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Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2015, Volume 372, Issue 3, pp. 232 - 240
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2018, Volume 379, Issue 1, pp. 22 - 31
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 508, Issue 7495, pp. 258 - 262
In obesity and type 2 diabetes, Glut4 glucose transporter expression is decreased selectively in adipocytes(1). Adipose-specific knockout or overexpression of... 
METABOLISM | MULTIDISCIPLINARY SCIENCES | MOUSE | LIVER | RESISTANCE | MICE | CDNA CLONING | EXPRESSION | SIRT1 | CANCER | ADIPOSE-TISSUE | Sirtuin 1 - metabolism | Acetyltransferases - metabolism | Adipocytes - secretion | Ornithine Decarboxylase - metabolism | Liver - enzymology | Glucose Transporter Type 4 - metabolism | Adipose Tissue, White - metabolism | Male | Diabetes Mellitus, Type 2 - metabolism | Nicotinamide N-Methyltransferase - metabolism | Glucose Intolerance | Glucose Transporter Type 4 - deficiency | Obesity - genetics | Thinness - metabolism | Gene Knockdown Techniques | Adipose Tissue - metabolism | Nicotinamide N-Methyltransferase - deficiency | Obesity - etiology | NAD - metabolism | Spermine - analogs & derivatives | Nicotinamide N-Methyltransferase - genetics | Thinness - enzymology | Glucose Transporter Type 4 - genetics | Niacinamide - metabolism | Mice, Inbred C57BL | Diabetes Mellitus, Type 2 - enzymology | Insulin Resistance | Oxidoreductases Acting on CH-NH Group Donors - metabolism | Fatty Liver | Animals | Diet | Energy Metabolism | Adipocytes - metabolism | Obesity - prevention & control | Spermine - metabolism | Adipose Tissue, White - enzymology | Adipose Tissue - enzymology | Mice | Obesity - enzymology | S-Adenosylmethionine - metabolism | Adipose tissues | Type 2 diabetes | Obesity | Care and treatment | Analysis | Transferases | Physiological aspects | Genetic aspects | Research | Gene expression | Enzymes | Body fat | Adipocytes | Polyamines | Variance analysis | Proteins | Weight control | Metabolites | Rodents | Insulin resistance | Diabetes | Mass spectrometry | Food
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e66923
Obesity is a primary risk factor for multiple metabolic disorders. Many drugs for the treatment of obesity, which mainly act through CNS as appetite... 
FIBROBLAST GROWTH FACTOR-19 | INDUCED HEPATIC STEATOSIS | ENERGY-EXPENDITURE | INSULIN-RESISTANCE | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | EMERGING DRUGS | WEIGHT-LOSS | ACID SYNTHESIS | SUPPRESSION | BILE-ACIDS | Receptor, Fibroblast Growth Factor, Type 4 - metabolism | Pyrazoles - therapeutic use | Obesity - drug therapy | Caloric Restriction | Fatty Liver - pathology | Body Weight - drug effects | Basal Metabolism - drug effects | Hepatocytes - metabolism | Obesity - blood | Obesity - genetics | Liver - drug effects | Piperidines - pharmacology | Oligonucleotides, Antisense - therapeutic use | Oxidation-Reduction - drug effects | Drug Therapy, Combination | Receptor, Fibroblast Growth Factor, Type 4 - genetics | Fatty Acids - metabolism | Hepatocytes - drug effects | Pyrazoles - pharmacology | Fatty Liver - genetics | Insulin - pharmacology | Adiposity - drug effects | Oligonucleotides, Antisense - pharmacology | Fatty Liver - blood | Liver - metabolism | Mice, Inbred C57BL | Bile Acids and Salts - metabolism | Feeding Behavior - drug effects | Obesity - metabolism | Gene Expression Regulation - drug effects | Receptor, Cannabinoid, CB1 - metabolism | Animals | Diet | Fibroblast Growth Factors - blood | Piperidines - therapeutic use | Mice, Obese | Mice | Receptor, Cannabinoid, CB1 - antagonists & inhibitors | Weight reducing preparations | Type 2 diabetes | Obesity | Body weight | Fibroblast growth factors | Fatty acids | Metabolic rate | Drugs | Appetite suppressants | Fibroblast growth factor | Adipose tissue | Liver | Central nervous system | Oligonucleotides | Disorders | Risk factors | Dietary restrictions | Reduction | Fatty liver | Rodents | Animal tissues | Fibroblast growth factor receptor 4 | Oxidation | Lipogenesis | Energy expenditure | Antisense oligonucleotides | Insulin | Feeding | Steatosis | Side effects | Insulin resistance | Metabolic disorders | Bile | Pharmaceuticals
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2016, Volume 11, Issue 9, p. e0161455
Journal Article