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Journal of Neurochemistry, ISSN 0022-3042, 02/2005, Volume 92, Issue 3, pp. 628 - 636
Journal Article
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 06/2014, Volume 71, pp. 427 - 436
Journal Article
Journal of Gastroenterology and Hepatology, ISSN 0815-9319, 03/2017, Volume 32, Issue 3, pp. 708 - 715
Background and Aim: It has been suggested in several studies that an increased translocation of bacterial lipopolysaccharide (LPS) and, subsequently, an... 
iNOS | NAFLD | LBP | endotoxin | INDUCED HEPATIC STEATOSIS | ACTIVATION | RECEPTOR 4 | INTESTINAL BARRIER FUNCTION | PATHOGENESIS | FRUCTOSE | INSULIN-RESISTANCE | INFLAMMATION | STEATOHEPATITIS | GASTROENTEROLOGY & HEPATOLOGY | Carrier Proteins - physiology | Non-alcoholic Fatty Liver Disease - genetics | Liver - metabolism | Lipopolysaccharides - metabolism | Non-alcoholic Fatty Liver Disease - etiology | Lipid Metabolism | Acute-Phase Proteins - physiology | Mice, Knockout | Membrane Glycoproteins - physiology | Animals | Glucose - metabolism | Signal Transduction - physiology | Mice, Inbred BALB C | Acute-Phase Proteins - deficiency | Toll-Like Receptors - metabolism | Membrane Glycoproteins - deficiency | Disease Models, Animal | Fatty liver | Synthesis | RNA | Blood sugar | Nitric oxide | Physiological aspects | Fatty acids | Mitogens | Fructose | Protein binding | 4-Hydroxynonenal | mRNA | Protein turnover | Lipopolysaccharides | Proteins | Glucose metabolism | Signal transduction | Protein adducts | Rodents | Sterol regulatory element-binding protein | Toll-like receptors | Lipid metabolism | Adducts | Lipopolysaccharide-binding protein | Liver diseases | Fasting | Leukocytes (neutrophilic) | Metabolism | Fatty-acid synthase | Cholesterol | Nitric-oxide synthase | Sterol regulatory element-binding protein 1c | Index Medicus
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, pp. e29789 - e29789
In order to study oxidative stress in peripheral cells of Alzheimer's disease (AD) patients, immortalized lymphocytes derived from two peculiar cohorts of... 
WILD-TYPE P53 | GLUTATHIONE-REDUCTASE | DNA-BINDING | LIPID-PEROXIDATION | MANGANESE-SUPEROXIDE-DISMUTASE | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | NITRATED PROTEINS | TUMOR-SUPPRESSOR PROTEIN | MILD COGNITIVE IMPAIRMENT | REDOX PROTEOMICS | Demography | Glutathione Reductase - metabolism | Protein Unfolding - drug effects | Humans | Middle Aged | Male | Molsidomine - analogs & derivatives | Case-Control Studies | Alzheimer Disease - pathology | Oxidation-Reduction - drug effects | Adult | Female | Superoxide Dismutase - metabolism | Biomarkers - metabolism | Glutathione Peroxidase - metabolism | Tumor Suppressor Protein p53 - metabolism | Alzheimer Disease - enzymology | Mutation - genetics | Lymphocytes - pathology | Peroxynitrous Acid - pharmacology | Lymphocytes - drug effects | Nitrosation - drug effects | Age of Onset | Alzheimer Disease - metabolism | Molsidomine - pharmacology | Lymphocytes - enzymology | Protein Conformation | Tumor Suppressor Protein p53 - chemistry | Oxidative Stress - drug effects | Biomarkers - chemistry | Tyrosine | Oxidative stress | Enzymes | Medical research | Superoxide | B cells | Antioxidants | Advertising executives | Analysis | Monoclonal antibodies | Medicine, Experimental | Tumor proteins | Alzheimer's disease | Residues | Reactive oxygen species | Immunoprecipitation | 4-Hydroxynonenal | p53 Protein | Immunoblotting | Superoxide dismutase | Proteins | Neurodegeneration | Lymphocytes | Glutathione reductase | Rodents | Cell cycle | Aging | Peroxidase | Oxidation | Glutathione | Adducts | Carbonyls | Glutathione peroxidase | Stresses | Neurodegenerative diseases | Tertiary structure | Pharmacology | Patients | Stress | Brain research | Lymphocytes B | Nitrotyrosine | Mutation | Alzheimers disease | Protein structure | Cancer | Reductase | Index Medicus
Journal Article
American Journal of Physiology - Gastrointestinal and Liver Physiology, ISSN 0193-1857, 2015, Volume 308, Issue 5, pp. G403 - G415
To test the significance of lipid peroxidation in the development of alcoholic liver injury, an ethanol (EtOH) liquid diet was fed to male 129/SvJ mice... 
Lipid peroxidation | Alcohol | Peroxisome proliferator-activated receptor-α | Glutathione S-transferase A4–4 | Liver | 4-hydroxynonenal | alcohol | ACTIVATION | PHYSIOLOGY | liver | LIPID-PEROXIDATION PRODUCTS | TRANSFERASES | peroxisome proliferator-activated receptor-alpha | MODEL | lipid peroxidation | TOTAL ENTERAL NUTRITION | FATTY LIVER | glutathione S-transferase A4-4 | ETHANOL | TISSUES | GASTROENTEROLOGY & HEPATOLOGY | CONTRIBUTES | INDUCED HEPATOTOXICITY | Tumor Necrosis Factor-alpha - metabolism | Liver - pathology | Matrix Metalloproteinases - genetics | Tumor Necrosis Factor-alpha - genetics | Actins - metabolism | Male | Alanine Transaminase - blood | Aldehydes - metabolism | Fibrosis - metabolism | RNA, Messenger - metabolism | Receptor, Platelet-Derived Growth Factor beta - genetics | Actins - genetics | Lipopolysaccharide Receptors - metabolism | Glutathione Transferase - genetics | Gene Deletion | Chemokine CXCL2 - genetics | Chemokine CXCL2 - metabolism | Cytokines - genetics | Receptor, Platelet-Derived Growth Factor beta - metabolism | Cytokines - metabolism | Liver - metabolism | RNA, Messenger - genetics | Glutathione Transferase - metabolism | PPAR alpha - genetics | Liver Diseases, Alcoholic - metabolism | Animals | Transforming Growth Factor beta - genetics | Liver Diseases, Alcoholic - immunology | Aldehydes - immunology | Lipopolysaccharide Receptors - genetics | Antibodies - blood | Mice | Matrix Metalloproteinases - metabolism | PPAR alpha - metabolism | Lipid Peroxidation | Transforming Growth Factor beta - metabolism | Index Medicus | glutathione S-transferase A4–4 | Mediators | Inflammation | peroxisome proliferator-activated receptor-α | Immunity
Journal Article
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 10/2011, Volume 51, Issue 8, pp. 1575 - 1582
The superoxide free radical (O ) has been viewed as a likely major contributor to aging. If this is correct, then superoxide dismutase (SOD), which removes O ,... 
Caenorhabditis elegans | Free radicals | Oxidative damage | daf-16/FoxO | Aging | ER stress | Superoxide dismutase | BIOCHEMISTRY & MOLECULAR BIOLOGY | TISSUE | EXTENSION | STRESS RESISTANCE | LONGEVITY | HORMESIS | MUTANTS | ROS-GENERATOR | DAF-16 | ENDOCRINOLOGY & METABOLISM | EXPRESSION | C. ELEGANS | Superoxide Dismutase - genetics | Oxidation-Reduction | Animals, Genetically Modified | Heat-Shock Proteins - metabolism | Transcriptional Activation | Transgenes - genetics | Cells, Cultured | Oxidative Stress - genetics | Protein-Serine-Threonine Kinases - genetics | Caenorhabditis elegans Proteins - metabolism | Hydrogen Peroxide - metabolism | Catalase - metabolism | Transcription Factors - metabolism | Caenorhabditis elegans - physiology | Carrier Proteins - genetics | Heat-Shock Proteins - genetics | Animals | Carrier Proteins - metabolism | Superoxide Dismutase-1 | Caenorhabditis elegans Proteins - genetics | Forkhead Transcription Factors | Protein-Serine-Threonine Kinases - metabolism | Superoxide Dismutase - metabolism | Heat shock proteins | Acetylcysteine | Peroxides | Superoxide | Index Medicus | CML, carboxymethyllysine | FoxO | daf-16 | IIS, insulin | Original Contribution | HNE, 4-hydroxynonenal | NAC, N-acetylcysteine | RNAi, RNA-mediated interference | co-OE, co-overexpression | HSF-1, heat shock factor-1 | SOD, superoxide dismutase | OE, overexpression | IGF-1 signaling | O2•−, superoxide anion | AMPK, AMP-dependent kinase | ROS, reactive oxygen species
Journal Article