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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 | MITOCHONDRIAL IRON | iron-regulatory protein 2 (IRP2) | HEME-SYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | iron-regulatory protein 1 (IRP1) | ferroportin | AMYLOID PRECURSOR PROTEIN | RESPONSIVE ELEMENT | TRANSFERRIN-BOUND IRON | RNA-BINDING | H-FERRITIN | HEPCIDIN EXPRESSION | 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
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, p. e0176363
Mitochondrial respiratory chain dysfunction has been identified in a number of neurodegenerative disorders. Infantile cerebellar-retinal degeneration... 
ACID | RAT | MALONYL-COA | MULTIDISCIPLINARY SCIENCES | CITRATE | IRON | DYSFUNCTION | ENERGY-METABOLISM | PROTEINS | HUNTINGTONS-DISEASE | CYCLE | Aconitic Acid - blood | Humans | Ketoglutaric Acids - blood | Child, Preschool | Heredodegenerative Disorders, Nervous System - diagnosis | Male | Aconitate Hydratase - deficiency | Biomarkers - blood | Hydroxybutyrates - blood | Heredodegenerative Disorders, Nervous System - blood | Metabolomics - methods | Isocitrates - blood | Phosphoenolpyruvate - blood | Adolescent | Female | Aconitate Hydratase - genetics | Child | Metabolomics | Mitochondria | Analysis | Research | Aconitase | Health aspects | Blood plasma | Cerebellum | Brain | Pediatrics | Dehydrogenases | 4-Hydroxynonenal | Liver | Carbon dioxide | Retina | Mitochondrial DNA | Assaying | Dehydrogenase | Inactivation | Genetic screening | Proteins | Antioxidants | Enzymatic activity | Neurodegeneration | Aging | Genetics | Biocompatibility | Ataxia | Bioindicators | Diagnosis | Catalysis | Alzheimer's disease | Movement disorders | Deoxyribonucleic acid--DNA | Carbohydrates | Enzymes | AMP | Neurodegenerative diseases | Abnormalities | Cultures | Metabolism | Gene expression | Fatty acids | Children & youth | Diseases | Neurology | Hospitals | Insects | Biomarkers | Guardians | Poisoning | Mutation | Acetic acid | Kidney transplantation | Huntingtons disease | Oxidative stress | Families & family life | Iron | Biosynthesis | Infections | Kinases | AMP-activated protein kinase | Control | Missense mutation | Metabolites | Children | Paralysis | Adenosine triphosphate | Urine | Alanine | Kidneys | Aging (artificial) | Adenine | Pharmacology | Standards | Computer programs | Lobes | Medicine | Brain research | Proteomics | Acidosis | Respiration | Alzheimers disease | ATP | Plasmas (physics) | Cancer | Deoxyribonucleic acid | DNA
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 02/2019, Volume 55, Issue 16, pp. 2297 - 2300
The first molecular solid solution of lithium and sodium ions is reported. In spite of the different chemical and structural properties of the parent... 
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 07/2018, Volume 46, Issue W1, pp. W205 - W208
Abstract Patterns in biological sequences frequently signify interesting features in the underlying molecule. Many tools exist to search for well-known... 
ACONITASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | IRON | Web Server Issue
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 06/2019, Volume 141, Issue 25, pp. 10091 - 10098
Molybdenum nitrogenase catalyzes the reduction of dinitrogen into ammonia, which requires the coordinated transfer of eight electrons to the active site... 
TRANSFORMATION | SYSTEM | ELECTRON-TRANSFER | CARBON | MECHANISM | CRYSTAL-STRUCTURE | ACONITASE | LIGHT | MOFE-PROTEIN | IRON | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Chemical Communications, ISSN 1359-7345, 2019, Volume 55, Issue 16, pp. 2297 - 2300
The first molecular solid solution of lithium and sodium ions is reported. In spite of the different chemical and structural properties of the parent... 
RAY CRYSTAL ANALYSIS | COMPLEX | CHEMISTRY, MULTIDISCIPLINARY | ACONITASE | CERAMICS
Journal Article
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 09/2018, Volume 39, Issue 5, pp. 648 - 651
Inherited optic neuropathy is a rare cause of debilitating vision loss. It may occur in constellation with other syndromic features of neurological impairment,... 
aconitase 2 | optic atrophy | optic neuropathy | neuro-ophthalmology | ophthalmology | ACO2 | mitochondrial | pediatric ophthalmology | neuroophthalmology | GENETICS & HEREDITY | MITOCHONDRIAL ACONITASE | MUTATIONS
Journal Article