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Journal Article
Chemico-Biological Interactions, ISSN 0009-2797, 02/2013, Volume 202, Issue 1-3, pp. 210 - 217
► In endometrial cancer progesterone biosynthesis genes are down-regulated. ► Expression of most progesterone metabolism genes is not altered in cancerous... 
Steroidogenic acute regulatory protein | 5α-Reductase | Pre-receptor metabolism | Side-chain cleavage enzyme | 3-Keto/20-keto-reductase | 3-ALPHA-HYDROXYSTEROID DEHYDROGENASES | ADENOCARCINOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | STEROID 5-ALPHA-REDUCTASE | RECEPTOR-A | 5 alpha-Reductase | ER-ALPHA | 17-BETA-HYDROXYSTEROID-DEHYDROGENASE | KETO REDUCTASE SUPERFAMILY | ESTROGEN | PHARMACOLOGY & PHARMACY | TOXICOLOGY | YOUNG-WOMEN | TYPE-2 | Cholesterol Side-Chain Cleavage Enzyme - metabolism | Progesterone Reductase - metabolism | Humans | Middle Aged | Endometrial Neoplasms - metabolism | Multienzyme Complexes - metabolism | Receptors, Progesterone - genetics | Hydroxyprostaglandin Dehydrogenases - metabolism | Receptors, Progesterone - metabolism | Cholesterol Side-Chain Cleavage Enzyme - genetics | Endometrial Neoplasms - genetics | Phosphoproteins | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - metabolism | Aged, 80 and over | 3-Hydroxysteroid Dehydrogenases - metabolism | Adult | Female | Progesterone - biosynthesis | Membrane Proteins - metabolism | Steroid Isomerases - genetics | Endometrium - metabolism | 20-Hydroxysteroid Dehydrogenases - genetics | Membrane Proteins - genetics | Steroid Isomerases - metabolism | RNA, Messenger - genetics | Multienzyme Complexes - genetics | Progesterone Reductase - genetics | 20-Hydroxysteroid Dehydrogenases - metabolism | Down-Regulation - genetics | Hydroxyprostaglandin Dehydrogenases - genetics | Aldo-Keto Reductase Family 1 Member C3 | Estradiol Dehydrogenases - genetics | 17-Hydroxysteroid Dehydrogenases - genetics | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - genetics | Estradiol Dehydrogenases - metabolism | Progesterone - metabolism | Aged | Progesterone - genetics | 3-Hydroxysteroid Dehydrogenases - genetics | 17-Hydroxysteroid Dehydrogenases - metabolism | Endometrial cancer | RNA | Genes | Cytochrome P-450 | Physiological aspects | Genetic aspects | Progesterone | Cancer | Index Medicus
Journal Article
Animal Science Journal, ISSN 1344-3941, 11/2018, Volume 89, Issue 11, pp. 1540 - 1548
The spleen is a unique lymphoid organ that plays a key role in immune regulation. Interferon‐tau induces upregulation of interferon‐stimulated gene 15‐kDa... 
prostaglandin synthase | ISG15 | spleen | sheep | pregnancy | CELLS | AGRICULTURE, DAIRY & ANIMAL SCIENCE | PROGESTERONE | UTERUS | BONE-MARROW | TAU | RECEPTOR | MECHANISMS | MATERNAL RECOGNITION | IDENTIFICATION | Up-Regulation | Aldehyde Reductase - genetics | Spleen - immunology | Ubiquitins - genetics | Uterus - metabolism | Pregnancy, Animal - genetics | Cyclooxygenase 2 - genetics | Prostaglandin-E Synthases - genetics | Pregnancy, Animal - immunology | Aldehyde Reductase - metabolism | Female | Placentation - genetics | Sheep - genetics | Cytokines - genetics | Ubiquitins - metabolism | Cyclooxygenase 1 - genetics | Gene Expression | Cytokines - metabolism | Prostaglandin-E Synthases - metabolism | Placentation - physiology | Pregnancy | Animals | Spleen - metabolism | Cyclooxygenase 2 - metabolism | Sheep - metabolism | Cyclooxygenase 1 - metabolism | COX-2 inhibitors | Pregnant women | Prostaglandins E | Genes | Genetic research | Interferon | Biological response modifiers | Spleen | Immunohistochemistry | Estrus | Immune response | Immunoregulation | Paracrine signalling | mRNA | Estrus cycle | Gene expression | Prostaglandin endoperoxide synthase | Proteins | Immune systems | Cords | Prostaglandins | Uterus | Cyclooxygenase-1 | Sheep | Dimers | Prostaglandin E | Autocrine signalling | Reductase | Index Medicus
Journal Article
Cancer Research, ISSN 0008-5472, 02/2010, Volume 70, Issue 3, pp. 1256 - 1264
textabstractAndrogen-deprivation therapy for prostate cancer (PC) eventually leads to castration-resistant PC (CRPC). Intratumoral androgen production might... 
XENOGRAFT MODELS | INCREASED EXPRESSION | ONCOLOGY | PATHWAY | IN-VIVO | 5 17-BETA-HYDROXYSTEROID-DEHYDROGENASE | AGGRESSIVENESS | RECEPTOR GENE | PROGRESSION | DIHYDROTESTOSTERONE | ANDROGEN DEPRIVATION THERAPY | Progesterone Reductase - metabolism | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Neoplasms, Experimental - enzymology | Male | Transplantation, Heterologous | RNA, Messenger - metabolism | Hydroxyprostaglandin Dehydrogenases - metabolism | Androstenedione - metabolism | Pregnenolone - metabolism | Neoplasms, Experimental - pathology | Testosterone - metabolism | Prostatic Neoplasms - genetics | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - metabolism | Neoplasms, Experimental - genetics | Aged, 80 and over | 3-Hydroxysteroid Dehydrogenases - metabolism | Dihydrotestosterone - metabolism | Prostatic Neoplasms - pathology | RNA, Messenger - genetics | Progesterone Reductase - genetics | Reverse Transcriptase Polymerase Chain Reaction | Hydroxyprostaglandin Dehydrogenases - genetics | Orchiectomy | Gene Expression Regulation, Enzymologic | Animals | Aldo-Keto Reductase Family 1 Member C3 | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - genetics | Cell Line, Tumor | Prostatic Neoplasms - enzymology | Steroid 17-alpha-Hydroxylase - genetics | Aged | Mice | Steroid 17-alpha-Hydroxylase - metabolism | 3-Hydroxysteroid Dehydrogenases - genetics | Androgens - metabolism | Index Medicus
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
Journal of Biological Chemistry, ISSN 0021-9258, 05/2012, Volume 287, Issue 19, pp. 15174 - 15192
Journal Article
Molecules, ISSN 1420-3049, 08/2017, Volume 22, Issue 8, p. 1387
Swertia mussotii is an important medicinal plant found on the Qinghai Tibetan Plateau that has great economic and medicinal value. This plant has enjoyed a... 
Progesterone 5-β-reductase | Swertia mussotii | Iridoid synthase | Functional characterization | Secoiridoid biosynthesis | Heterologous expression | Medicinal plant | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT PROGESTERONE 5-BETA-REDUCTASE | heterologous expression | IDENTIFICATION | CHEMISTRY, MULTIDISCIPLINARY | progesterone 5-beta-reductase | iridoid synthase | GENTIOPICROSIDE | BIOSYNTHESIS | secoiridoid biosynthesis | medicinal plant | METABOLITE | EXPRESSION | CYCLIZATION | functional characterization | Progesterone Reductase - metabolism | Escherichia coli | Genes | Humans | Gene Expression Profiling | Iridoids - metabolism | Phylogeny | Iridoid Glucosides - chemistry | Pyrones - chemistry | Iridoids - chemistry | Plant Proteins - chemistry | Swertia - enzymology | Swertia - genetics | Cloning, Molecular | Iridoid Glucosides - metabolism | Plant Proteins - metabolism | Progesterone Reductase - chemistry | Gene Expression | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Progesterone Reductase - genetics | Plant Proteins - genetics | Kinetics | Pyrones - metabolism | Plants, Medicinal | Medicinal plants | Transcription | Cloning | Homology | Tissues | Stems | Biological activity | Proteins | Polymerase chain reaction | Hepatitis | Leaves | Recombinant | Reductase | Index Medicus | progesterone 5-β-reductase
Journal Article
Molecular Human Reproduction, ISSN 1360-9947, 05/2017, Volume 23, Issue 5, pp. 271 - 281
STUDY QUESTION: Do intraluteal prostaglandins (PG) contribute to luteal regulation in women? SUMMARY ANSWER: Prostaglandin E (PGE), which is produced in human... 
Corpus luteum | Luteinized granulosa cell | Prostaglandin | HCG | Luteolysis | PROGESTERONE | prostaglandin | luteinized granulosa cell | DEVELOPMENTAL BIOLOGY | HUMAN CHORIONIC-GONADOTROPIN | hCG | luteolysis | OBSTETRICS & GYNECOLOGY | DEHYDROGENASE GENE | ACTIVIN-A | IN-VITRO | REPRODUCTIVE BIOLOGY | EARLY-PREGNANCY | corpus luteum | RECEPTORS | HUMAN CORPUS-LUTEUM | LUTEINIZED GRANULOSA-CELLS | EXPRESSION | Aldehyde Reductase - genetics | Progesterone Reductase - metabolism | Corpus Luteum - drug effects | Luteinization - physiology | Humans | Prostaglandins E - pharmacology | Multienzyme Complexes - metabolism | Phosphoproteins - metabolism | Granulosa Cells - drug effects | Granulosa Cells - metabolism | Chorionic Gonadotropin - pharmacology | Isoenzymes - metabolism | Luteal Phase - physiology | Prostaglandin-E Synthases - genetics | Aldehyde Reductase - metabolism | Female | Progesterone - biosynthesis | Steroid Isomerases - genetics | Inhibin-beta Subunits - genetics | Inhibin-beta Subunits - metabolism | Progesterone - secretion | 20-Hydroxysteroid Dehydrogenases - genetics | Prostaglandin-E Synthases - metabolism | Signal Transduction | Isoenzymes - genetics | Menstruation - physiology | Steroid Isomerases - metabolism | Gene Expression Regulation | Multienzyme Complexes - genetics | Phosphoproteins - genetics | Progesterone Reductase - genetics | 20-Hydroxysteroid Dehydrogenases - metabolism | Corpus Luteum - cytology | Animals | Corpus Luteum - metabolism | Luteolysis - genetics | Primary Cell Culture | Prostaglandins E - genetics | Placenta Growth Factor - pharmacology | Prostaglandins E - deficiency | Granulosa Cells - cytology | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, pp. e51301 - e51301
Bladder cancer is the 4th most common cancer among men in the U.S. We analyzed variant genotypes hypothesized to modify major biological processes involved in... 
CONFERS SUSCEPTIBILITY | BREAST-CANCER | MULTIFACTOR-DIMENSIONALITY REDUCTION | METABOLISM GENES | POLYMORPHISMS | MULTIDISCIPLINARY SCIENCES | PROSTATE-CANCER | TUMOR | RISK | DNA-REPAIR | ASSOCIATION | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Male | Multienzyme Complexes - genetics | Signal Transduction - genetics | Progesterone Reductase - genetics | Case-Control Studies | Urinary Bladder Neoplasms - genetics | Epistasis, Genetic | Urinary Bladder Neoplasms - pathology | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Steroid Isomerases - genetics | Telomeres | Oncology, Experimental | Genes | Physiological aspects | Genetic aspects | Disease susceptibility | Research | Bladder cancer | Apoptosis | Cancer | Dehydrogenases | Bladder | Lymphocytes T | Epistasis | Single-nucleotide polymorphism | Hormones | Males | Medical diagnosis | DNA repair | Carcinogenesis | Signal transduction | Carcinogens | Cell activation | Cell growth | Urinary bladder | Transcription activation | Network analysis | Cell cycle | Population | Genotypes | Deoxyribonucleic acid--DNA | Enzymes | Statistical analysis | Health risks | Cell division | Immunosurveillance | Genetic diversity | Regression analysis | Metabolism | Gene expression | Biological activity | Medicine | Studies | Population (statistical) | Surveillance | GATA-3 protein | Biomarkers | CD81 antigen | Health risk assessment | Females | Prostate cancer | Tumors | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 2016, Volume 36, Issue 6, pp. 1032 - 1047
Journal Article