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1. Full Text Vitamin D receptor and vitamin D metabolizing enzymes are expressed in the human male reproductive tract
by Blomberg Jensen, Martin and Nielsen, John E and Jørgensen, Anne and Rajpert-De Meyts, Ewa and Kristensen, David Møbjerg and Jørgensen, Niels and Skakkebaek, Niels E and Juul, Anders and Leffers, Henrik
Human Reproduction, ISSN 0268-1161, 5/2010, Volume 25, Issue 5, pp. 1303 - 1311
BACKGROUND The vitamin D receptor (VDR) is expressed in human testis, and vitamin D (VD) has been suggested to affect survival and function of mature... 
Testis | Reproduction | CYP | Hydroxylase | Vitamin D receptor | RAT | testis | hydroxylase | CANCER | FERTILITY | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE BIOLOGY | D-3 RECEPTOR | CALCIUM | 1,25-DIHYDROXYVITAMIN-D3 | vitamin D receptor | HUMAN MALE GAMETE | SPERM MOTILITY | CELL-LINE | reproduction | Epididymis - metabolism | Immunohistochemistry | Steroid Hydroxylases - metabolism | Testis - metabolism | Seminal Vesicles - metabolism | Spermatogenesis | Humans | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - genetics | Male | DNA Primers - genetics | Spermatozoa - metabolism | RNA, Messenger - metabolism | Prostate - metabolism | Tissue Distribution | Cytochrome P450 Family 2 | Base Sequence | Adult | Steroid Hydroxylases - genetics | Gene Expression | RNA, Messenger - genetics | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - metabolism | Rats | Vitamin D3 24-Hydroxylase | Genitalia, Male - metabolism | Receptors, Calcitriol - metabolism | Animals | Cholestanetriol 26-Monooxygenase - genetics | Cholestanetriol 26-Monooxygenase - metabolism | Vitamin D - metabolism | Mice | Index Medicus
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2. Full Text The Cholesterol Metabolite 27-Hydroxycholesterol Promotes Atherosclerosis via Proinflammatory Processes Mediated by Estrogen Receptor Alpha
by Umetani, Michihisa and Umetani, Junko and Ghosh, Pritam and Ishikawa, Tomonori and Ahmed, Mohamed and Mineo, Chieko and Shaul, Philip W
Cell Metabolism, ISSN 1550-4131, 07/2014, Volume 20, Issue 1, pp. 172 - 182
Oxysterols are cholesterol metabolites that serve multiple functions in lipid metabolism, including as liver X receptor (LXR) ligands. 27-hydroxycholesterol... 
ADHESION | SIGNALING PATHWAYS | HEART-DISEASE | DNA-BINDING | LIVER X RECEPTORS | INFLAMMATION | TRANSCRIPTION | ENDOCRINOLOGY & METABOLISM | NF-KAPPA-B | INTERLEUKIN-6 GENE-EXPRESSION | STEROL 27-HYDROXYLASE | CELL BIOLOGY | Steroid Hydroxylases - metabolism | Apolipoproteins E - deficiency | JNK Mitogen-Activated Protein Kinases - metabolism | Male | NF-kappa B - metabolism | I-kappa B Proteins - metabolism | Apolipoproteins E - metabolism | Cytochrome P450 Family 7 | RNA Interference | Estrogen Receptor alpha - metabolism | Female | Cytokines - genetics | Steroid Hydroxylases - genetics | Macrophages - immunology | Cell Line | Atherosclerosis - pathology | NF-KappaB Inhibitor alpha | Cytokines - metabolism | Endothelial Cells - metabolism | Inflammation | Cell Adhesion - drug effects | Cholesterol - metabolism | Hydroxycholesterols - pharmacology | Atherosclerosis - metabolism | Mice, Knockout | Macrophages - metabolism | Animals | Estrogen Receptor alpha - genetics | Mitogen-Activated Protein Kinase 3 - metabolism | Endothelial Cells - cytology | Apolipoproteins E - genetics | Steroid Hydroxylases - deficiency | Hydroxycholesterols - metabolism | Macrophages - drug effects | Mice | Endothelial Cells - drug effects | Mitogen-Activated Protein Kinase 1 - metabolism | RNA, Small Interfering - metabolism | Metabolites | Atherosclerosis | Estrogen | Cytochrome P-450 | Physiological aspects | Phenols | Cholesterol | Prevention | Blood circulation disorders | Liver | Endothelium | Index Medicus
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3. Full Text T-cell cytokines differentially control human monocyte antimicrobial responses by regulating vitamin D metabolism
by Kristina Edfeldt and Philip T. Liu and Rene Chun and Mario Fabri and Mirjam Schenk and Matthew Wheelwright and Caroline Keegan and Stephan R. Krutzik and John S. Adams and Martin Hewison and Robert L. Modlin and Diane E. Griffin
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2010, Volume 107, Issue 52, pp. 22593 - 22598
We investigated the mechanisms by which T-cell cytokines are able to influence the Toll-like receptor (TLR)-induced, vitamin D-dependent antimicrobial pathway... 
T lymphocytes | Up regulation | Monocytes | Messenger RNA | Cytokines | Vitamin D | Mycobacterium tuberculosis | Antimicrobials | Small interfering RNA | Physiological regulation | Interleukin-4 | Interferon-γ | Innate immune response | interleukin-4 | MYCOBACTERIUM-TUBERCULOSIS | ACTIVATION | CATHELICIDIN | IFN-GAMMA | MACROPHAGES | MULTIDISCIPLINARY SCIENCES | AUTOPHAGY | CUTTING EDGE | TOLL-LIKE RECEPTOR-2 | innate immune response | MICROBIAL LIPOPROTEINS | interferon-gamma | Steroid Hydroxylases - metabolism | Gene Expression - drug effects | Monocytes - cytology | Humans | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - genetics | Monocytes - metabolism | Antimicrobial Cationic Peptides - metabolism | Th1 Cells - metabolism | Interleukin-4 - pharmacology | T-Lymphocytes - metabolism | Calcitriol - metabolism | beta-Defensins - metabolism | Antimicrobial Cationic Peptides - genetics | Steroid Hydroxylases - genetics | beta-Defensins - genetics | Toll-Like Receptor 1 - metabolism | Cells, Cultured | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - metabolism | Vitamin D3 24-Hydroxylase | Toll-Like Receptor 2 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Th2 Cells - metabolism | Blotting, Western | Monocytes - drug effects | Signal Transduction - drug effects | Vitamin D - analogs & derivatives | Vitamin D - metabolism | Cytokines - pharmacology | Interferon-gamma - pharmacology | Immune response | Calcifediol | Regulation | Alfacalcidol | Research | T cells | Properties | Health aspects | Signal transduction | Peptides | Metabolism | Gene expression | Cells | Index Medicus | Biological Sciences | interferon-γ
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4. Full Text Metabolism of vitamin D3 in human osteoblasts: Evidence for autocrine and paracrine activities of 1α,25-dihydroxyvitamin D3
by Atkins, Gerald J and Anderson, Paul H and Findlay, David M and Welldon, Katie J and Vincent, Cristina and Zannettino, Andrew C.W and O'Loughlin, Peter D and Morris, Howard A
Bone, ISSN 8756-3282, 2007, Volume 40, Issue 6, pp. 1517 - 1528
Abstract Circulating 1α,25-dihydroxyvitamin D3 (1,25D) derives from renal conversion of 25-hydroxyvitamin D3 (25D), by the 25D 1α-hydroxylase (CYP27B1). Blood... 
Orthopedics | CYP27B1 | Vitamin D | CYP24 | Osteoblasts | 25-Hydroxyvitamin D | Steroid Hydroxylases - metabolism | RANK Ligand - metabolism | Osteocalcin - metabolism | Humans | Cells, Cultured | Gene Expression Regulation | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - genetics | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - metabolism | Receptors, Cell Surface - metabolism | Low Density Lipoprotein Receptor-Related Protein-2 - metabolism | Vitamin D3 24-Hydroxylase | Osteopontin - metabolism | Calcifediol - genetics | RNA, Messenger - metabolism | Calcitriol - blood | Cholecalciferol - metabolism | Polymerase Chain Reaction | Cell Line, Tumor | Calcifediol - metabolism | Transcription, Genetic | Osteoblasts - metabolism | Steroid Hydroxylases - genetics | Osteosarcoma - pathology | RNA, Small Interfering - metabolism | Index Medicus
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5. Full Text Mutations in CYP24A1 and Idiopathic Infantile Hypercalcemia
by Schlingmann, Karl P and Kaufmann, Martin and Weber, Stefanie and Irwin, Andrew and Goos, Caroline and John, Ulrike and Misselwitz, Joachim and Klaus, Günter and Kuwertz-Bröking, Eberhard and Fehrenbach, Henry and Wingen, Anne M and Güran, Tülay and Hoenderop, Joost G and Bindels, René J and Prosser, David E and Jones, Glenville and Konrad, Martin
The New England Journal of Medicine, ISSN 0028-4793, 08/2011, Volume 365, Issue 5, pp. 410 - 421
Mutations in a vitamin D–metabolizing enzyme were found in patients with idiopathic infantile hypercalcemia. The mutations may explain the patients' vitamin D... 
CALCITROIC ACID | INACTIVATION | VITAMIN-D | MEDICINE, GENERAL & INTERNAL | SUPRAVALVULAR AORTIC STENOSIS | METABOLISM | PHARMACOKINETICS | MECHANISM | PATHWAY | 1,25-DIHYDROXYVITAMIN-D3 | SITE-DIRECTED MUTAGENESIS | Hypercalcemia - genetics | Steroid Hydroxylases - metabolism | Cricetinae | Genetic Predisposition to Disease | Cricetulus | Genetic Association Studies | Humans | Risk Factors | Cells, Cultured | Infant | Male | Vitamin D3 24-Hydroxylase | Hypercalcemia - chemically induced | Genes, Recessive | Vitamin D - adverse effects | Animals | DNA Mutational Analysis | Pedigree | Female | Vitamin D - metabolism | Mutation | Vitamin D - therapeutic use | Steroid Hydroxylases - genetics | Hypercalcemia | Care and treatment | Gene mutations | Vitamin D | Calcifediol | Genetic aspects | Research | Alfacalcidol | Health aspects | Risk factors | Milk products | Laboratories | Pathogenesis | Prophylaxis | Calcitriol | Families & family life | Homeostasis | Infants | Family medical history | Dehydration | Ultrasonic imaging | Dihydroxyvitamin D3 | Rickets | Metabolites | Vomiting | Fibroblasts | Supplementation | Children | 25-Hydroxyvitamin D | Enzymes | Hydroxylase | Vitamin deficiency | Heredity | Metabolism | Patients | Calcinosis | Kidney diseases | Index Medicus | Abridged Index Medicus
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6. Full Text Screening for strains with 11α-hydroxylase activity for 17α-hydroxy progesterone biotransformation
by Gao, Qian and Qiao, Yuqian and Shen, Yanbing and Wang, Xibo and Wang, Min and Liu, Yang
Steroids, ISSN 0039-128X, 08/2017, Volume 124, pp. 67 - 71
Various corticosteroids are prepared by using 11α,17α-diOH-progesterone (11α,17α-diOH-PROG) as an important intermediate and raw material. Hence, strains that... 
17α-Hydroxy progesterone | Hydroxylation | Biotransformation | Cunninghamella elegans | STEROIDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENDOCRINOLOGY & METABOLISM | IMPROVEMENT | RHIZOPUS-NIGRICANS | COSUBSTRATE-COUPLED SYSTEM | 17 alpha-Hydroxy progesterone | EFFICIENT | Hydroxyprogesterones - metabolism | Steroid Hydroxylases - metabolism | Cunninghamella - metabolism | Index Medicus
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7. Full Text Oxysterol Gradient Generation by Lymphoid Stromal Cells Guides Activated B Cell Movement during Humoral Responses
by Yi, Tangsheng and Wang, Xiaoming and Kelly, Lisa M and An, Jinping and Xu, Ying and Sailer, Andreas W and Gustafsson, Jan-Ake and Russell, David W and Cyster, Jason G
Immunity, ISSN 1074-7613, 09/2012, Volume 37, Issue 3, pp. 535 - 548
7α,25-dihydroxycholesterol (7α,25-OHC) is a ligand for the G protein-coupled receptor EBI2; however, the cellular sources of this oxysterol are undefined.... 
MIGRATION | DENDRITIC CELLS | CHOLESTEROL | METABOLISM | MARGINAL ZONE | EBI2 | MACROPHAGES | FOLLICLES | GERMINAL CENTER | IMMUNOLOGY | KNOCKOUT MICE | Steroid Hydroxylases - metabolism | Receptors, G-Protein-Coupled - metabolism | Immunity, Humoral - immunology | Humans | Male | Lymphoid Tissue - immunology | Receptors, G-Protein-Coupled - immunology | Cell Movement - immunology | Lymphocyte Activation - immunology | Flow Cytometry | Cytochrome P450 Family 7 | Hydroxycholesterols - immunology | Bone Marrow Cells - immunology | HEK293 Cells | 3-Hydroxysteroid Dehydrogenases - metabolism | Female | Steroid Hydroxylases - genetics | Steroid Hydroxylases - immunology | Gene Expression | Mice, Inbred C57BL | Stromal Cells - metabolism | Cells, Cultured | Lymphoid Tissue - metabolism | Stromal Cells - immunology | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Animals | B-Lymphocytes - immunology | Hydroxycholesterols - metabolism | Mice | Receptors, G-Protein-Coupled - genetics | 3-Hydroxysteroid Dehydrogenases - genetics | 3-Hydroxysteroid Dehydrogenases - immunology | Bone Marrow Cells - metabolism | Dendritic cells | Cytochrome P-450 | Membrane proteins | Vitamin deficiency | Acids | Rodents | Cholesterol | Bile | Index Medicus
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8. Full Text Upregulation of calcitriol during pregnancy and skeletal recovery after lactation do not require parathyroid hormone
by Kirby, Beth J and Ma, Yue and Martin, Heather M and Buckle Favaro, Kerri L and Karaplis, Andrew C and Kovacs, Christopher S
Journal of Bone and Mineral Research, ISSN 0884-0431, 09/2013, Volume 28, Issue 9, pp. 1987 - 2000
Pregnancy invokes a doubling of intestinal calcium absorption whereas lactation programs skeletal resorption to provide calcium to milk. Postweaning bone... 
ANIMAL MODELS, RODENT | BONE MINERALIZATION | KNOCKOUT | FGF23 | LACTATION | GROWTH AND DEVELOPMENT | PREGNANCY | PTH/PTHRP | CALCITRIOL | RODENT | VITAMIN-D METABOLISM | INTESTINAL CALCIUM | BONE-MINERAL DENSITY | PTH | PTHRP | HUMAN SYNCYTIOTROPHOBLAST CELLS | PHOSPHATE HOMEOSTASIS | ENDOCRINOLOGY & METABOLISM | 25-HYDROXYVITAMIN D-3 1-ALPHA-HYDROXYLASE | 1,25-DIHYDROXYVITAMIN-D CONCENTRATIONS | FIBROBLAST GROWTH FACTOR-23 | D-RECEPTOR | ANIMAL MODELS | CALCIUM-TRANSPORT | Steroid Hydroxylases - metabolism | Vitamin D-Binding Protein - metabolism | Glucuronidase - metabolism | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - genetics | Fibroblast Growth Factors - genetics | Lactation - drug effects | Parathyroid Hormone - deficiency | RNA, Messenger - metabolism | Bone Remodeling - drug effects | Bone and Bones - drug effects | Calcium - blood | Fibroblast Growth Factors - metabolism | Kidney - metabolism | Parathyroid Hormone - metabolism | Bone and Bones - metabolism | Lactation - blood | Female | Calcitriol - metabolism | Steroid Hydroxylases - genetics | Biomarkers - metabolism | Calcium - pharmacology | Kidney - drug effects | RNA, Messenger - genetics | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - metabolism | Up-Regulation - genetics | Vitamin D3 24-Hydroxylase | Placenta - drug effects | Placenta - metabolism | Pregnancy | Reproduction - drug effects | Up-Regulation - drug effects | Bone Density - drug effects | Animals | Diet | Glucuronidase - genetics | Lactation - metabolism | Mice | Vitamin D | Pregnant women | Parathyroid hormone | Calcifediol | Alfacalcidol | Protein binding | Calcium | Rodents | Index Medicus
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9. Full Text CYP260B1 acts as 9α-hydroxylase for 11-deoxycorticosterone
by Litzenburger, Martin and Bernhardt, Rita
Steroids, ISSN 0039-128X, 11/2017, Volume 127, pp. 40 - 45
Steroids and their oxyfunctionalized counterparts are valuable compounds for the pharmaceutical industry; however, the regio- and stereoselective introduction... 
9α-Hydroxylase | CYP260B1 | Steroids | 11-Deoxycorticosterone | Sorangium cellulosum So ce56 | Cytochromes P450 | SYSTEM | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | HYDROXYLATION | CYP106A2 | 9 alpha-Hydroxylase | IDENTIFICATION | HYDROCORTISONE | BACILLUS-MEGATERIUM | ENDOCRINOLOGY & METABOLISM | MYXOBACTERIAL CYP260B1 | Steroid Hydroxylases - metabolism | Oxidation-Reduction | Myxococcales - enzymology | Desoxycorticosterone - metabolism | Substrate Specificity | Kinetics | Mutation | Steroid Hydroxylases - genetics | Index Medicus
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10. Full Text Cold-induced conversion of cholesterol to bile acids in mice shapes the gut microbiome and promotes adaptive thermogenesis
by Worthmann, Anna and John, Clara and Rühlemann, Malte C and Baguhl, Miriam and Heinsen, Femke-Anouska and Schaltenberg, Nicola and Heine, Markus and Schlein, Christian and Evangelakos, Ioannis and Mineo, Chieko and Fischer, Markus and Dandri, Maura and Kremoser, Claus and Scheja, Ludger and Franke, Andre and Shaul, Philip W and Heeren, Joerg
Nature Medicine, ISSN 1078-8956, 07/2017, Volume 23, Issue 7, pp. 839 - 849
Adaptive thermogenesis is an energy-demanding process that is mediated by cold-activated beige and brown adipocytes, and it entails increased uptake of... 
MEDICINE, RESEARCH & EXPERIMENTAL | HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ATHEROSCLEROSIS | ADULT HUMANS | BROWN ADIPOSE-TISSUE | INSULIN SENSITIVITY | CELL BIOLOGY | OBESITY | ENERGY-EXPENDITURE | METABOLISM | FAT | EXPOSURE | Steroid Hydroxylases - metabolism | Humans | Gene Expression Profiling | Case-Control Studies | ATP Binding Cassette Transporter, Subfamily B - genetics | Steroid Hydroxylases - genetics | Obesity | Receptors, LDL - genetics | Cold Temperature | Liver - metabolism | Bile Acids and Salts - metabolism | Calorimetry, Indirect | Cholesterol - metabolism | Gastrointestinal Microbiome - genetics | Reverse Transcriptase Polymerase Chain Reaction | Cytochrome P450 Family 7 - genetics | Blotting, Western | Aspartate Aminotransferases - metabolism | Mice, Knockout | Animals | Thermogenesis | Cytochrome P450 Family 7 - metabolism | RNA, Ribosomal, 16S - genetics | Adipose Tissue, Brown - metabolism | Mice | Alanine Transaminase - metabolism | Adipose tissues | Microbiota (Symbiotic organisms) | Cytochrome P-450 | Physiological aspects | Triglycerides | Research | Health aspects | Cholesterol | Cytochrome | Energy metabolism | Adipose tissue | Liver | Adipocytes | Synthesis | Energy | Rodents | Bacteria | Lipid metabolism | Adipose tissue (brown) | Digestive tract | Carbohydrates | Stomach | Excretion | Bile acids | Cytochrome P450 | Pharmacology | Metabolism | Conversion | Heat | Acids | Effectors | Plasma levels | Bile | Index Medicus
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11. Full Text Vitamin D: An innate antiviral agent suppressing hepatitis C virus in human hepatocytes
by Gal‐Tanamy, Meital and Bachmetov, Larisa and Ravid, Amiram and Koren, Ruth and Erman, Arie and Tur‐Kaspa, Ran and Zemel, Romy
Hepatology, ISSN 0270-9139, 11/2011, Volume 54, Issue 5, pp. 1570 - 1579
Vitamin D supplementation was reported to improve the probability of achieving a sustained virological response when combined with antiviral treatment against... 
SIGNALING PATHWAYS | INTERFERON | INHIBITION | RNA | RECEPTOR | 1,25-DIHYDROXYVITAMIN D-3 | D PATHWAY | GASTROENTEROLOGY & HEPATOLOGY | Interferon-alpha - pharmacology | Steroid Hydroxylases - metabolism | Humans | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - genetics | Hepatitis C, Chronic - virology | Antiviral Agents - metabolism | Hepatocytes - metabolism | Liver Neoplasms | Calcitriol - metabolism | Steroid Hydroxylases - genetics | Hepatocytes - drug effects | Hepacivirus - drug effects | Antiviral Agents - pharmacology | 25-Hydroxyvitamin D3 1-alpha-Hydroxylase - metabolism | Vitamin D3 24-Hydroxylase | Hepatitis C, Chronic - drug therapy | Cholecalciferol - pharmacokinetics | Drug Synergism | Vitamins - pharmacokinetics | Signal Transduction - drug effects | Calcitriol - biosynthesis | Cell Line, Tumor | Hepatocytes - virology | Hepacivirus - growth & development | Signal Transduction - physiology | Carcinoma, Hepatocellular | Vitamin D | Hepatitis | Enzymes | Index Medicus
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12. Full Text Development of monoclonal antibodies against human CYP11B1 and CYP11B2
by Gomez-Sanchez, Celso E and Gomez-Sanchez, Elise P and Qi, Xin and Velarde-Miranda, Carolina and Plonczynski, Maria W and Parker, C. Richard and Rainey, William and Satoh, Fumitoshi and Maekawa, Takashi and Nakamura, Yasuhiro and Sasano, Hironobu
Molecular and Cellular Endocrinology, ISSN 0303-7207, 03/2014, Volume 383, Issue 1-2, pp. 111 - 117
1.The final enzymes in the biosynthesis of aldosterone and cortisol are by the cytochrome P450 CYP11B2 and CYP11B1, respectively. The enzymes are 93%... 
Monoclonal antibodies | Immunofluorescence | CYP11B2 | CYP11B1 | Adrenal cortex | 17α-Hydroxylase | 17 alpha-Hydroxylase | lmmunofluorescence | DIAGNOSIS | MESSENGER-RNA EXPRESSION | HYPERPLASIA | PARTIAL ALDOSTERONE RESISTANCE | CELL BIOLOGY | SYNTHASE | RAT ADRENAL-CORTEX | GENE | ZONA GLOMERULOSA | BIOSYNTHESIS | ENDOCRINOLOGY & METABOLISM | ADENOMA | Antibodies, Monoclonal - biosynthesis | Humans | Steroid 11-beta-Hydroxylase - immunology | Molecular Sequence Data | Peptides - administration & dosage | Peptides - chemical synthesis | Zona Fasciculata - immunology | Steroid 17-alpha-Hydroxylase - immunology | Adult | Cytochrome P-450 CYP11B2 - metabolism | Infant, Newborn | Amino Acid Sequence | Zona Glomerulosa - ultrastructure | Peptides - immunology | Rats | Zona Glomerulosa - metabolism | Antibodies, Monoclonal - isolation & purification | Immunohistochemistry - methods | Sequence Homology, Amino Acid | Sequence Alignment | Animals | Steroid 11-beta-Hydroxylase - metabolism | Cytochrome P-450 CYP11B2 - immunology | Zona Glomerulosa - immunology | Zona Fasciculata - metabolism | Mice | Steroid 17-alpha-Hydroxylase - metabolism | Zona Fasciculata - ultrastructure | Cytochrome P-450 | Index Medicus
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