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American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 06/2009, Volume 296, Issue 6, pp. 1258 - 1270
Myostatin is a negative regulator of skeletal muscle size, previously shown to inhibit muscle cell differentiation. Myostatin requires both Smad2 and Smad3... 
MAFbx | Mammalian target of rapamycin complex signaling | MuRF1 | S6 kinase | Smad signaling | Human skeletal muscle cells | Transducer of regulated Ca | responsive element-binding protein activity | MuRF-1 | Atrogin | Transforming growth factor-β-like molecules | IGF-I | PHYSIOLOGY | ATROPHY | RAPID DISUSE | human skeletal muscle cells | transforming growth factor-beta-like molecules | SKELETAL-MUSCLE HYPERTROPHY | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | transducer of regulated Ca2+-responsive element-binding protein activity | CELL BIOLOGY | atrogin | PATHWAY | GROWTH | GENE-EXPRESSION | mammalian target of rapamycin complex signaling | CONDITIONAL ACTIVATION | Activin Receptors, Type I - antagonists & inhibitors | Protein Kinases - metabolism | Phosphorylation | Protein Kinases - genetics | Humans | Smad3 Protein - metabolism | Muscle Fibers, Skeletal - drug effects | Tripartite Motif Proteins | Smad3 Protein - genetics | Transfection | RNA Interference | Myoblasts, Skeletal - pathology | Smad2 Protein - genetics | Muscle Proteins - metabolism | Dioxoles - pharmacology | Regulatory-Associated Protein of mTOR | Benzamides - pharmacology | Myostatin - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Rapamycin-Insensitive Companion of mTOR Protein | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Signal Transduction | Cell Size - drug effects | Cells, Cultured | Smad2 Protein - metabolism | Ubiquitin-Protein Ligases - metabolism | Organ Size | Activin Receptors, Type I - metabolism | Myoblasts, Skeletal - enzymology | SKP Cullin F-Box Protein Ligases - metabolism | Mice, SCID | Myostatin - antagonists & inhibitors | Adaptor Proteins, Signal Transducing | Animals | Carrier Proteins - metabolism | Proteins - metabolism | Cell Differentiation - drug effects | Follistatin - pharmacology | Muscle Fibers, Skeletal - pathology | Creatine Kinase - metabolism | Mice | Protein Kinase Inhibitors - pharmacology | TOR Serine-Threonine Kinases | Myoblasts, Skeletal - drug effects | Insulin-Like Growth Factor I - metabolism | Muscle Fibers, Skeletal - enzymology | RNA, Small Interfering - metabolism | Abdominal surgery | Musculoskeletal system | Signal transduction | Cell growth | Kinases | Gene expression | Cells | Index Medicus
Journal Article
Journal Article
Nature, ISSN 0028-0836, 01/2012, Volume 481, Issue 7382, pp. 463 - 468
Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional... 
SKELETAL-MUSCLE | COACTIVATOR | PHOSPHORYLATION | PGC-1-ALPHA | MULTIDISCIPLINARY SCIENCES | DISEASE | MYOBLAST | EXPRESSION | EXERCISE | ADIPOSE-TISSUE | PROTECTS | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Adipocytes - drug effects | Obesity - blood | Adipose Tissue, White - cytology | Mitochondrial Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Models, Animal | Energy Metabolism - physiology | Intracellular Signaling Peptides and Proteins - genetics | Obesity - chemically induced | Mice, Transgenic | Trans-Activators - deficiency | Obesity - prevention & control | Plasma - chemistry | Adipose Tissue, Brown - drug effects | Exercise - physiology | Mice | Mice, Inbred BALB C | Transcription Factors | Energy Metabolism - drug effects | Thermogenesis - genetics | Adipose Tissue, White - metabolism | Adipocytes - cytology | Culture Media, Conditioned - pharmacology | Subcutaneous Fat - metabolism | Insulin Resistance - physiology | Cell Respiration - drug effects | Subcutaneous Fat - drug effects | Trans-Activators - genetics | Energy Metabolism - genetics | Gene Expression Regulation - genetics | Cells, Cultured | Hormones - secretion | Muscle Cells - metabolism | Physical Conditioning, Animal - physiology | Subcutaneous Fat - cytology | Gene Expression Regulation - drug effects | Adipose Tissue, Brown - cytology | Animals | Hormones - metabolism | Ion Channels - metabolism | Adipocytes - metabolism | Trans-Activators - secretion | Trans-Activators - metabolism | Adipose Tissue, Brown - metabolism | Thermogenesis - drug effects | Uncoupling Protein 1 | Adipose Tissue, White - drug effects | Index Medicus
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 06/2009, Volume 296, Issue 6, pp. 1248 - 1257
Loss of muscle mass occurs in a variety of diseases, including cancer, chronic heart failure, aquired immunodeficiency syndrome, diabetes, and renal failure,... 
Myostatin | Muscle atrophy | Akt | Hypertrophy | MYOBLAST DIFFERENTIATION | PHYSIOLOGY | hypertrophy | MYOSTATIN GENE | UBIQUITIN LIGASES | myostatin | CELL BIOLOGY | SKELETAL-MUSCLE | IN-VIVO | GROWTH | ATROPHY INVOLVE | MICE | muscle atrophy | EXPRESSION | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Age Factors | Muscle Denervation | Male | Muscle, Skeletal - innervation | Muscle, Skeletal - metabolism | Smad3 Protein - metabolism | Proto-Oncogene Proteins c-akt - genetics | Tripartite Motif Proteins | Muscle Development | Muscular Atrophy - physiopathology | Transfection | RNA Interference | Muscle Proteins - metabolism | Cell Differentiation | Muscular Atrophy - prevention & control | Myostatin - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Muscular Atrophy - metabolism | Signal Transduction | Muscular Atrophy - pathology | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Smad2 Protein - metabolism | Ubiquitin-Protein Ligases - metabolism | Mice, Transgenic | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Animals | Carrier Proteins - metabolism | Receptors, Transforming Growth Factor beta - metabolism | Sciatic Nerve - surgery | Muscle, Skeletal - physiopathology | Mice | TOR Serine-Threonine Kinases | Muscle, Skeletal - pathology | Mutation | Transforming Growth Factor beta - metabolism | RNA, Small Interfering - metabolism | Proteins | Signal transduction | Musculoskeletal system | Adults | Cells | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2006, Volume 281, Issue 36, pp. 26602 - 26614
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2016, Volume 11, Issue 5, pp. e0155108 - e0155108
Background The regulation of microRNAs (miRNAs) at different stages of the progression of type 2 diabetes mellitus (T2DM) and their role in glucose homeostasis... 
OFFSPRING HYPERPHAGIA | MITOCHONDRIAL BIOGENESIS | PHOSPHORYLATION | INSULIN-RESISTANCE | MULTIDISCIPLINARY SCIENCES | GLYCOGEN-SYNTHASE KINASE-3 | DISEASE | RATS | LEADS | ADIPOSITY | DIET-INDUCED OBESITY | Prediabetic State - metabolism | Prediabetic State - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Diet, High-Fat - adverse effects | Male | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Diabetes Mellitus, Type 2 - metabolism | Proto-Oncogene Proteins c-akt - genetics | Myoblasts - metabolism | Glycogen - metabolism | Female | Prediabetic State - pathology | Prediabetic State - etiology | Proto-Oncogene Proteins c-akt - metabolism | Disease Models, Animal | Cell Line | Signal Transduction | Mice, Inbred C57BL | Gene Expression Regulation | Insulin Resistance | Oxidative Phosphorylation | Rats | Mitochondria - metabolism | Glycogen Synthase Kinase 3 - metabolism | Myoblasts - pathology | Rats, Sprague-Dawley | Insulin - metabolism | Animals | Glycogen Synthase Kinase 3 - genetics | Glucose - metabolism | MicroRNAs - genetics | Diabetes Mellitus, Type 2 - pathology | Muscle, Skeletal - pathology | Type 2 diabetes | Glucose metabolism | Complications and side effects | MicroRNA | Genetic aspects | Research | Comparative analysis | Diabetes therapy | Heart | Plasma | Phosphorylation | Sucrose | Homeostasis | AKT protein | Biosynthesis | Glucose | High fat diet | Proteins | Mitochondria | Control | Rodents | Oxidation | Diabetes mellitus (non-insulin dependent) | Medical research | Obesity | Glycogen | Diabetes mellitus | MiRNA | Muscles | Metabolism | Gene expression | Insulin | Patients | Skeletal muscle | Pregnancy | Musculoskeletal system | Progeny | Offspring | Oxidative phosphorylation | Ribonucleic acids | Biopsy | MicroRNAs | Glycolysis | Insulin resistance | Diabetes | Lactic acid | Laboratory animals | Index Medicus
Journal Article
American Journal of Physiology. Endocrinology and Metabolism, ISSN 0193-1849, 2014, Volume 306, Issue 5, pp. E469 - E482
UCP1-Tg mice with ectopic expression of uncoupling protein 1 (UCP1) in skeletal muscle (SM) are a model of improved substrate metabolism and increased... 
Myokine | Browning | Energy metabolism | Fibroblast growth factor 21 | Uncoupling protein 1 | fibroblast growth factor 21 | BETA-KLOTHO | PPAR-ALPHA | ANTIDIABETIC ACTIONS | PHYSIOLOGY | LIPID-METABOLISM | browning | uncoupling-protein 1 | myokine | AUTOPHAGY | INSULIN SENSITIVITY | OBESITY | PROTEIN-1 EXPRESSION | ENDOCRINOLOGY & METABOLISM | energy metabolism | GROWTH-FACTOR 21 | TRANSGENIC MICE | Cell Line | Phosphorylation | Uncoupling Agents - pharmacology | Bone Density - physiology | Adipose Tissue, White - metabolism | Ion Channels - genetics | Mice, Transgenic | Muscle, Skeletal - metabolism | Mitochondria - metabolism | Mitochondrial Proteins - genetics | Mitochondria - drug effects | Fibroblast Growth Factors - metabolism | Myoblasts - drug effects | Myoblasts - metabolism | Animals | Ion Channels - metabolism | Mitochondrial Proteins - metabolism | Muscle, Skeletal - drug effects | Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology | Mice | Uncoupling Protein 1 | Adipose Tissue, White - drug effects | Energy Metabolism - drug effects | Body Composition - physiology | Cell research | Cytokines | Physiological aspects | Muscles | Muscle cells | Fibroblast growth factors | Research | Metabolism | Genotype & phenotype | Musculoskeletal system | Rodents | Cells | Index Medicus | growth-factor 21 | insulin sensitivity | lipid-metabolism | activated-receptor-gamma | adaptive thermogenesis | protein-1 expression | white adipose-tissues | respiratory-chain | ppar-alpha | glucose-homeostasis
Journal Article
Journal Article