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Journal Article
Journal Article
Molecular Endocrinology, ISSN 0888-8809, 12/2011, Volume 25, Issue 12, pp. 2041 - 2053
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 07/2015, Volume 125, Issue 7, pp. 2808 - 2824
The precise mechanisms that lead to parturition are incompletely defined. Surfactant protein-A (SP-A), which is secreted by fetal lungs into amniotic fluid... 
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN MYOMETRIAL CELLS | ACUTE REGULATORY PROTEIN | A SP-A | PRETERM BIRTH | II CELLS | SURFACTANT-PROTEIN | PLATELET-ACTIVATING-FACTOR | AMNIOTIC-FLUID | UTERINE CERVICAL FIBROBLASTS | CORPUS-LUTEUM | Nuclear Receptor Coactivator 2 - deficiency | Nuclear Receptor Coactivator 1 - deficiency | 1-Acylglycerophosphocholine O-Acyltransferase - deficiency | Transcriptional Activation | Male | Maternal-Fetal Exchange - genetics | Nuclear Receptor Coactivator 1 - genetics | Uterus - physiology | Female | Models, Animal | Promoter Regions, Genetic | 1-Acylglycerophosphocholine O-Acyltransferase - genetics | Signal Transduction | Nuclear Receptor Coactivator 1 - physiology | Mice, Inbred C57BL | Maternal-Fetal Exchange - physiology | Platelet Activating Factor - deficiency | Lung - physiology | Mice, Knockout | Parturition - physiology | Pregnancy | Animals | Heterozygote | Lung - embryology | Mice | Nuclear Receptor Coactivator 2 - physiology | Pulmonary Surfactant-Associated Protein A - deficiency | Luteolysis | Nuclear Receptor Coactivator 2 - genetics | Fetal Organ Maturity | Cytokines | Laboratories | Fetuses | Lipids | Kinases | Gene expression | Surfactants | Cell adhesion & migration | Proteins | Studies | Respiratory distress syndrome | Physiology | Females | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 07/2015, Volume 290, Issue 30, pp. 18596 - 18608
Journal Article
Cancer Cell, ISSN 1535-6108, 08/2015, Volume 28, Issue 2, pp. 240 - 252
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 03/2015, Volume 459, Issue 1, pp. 143 - 147
The constitutive androstane receptor (CAR) plays a key role in the expression of xenobiotic/steroid and drug metabolizing enzymes and their transporters. In... 
PRMT5 | Nuclear receptor | CYP2B6 | CYP3A4 | CAR | METHYLATION | ACTIVATION | ENHANCER MODULE | NUCLEAR | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | SIGNALS | IDENTIFICATION | BIOPHYSICS | GENES | RETINOID-X-RECEPTOR | EXPRESSION | Cell Line | Cytochrome P-450 CYP2B6 - genetics | Humans | Transcriptional Activation | Gene Expression Regulation | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | Neoplasm Proteins - metabolism | Cytochrome P-450 CYP2B6 - metabolism | Cytochrome P-450 CYP2C9 - genetics | Gene Knockdown Techniques | Nuclear Receptor Coactivator 1 - metabolism | Protein-Arginine N-Methyltransferases - metabolism | Transcription Factors - metabolism | DEAD-box RNA Helicases - genetics | Nuclear Receptor Coactivator 1 - genetics | Cytochrome P-450 CYP3A - genetics | Cytochrome P-450 CYP3A - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Protein-Arginine N-Methyltransferases - genetics | DEAD-box RNA Helicases - metabolism | Neoplasm Proteins - genetics | Cytochrome P-450 CYP2C9 - metabolism | Receptors, Cytoplasmic and Nuclear - metabolism | Phenobarbital | Arginine | RNA | Transferases | Cytochrome P-450 | Index Medicus | STEROIDS | RATS | PHENOBARBITAL | 60 APPLIED LIFE SCIENCES | MESSENGER-RNA | TETRACYCLINES | DNA | LIVER CELLS | ARGININE | AUTOMOBILES | METHYL TRANSFERASES | RECEPTORS
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 01/2018, Volume 115, Issue 3, pp. E458 - E467
Th17 cells are major players in multiple autoimmune diseases and are developmentally contingent on reciprocal functionality between the transcription factor... 
EAE | Th17 | T cell differentiation | Treg | ACTIVATION | TGF-BETA | PROTECTION | STEROID-RECEPTOR COACTIVATORS | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | DEFICIENT | IL-17 | PROTEIN METHYLTRANSFERASE | CELL-DIFFERENTIATION | PLASTICITY | Amino Acid Sequence | Th17 Cells - physiology | Nuclear Receptor Coactivator 1 - chemistry | Gene Expression Regulation, Enzymologic - physiology | Forkhead Transcription Factors - genetics | Interleukins - metabolism | Nuclear Receptor Coactivator 1 - metabolism | Interleukins - genetics | Nuclear Receptor Coactivator 1 - genetics | Animals | Forkhead Transcription Factors - metabolism | Protein Kinase C-theta - metabolism | Gene Deletion | Nuclear Receptor Subfamily 1, Group F, Member 3 - metabolism | Protein Kinase C-theta - genetics | Mice | Cell Differentiation - physiology | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Binding | Ubiquitin | Phosphorylation | Protein kinase C | Encephalomyelitis | Medical treatment | Helper cells | Reversing | Dominance | T cell receptors | Lymphocytes T | Cells | Experimental allergic encephalomyelitis | Interleukin 17 | T-cell receptor | Signaling | Steroid receptor coactivator 1 | Foxp3 protein | Forkhead protein | Autoimmune diseases | Differentiation | Methylation | Deoxyribonucleic acid--DNA | Index Medicus | Biological Sciences | PNAS Plus
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7, pp. e36961 - e36961
Three p160 family members, p/CIP, SRC1, and TIF2, have been identified as transcriptional coactivators for nuclear hormone receptors and other transcription... 
ENERGY-BALANCE | ADIPONECTIN RECEPTORS | DISRUPTION | GROWTH | SUBSTRATE-1 | BIOLOGY | SENSITIVITY | PPAR-GAMMA | MICE | CELL | EXPRESSION | NIH 3T3 Cells | RNA, Small Interfering - genetics | Adipose Tissue, White - metabolism | Diet, High-Fat - adverse effects | Male | Muscle, Skeletal - metabolism | Insulin Receptor Substrate Proteins - metabolism | Obesity - blood | Gene Knockdown Techniques | Nuclear Receptor Coactivator 1 - metabolism | Nuclear Receptor Coactivator 1 - genetics | Obesity - etiology | Insulin Receptor Substrate Proteins - genetics | Disease Models, Animal | Gene Expression | Glucose Tolerance Test | Signal Transduction | Nuclear Receptor Coactivator 1 - physiology | Insulin Resistance | Blood Glucose | Nuclear Receptor Coactivator 3 - genetics | Mice, Knockout | Obesity - metabolism | Adiponectin - blood | Animals | Nuclear Receptor Coactivator 3 - metabolism | Mice | Nuclear Receptor Coactivator 3 - physiology | Obesity | Glucose metabolism | Physiological aspects | Muscles | Insulin resistance | Genetic aspects | Genetic transcription | Glucose | Dextrose | Diabetes therapy | Animal models | Transcription factors | Adipose tissue | Kinases | High fat diet | Receptors | Clonal deletion | Rodents | Deletion | Age | Diabetes mellitus | Energy expenditure | Metabolism | Nuclear receptors | Insulin | Skeletal muscle | Glucose tolerance | Intolerance | Signaling | Sensitivity | Insulin receptor substrate 1 | Food intake | Cell lines | Steroid receptor coactivator 1 | Sensitivity enhancement | Index Medicus
Journal Article
Molecular and Cellular Endocrinology, ISSN 0303-7207, 09/2015, Volume 412, Issue C, pp. 26 - 35
Journal Article