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The EMBO Journal, ISSN 0261-4189, 11/2004, Volume 23, Issue 23, pp. 4679 - 4689
Journal Article
Cell Metabolism, ISSN 1550-4131, 07/2011, Volume 14, Issue 1, pp. 80 - 90
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2008, Volume 14, Issue 10, pp. 1097 - 1105
Journal Article
Annals of Neurology, ISSN 0364-5134, 08/2019, Volume 86, Issue 2, pp. 193 - 202
Objective Cytochrome c oxidase (COX) deficiency is a major mitochondrial respiratory chain defect that has vast genetic and phenotypic heterogeneity. This... 
MITOCHONDRIAL-DNA DEPLETION | COMPLEXES | GENES | MUTATIONS | MYOPATHY | NEUROSCIENCES | CLINICAL NEUROLOGY | SUBUNIT | Cytochrome | Heart | Signs and symptoms | Cardiac muscle | Cardiomyopathy | Oxidase | Organs | Cytochrome-c oxidase | Muscles | Chains | Skeletal muscle | Heterogeneity | Musculoskeletal system | Mitochondria | Hypotonia | Enzymatic activity | Cytochromes | Electron transport | Assembly | Myopathy
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 08/2018, Volume 115, Issue 32, pp. 8161 - 8166
Copper is an essential cofactor of cytochrome c oxidase (CcO), the terminal enzyme of the mitochondrial respiratory chain. Inherited loss-of-function mutations... 
elesclomol | cytochrome c oxidase | Copper | mitochondria | MATRIX | MULTIDISCIPLINARY SCIENCES | BINDING PROTEIN | CYTOCHROME-C-OXIDASE | HYPERTROPHIC CARDIOMYOPATHY | DRUG ELESCLOMOL | BIOGENESIS | SCO2 | DISEASE | copper | MUTATIONS | COA6 | Drugs, Investigational - pharmacology | Humans | Drugs, Investigational - therapeutic use | Antineoplastic Agents - therapeutic use | Mitochondrial Proteins - genetics | Electron Transport Complex IV - metabolism | Membrane Transport Proteins - genetics | Coenzymes - deficiency | Fibroblasts | Antineoplastic Agents - pharmacology | Biological Transport - genetics | Copper - deficiency | Disease Models, Animal | Cell Line | Hydrazines - pharmacology | Hydrazines - therapeutic use | Mutagenesis, Site-Directed | Metabolism, Inborn Errors - metabolism | Rats | Zebrafish | Mitochondria - metabolism | Drug Repositioning | Mitochondria - drug effects | Metabolism, Inborn Errors - genetics | Carrier Proteins - genetics | Animals | Copper - therapeutic use | Metabolism, Inborn Errors - drug therapy | Mutation | Zebrafish Proteins - genetics | Dietary Supplements | Saccharomyces cerevisiae | Antimitotic agents | Copper in the body | Mitochondria | Physiological aspects | Genetic aspects | Minerals in nutrition | Models | Dosage and administration | Drug therapy | Antineoplastic agents | Biological Sciences
Journal Article
BBA - Molecular and Cell Biology of Lipids, ISSN 1388-1981, 10/2017, Volume 1862, Issue 10, pp. 1044 - 1055
Journal Article