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Oxidoreductase
Altered Expression and Function of Mitochondrial Я-Oxidation Enzymes
Isocitrate Dehydrogenase 1 (NADP+) (I5036)
Pro-Aging Effects of Xanthine Oxidoreductase Products
RESEARCH COMMUNICATION HADHA Is a Potential Predictor Of
Glyoxysomal Malate Dehydrogenase from Watermelon Is Synthesized
Cholic Acid for Treating Inborn Errors of Primary Bile Acid Synthesis NHS England Unique Reference Number URN1623 / NICE ID004
Additional File 1
Bioactivity of Curcumin on the Cytochrome P450 Enzymes of the Steroidogenic Pathway
Flavonoids, Cinnamic Acid Derivatives As Inhibitors of 17(-Hydroxysteroid
Structural Basis for the Electron Transfer from an Open Form of NADPH-Cytochrome P450 Oxidoreductase to Heme Oxygenase
Significance to Female Reproductive Physiology1
Partial Purification and Characterization of an Ls-NADP: Isocitrate Oxidoreductase from Embryonic Chick Liver
Role of NAD+-Dependent Malate Dehydrogenase in the Metabolism of Methylomicrobium Alcaliphilum 20Z and Methylosinus Trichosporium Ob3b
Inborn Errors of Bile Acid Metabolism
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Physiological and Biochemical Aspects of 17Β-Hydroxysteroid Dehydrogenase Type 2 and 3
Microbial Hydroxysteroid Dehydrogenases: from Alpha to Omega
Expression of the Mouse Tyrosinase Gene During Embryonic Development
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All Enzymes in BRENDA™ the Comprehensive Enzyme Information System
46,XX DSD Due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features
Steroid 21-Hydroxylasedeficiency: Three Additional Mutated Alleles
Dopachrome Oxidoreductase: a New Enzyme in the Pigment Pathway
Tyrosinase Maturation Through the Mammalian Secretory Pathway: Bringing Color to Life
Alternative Androgen Pathway Biosynthesis Drives Fetal Female Virilization in P450 Oxidoreductase Deficiency Nicole Reischa,B, Richard J
(Cyp8b1) Gene; an Alternative Mechanism for Bile Acid
Human Cholesterol 7Α-Hydroxylase (CYP7A1) Deficiency Has a Hypercholesterolemic Phenotype
Cytochrome P450 Oxidoreductase Deficiency in Three Patients Initially
Enzyme Classification
17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency
Structural Characterization of 17Β-Hydroxysteroid Dehydrogenase Type 14 and Inhibitor Optimization Using Crystallography and Computational Techniques
Rare Defects in Adrenal Steroidogenesis
Differential Effects of Variations in Human P450 Oxidoreductase on the Aromatase Activity of CYP19A1 Polymorphisms R264C and R264H
The Mechanism of Superoxide Production by NADH:Ubiquinone Oxidoreductase (Complex I) from Bovine Heart Mitochondria
Supplementary Table 2 - in Silico Reconstruction of the Metabolic Pathways of S
Long-Term Follow-Up of a Female with Congenital Adrenal Hyperplasia Due
Molecular and Structural Evolution of Cytochrome P450 Aromatase
17Β-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotypic Variability and Molecular Findings
6-Phosphogluconate Dehydrogenase (Central Intermediary Metabolism/Cell-Free Protein Synthesis/Gnd/3':5'-Cyclic AMP) TOMAS ISTURIZ* and RICHARD E
Reconsidering Aromatase for Breast Cancer Treatment: New Roles for an Old Target
Tyrosinase (T3824)
Update Review About Metabolic Myopathies
The Tyrosinase Protein Families Chem184 May 13, 2008
Differential Effects of Variations in Human P450 Oxidoreductase on the Aromatase Activity of CYP19A1 Polymorphisms R264C and R264H
Measurement of Tyrosinase Activity Using the LAMBDA 465 UV/Vis
LINC00116 Codes for a Mitochondrial Peptide Linking Respiration and Lipid Metabolism
Molecular Mechanism Study on Stereo-Selectivity of Α Or Β Hydroxysteroid Dehydrogenases
Structural and Stereoelectronic Insights Into Oxygenase-Catalyzed Formation of Ethylene from 2-Oxoglutarate
REVIEW 17Β-Hydroxysteroid Dehydrogenase (HSD)/17
(12) Patent Application Publication (10) Pub. No.: US 2013/0273277 A1 Lee Et Al
Mutational Analysis of the Catalytic Residues Lysine 230 and Tyrosine 160 in the Nadpf-Dependent Isocitrate Dehydrogenase from Escherichia Colit Myoung E
Generate Metabolic Map Poster
Clinical and Molecular Review of Atypical Congenital Adrenal Hyperplasia
Minor Activities and Transition State Properties of the Human Steroid
Structure of a Bacterial Enzyme Regulated by Phosphorylation
Pharmacological and Clinical Significance of Heme Oxygenase-1
Molecular Basis of CYP19A1 Deficiency in a 46, XX Patient with R550W Mutation in POR: Expanding the PORD Phenotype