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Journal Article
BJU International, ISSN 1464-4096, 03/2008, Volume 101, Issue 6, pp. 775 - 780
Journal Article
Frontiers in Pharmacology, ISSN 1663-9812, 2014, Volume 5
In living systems iron appears predominantly associated with proteins, but can also be detected in forms referred as labile iron, which denotes the combined... 
Iron overload | Oxidative stress | Chelator | Iron metabolism | Mitochondria | Siderophore | Fluorescence | Iron | OVERLOAD | iron overload | NONSPECIFIC SERUM IRON | mitochondria | REDOX ACTIVITY | siderophore | iron metabolism | TRANSFERRIN-BOUND IRON | PLASMA IRON | fluorescence | chelator | THALASSEMIA | iron | POOL | PHARMACOLOGY & PHARMACY | oxidative stress | CHELATION | CHELATABLE IRON | Oxidative Stress | Iron Overload
Journal Article
Journal of Antimicrobial Chemotherapy, ISSN 0305-7453, 2017, Volume 72, Issue 6, pp. 1704 - 1708
Journal Article
International Journal of Cancer, ISSN 0020-7136, 10/2013, Volume 133, Issue 7, pp. 1732 - 1742
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e45906
The search for new antimalarial chemotherapy has become increasingly urgent due to parasite resistance to current drugs. Ellagic acid (EA) is a polyphenol,... 
PARASITES | ERYTHROCYTES | POTENTIATION | PLASMODIUM-FALCIPARUM | ANTIOXIDANT | MULTIDISCIPLINARY SCIENCES | ANTIMALARIAL ACTION | CHLOROQUINE | IDENTIFICATION | EXTRACTS | MALARIA TREATMENT | Buthionine Sulfoximine - pharmacology | Reactive Oxygen Species | Glutathione - metabolism | Antioxidants - metabolism | Humans | Plasmodium falciparum - drug effects | Glutathione - pharmacology | Plasmodium yoelii - drug effects | Inhibitory Concentration 50 | Plasmodium falciparum - metabolism | Deferoxamine - pharmacology | Ellagic Acid - pharmacology | Oxidation-Reduction | Cells, Cultured | Enzyme Inhibitors - pharmacology | Antioxidants - pharmacology | Siderophores - pharmacology | Antimalarials - pharmacology | Erythrocytes - drug effects | Glutathione - physiology | Drug Synergism | Animals | Antioxidants - physiology | Acetylcysteine - pharmacology | Ascorbic Acid - pharmacology | Erythrocytes - metabolism | Mice | Plasmodium falciparum - growth & development | Erythrocytes - parasitology | Usage | Malaria | Research | Risk factors | Prevention | Chemotherapy | Analysis | Ellagic acid | Polyphenols | Diagnosis | Health aspects | Public health | Glutathione | Cancer | Drugs | Reactive oxygen species | Animal models | Ascorbic acid | Toxicity | Erythrocytes | Acetylcysteine | Parasites | Drug resistance | Urology | Deferoxamine | Antioxidants | Consolidation | Red blood cells | Rodents | Biocompatibility | Parasite resistance | Antimalarial activity | Acids | Antimalarial agents | N-Acetyl-L-cysteine | Antiprotozoal agents
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2016, Volume 11, Issue 6, p. e0157799
Microorganisms produce siderophores to facilitate iron uptake and even though this trait has been extensively studied, there is growing evidence suggesting... 
SMALL RNA | IRON-METABOLISM | BACTERIAL SIDEROPHORES | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | GENES | CATECHOLATE SIDEROPHORES | AZOTOBACTER-VINELANDII | PROMOTER | PEROXIDE STRESS | E. COLI | Oxidants - pharmacology | Oxidative Stress | Escherichia coli - drug effects | Ligases - genetics | Siderophores - genetics | Paraquat - antagonists & inhibitors | Siderophores - biosynthesis | Escherichia coli - metabolism | Enterobactin - biosynthesis | Transcription, Genetic | Carboxylic Ester Hydrolases - genetics | Paraquat - pharmacology | Oxidation-Reduction | Chlorides - pharmacology | Stress, Physiological - genetics | Gene Expression Regulation | Hydrogen Peroxide - pharmacology | Ligases - metabolism | Escherichia coli Proteins - metabolism | Ferric Compounds - pharmacology | Oxidants - antagonists & inhibitors | Antioxidants - pharmacology | Enterobactin - genetics | Iron - metabolism | Hydrolysis | Escherichia coli - genetics | Ascorbic Acid - pharmacology | Escherichia coli Proteins - genetics | Mutation | Hydrogen Peroxide - antagonists & inhibitors | Carboxylic Ester Hydrolases - metabolism | Oxidative stress | Siderophores | Hydrogen peroxide | Ascorbic acid | Transcription | Laboratories | Genes | Reducing agents | Iron | Biosynthesis | Enterobactin | Metabolism | Mutants | Strain | Sensitivity | Microorganisms | E coli | Paraquat | Supplementation | Stress response | Strains (organisms) | Hydrogen ion concentration | Cytoplasm | Hydroxyl groups
Journal Article
Journal of Periodontal Research, ISSN 0022-3484, 10/2014, Volume 49, Issue 5, pp. 563 - 573
Background and Objective Recently it was reported that deferoxamine (DFO), an iron chelator, stimulates bone formation from MG63 and mesenchymal stem cells,... 
periodontal ligament cells | antioxidant | deferoxamine | osteoblastic differentiation | iron chelator | nuclear factor erythroid 2‐related factor | Osteoblastic differentiation | Nuclear factor erythroid 2-related factor | Periodontal ligament cells | Antioxidant | Iron chelator | Deferoxamine | STEM-CELLS | ORAL KERATINOCYTES | IRON CHELATION | COLLAGENASE EXPRESSION | DENTISTRY, ORAL SURGERY & MEDICINE | ENDOTHELIAL-CELLS | BONE REGENERATION | HYDROGEN-PEROXIDE | HEME OXYGENASE-1 | GLUTATHIONE DEPLETION | nuclear factor erythroid 2-related factor | NF-KAPPA-B | osteoblastic dierentiation | Free Radical Scavengers - pharmacology | Buthionine Sulfoximine - pharmacology | RNA, Small Interfering - genetics | Maleates - pharmacology | Glutathione Peroxidase - analysis | Humans | Calcium - analysis | Antioxidant Response Elements - drug effects | Periodontal Ligament - drug effects | Dose-Response Relationship, Drug | Periodontal Ligament - cytology | Glutathione - analysis | NF-E2-Related Factor 2 - genetics | Glutamate-Cysteine Ligase - analysis | NF-E2-Related Factor 2 - pharmacology | Cell Line | Deferoxamine - pharmacology | Calcification, Physiologic - drug effects | Osteoblasts - drug effects | Enzyme Inhibitors - pharmacology | Glutathione - antagonists & inhibitors | Reactive Oxygen Species - analysis | Siderophores - pharmacology | Glutathione Transferase - analysis | MAP Kinase Signaling System - drug effects | Signal Transduction - drug effects | Cell Differentiation - drug effects | Glutathione Reductase - analysis | Acetylcysteine - pharmacology | Glutamate-Cysteine Ligase - antagonists & inhibitors | NF-kappa B - drug effects | Vitamin E - pharmacology | Antioxidants | RNA | Glutathione transferase | Analysis | Stem cells | Acetylcysteine | Cellular signal transduction
Journal Article