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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 | 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) | Cultures | Deoxyribonucleic acid | DNA
Journal Article
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 2011, Volume 659, Issue 1, pp. 89 - 93
Journal Article
Redox Biology, ISSN 2213-2317, 2013, Volume 1, Issue 1, pp. 258 - 264
The elimination of oxidatively modified proteins is a crucial process in maintaining cellular home-ostasis, especially during stress. Mitochondria are... 
Oxidative stress | Lon Protease | Mitochondria | Hormesis | Protein degradation and oxidation | Adaptation | BIOCHEMISTRY & MOLECULAR BIOLOGY | Mitochondria - enzymology | Up-Regulation | Animals | Disease | Oxidative Stress | Humans | Adaptation, Biological | Mitochondria - metabolism | Protease La - metabolism | Aging - metabolism
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2018, Volume 140, Issue 37, pp. 11800 - 11810
Here we characterize the [Fe4S4] cluster nitrosylation of a DNA repair enzyme, endonuclease III (EndoIII), using DNA-modified gold electrochemistry and protein... 
REPAIR PROTEINS | SENSING 4FE-4S CLUSTER | DINITROSYL-IRON COMPLEXES | EPR | ESCHERICHIA-COLI | ACTIVATED MACROPHAGES | DNA CHARGE-TRANSPORT | CANCER PROGRESSION | CHEMISTRY, MULTIDISCIPLINARY | MITOCHONDRIAL ACONITASES | GUANYLATE-CYCLASE
Journal Article
1992, ISBN 0120236389, Volume 38, Issue C, 17
This chapter describes an iron–sulfur enzyme—aconitase. Although the presence and function of the Krebs cycle enzyme aconitase has been known for over 50... 
ACTIVATED ACONITASE | <4FE-4S>+ CLUSTER | MESSENGER-RNA | BEEF-HEART ACONITASE | DOUBLE-RESONANCE CHARACTERIZATION | ELECTRON-PARAMAGNETIC-RES | INHIBITOR BINDING | RESPONSIVE ELEMENT | RNA-BINDING PROTEIN | 4FE-4S CLUSTER | CHEMISTRY, INORGANIC & NUCLEAR
Book Chapter
Human Molecular Genetics, ISSN 0964-6906, 01/2014, Volume 23, Issue 1, pp. 24 - 39
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 6/2015, Volume 74, Issue 6, pp. 527 - 537
Journal Article
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 08/2014, Volume 73, pp. 21 - 33
Friedreich ataxia (FRDA) is a hereditary disease caused by deficient frataxin expression. This mitochondrial protein has been related to iron homeostasis,... 
Oxidative stress |