose.
- Enzymatic Characteristics and Subcellular Distribution of A Short-Chain Dehydrogenase/Reductase Family Protein, P26h, in Hamster Testis and epididymis.
- Crystallization and Preliminary X-ray Diffraction Analysis of Monkey Dimeric Dihydrodiol Dehydrogenase.
- Identity of Dimeric Dihydrodiol Dehydrogenase as NADP^+-dependent D-Xylose Dehydrogenase in Pig Liver.
- Roles of His-79 and Tyr-180 of D-Kylose/Dihydrodiol Dehydrogenase in Catalytic Function.
- Kinetic Alteration of Human Dihydrodiol/3α-Hydroxysteroid Dehydrogenase Isoenzyme, AKR1C4,by Replacement of Histidine-216 with Tyrosine or Phenylalanine.
- Structure-Specifis Effects of Thyroxine Analogs on Human Liver 3α-Hydroxysteroid Dehydrogenase
- Cloning and Sequencing of the cDNA Species for Mammalian Dimeric Dihydrodiol Dehydrogenases.
- Inhibition of Human Aldehyde Reductase by Drugs for Testing the Function of Liver and Kidney.
- Inhibition of Human Aldehyde Reductase by Drugs for Testing the Function of Liver and Kidney