Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5675) 5675
Book Chapter (3) 3
Conference Proceeding (2) 2
Dissertation (2) 2
Book / eBook (1) 1
Magazine Article (1) 1
Publication (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
female (3737) 3737
humans (3208) 3208
animals (2543) 2543
science & technology (2116) 2116
life sciences & biomedicine (2030) 2030
estrone - metabolism (1876) 1876
biological and medical sciences (1495) 1495
male (1329) 1329
estradiol - metabolism (1311) 1311
estrone - blood (1263) 1263
estradiol - blood (1064) 1064
estrone - analogs & derivatives (1043) 1043
rats (982) 982
pregnancy (961) 961
estrone (953) 953
adult (925) 925
middle aged (919) 919
abridged index medicus (886) 886
medical sciences (856) 856
estrone - pharmacology (780) 780
fundamental and applied biological sciences. psychology (717) 717
endocrinology & metabolism (697) 697
estradiol (631) 631
tritium (595) 595
aged (549) 549
estrogens - metabolism (545) 545
kinetics (514) 514
estrogens (504) 504
in vitro techniques (482) 482
testosterone - blood (468) 468
estradiol - pharmacology (458) 458
estrone - biosynthesis (445) 445
time factors (402) 402
testosterone - metabolism (397) 397
estrone - urine (380) 380
estradiol - biosynthesis (368) 368
biochemistry & molecular biology (348) 348
androstenedione - metabolism (345) 345
estrogen (345) 345
pharmacology. drug treatments (331) 331
menopause (329) 329
luteinizing hormone - blood (324) 324
liver - metabolism (304) 304
carbon isotopes (303) 303
pharmacology & pharmacy (288) 288
estrone - analysis (287) 287
androstenedione - blood (286) 286
vertebrates: reproduction (285) 285
mice (282) 282
follicle stimulating hormone - blood (273) 273
progesterone - blood (273) 273
testosterone (273) 273
progesterone - metabolism (271) 271
gynecology. andrology. obstetrics (267) 267
breast neoplasms - metabolism (266) 266
estrogens - blood (264) 264
old medline (255) 255
hormones (249) 249
estradiol - analogs & derivatives (237) 237
estradiol - urine (233) 233
metabolism (233) 233
radioimmunoassay (232) 232
uterus - metabolism (231) 231
chromatography, thin layer (229) 229
dehydroepiandrosterone - metabolism (225) 225
progesterone - pharmacology (225) 225
ovary - metabolism (224) 224
estradiol - analysis (223) 223
oncology (220) 220
castration (218) 218
tumors (218) 218
aromatase - metabolism (214) 214
hormone metabolism and regulation (213) 213
estrogens - biosynthesis (209) 209
estrogens - pharmacology (207) 207
breast cancer (206) 206
progesterone (203) 203
research (203) 203
dose-response relationship, drug (202) 202
estriol - metabolism (202) 202
placenta - metabolism (197) 197
adolescent (190) 190
steroids (182) 182
cells, cultured (181) 181
analysis (177) 177
chromatography (177) 177
receptors, estrogen - metabolism (172) 172
protein binding (170) 170
vertebrates: endocrinology (170) 170
sex hormone-binding globulin - metabolism (168) 168
chemistry (166) 166
obstetrics & gynecology (162) 162
dehydroepiandrosterone - blood (161) 161
sex hormones (160) 160
estriol - urine (158) 158
physiological aspects (156) 156
cell line (154) 154
androgens - metabolism (149) 149
gonadal steroid hormones - blood (148) 148
rabbits (147) 147
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (5347) 5347
German (126) 126
Japanese (93) 93
French (90) 90
Russian (47) 47
Italian (22) 22
Polish (14) 14
Spanish (8) 8
Ukrainian (7) 7
Chinese (5) 5
Czech (4) 4
Bulgarian (2) 2
Dutch (2) 2
Catalan (1) 1
Hungarian (1) 1
Slovak (1) 1
Swedish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Aldo-keto reductase 1C3 expression in MCF-7 cells reveals roles in steroid hormone and prostaglandin metabolism that may explain its over-expression in breast cancer
by Byrns, Michael C and Duan, Ling and Lee, Seon Hwa and Blair, Ian A and Penning, Trevor M
The Journal of steroid biochemistry and molecular biology, ISSN 0960-0760, 2010, Volume 118, Issue 3, pp. 177 - 187
Estrogen receptor | Peroxisome proliferator activated receptor γ | Prostaglandin F synthase | Prostaglandin D 2 | 17β-Hydroxysteroid dehydrogenase | Prostaglandin D | Biochemistry & Molecular Biology | Endocrinology & Metabolism | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Vertebrates: endocrinology | Vertebrates: reproduction | Biological and medical sciences | Medical sciences | Tumors | Up-Regulation | Prostaglandins - pharmacology | Humans | Gene Expression Regulation, Neoplastic | Dinoprost - metabolism | Hydroxyprostaglandin Dehydrogenases - metabolism | Androstenedione - metabolism | Breast Neoplasms - metabolism | Testosterone - metabolism | Breast Neoplasms - enzymology | Transfection | Prostaglandin D2 - metabolism | Prostaglandin D2 - analogs & derivatives | 3-Hydroxysteroid Dehydrogenases - metabolism | Female | 5-alpha-Dihydroprogesterone - metabolism | Dinoprost - pharmacology | Etiocholanolone - metabolism | Estradiol - pharmacology | Dihydrotestosterone - metabolism | Recombinant Proteins - metabolism | Estradiol - metabolism | Estrone - pharmacology | Gonadal Steroid Hormones - metabolism | Biocatalysis | Etiocholanolone - analogs & derivatives | Gonadal Steroid Hormones - pharmacology | Progesterone - analogs & derivatives | Recombinant Proteins - genetics | 20-alpha-Dihydroprogesterone - metabolism | Androsterone - metabolism | Hydroxyprostaglandin Dehydrogenases - genetics | Breast Neoplasms - genetics | Aldo-Keto Reductase Family 1 Member C3 | Estrone - metabolism | Progesterone - metabolism | Cell Line, Tumor | Cell Proliferation - drug effects | Prostaglandin D2 - pharmacology | Ketosteroids - metabolism | Kinetics | 3-Hydroxysteroid Dehydrogenases - genetics | Prostaglandins - metabolism | Physiological aspects | Testosterone | Breast cancer | Progesterone | Estradiol | Synthetic prostaglandins F | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Substrate-Dependent Drug-Drug Interactions between Gemfibrozil, Fluvastatin and Other Organic Anion-Transporting Peptide (OATP) Substrates on OATP1B1, OATP2B1, and OATP1B3
by Johannes Noà and Renée Portmann and Marie-Elise Brun and Christoph Funk
Drug metabolism and disposition, ISSN 0090-9556, 08/2007, Volume 35, Issue 8, pp. 1308 - 1314
Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Biological and medical sciences | Pharmacology. Drug treatments | Medical sciences | Organic Anion Transporters, Sodium-Independent - genetics | Fatty Acids, Monounsaturated - pharmacology | Cricetulus | Hypolipidemic Agents - metabolism | Hypoglycemic Agents - metabolism | Taurocholic Acid - metabolism | Humans | Hepatocytes - metabolism | Simvastatin - pharmacology | Organic Anion Transporters - metabolism | Chromans - metabolism | Hepatocytes - cytology | Indoles - metabolism | Organic Anion Transporters - genetics | Drug Interactions | Anticholesteremic Agents - metabolism | Chromans - pharmacology | Fatty Acids, Monounsaturated - metabolism | Organic Anion Transporters, Sodium-Independent - metabolism | Indoles - pharmacology | Biological Transport - drug effects | Thiazolidinediones - pharmacology | Hepatocytes - drug effects | Solute Carrier Organic Anion Transporter Family Member 1B3 | CHO Cells | Pravastatin - pharmacology | Recombinant Proteins - metabolism | Taurocholic Acid - pharmacology | Cell Line | Cricetinae | Pravastatin - metabolism | Simvastatin - metabolism | Gemfibrozil - pharmacokinetics | Gemfibrozil - pharmacology | Hypolipidemic Agents - pharmacology | Thiazolidinediones - metabolism | Hypoglycemic Agents - pharmacology | Animals | Estrone - analogs & derivatives | Estrone - metabolism | Protein Binding | Fatty Acids, Monounsaturated - pharmacokinetics | Indoles - pharmacokinetics | Kinetics | Solute Carrier Organic Anion Transporter Family Member 1b1 | Anticholesteremic Agents - pharmacology | Gemfibrozil - metabolism | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Multiple Human Isoforms of Drug Transporters Contribute to the Hepatic and Renal Transport of Olmesartan, a Selective Antagonist of the Angiotensin II AT1-Receptor
by Akihiro Yamada and Kazuya Maeda and Emi Kamiyama and Daisuke Sugiyama and Tsunenori Kondo and Yoshiyuki Shiroyanagi and Hayakazu Nakazawa and Teruo Okano and Masashi Adachi and John D. Schuetz and Yasuhisa Adachi and Zhuohan Hu and Hiroyuki Kusuhara and Yuichi Sugiyama
Drug metabolism and disposition, ISSN 0090-9556, 12/2007, Volume 35, Issue 12, pp. 2166 - 2176
Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Biological and medical sciences | Pharmacology. Drug treatments | Medical sciences | ATP Binding Cassette Transporter, Sub-Family G, Member 2 | Humans | ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism | Membrane Transport Proteins - drug effects | Hepatocytes - metabolism | Imidazoles - pharmacokinetics | Neoplasm Proteins - metabolism | Angiotensin II Type 1 Receptor Blockers - pharmacokinetics | Sincalide - metabolism | Angiotensin II Type 1 Receptor Blockers - metabolism | Organic Anion Transporters - metabolism | Prodrugs - metabolism | Tetrazoles - metabolism | Dose-Response Relationship, Drug | Kidney - metabolism | Protein Isoforms - metabolism | Transfection | Liver - drug effects | Membrane Transport Proteins - genetics | Organic Anion Transporters, Sodium-Independent - metabolism | Adenosine Triphosphate - metabolism | ATP-Binding Cassette Transporters - metabolism | Female | Membrane Transport Proteins - metabolism | Hepatocytes - drug effects | Solute Carrier Organic Anion Transporter Family Member 1B3 | Imidazoles - metabolism | Olmesartan Medoxomil | Cell Line | Liver - metabolism | Probenecid - pharmacology | Penicillin G - pharmacology | Mice, Knockout | p-Aminohippuric Acid - pharmacology | Animals | Estrone - analogs & derivatives | Multidrug Resistance-Associated Proteins - deficiency | Prodrugs - pharmacokinetics | Estrone - metabolism | Dogs | Protein Binding | ATP Binding Cassette Transporter, Sub-Family B | Mice | Kinetics | In Vitro Techniques | Solute Carrier Organic Anion Transporter Family Member 1b1 | Multidrug Resistance-Associated Proteins - metabolism | Tetrazoles - pharmacokinetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Estrogen Metabolism in Abdominal Subcutaneous and Visceral Adipose Tissue in Postmenopausal Women
by Hetemäki, Natalia and Savolainen-Peltonen, Hanna and Tikkanen, Matti J and Wang, Feng and Paatela, Hanna and Hämäläinen, Esa and Turpeinen, Ursula and Haanpää, Mikko and Vihma, Veera and Mikkola, Tomi S
The journal of clinical endocrinology and metabolism, ISSN 0021-972X, 09/2017, Volume 102, Issue 12, pp. 4588 - 4595
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Estradiol - metabolism | Humans | Middle Aged | RNA, Messenger - genetics | Intra-Abdominal Fat - metabolism | RNA, Messenger - biosynthesis | Abdominal Fat - metabolism | Subcutaneous Fat - metabolism | Waist Circumference | 17-Hydroxysteroid Dehydrogenases - biosynthesis | Postmenopause - metabolism | 17-Hydroxysteroid Dehydrogenases - genetics | Estrone - metabolism | Aged, 80 and over | Female | Steryl-Sulfatase - metabolism | Aged | Estrogens - metabolism | 17-Hydroxysteroid Dehydrogenases - metabolism | Correlation | Adipose tissue | Menopause | Estrogens | Reverse transcription | Sulfates | Estradiol | Body mass index | Steroid sulfatase | Surgery | Enzymes | Mass spectroscopy | Liquid chromatography | Exposure | Metabolism | Gene expression | Ribonucleic acid--RNA | Post-menopause | Polymerase chain reaction | Sex hormones | Body mass | Womens health | Body size | Estrone | Hormone replacement therapy | Metabolic pathways | Mass spectrometry | Metabolic disorders | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text The endometrial cancer cell lines Ishikawa and HEC-1A, and the control cell line HIEEC, differ in expression of estrogen biosynthetic and metabolic genes, and in androstenedione and estrone-sulfate metabolism
by Hevir-Kene, Neli and Rižner, Tea Lanišnik
Chemico-biological interactions, ISSN 0009-2797, 06/2015, Volume 234, pp. 309 - 319
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) | Pharmacology & Pharmacy | Biochemistry & Molecular Biology | Toxicology | Life Sciences & Biomedicine | Science & Technology | 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
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Transport of Estrone 3-sulfate Mediated by Organic Anion Transporter OATP4C1: Estrone 3-sulfate binds to the Different Recognition Site for Digoxin in OATP4C1
by Yamaguchi, Hiroaki and Sugie, Misa and Okada, Masahiro and Mikkaichi, Tsuyoshi and Toyohara, Takafumi and Abe, Takaaki and Goto, Junichi and Hishinuma, Takanori and Shimada, Miki and Mano, Nariyasu and Graduate School of Pharmaceutical Sciences and Hokkaido University and Department of Pharmaceutical Sciences and Endocrinology and Faculty of Pharmaceutical Sciences and Tohoku University Hospital and and Vascular Medicine and Laboratory of Clinical Pharmaceutics and Therapeutics and Division of Pharmacotherapy and Tohoku University and Division of Clinical Pharmacy and Division of Nephrology and Tohoku University Graduate School of Biomedical Engineering and Division of Pharmasciences
Drug metabolism and pharmacokinetics, ISSN 1347-4367, 2010, Volume 25, Issue 3, pp. 314 - 317
mutual inhibition | OATP4C1 | estrone 3-sulfate | digoxin | recognition site | Recognition site | Digoxin | Mutual inhibition | Estrone 3-sulfate | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Binding, Competitive | Cell Line | Organic Anion Transporters - antagonists & inhibitors | Digoxin - metabolism | Humans | Epithelial Cells | Kidney - cytology | Organic Anion Transporters - metabolism | Ouabain - metabolism | Kidney - metabolism | Animals | Estrone - analogs & derivatives | Triiodothyronine - metabolism | Sulfobromophthalein - metabolism | Estrone - metabolism | Chenodeoxycholic Acid - metabolism | Dogs | Biological Transport - drug effects | Pharmacokinetics | Cyclosporine - metabolism | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Association between up-regulated expression proteins and circulating steroidal hormones in leiomyoma
by Ura, Blendi and Scrimin, Federica and Monasta, Lorenzo and Radillo, Oriano and Ricci, Giuseppe
Medical hypotheses, ISSN 0306-9877, 2015, Volume 85, Issue 4, pp. 515 - 515
Internal Medicine | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Estradiol - metabolism | Up-Regulation | Uterine Neoplasms - metabolism | Humans | Peroxiredoxins - metabolism | Gene Expression Regulation | Inflammation | Leiomyoma - metabolism | Lamin Type A - metabolism | HSP70 Heat-Shock Proteins - metabolism | Extracellular Fluid - metabolism | Hormones - metabolism | Desmin - metabolism | Estrone - metabolism | Myometrium - metabolism | Steroids - metabolism | Leiomyoma - drug therapy | Muscle Proteins - metabolism | Progesterone - metabolism | Uterine Neoplasms - drug therapy | Female | Microfilament Proteins - metabolism | alpha 1-Antitrypsin - metabolism | Actinin - metabolism | Hormones | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation
by Yan, Ming and Gingras, Marie-Claude and Dunlop, Elaine A and Nouet, Yann and Dupuy, Fanny and Jalali, Zahra and Possik, Elite and Coull, Barry J and Kharitidi, Dmitri and Dydensborg, Anders Bondo and Faubert, Brandon and Kamps, Miriam and Sabourin, Sylvie and Preston, Rachael S and Davies, David Mark and Roughead, Taren and Chotard, Laetitia and van Steensel, Maurice A. M and Jones, Russell and Tee, Anew R and Pause, Arnim
The Journal of clinical investigation, ISSN 0021-9738, 06/2014, Volume 124, Issue 6, pp. 2640 - 2650
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Proto-Oncogene Proteins - metabolism | Cell Line | AMP-Activated Protein Kinases - metabolism | Tumor Suppressor Proteins - metabolism | Reactive Oxygen Species - metabolism | Proto-Oncogene Proteins - genetics | Mitochondria - metabolism | Proto-Oncogene Proteins - deficiency | Hypoxia-Inducible Factor 1 - metabolism | Birt-Hogg-Dube Syndrome - genetics | Mice, Knockout | Transcription Factors - metabolism | Animals | Energy Metabolism | Cell Transformation, Neoplastic | Tumor Suppressor Proteins - deficiency | Adenosine Triphosphate - metabolism | Birt-Hogg-Dube Syndrome - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Tumor Suppressor Proteins - genetics | Birt-Hogg-Dube Syndrome - etiology | Mice | Mitochondria | Cancer cells | Physiological aspects | Drug metabolism | Tumor suppressor genes | Estrone | Genetic aspects | Properties | Medical research | Muscular system | Metabolites | Kinases | Metabolic disorders | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Interactions of green tea catechins with organic anion-transporting polypeptides
by Roth, Megan and Timmermann, Barbara N and Hagenbuch, Bruno
Drug metabolism and disposition, ISSN 0090-9556, 05/2011, Volume 39, Issue 5, pp. 920 - 926
Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Biological and medical sciences | Pharmacology. Drug treatments | Medical sciences | Cell Line | Estradiol - metabolism | Cricetinae | Estradiol - analogs & derivatives | Cricetulus | Aniline Compounds - metabolism | Enterocytes - metabolism | Antioxidants - metabolism | Humans | Fluorescent Dyes - metabolism | Hepatocytes - metabolism | Organic Anion Transporters - metabolism | Tea | Camellia sinensis | Animals | Drug Interactions | Estrone - analogs & derivatives | Biological Transport | Xanthenes - metabolism | Estrone - metabolism | Catechin - analogs & derivatives | Catechin - metabolism | CHO Cells | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Intracrine androgen biosynthesis, metabolism and action revisited
by Schiffer, Lina and Arlt, Wiebke and Storbeck, Karl-Heinz
Molecular and cellular endocrinology, ISSN 0303-7207, 04/2018, Volume 465, Issue C, pp. 4 - 26
Testosterone | Androgens | Steroid biosynthesis | Hormone-dependent cancer | 11-oxygenated androgens | Intracrinology | Endocrinology & Metabolism | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Reproduction | Animals | Humans | Androgens - biosynthesis | Biosynthetic Pathways | Androgens - metabolism | Organ Specificity | Steroids - biosynthesis | Dehydroepiandrosterone | Corticosteroids | Metabolites | Stein-Leventhal syndrome | Cytochrome P-450 | Physiological aspects | Progesterone | Hormones | Sulfates | Estradiol | Blood proteins | Index Medicus | 11OHT, 11β-hydroxy-testosterone | E1S, estrone sulfate | STS, steroid sulfatase | CRPC, castration resistant prostate cancer | 17αHP, 5α-pregnane-17α-ol-3,20-one | CHOL, cholesterol | 11KA4, 11-keto-androstenedione | DHEA, dehydroepiandrosterone (androst-5-ene-3β-ol-17-one) | EpiAST, 5α-androstan-3β-ol-17-one | 5-diol, androst-5-ene-3β,17β-diol | Pdiol, 5α-pregnane-3α,17α-diol-20-one | PORD, cytochrome P450 oxidoreductase deficiency | 5α-dione, 5α-androstane-3,17-dione | EpiT, epitestosterone (17α-hydroxy-testosterone, androst-4-ene-17α-ol-3-one) | OATP, organic anion-transporting polypeptide | A4, androstenedione (androst-4-ene-3,17-dione) | SULT, sulfotransferase | ETIO, etiochonanolone (5β-androstan-3α-ol-17-one) | SHBG, sex hormone-binding globulin | T, testosterone (androst-4-ene-17β-ol-3-one) | CYP, cytochrome P450 | 3α-adiol, 5α-androstan-3α,17β-diol | 17OHPROG, 17α-hydroxy-progesterone | StAR, steroidogenic acute regulatory protein | UGT, uridine diphosphate-glucuronosyl transferase | PAPS, 3′-phospho-adenosine-5′-phosphosulfate | 11OHDHT, 11β-hydroxy-5α-dihydrotestosterone | DHEAS, dehydroepiandrosterone sulfate | 11KT, 11-keto-testosterone | HSD, hydroxysteroid dehydrogenase | 11OHA4, 11β-hydroxy-androstenedione | PROG, progesterone | AST, androsterone (5α-androstan-3α-ol-17-one) | AKR, aldo-keto reductase | PCOS, polycystic ovary syndrome | PREG, pregnenolone | E1, estrone | 11KDHT, 11-keto-5α-dihydrotestosterone | AR, androgen receptor | E2, estradiol | DHT, 5α-dihydrotestosterone (5α-androstan-17β-ol-3-one)
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights