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Nature, ISSN 0028-0836, 11/2014, Volume 515, Issue 7527, pp. 431 - 435
Journal Article
Cell, ISSN 0092-8674, 10/2016, Volume 167, Issue 2, pp. 457 - 470.e13
Activated macrophages undergo metabolic reprogramming, which drives their pro-inflammatory phenotype, but the mechanistic basis for this remains obscure. Here,... 
succinate | reverse electron transport | toll-like receptors | innate immunity | immunometabolism | macrophage | succinate dehydrogenase | RESPIRATORY-CHAIN | DENDRITIC CELL | BIOCHEMISTRY & MOLECULAR BIOLOGY | REPERFUSION INJURY | ALPHA | IL-1-BETA | INTERLEUKIN-10 IL-10 | DIMETHYL FUMARATE | HYPOXIA | ELECTRON-TRANSPORT | CELL-ACTIVATION | CELL BIOLOGY | Mitochondria - enzymology | Reactive Oxygen Species - metabolism | Transcriptome | Malonates - pharmacology | Lipopolysaccharides - immunology | Oxidative Phosphorylation - drug effects | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Mitochondrial Proteins - metabolism | Adenosine Triphosphate - metabolism | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Membrane Potential, Mitochondrial | Oxidation-Reduction - drug effects | Interleukin-10 - metabolism | Plant Proteins - metabolism | Macrophages - immunology | Oxidoreductases - metabolism | Mice, Inbred C57BL | Inflammation - immunology | Mitochondria - drug effects | Citric Acid Cycle | Macrophage Activation | Macrophages - metabolism | Succinate Dehydrogenase - genetics | Animals | Sequence Analysis, RNA | Succinic Acid - metabolism | Glycolysis | Inflammation - genetics | Succinate Dehydrogenase - metabolism | Mice | Oxidases | RNA sequencing | Glucose metabolism | Medical colleges | RNA | Gastrointestinal diseases | Genes | Research institutes | Macrophages | Gene expression | Mitogens
Journal Article
Nature, ISSN 0028-0836, 04/2000, Volume 404, Issue 6779, pp. 787 - 790
Diabetic hyperglycaemia causes a variety of pathological changes in small vessels, arteries and peripheral nerves. Vascular endothelial cells are an important... 
OVEREXPRESSION | IN-VITRO | ACTIVATION | PROTEIN | RAT | BOVINE ENDOTHELIAL-CELLS | MULTIDISCIPLINARY SCIENCES | ADVANCED GLYCATION ENDPRODUCTS | KAPPA-B | EXPRESSION | ALDOSE REDUCTASE | Electron Transport | Reactive Oxygen Species - metabolism | Uncoupling Agents - pharmacology | Ion Channels | Multienzyme Complexes - metabolism | Endothelium, Vascular - drug effects | NF-kappa B - metabolism | Membrane Proteins - pharmacology | Mitochondrial Proteins | Electron Transport Complex II | Sorbitol - metabolism | Cattle | Protein Kinase C - metabolism | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Carrier Proteins - pharmacology | Hyperglycemia - pathology | Malates - metabolism | Rotenone - pharmacology | Superoxide Dismutase - metabolism | Superoxide Dismutase - pharmacology | Oxidoreductases - metabolism | Thenoyltrifluoroacetone - analogs & derivatives | Mitochondria - metabolism | Hyperglycemia - metabolism | Animals | Thenoyltrifluoroacetone - pharmacology | Endothelium, Vascular - metabolism | Glycation End Products, Advanced - metabolism | Aspartic Acid - metabolism | Endothelium, Vascular - pathology | Succinate Dehydrogenase - metabolism | Hyperglycemia - etiology | Enzyme Activation | Uncoupling Protein 1 | Blood Glucose - metabolism | Oxidation | Pharmacology | Glucose | Diabetes | Metabolism | Cells | Electrons
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2013, Volume 288, Issue 3, pp. 1696 - 1705
Journal Article
Biochemical Journal, ISSN 0264-6021, 03/2011, Volume 434, Issue 3, pp. 365 - 381
Iron is an essential but potentially hazardous biometal. Mammalian cells require sufficient amounts of iron to satisfy metabolic needs or to accomplish... 
Ferroportin | Iron-sulfur cluster (ISC) | Transferrin receptor (TfR) | Iron-regulatory protein 2 (IRP2) | Ferritin | Iron-regulatory protein 1 (IRP1) | ferritin | iron-sulfur cluster (ISC) | transferrin receptor (TfR) | OXIDATIVE STRESS | MAMMALIAN IRON | FE-S CLUSTER | iron-regulatory protein 2 (IRP2) | HEME-SYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | iron-regulatory protein 1 (IRP1) | ferroportin | AMYLOID PRECURSOR PROTEIN | RESPONSIVE ELEMENT | TRANSFERRIN-BOUND IRON | SULFUR CLUSTER BIOGENESIS | HEPCIDIN EXPRESSION | UBIQUITIN-PROTEASOME PATHWAY | Neoplasms - metabolism | Oxidation-Reduction | Response Elements | Humans | RNA, Messenger - genetics | RNA, Messenger - physiology | Mitochondria - metabolism | Iron - metabolism | Iron-Regulatory Proteins - genetics | Animals | Ferritins - metabolism | Biological Transport | Iron-Regulatory Proteins - physiology | Transferrin - metabolism | DHBA, dihydroxybenzoic acid | IRP, iron-regulatory protein | UTR, untranslated region | SLC, solute carrier | iron–sulfur cluster (ISC) | MRCKα, myotonic dystrophy kinase-related Cdc42 (cell division cycle 42)-binding kinase α | LIP, labile iron pool | Lcn2, lipocalin 2 | FLVCR, feline leukaemia virus, subgroup C, receptor | CIA, cytosolic ISC assembly | Cfd1, cytosolic Fe–S cluster-deficient protein 1 | BMP, bone morphogenetic protein | PCBP1, poly(rC)-binding protein 1 | Abcb, ATP-binding cassette, subfamily B | STAT3, signal transducer and activator of transcription 3 | SDH, succinate dehydrogenase | TfR, Tf receptor | c-aconitase, cytosolic aconitase | HIF, hypoxia-inducible factor | HO-1, haem oxygenase 1 | IRIDA, iron-refractory iron deficiency anaemia | ISC, iron–sulfur cluster | m-aconitase, mitochondrial aconitase | DMT1, divalent metal transporter 1 | Review | EBPα, CCAAT | IRE, iron-responsive element | IOP1, iron-only hydrogenase-like protein 1 | Nbp35, nucleotide-binding protein 35 | Skp1, S-phase kinase-associated protein 1 | Nfs, nitrogen fixation homologue | FBXL5, F-box and leucine-rich repeat protein 5 | ROS, reactive oxygen species | Tf, transferrin | enhancer-binding protein α | H, heavy | Isu, iron–sulfur cluster scaffold homologue | Rbx1, Ring-box 1 | β-APP, β-amyloid precursor protein | Dcytb, duodenal cytochrome b | Nar1, nuclear architecture-related protein 1 | ALAS, ALA synthase | NTBI, non-transferrin-bound iron | ALA, 5-aminolevulinic acid | Hpx, haemopexin | Cul1, Cullin 1 | Grx, glutaredoxin | ER, endoplasmic reticulum | L, light
Journal Article
Journal Article
Developmental Cell, ISSN 1534-5807, 03/2017, Volume 40, Issue 6, pp. 583 - 594.e6
Mitochondrial fission mediated by the GTPase dynamin-related protein 1 (Drp1) is an attractive drug target in numerous maladies that range from heart disease... 
succinate | bioenergetics | mitochondria | fission | neuron | reverse electron transfer | respiration | superoxide | brain | fragmentation | ISCHEMIA-REPERFUSION INJURY | BRAIN MITOCHONDRIA | LIFE-SPAN | CELLS | ROS | DYNAMIN-RELATED PROTEIN-1 | DEVELOPMENTAL BIOLOGY | RAT-BRAIN | FISSION | DIVISION | DAMAGE | CELL BIOLOGY | Dynamins - metabolism | Reactive Oxygen Species - metabolism | Microtubule-Associated Proteins - metabolism | Humans | Cercopithecus aethiops | Saccharomyces cerevisiae - drug effects | GTP Phosphohydrolases - antagonists & inhibitors | Electron Transport Complex I - metabolism | Fibroblasts - ultrastructure | Saccharomyces cerevisiae - metabolism | Mitochondrial Proteins - metabolism | Cell Respiration - drug effects | Oxidation-Reduction - drug effects | Neurons - metabolism | NAD - metabolism | Quinazolinones - pharmacology | Fibroblasts - metabolism | Dynamins - antagonists & inhibitors | Electron Transport Complex I - antagonists & inhibitors | Mitochondrial Proteins - antagonists & inhibitors | Mitochondria - metabolism | Microtubule-Associated Proteins - antagonists & inhibitors | Mitochondria - drug effects | Rats, Sprague-Dawley | Mice, Knockout | Animals | GTP Phosphohydrolases - metabolism | Oxygen Consumption - drug effects | Saccharomyces cerevisiae Proteins - metabolism | Mice | COS Cells | Brain | Medical colleges | Nervous system diseases | Heart diseases | Injuries | Biomedical engineering | Neurons | Superoxide
Journal Article
Nature, ISSN 0028-0836, 04/2018, Volume 556, Issue 7702, pp. 501 - 504
Journal Article