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Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 04/2014, Volume 146, Issue 4, pp. 1060 - 1069.e3
Background & Aims Hepatic gluconeogenesis provides fuel during starvation, and is abnormally induced in obese individuals or those with diabetes. Common... 
Gastroenterology and Hepatology | cAMP Response Element-Binding Protein-H (CREBH) | Glucagon | Peroxisome Proliferator-Activated Receptor-Gamma Co-activator 1-Alpha (PGC1A) | Mouse Model | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Up-Regulation | Humans | Phosphoenolpyruvate Carboxykinase (GTP) - metabolism | Homeostasis | Male | Hepatocytes - metabolism | Mice, 129 Strain | Phosphoenolpyruvate Carboxykinase (GTP) - genetics | Transfection | RNA Interference | Time Factors | Cation Transport Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Transcription, Genetic | Binding Sites | Starvation - genetics | Disease Models, Animal | Gluconeogenesis | Iron - blood | Promoter Regions, Genetic | Signal Transduction | Starvation - blood | Liver - metabolism | Mice, Inbred C57BL | Insulin Resistance | Hemoglobins - metabolism | Hepcidins - blood | Transcription Factors - genetics | Hep G2 Cells | Mice, Knockout | Transcription Factors - metabolism | Cyclic AMP Response Element-Binding Protein - genetics | Animals | Spleen - metabolism | Mice | Mice, Inbred BALB C | Blood Glucose - metabolism | Cyclic AMP Response Element-Binding Protein - deficiency | Insulin resistance | Starvation | Iron | Analysis | Index Medicus | Abridged Index Medicus | Original Research | CREBH, cyclic adenosine monophosphate response element binding protein 3–like 3 | CREBBL3 | HAMP, hepcidin | NAFLD, nonalcoholic fatty liver disease | PPARGC1A, peroxisome proliferator-activated receptor gamma coactivator 1-α | siRNA, small interfering RNA | qRT-PCR, quantitative reverse-transcription polymerase chain reaction | cAMP, cyclic adenosine monophosphate | ChIP, chromatin immunoprecipitation | Pck1, phosphoenolpyruvate carboxykinase 1 | IL, interleukin | FPN1, ferroportin | ER, endoplasmic reticulum
Journal Article
Journal of cellular and molecular medicine, ISSN 1582-1838, 12/2018, Volume 22, Issue 12, pp. 5847 - 5861
Increasing evidence highlights that senescence plays an important role in idiopathic pulmonary fibrosis (IPF). This study delineates the specific contribution... 
lung fibroblast | reactive oxygen species and mitoTEMPO | DNA damage response | primary culture | endogenous compound | senescence | fibroblasts | enzyme activity | human | mammalian target of rapamycin complex 1 | fibrosing alveolitis | phenotype | stress | antioxidant | signal transduction | mitochondria | rotenone | human cell | idiopathic pulmonary fibrosis | article | mitochondrion | homeostasis | peroxisome proliferator-activated receptor gamma coactivator 1-alpha | mechanistic target of rapamycin complex 1 | peroxisome proliferator activated receptor gamma coactivator 1alpha | controlled study | cyclin dependent kinase inhibitor | etoposide | cyclin-dependent kinase inhibitors | adult | superoxide | rapamycin | reactive oxygen metabolite | peroxisome proliferator‐activated receptor gamma coactivator 1‐alpha | cyclin‐dependent kinase inhibitors | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Biomarkers - metabolism | Lung - pathology | Humans | Cellular Senescence - drug effects | Etoposide - pharmacology | Mitochondria - pathology | Down-Regulation - drug effects | Fibroblasts - pathology | Myofibroblasts - drug effects | Sirolimus - pharmacology | Myofibroblasts - metabolism | Fibroblasts - drug effects | Acetylcysteine - pharmacology | Rotenone - pharmacology | Cyclic N-Oxides - metabolism | Idiopathic Pulmonary Fibrosis - pathology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism | Fibroblasts - metabolism | Respiratory tract diseases | Genetic aspects | Superoxide | Phenotypes | Senescence | Deceleration | DNA damage | Lung diseases | Etoposide | Pharmacology | Mitochondrial DNA | Perturbation | Rotenone | Antioxidants | Mitochondria | Nitric oxide | Fibrosis | Fibroblasts | Damage | Deoxyribonucleic acid--DNA | Prolongation | Index Medicus | Original
Journal Article
Science signaling, ISSN 1937-9145, 01/2017, Volume 10, Issue 464, p. eaaf7478
Journal Article
Biochemical and biophysical research communications, ISSN 0006-291X, 09/2017, Volume 491, Issue 2, pp. 436 - 441
Mitochondrial dysfunction has been associated with insulin resistance and diabetes. Decreased mitochondrial density and mitochondrial copy numbers have been... 
Salicylate | PGC-1α | Diabetes | Mitochondria biogenesis | mtDNA | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - agonists | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | RNA, Small Interfering - genetics | AMP-Activated Protein Kinases - metabolism | Adipocytes - cytology | Adipocytes - drug effects | Electron Transport Complex I - metabolism | Nuclear Respiratory Factor 1 - genetics | DNA-Binding Proteins - metabolism | Organelle Biogenesis | Salicylic Acid - pharmacology | DNA, Mitochondrial - genetics | DNA-Binding Proteins - agonists | Mitochondria - genetics | Electron Transport Complex I - genetics | Nuclear Respiratory Factor 1 - agonists | High Mobility Group Proteins - agonists | Nuclear Respiratory Factor 1 - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism | Citrate (si)-Synthase - metabolism | Phosphorylation - drug effects | Pyrazoles - pharmacology | DNA, Mitochondrial - metabolism | High Mobility Group Proteins - metabolism | Signal Transduction | AMP-Activated Protein Kinases - antagonists & inhibitors | Gene Expression Regulation | Mitochondria - metabolism | Mitochondria - drug effects | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - antagonists & inhibitors | Pyrimidines - pharmacology | 3T3-L1 Cells | DNA-Binding Proteins - genetics | Hypoglycemic Agents - pharmacology | Animals | Cell Differentiation - drug effects | Adipocytes - metabolism | Citrate (si)-Synthase - genetics | Mice | Protein Kinase Inhibitors - pharmacology | AMP-Activated Protein Kinases - genetics | High Mobility Group Proteins - genetics | RNA, Small Interfering - metabolism | Index Medicus | TRANSCRIPTION FACTORS | RNA | PHOSPHORYLATION | MITOCHONDRIA | TRANSCRIPTION | CITRATES | 60 APPLIED LIFE SCIENCES | ACETYLSALICYLIC ACID | INSULIN | BIOLOGICAL RECOVERY | DISEASES | INHIBITION | RECEPTORS
Journal Article
Journal of pineal research, ISSN 0742-3098, 09/2018, Volume 65, Issue 2, pp. e12491 - n/a
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 02/2012, Volume 120, Issue 3, pp. 419 - 429
J. Neurochem. (2012) 120, 419–429. Mitochondrial dysfunction is a prominent feature of Alzheimer’s disease (AD) brain. Our prior studies demonstrated reduced... 
mitochondrial transcription factor A | nuclear respiratory factors | proliferator‐activated receptor gamma coactivator 1α | Alzheimer’s disease | mitochondrial biogenesis | proliferator-activated receptor gamma coactivator 1α | Alzheimer's disease | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Middle Aged | Male | Mitochondrial Proteins - genetics | Nuclear Respiratory Factors - metabolism | Alzheimer Disease - pathology | Electron Transport Complex IV - metabolism | Dose-Response Relationship, Drug | CREB-Binding Protein - metabolism | Organelle Biogenesis | Transfection - methods | Mitochondrial Proteins - metabolism | Adenosine Triphosphate - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Amyloid beta-Protein Precursor - metabolism | Aged, 80 and over | Female | Hippocampus - ultrastructure | RNA Interference - physiology | Neuroblastoma - pathology | Alzheimer Disease - physiopathology | DNA, Mitochondrial - metabolism | Heat-Shock Proteins - metabolism | Enzyme Inhibitors - pharmacology | Gene Expression Regulation - physiology | Mitochondria - metabolism | Gene Expression Regulation - drug effects | Transcription Factors - metabolism | Neuroblastoma - ultrastructure | Cell Line, Tumor | Trans-Activators - metabolism | Aged | Cytochrome c | Neurons | Amyloid beta-protein | Cytochrome oxidase | Mitochondrial DNA | Disease susceptibility | Biosynthesis | Neurochemistry | Mitochondria | Cellular biology | Alzheimers disease | Molecular biology | Index Medicus | mitochondrial transcription factor A (TFAM) | nuclear respiratory factors (NRF) | proliferator-activated receptor gamma coactivator 1alpha (PGC-1a)
Journal Article