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Current opinion in gastroenterology, ISSN 0267-1379, 03/2015, Volume 31, Issue 2, pp. 159 - 165
microbiota | bile acids | diabetes | incretin | FGF15/FGF19 | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Liver - pathology | Intestine, Small - pathology | Signal Transduction | Humans | Liver - metabolism | Homeostasis | Bile Acids and Salts - metabolism | Diabetes Mellitus, Type 2 - metabolism | Obesity - metabolism | Inflammation - metabolism | Biological Transport | Energy Metabolism | Cholesterol 7-alpha-Hydroxylase - metabolism | Intestine, Small - metabolism | Receptors, Cytoplasmic and Nuclear - metabolism | Index Medicus | 19 | FGF15
Journal Article
Journal of hepatology, ISSN 0168-8278, 2012, Volume 58, Issue 1, pp. 155 - 168
Gastroenterology and Hepatology | Gallstones | Liver cancer | Bile acids | Fatty liver disease | Cholestasis | Liver regeneration | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Animals | Carrier Proteins - metabolism | Cholestasis - metabolism | Membrane Glycoproteins - metabolism | Humans | Liver - metabolism | Bile Acids and Salts - metabolism | Liver Diseases - metabolism | Liver Regeneration - physiology | Receptors, Cytoplasmic and Nuclear - metabolism | Drug resistance in microorganisms | Corticosteroids | Glucagon | Calcifediol | Ursodiol | Deoxycholic acid | Epidermal growth factor | Vitamin D | Physiological aspects | Fibroblast growth factors | Alfacalcidol | Index Medicus | IBABP (FABP6, ILBP), intestinal bile acid-binding protein, fatty acid-binding protein 6 | PFIC, progressive familial intrahepatic cholestasis | TNFα, tumor necrosis factor α | 3 (human) | SRC2, p160 steroid receptor coactivator | NAFLD, non-alcoholic fatty liver disease | BA, bile acid | bile acid receptor | 8, cholesterol efflux pump, ATP-binding cassette, subfamily G, member 5 | UDCA, ursodeoxycholic acid | LRH-1 (NR5A2), liver receptor homolog-1 | LCA, lithocholic acid | LXRα (NR1H3), liver X receptor alpha | PPARγ (NR1C3), peroxisome proliferator-activated receptor gamma | OSTαβ, organic solute transporter alpha | ABCG5 | AMPK, AMP activated protein kinase | NASH, non-alcoholic steatohepatitis | SHP (NR0B2), short heterodimer partner | OATP1A2 (SLCO1A2, OATP1, OATP-A, SLC21A3), solute carrier organic anion transporter family, member 1A2 | EGFR, epidermal growth factor receptor | IL6, interleukin 6 | TGR5, G protein-coupled bile acid receptor | PH, partial hepatectomy | AE2, anion exchanger 2 | PSC, primary sclerosing cholangitis | OATP1B1 (SLCO1B1, OATP2, OATP-C, SLC21A6), solute carrier organic anion transporter family, member 1B1 | RARα (NR1B1), retinoic acid receptor alpha | GLP-1, glucagon like peptide 1 | VDR (NR1I1), vitamin D receptor. Please note that for the convenience of better readability and clarity, abbreviations for transporters and nuclear receptors were capitalized throughout this article when symbols were identical for human and rodents | MRP2 (ABCC2), multidrug resistance-associated protein 2, ATP-binding cassette, subfamily C, member 2 | NTCP (SLC10A1), sodium | CAR (NR1I3), constitutive androstane receptor | taurocholate cotransporting polypeptide, solute carrier family 10, member 1 | PPARα (NR1C1), peroxisome proliferator-activated receptor alpha | Review | GR (NR3C1), glucocorticoid receptor | Bile acids, Cholestasis, Fatty liver disease, Gallstones, Liver regeneration, Liver cancer | 19, fibroblast growth factor 15 | Mdr2 | ICP, intrahepatic cholestasis of pregnancy | BRIC, benign recurrent intrahepatic cholestasis | OATP1B3 (SLCO1B3, OATP8, SLC21A8), solute carrier organic anion transporter family, member 1B3 | MRP3 (ABCC3), multidrug resistance-associated protein 3, ATP-binding cassette, subfamily C, member 3 | beta | MDR1 (ABCB1), p-glycoprotein, ATP-binding cassette, subfamily B, member 1 | norUDCA, norursodeoxycholic acid | 6-ECDCA, 6-ethylchenodeoxycholic acid | FXR (NR1H4), farnesoid X receptor | BCRP (ABCG2), breast cancer resistance protein, ATP-binding cassette, subfamily G, member 2 | HNF4α (NR2A1), hepatocyte nuclear factor 4 alpha | PBC, primary biliary cirrhosis | MDR3 (ABCB4), multidrug resistance protein 2 (rodents) | HNF1α, hepatocyte nuclear factor 1 alpha | NR, nuclear receptor | FGF15 | RXRα (NR2B1), retinoid X receptor alpha | PXR (NR1I2), pregnane X receptor | BSEP (ABCB11), bile salt export pump | HCC, hepatocellular carcinoma | MRP4 (ABCC4), multidrug resistance-associated protein 4, ATP-binding cassette, subfamily C, member 4 | TPN, total parenteral nutrition
Journal Article
Hepatology (Baltimore, Md.), ISSN 0270-9139, 2/2020, Volume 71, Issue 2, pp. 670 - 685
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Genes & development, ISSN 0890-9369, 02/2012, Volume 26, Issue 4, pp. 312 - 324
Obesity | FGF15 | Bile acids | Diabetes | FGF19 | FGF21 | Genetics & Heredity | Life Sciences & Biomedicine | Developmental Biology | Science & Technology | Cell Biology | Neoplasms - metabolism | Fibroblast Growth Factors - metabolism | Animals | Fasting - physiology | Homeostasis - physiology | Humans | Bile Acids and Salts - metabolism | Fibroblast Growth Factors - pharmacology | Homeostasis - drug effects | Prevention | Care and treatment | Liver | Physiological aspects | Endocrine glands | Metabolic diseases | Fibroblast growth factors | Research | Index Medicus | bile acids | Review | diabetes | obesity
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Hepatology (Baltimore, Md.), ISSN 0270-9139, 09/2012, Volume 56, Issue 3, pp. 1034 - 1043
Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Gastroenterology. Liver. Pancreas. Abdomen | Biological and medical sciences | Medical sciences | Liver. Biliary tract. Portal circulation. Exocrine pancreas | Gene Expression | Animals | Bile Acids and Salts - biosynthesis | Bile Acids and Salts - genetics | Receptors, Cytoplasmic and Nuclear - physiology | Mice | Mice, Knockout | Acids | Kinases | Gene expression | Rodents | Hepatology | Index Medicus | FXR | FGF15 | SHP | Bile Acids | MAPK
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Hepatology (Baltimore, Md.), ISSN 0270-9139, 10/2019, Volume 70, Issue 4, pp. 1168 - 1184
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Current molecular medicine, ISSN 1566-5240, 2014, Volume 14, Issue 6, pp. 703 - 711
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Full Text
FGF15 Activates Hippo Signaling to Suppress Bile Acid Metabolism and Liver Tumorigenesis
Developmental cell, ISSN 1534-5807, 02/2019, Volume 48, Issue 4, pp. 460 - 474.e9
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Journal of anatomy, ISSN 0021-8782, 05/2011, Volume 218, Issue 5, pp. 534 - 543
tooth development | Fgf15 mutant | mesenchyme | secondary enamel knot | Fgf ligand | Fgf15/Fgf8 mutant | epithelium | primary enamel knot | cervical loop | Mesenchyme | Tooth development | Secondary enamel knot | Epithelium | Primary enamel knot | Cervical loop | Life Sciences & Biomedicine | Anatomy & Morphology | Science & Technology | Dental Enamel - metabolism | Epithelium - metabolism | Rats | Tooth - growth & development | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Fibroblast Growth Factors - metabolism | Animals | In Situ Hybridization | Signal Transduction - physiology | Trans-Activators - metabolism | Mesoderm - metabolism | Odontogenesis - physiology | Tooth - metabolism | Analysis | Fibroblast growth factors | Stem cells | Evolution | Ligands | Enamel | Hominids | Index Medicus | Fibroblast growth factor | Fibroblast growth factor 20 | Transcription | Teeth | Molars | Signal transduction | Dental enamel | Ameloblasts | Development | Fibroblast growth factor 16 | Incisors | Fibroblast growth factor 18 | Fibroblast growth factor 17 | Fgf8 mutant | Fgf15 | Original
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