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Immunity, ISSN 1074-7613, 10/2016, Volume 45, Issue 4, pp. 761 - 773
Journal Article
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 12/2010, Volume 335, Issue 3, pp. 533 - 545
Doxorubicin (DOX) and daunorubicin (DAUN) are effective anticancer drugs; however, considerable interpatient variability exists in their pharmacokinetics. This... 
DIHYDRODIOL DEHYDROGENASE ISOFORMS | QUINONE REDUCTASE | HUMAN CARBONYL REDUCTASE | ENZYMES | ANTHRACYCLINE-INDUCED CARDIOTOXICITY | SUPERFAMILY | PHARMACOLOGY & PHARMACY | HUMAN LIVER | ALDEHYDE REDUCTASE | SINGLE NUCLEOTIDE POLYMORPHISMS | PROSTAGLANDIN-F SYNTHASE | Aldehyde Reductase - genetics | Humans | Polymorphism, Single Nucleotide - physiology | Mitochondrial Proteins - genetics | NAD(P)H Dehydrogenase (Quinone) - genetics | Hydroxyprostaglandin Dehydrogenases - metabolism | Alcohol Oxidoreductases - genetics | Recombinant Proteins - isolation & purification | Mitochondrial Proteins - metabolism | 3-Hydroxysteroid Dehydrogenases - metabolism | Aldehyde Reductase - metabolism | Hydroxysteroid Dehydrogenases - metabolism | Doxorubicin - metabolism | Daunorubicin - metabolism | Glyceraldehyde - metabolism | Phenanthrenes - metabolism | Recombinant Proteins - metabolism | 20-Hydroxysteroid Dehydrogenases - genetics | Biocatalysis | Oxidoreductases - metabolism | Oxidoreductases - genetics | Gene Frequency | Indans - metabolism | Models, Molecular | Alcohol Oxidoreductases - metabolism | Recombinant Proteins - genetics | Hydroxysteroid Dehydrogenases - genetics | 20-Hydroxysteroid Dehydrogenases - metabolism | Hydroxyprostaglandin Dehydrogenases - genetics | Aldo-Keto Reductases | Vitamin K 3 - metabolism | Aldo-Keto Reductase Family 1 Member C3 | NAD(P)H Dehydrogenase (Quinone) - metabolism | Kinetics | 3-Hydroxysteroid Dehydrogenases - genetics | Index Medicus
Journal Article
Journal Article
Chemico-Biological Interactions, ISSN 0009-2797, 06/2015, Volume 234, pp. 309 - 319
Estrogens have important roles in the pathogenesis of endometrial cancer. They can have carcinogenic effects through stimulation of cell proliferation or... 
Aromatase pathway | Sulfatase pathway | Phase I and phase II estrogen metabolism | Aldo–keto reductase 1C3 (AKR1C3) | 17β-Hydroxysteroid dehydrogenases (17β-HSDs, HSD17B) | Catechol-O-methyl transferase (COMT) | 17b-Hydroxysteroid dehydrogenases | (17b-HSDs HSD17B)Aldoketo reductase 1C3 (AKR1C3) | 17 beta-Hydroxysteroid dehydrogenases (17 beta-HSDs, HSD17B) | DEHYDROGENASES | QUINONES | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROGESTERONE ACTION | 17-BETA-ESTRADIOL | CARCINOGENESIS | OVARIAN ENDOMETRIOSIS | Aldo-keto reductase 1C3 (AKR1C3) | ENZYMES | PHARMACOLOGY & PHARMACY | TOXICOLOGY | PHASE-I | CARCINOMA | PRE-RECEPTOR REGULATION | Sulfatases - genetics | Progesterone Reductase - metabolism | Humans | Endometrial Neoplasms - metabolism | Aromatase - metabolism | Catechol O-Methyltransferase - genetics | Hydroxyprostaglandin Dehydrogenases - metabolism | Androstenedione - metabolism | Catechol O-Methyltransferase - metabolism | Aromatase - genetics | Endometrial Neoplasms - genetics | Sulfatases - metabolism | Estrogens - genetics | 3-Hydroxysteroid Dehydrogenases - metabolism | Female | Sulfotransferases - metabolism | Estrogens - metabolism | Quinones - pharmacology | Glutathione S-Transferase pi - genetics | Sulfotransferases - genetics | Estrone - genetics | Quinone Reductases - metabolism | Androstenedione - genetics | Glutathione S-Transferase pi - metabolism | Estrogens - biosynthesis | RNA, Messenger - genetics | Transcriptome - genetics | Progesterone Reductase - genetics | Arylsulfotransferase - genetics | Hydroxyprostaglandin Dehydrogenases - genetics | Estrone - analogs & derivatives | Aldo-Keto Reductase Family 1 Member C3 | Estrone - metabolism | Cell Line, Tumor | Quinone Reductases - genetics | 3-Hydroxysteroid Dehydrogenases - genetics | Arylsulfotransferase - metabolism | Physiological aspects | Endometrial cancer | Sulfates | Genes | Estrogen | Steroids | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, pp. e0135285 - e0135285
To identify novel susceptibility variants for osteoporosis in Korean postmenopausal women, we performed a genome-wide association analysis of 1180... 
PROGENITOR CELLS | POLYMORPHISMS | BONE-MINERAL DENSITY | ULTRASOUND | MULTIDISCIPLINARY SCIENCES | MASS | DIFFERENTIATION | TRAITS | IDENTIFICATION | CHALLENGES | GENOME-WIDE ASSOCIATION | Osteoporosis, Postmenopausal - epidemiology | Postmenopause - genetics | Humans | Middle Aged | Alkaline Phosphatase - metabolism | Osteoporosis, Postmenopausal - metabolism | Monocytes - metabolism | Osteoporosis, Postmenopausal - pathology | Core Binding Factor Alpha 1 Subunit - metabolism | Case-Control Studies | Postmenopause - metabolism | Monocytes - pathology | Female | Cell Differentiation | Republic of Korea - epidemiology | Biomarkers - metabolism | Oxidoreductases Acting on Sulfur Group Donors - metabolism | Quinone Reductases - metabolism | Gene Expression | Genome-Wide Association Study | Hydrogen Sulfide - pharmacology | Osteoclasts - pathology | Alkaline Phosphatase - genetics | Bone Density | Osteoblasts - drug effects | Genotype | Logistic Models | Osteoporosis, Postmenopausal - genetics | Transcription Factors - genetics | Osteoclasts - metabolism | Transcription Factors - metabolism | Osteoblasts - pathology | Calcification, Physiologic | Oxidoreductases Acting on Sulfur Group Donors - genetics | Sp7 Transcription Factor | Quinone Reductases - genetics | Aged | Polymorphism, Single Nucleotide | Primary Cell Culture | Osteoblasts - metabolism | Core Binding Factor Alpha 1 Subunit - genetics | Osteoclasts - drug effects | Hydrogen sulfide | Osteoporosis | Analysis | Genes | Genomics | Genomes | Postmenopausal women | Single nucleotide polymorphisms | Alkaline phosphatase | Disease | Laboratories | Pathogenesis | Hydrogen | Association analysis | Single-nucleotide polymorphism | Remodeling | Epidemiology | Data bases | Proteins | Biomedical materials | Conserved sequence | Metabolites | Mineralization | Genetics | Biocompatibility | Bone density | Oxidation | University graduates | Cbfa-1 protein | Statistical analysis | Bone remodelling | Quinone | Amino acid sequence | Regression analysis | Metabolism | Gene expression | Post-menopause | Medicine | Studies | Osteoclastogenesis | Genetic variance | Monocytes | Osteoblastogenesis | Fractures | Acids | Womens health | Bone | Differentiation | Reductase | Index Medicus
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 04/2012, Volume 165, Issue 7, pp. 2178 - 2190
BACKGROUND AND PURPOSE Hydrogen sulphide (H 2 S) is gaining acceptance as a gaseous signal molecule. However, mechanisms regarding signal termination are not... 
hydrogen sulfide (H | protein sequestration | thiosulphate | sulphide oxidase | gasotransmitter | disulphide oxidoreductase (DiSR) | sulphide quinone reductase | sulphide metabolism | enteric nervous system | gas chromatography | RESPIRATORY-CHAIN | hydrogen sulfide (H2S) | SMOOTH-MUSCLE RELAXANT | GASTROINTESTINAL-TRACT | MITOCHONDRIAL-FUNCTION | MYOCARDIAL-ISCHEMIA | GLIDING BACTERIA | IN-VITRO | ELECTRON-TRANSFER | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | SODIUM SULFIDE | Hydrogen Sulfide - metabolism | Immunohistochemistry | Dioxygenases - metabolism | Thiosulfate Sulfurtransferase - genetics | Colon - drug effects | Male | Mitochondrial Proteins - genetics | Mice, 129 Strain | RNA, Messenger - metabolism | Antimycin A - pharmacology | Brain - metabolism | Tissue Distribution | Thiosulfate Sulfurtransferase - metabolism | Liver - drug effects | Mitochondrial Proteins - metabolism | Female | Quinone Reductases - metabolism | Sulfates - metabolism | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Polyenes - pharmacology | RNA, Messenger - genetics | Enzyme Inhibitors - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Colon - metabolism | Thiosulfates - metabolism | Brain - drug effects | Animals | Dioxygenases - genetics | Quinone Reductases - antagonists & inhibitors | Quinone Reductases - genetics | Mice | Metabolism | Rodents | Index Medicus | Research Papers
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2015, Volume 112, Issue 17, pp. 5539 - 5544
Cyclic electron flow (CEF) around photosystem I is thought to balance the ATP/NADPH energy budget of photosynthesis, requiring that its rate be finely... 
Cyclic electron flow | Reactive oxygen species | Hydrogen peroxide | Photosynthesis | Stress | stress | CYTOCHROME BF COMPLEX | CHLOROPHYLL FLUORESCENCE | C3 PLANTS | MULTIDISCIPLINARY SCIENCES | cyclic electron flow | hydrogen peroxide | FERREDOXIN-PLASTOQUINONE REDUCTASE | PROTON CIRCUIT | photosynthesis | CHLAMYDOMONAS-REINHARDTII | reactive oxygen species | STATE TRANSITIONS | CHLOROPLASTIC NDH COMPLEX | PHOTOSYSTEM-I | Quinone Reductases - metabolism | Arabidopsis Proteins - genetics | Oxidants - pharmacology | Photosynthetic Reaction Center Complex Proteins - metabolism | Electron Transport - drug effects | Membrane Proteins - genetics | Stress, Physiological - genetics | Hydrogen Peroxide - pharmacology | Alcohol Oxidoreductases - metabolism | Photosystem I Protein Complex - genetics | Chloroplasts - metabolism | Arabidopsis - metabolism | Alcohol Oxidoreductases - genetics | Arabidopsis - genetics | Arabidopsis Proteins - metabolism | Photosynthetic Reaction Center Complex Proteins - genetics | Photosystem I Protein Complex - metabolism | Quinone Reductases - genetics | Membrane Proteins - metabolism | Stress, Physiological - drug effects | Mutation | Chloroplasts - genetics | Observations | Health aspects | Enzymes | Gene expression | Metabolism | Electrons | Index Medicus | INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY | Biological Sciences
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