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1. Full Text Sodium‐glucose co‐transporter (SGLT) and glucose transporter (GLUT) expression in the kidney of type 2 diabetic subjects
by Norton, Luke and Shannon, Christopher E and Fourcaudot, Marcel and Hu, Cheng and Wang, Niansong and Ren, Wei and Song, Jun and Abdul‐Ghani, Muhammad and DeFronzo, Ralph A and Ren, Jimmy and Jia, Weiping
Diabetes, Obesity and Metabolism, ISSN 1462-8902, 09/2017, Volume 19, Issue 9, pp. 1322 - 1326
The sodium‐glucose co‐transporters ( SGLTs ) are responsible for the tubular reabsorption of filtered glucose from the kidney into the bloodstream. The... 
kidney | glucose transporters (GLUT) | type 2 diabetes | sodium‐glucose co‐transporters (SGLT) | sodium-glucose co-transporters (SGLT) | INHIBITORS INHIBIT | DAPAGLIFLOZIN | RATS | PROXIMAL TUBULAR CELLS | 30-50-PERCENT | NEPHROPATHY | GENE | ENDOCRINOLOGY & METABOLISM | FILTRATION-RATE | MICE | REABSORPTION | Glycated Hemoglobin A - analysis | Glucose Transporter Type 2 - genetics | Kidney - pathology | Humans | Glucose Transporter Type 1 - metabolism | Male | Diabetes Mellitus, Type 2 - metabolism | RNA, Messenger - metabolism | Glucose Transporter Type 2 - metabolism | Sodium-Glucose Transporter 1 - genetics | Kidney - metabolism | China | Postprandial Period | Adult | Female | Sodium-Glucose Transporter 1 - metabolism | Sodium-Glucose Transporter 2 - genetics | Hypoglycemic Agents - therapeutic use | Reproducibility of Results | Fasting | Kidney - drug effects | Blood Glucose - analysis | Sodium-Glucose Transporter 2 - metabolism | Gene Expression Regulation - drug effects | Diabetes Mellitus, Type 2 - blood | Glucose Transporter Type 1 - genetics | Biopsy | Diabetes Mellitus, Type 2 - pathology | Diabetes Mellitus, Type 2 - drug therapy | Type 2 diabetes | Diabetics | Hyperglycemia | RNA | Glycosylated hemoglobin | Glucose | Dextrose | Diabetes | Index Medicus
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2. Full Text The role of SGLT1 and GLUT2 in intestinal glucose transport and sensing
by Röder, Pia V and Geillinger, Kerstin E and Zietek, Tamara S and Thorens, Bernard and Koepsell, Hermann and Daniel, Hannelore
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e89977 - e89977
Intestinal glucose absorption is mediated by SGLT1 whereas GLUT2 is considered to provide basolateral exit. Recently, it was proposed that GLUT2 can be... 
CALCIUM-ABSORPTION | DIFFUSIVE COMPONENT | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | SUGAR ABSORPTION | APICAL GLUT2 | COTRANSPORTER | RAT SMALL-INTESTINE | MICE | BRUSH-BORDER MEMBRANE | INCRETIN SECRETION | Intestines - drug effects | Intestinal Mucosa - metabolism | Incretins - blood | Intestinal Absorption - drug effects | Incretins - metabolism | Glucose - pharmacology | Insulin - blood | Glucose Transporter Type 2 - metabolism | Glucose Transporter Type 2 - deficiency | Sodium-Glucose Transporter 1 - deficiency | Insulin - metabolism | Animals | Glucose - metabolism | Mice | Sodium-Glucose Transporter 1 - metabolism | Blood Glucose - metabolism | Insulin Secretion | Tracers (Biology) | Glucose metabolism | Blood sugar | Glucose transporter | Membranes | Secretion | Chemoreception | Glucose | Kinases | Glucose transport | Insulin | Small intestine | Contamination | Absorption | Clonal deletion | Rodents | Deletion | Transporter | Bulk transporters | Index Medicus
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3. Full Text Na+/H+ exchanger 3 blockade ameliorates type 2 diabetes mellitus via inhibition of sodium-glucose co-transporter 1-mediated glucose absorption in the small intestine
by Chan, Leo K. Y and Wang, Yi and Ng, Enders K. W and Leung, Po Sing
Diabetes, Obesity and Metabolism, ISSN 1462-8902, 03/2018, Volume 20, Issue 3, pp. 709 - 717
AimTo elucidate the role of Na+/H+ exchanger 3 (NHE3) in sodium-glucose co-transporter 1 (SGLT1)-mediated small intestinal brush border membrane (BBM) glucose... 
glucose intolerance | NHE3 inhibitor | postprandial hyperglycaemia | diabetes | TRANSPORTER SGLT1 | ACTIVATION | ENTEROCYTES | KINASE | HYPOGLYCEMIC AGENT | RECEPTOR | NHE3 | GROWTH | ENDOCRINOLOGY & METABOLISM | Intestinal Mucosa - metabolism | Humans | Amiloride - analogs & derivatives | Male | Diabetes Mellitus, Type 2 - metabolism | Glucose Transporter Type 2 - metabolism | Gene Knockdown Techniques | Dose-Response Relationship, Drug | Immediate-Early Proteins - metabolism | Postprandial Period | Epithelial Sodium Channel Blockers - pharmacology | Sodium-Glucose Transporter 1 - metabolism | Hyperglycemia - physiopathology | Glucose Intolerance - physiopathology | Protein-Serine-Threonine Kinases - metabolism | Intestinal Absorption - physiology | Caco-2 Cells | Sodium-Glucose Transporter 1 - antagonists & inhibitors | Mice, Inbred C57BL | Sodium-Hydrogen Exchanger 3 - antagonists & inhibitors | Down-Regulation - physiology | Animals | Glucose - pharmacokinetics | Amiloride - pharmacology | Intestine, Small - metabolism | Diabetes Mellitus, Type 2 - drug therapy | Type 2 diabetes | Glucose metabolism | Blood sugar monitoring | RNA | Analysis | Insulin resistance | Glucose | Glucose tolerance tests | Insulin | Dextrose | Glucose transporter | Glucocorticoids | Hydrogen | Na+/H+-exchanging ATPase | Diabetes mellitus | mRNA | siRNA | Gastrectomy | Small intestine | Glucose tolerance | Intolerance | Hyperglycemia | Jejunum | Sodium | Diabetes | Diabetes mellitus (non-insulin dependent) | Index Medicus
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4. Full Text Differential patterns of inhibition of the sugar transporters GLUT2, GLUT5 and GLUT7 by flavonoids
by Gauer, Julia S and Tumova, Sarka and Lippiat, Jonathan D and Kerimi, Asimina and Williamson, Gary
Biochemical Pharmacology, ISSN 0006-2952, 06/2018, Volume 152, pp. 11 - 20
Only limited data are available on the inhibition of the sugar transporter GLUT5 by flavonoids or other classes of bioactives. Intestinal GLUT7 is poorly... 
Polyphenols | Flavonoids | Caco-2 cells | Xenopus laevis oocytes | Sugar transporters | HOMEOSTASIS | ADIPOCYTES | DETERMINANT | IDENTIFICATION | FRUCTOSE TRANSPORTER | METABOLISM | INTESTINAL GLUCOSE | APICAL GLUT2 | PHARMACOLOGY & PHARMACY | ABSORPTION | HEXOSE TRANSPORTERS | Caco-2 Cells | Glucose Transport Proteins, Facilitative - metabolism | Glucose Transporter Type 2 - genetics | Glucose Transporter Type 5 - metabolism | Oocytes - metabolism | Humans | RNA, Messenger - genetics | Xenopus laevis | Glucose Transporter Type 2 - antagonists & inhibitors | RNA, Messenger - metabolism | Fructose - metabolism | Glucose Transporter Type 2 - metabolism | Gene Expression Regulation - drug effects | Animals | Glucose - metabolism | Oocytes - drug effects | Flavonoids - pharmacology | Glucose Transport Proteins, Facilitative - genetics | Glucose Transporter Type 5 - genetics | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Glucose Transporter Type 5 - antagonists & inhibitors | Sorbitol | Catechin | RNA | Analysis | Glucose | Fructose | Dextrose | Isoflavones | Index Medicus
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5. Full Text The regulation of K‐ and L‐cell activity by GLUT2 and the calcium‐sensing receptor CasR in rat small intestine
by Mace, Oliver J and Schindler, Marcus and Patel, Sonal
The Journal of Physiology, ISSN 0022-3751, 06/2012, Volume 590, Issue 12, pp. 2917 - 2936
•  In intestine, nutrients including glucose and amino acids and non‐nutrients including bile acids increase secretion of anti‐diabetic gut peptides such as... 
GASTRIC-ACID-SECRETION | PHYSIOLOGY | CHOLECYSTOKININ RELEASE | INSULIN-SECRETION | APICAL GLUT2 | GLUCOSE-ABSORPTION | BRUSH-BORDER MEMBRANE | TASTE RECEPTORS | PEPTIDE-1 SECRETION | NEUROSCIENCES | INCRETIN SECRETION | CA2+-SENSING RECEPTOR | Glucose Transporter Type 2 - agonists | Calcium - metabolism | Sucrose - analogs & derivatives | Incretins - metabolism | Sucrose - pharmacology | Male | Glucose Transporter Type 2 - antagonists & inhibitors | Receptors, Calcium-Sensing - metabolism | Phenethylamines | Glucose Transporter Type 2 - metabolism | Amino Acids - metabolism | Phloretin - pharmacology | Cyclohexylamines - pharmacology | Benzamides - pharmacology | Sodium-Glucose Transporter 1 - metabolism | Enteroendocrine Cells - metabolism | Phlorhizin - pharmacology | Receptors, Calcium-Sensing - antagonists & inhibitors | Sodium-Glucose Transporter 1 - antagonists & inhibitors | Cytochalasin B - pharmacology | Aniline Compounds - pharmacology | Sweetening Agents - pharmacology | Rats | Rats, Sprague-Dawley | Intestine, Small - secretion | Receptors, Calcium-Sensing - agonists | KATP Channels - metabolism | Animals | Incretins - secretion | Intestine, Small - metabolism | In Vitro Techniques | Propylamines | Amino acids | Peptides | Calcium | Small intestine | Index Medicus | Indexing in process | Renal and Endocrine
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6. Full Text Quantitative Atlas of Cytochrome P450, UDP-Glucuronosyltransferase, and Transporter Proteins in Jejunum of Morbidly Obese Subjects
by Miyauchi, Eisuke and Tachikawa, Masanori and Declèves, Xavier and Uchida, Yasuo and Bouillot, Jean-Luc and Poitou, Christine and Oppert, Jean-Michel and Mouly, Stéphane and Bergmann, Jean-François and Terasaki, Tetsuya and Scherrmann, Jean-Michel and Lloret-Linares, Célia
Molecular Pharmaceutics, ISSN 1543-8384, 08/2016, Volume 13, Issue 8, pp. 2631 - 2640
Protein expression levels of drug-metabolizing enzymes and transporters in human jejunal tissues excised from morbidly obese subjects during gastric bypass... 
morbid obesity | transporter | UGT2B17 | small intestine | CYP | BCRP/ABCG2 | drug-metabolizing enzymes | OATP2B1 | MEDICINE, RESEARCH & EXPERIMENTAL | TARGETED ABSOLUTE PROTEOMICS | HUMAN INTESTINE | DELETION POLYMORPHISM | MASS-SPECTROMETRY | GLUCURONIDATION ACTIVITY | P450-MEDIATED METABOLISM | ALPHA-OST-BETA | DRUG DEVELOPMENT | BARRIER TRANSPORTERS | PHARMACOLOGY & PHARMACY | SIMULTANEOUS QUANTIFICATION | Glucose Transporter Type 5 - metabolism | Peptide Transporter 1 | Humans | Cytochrome P-450 Enzyme System - metabolism | Male | Neoplasm Proteins - metabolism | ATP Binding Cassette Transporter, Sub-Family G, Member 2 - metabolism | Glucose Transporter Type 2 - metabolism | Organic Anion Transporters - metabolism | Jejunum - metabolism | Minor Histocompatibility Antigens - metabolism | Glucuronosyltransferase - metabolism | Cytochrome P-450 CYP3A - metabolism | Symporters | Cytochrome P-450 CYP2D6 - metabolism | Female | Sodium-Glucose Transporter 1 - metabolism | Intestine, Small - metabolism | In Vitro Techniques | Obesity, Morbid - metabolism | Cytochrome P-450 CYP2C9 - metabolism | Index Medicus
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7. Full Text Green and Chamomile Teas, but not Acarbose, Attenuate Glucose and Fructose Transport via Inhibition of GLUT2 and GLUT5
by Villa‐Rodriguez, Jose A and Aydin, Ebru and Gauer, Julia S and Pyner, Alison and Williamson, Gary and Kerimi, Asimina
Molecular Nutrition & Food Research, ISSN 1613-4125, 12/2017, Volume 61, Issue 12, pp. 1700566 - n/a
Dietary sugars can cause a large peak of glucose in the blood after a meal, which increases the risk of developing diabetes over time. Using enzymes and human... 
carbohydrates | polyphenols | tea | flavonoids | sugar | DIETARY POLYPHENOLS | ENDOTHELIAL DYSFUNCTION | TOLERANCE | FOOD SCIENCE & TECHNOLOGY | ALPHA-GLUCOSIDASE | SUGAR ABSORPTION | SUBSTRATE SELECTIVITY | BRUSH-BORDER MEMBRANE | TYPE-2 DIABETES-MELLITUS | EXPRESSION | CACO-2 CELLS | Acarbose - pharmacology | Caco-2 Cells | Xenopus | alpha-Amylases - antagonists & inhibitors | Glucose Transporter Type 2 - genetics | Glucose Transporter Type 5 - metabolism | Oocytes - metabolism | Humans | alpha-Amylases - metabolism | Glucose Transporter Type 2 - antagonists & inhibitors | Fructose - metabolism | Glucose Transporter Type 2 - metabolism | Animals | Cell Differentiation - drug effects | Chamomile - chemistry | Sucrose - metabolism | Glucose - metabolism | Oocytes - drug effects | Biological Transport - drug effects | Glucose Transporter Type 5 - genetics | Teas, Herbal | Glucose Transporter Type 5 - antagonists & inhibitors | Tea - chemistry | Type 2 diabetes | Hyperglycemia | Acarbose | Amylases | Liver | Physiological aspects | Polyphenols | Glucose | Green tea | Fructose | Dextrose | Isoflavones | Energy metabolism | Drug delivery systems | Syrups | Glucose transporter type 5 | Oocytes | Intestine | Digestive enzymes | Inhibition | Sugar | Sugars | Glucose transporter | Carbohydrates | Incubation | Diabetes mellitus | Metabolism | Glucose transport | Tea | Diabetes | Transport | Transporter | Index Medicus
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8. Full Text Campylobacter jejuni influences the expression of nutrient transporter genes in the intestine of chickens
by Awad, Wageha A and Aschenbach, Jörg R and Ghareeb, Khaled and Khayal, Basel and Hess, Claudia and Hess, Michael
Veterinary Microbiology, ISSN 0378-1135, 08/2014, Volume 172, Issue 1-2, pp. 195 - 201
The gastrointestinal tract represents the first barrier against pathogens. However, the interaction of with intestinal epithelial cells and its effects on the... 
Peptide transporter | Amino acid transporter | Chicken | Monosaccharide transporter | Campylobacter jejuni | CELLS | BROILER-CHICKENS | MICROBIOLOGY | GLUCOSE-TRANSPORT | COLONIZATION | IN-VITRO | EPITHELIUM | AMINO-ACIDS | GROWTH | VETERINARY SCIENCES | LAYING HENS | INFECTION | Glucose Transporter Type 2 - genetics | Body Weight | Campylobacter Infections - veterinary | Campylobacter Infections - metabolism | Cationic Amino Acid Transporter 2 - metabolism | Campylobacter jejuni - physiology | Cecum - microbiology | RNA, Messenger - metabolism | Poultry Diseases - metabolism | Glucose Transporter Type 2 - metabolism | Sodium-Glucose Transporter 1 - genetics | Jejunum - metabolism | Duodenum - microbiology | Cecum - metabolism | Duodenum - metabolism | Sodium-Glucose Transporter 1 - metabolism | Poultry Diseases - genetics | Specific Pathogen-Free Organisms | Peptide Transporter 1 | RNA, Messenger - genetics | Gene Expression Regulation | Jejunum - microbiology | Chickens - microbiology | Campylobacter Infections - genetics | Excitatory Amino Acid Transporter 3 - genetics | Campylobacter Infections - microbiology | Cationic Amino Acid Transporter 2 - genetics | Symporters - metabolism | Host-Pathogen Interactions | Animals | Excitatory Amino Acid Transporter 3 - metabolism | Symporters - genetics | Poultry Diseases - microbiology | Glucose | Bacterial genetics | Genes | Dextrose | Public health | Index Medicus
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9. Full Text Dietary and Genetic Control of Glucose Transporter 2 Glycosylation Promotes Insulin Secretion in Suppressing Diabetes
by Ohtsubo, Kazuaki and Takamatsu, Shinji and Minowa, Mari T and Yoshida, Aruto and Takeuchi, Makoto and Marth, Jamey D
Cell, ISSN 0092-8674, 2005, Volume 123, Issue 7, pp. 1307 - 1321
Pancreatic β cell-surface expression of glucose transporter 2 (Glut-2) is essential for glucose-stimulated insulin secretion, thereby controlling blood glucose... 
C57BL/6J MICE | HYPERGLYCEMIA | GLUCOSE-TRANSPORTER | HIGH-FAT DIET | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUT-2 | PANCREATIC BETA-CELLS | UDP-N-ACETYLGLUCOSAMINE | CDNA CLONING | EXPRESSION | FAMILY | CELL BIOLOGY | Glucose Transporter Type 2 - genetics | Up-Regulation | Diabetes Mellitus, Type 2 - genetics | Mice, Inbred C57BL | Cells, Cultured | Diabetes Mellitus, Type 2 - enzymology | Diabetes Mellitus, Type 2 - prevention & control | N-Acetylglucosaminyltransferases - genetics | Mice, Transgenic | Glycosylation | Insulin - biosynthesis | Glucose Transporter Type 2 - metabolism | Insulin-Secreting Cells - chemistry | N-Acetylglucosaminyltransferases - metabolism | Insulin - metabolism | Animals | Diet | N-Acetylglucosaminyltransferases - deficiency | Dietary Fats - pharmacology | Dietary Fats - administration & dosage | Mice | Insulin Secretion | Type 2 diabetes | Genetic research | Pancreatic beta cells | Genetic aspects | Research | Gene expression | Diet therapy | Blood sugar | Lectins | Insulin | Diabetes therapy | Index Medicus
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10. Full Text GLUT2 (SLC2A2) is not the principal glucose transporter in human pancreatic beta cells: Implications for understanding genetic association signals at this locus
by McCulloch, Laura J and van de Bunt, Martijn and Braun, Matthias and Frayn, Keith N and Clark, Anne and Gloyn, Anna L
Molecular Genetics and Metabolism, ISSN 1096-7192, 12/2011, Volume 104, Issue 4, pp. 648 - 653
encoding glucose transporter − 2 (GLUT2) acts as the primary glucose transporter and sensor in rodent pancreatic islets and is widely assumed to play a similar... 
Human islets | Diabetes | GWAS signal translation | Pancreatic beta-cells | Human genetics | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | INSULIN-SECRETION | MECHANISMS | GENETICS & HEREDITY | CHANNELS | EXPRESSION | REVEALS | Glucose Transporter Type 2 - genetics | Gene Expression | Humans | Liver - metabolism | RNA, Messenger - genetics | Glucose Transporter Type 1 - metabolism | Muscle, Skeletal - metabolism | Genetic Loci | Glucose Transporter Type 3 - metabolism | RNA, Messenger - metabolism | Glucose Transporter Type 2 - metabolism | Glucose Transporter Type 3 - genetics | Insulin-Secreting Cells - metabolism | Subcutaneous Fat - metabolism | Animals | Glucose Transporter Type 1 - genetics | Adipose Tissue, Brown - metabolism | Mice | Physiological aspects | Genetics | Pancreatic beta cells | Glucose | Dextrose | Index Medicus
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11. Full Text Apple Polyphenol Phloretin Inhibits Colorectal Cancer Cell Growth via Inhibition of the Type 2 Glucose Transporter and Activation of p53-Mediated Signaling
by Lin, Sheng-Tsai and Tu, Shih-Hsin and Yang, Po-Sheng and Hsu, Sung-Po and Lee, Wei- Hwa and Ho, Chi-Tang and Wu, Chih-Hsiung and Lai, Yu-Hsin and Chen, Ming-Yao and Chen, Li-Ching
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 09/2016, Volume 64, Issue 36, pp. 6826 - 6837
Glucose transporters (GLUTs) are required for glucose uptake in malignant cells, and they can be used as molecular targets for cancer therapy. An RT-PCR... 
phloretin | apple polyphenol | glucose transporter 2 | colon cancer | p53 | INDUCED APOPTOSIS | FOOD SCIENCE & TECHNOLOGY | CYCLE ARREST | TUMOR | LINES | COLON-CANCER | IN-VITRO | AGRICULTURE, MULTIDISCIPLINARY | CHEMISTRY, APPLIED | HUMAN HEPATOCELLULAR-CARCINOMA | MELANOMA 4A5 CELLS | EXPRESSION | Hepatocyte Nuclear Factor 6 - metabolism | Signal Transduction | Antioxidants - metabolism | Humans | Malus - chemistry | Tumor Suppressor Protein p53 - metabolism | Male | RNA, Messenger - metabolism | Glucose Transporter Type 2 - metabolism | Cell Cycle Checkpoints | Animals | Mice, Nude | Phloretin - chemistry | Polyphenols - chemistry | Cell Line, Tumor | Glucose - metabolism | Female | Aged | Mice | Mice, Inbred BALB C | Neoplasm Staging | Colorectal Neoplasms - metabolism | Apoptosis | Index Medicus
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12. Full Text The Effects of Critical Illness on Intestinal Glucose Sensing, Transporters, and Absorption
by Deane, Adam M and Rayner, Chris K and Keeshan, Alex and Cvijanovic, Nada and Marino, Zelia and Nguyen, Nam Q and Chia, Bridgette and Summers, Matthew J and Sim, Jennifer A and van Beek, Theresia and Chapman, Marianne J and Horowitz, Michael and Young, Richard L
Critical Care Medicine, ISSN 0090-3493, 01/2014, Volume 42, Issue 1, pp. 57 - 65
OBJECTIVES:Providing effective enteral nutrition is important during critical illness. In health, glucose is absorbed from the small intestine via... 
enteral nutrition | blood glucose | small intestine | intensive care | glucose absorption | SGLT1 | GUT | INJURY | GUSTDUCIN | SEPSIS | GLUCAGON-LIKE PEPTIDE-1 | MALABSORPTION | SECRETION | ILL PATIENTS | EXPRESSION | CRITICAL CARE MEDICINE | Prospective Studies | Receptors, G-Protein-Coupled - metabolism | Humans | Middle Aged | Critical Illness | Glucose Transporter Type 1 - metabolism | Male | Glucose Transporter Type 2 - metabolism | Young Adult | Glucose Transporter Type 2 - physiology | Glucose Transporter Type 1 - physiology | Adult | Duodenum - physiopathology | Female | Sodium-Glucose Transporter 1 - metabolism | Real-Time Polymerase Chain Reaction | Disease Models, Animal | Intestinal Absorption - physiology | Receptors, G-Protein-Coupled - physiology | 3-O-Methylglucose - metabolism | Sodium-Glucose Transporter 1 - physiology | Animals | Glucose - metabolism | Aged | Mice | Intestines - physiopathology | Index Medicus | Abridged Index Medicus
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13. Full Text Thyroid stimulating hormone stimulates the expression of glucose transporter 2 via its receptor in pancreatic β cell line, INS-1 cells
by Lyu, Jingya and Imachi, Hitomi and Yoshimoto, Takuo and Fukunaga, Kensaku and Sato, Seisuke and Ibata, Tomohiro and Kobayashi, Toshihiro and Dong, Tao and Yonezaki, Kazuko and Yamaji, Nao and Kikuchi, Fumi and Iwama, Hisakazu and Ishikawa, Ryou and Haba, Reiji and Sugiyama, Yasunori and Zhang, Huanxiang and Murao, Koji
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 1986 - 10
Thyroid stimulating hormone (TSH) stimulates the secretion of thyroid hormones by binding the TSH receptor (TSHR). TSHR is well-known to be expressed in... 
SIGNAL-TRANSDUCTION | GLUT2 | ACTIVATED PROTEIN-KINASE | INSULIN-RESISTANCE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | GRAVES-DISEASE | TSH RECEPTOR | CAMKK/CAMKIV PATHWAY | BINDING PROTEIN | GLUCOKINASE | Cell Line | Glucose Transporter Type 2 - genetics | Rats, Wistar | Receptors, Thyrotropin - metabolism | Glucokinase - metabolism | Promoter Regions, Genetic - genetics | Glucose Transporter Type 2 - metabolism | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Animals | Insulin-Secreting Cells - drug effects | Thyrotropin - pharmacology | Glucose - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Glucose transporter | Transcription | GLUT2 protein | Secretion | MAP kinase | Thyroid gland | Glucose | Gene expression | Insulin | Thyroid-stimulating hormone receptors | Signal transduction | Thyroid-stimulating hormone | Rodents | Glucokinase | Thyroid hormones | Pancreas | Thyroid | Index Medicus
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