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BBA - Molecular Basis of Disease, ISSN 0925-4439, 08/2013, Volume 1832, Issue 8, pp. 1194 - 1206
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 05/2013, Volume 54, Issue 5, pp. 1312 - 1325
Journal Article
Nature Chemical Biology, ISSN 1552-4450, 08/2016, Volume 12, Issue 8, pp. 641 - 647
Cardiolipin is a specific mitochondrial phospholipid that has a high affinity for proteins and that stabilizes the assembly of supercomplexes involved in... 
HEART | RESPIRATORY-CHAIN | STABLE-ISOTOPES | TURNOVER | SUPERCOMPLEXES | TAFAZZIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | FATTY-ACIDS | MITOCHONDRIAL-MEMBRANE | MODEL | PLURIPOTENT STEM-CELL | Humans | Cardiolipins - metabolism | Barth Syndrome - metabolism | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2015, Volume 10, Issue 6, pp. e0128561 - e0128561
Cardiolipin (CL) is a mitochondrial phospholipid essential for electron transport chain (ETC) integrity. CL-deficiency in humans is caused by mutations in the... 
ORGANIZATION | CARDIOLIPIN | MITOCHONDRIAL RESPIRATORY-CHAIN | PROTEIN | SUPERCOMPLEXES | POLYMORPHISMS | FATTY-ACID OXIDATION | MULTIDISCIPLINARY SCIENCES | MYOPATHY | DEFICIENCY | FOLATE | Barth Syndrome - metabolism | Acyl-CoA Dehydrogenase, Long-Chain - metabolism | Heart - physiology | Mice, Inbred C57BL | Oxidative Phosphorylation | Male | Cardiolipins - metabolism | Mitochondria - metabolism | Electron Transport Complex I - metabolism | Gene Knockdown Techniques - methods | Mitochondrial Membranes - metabolism | Transcription Factors - metabolism | Barth Syndrome - pathology | Animals | Myocardium - metabolism | Metabolic Networks and Pathways - physiology | Mice | Phospholipids - metabolism | Proteomics - methods | Disease Models, Animal | Myoglobin | Enzymes | Membrane lipids | Mitochondrial DNA | Cardiolipin | Electron transport | Fatty acids | Cytochrome | Heart | Pediatrics | Phosphorylation | Cardiomyopathy | NADH dehydrogenase | Amino acids | Biology | Phospholipids | Dehydrogenase | Acyl-CoA dehydrogenase | Folic acid | Proteins | Electron transport chain | ATP synthase | Mitochondria | NADH | Pathways | Vitamin B | Physiology | Oxidation | Catalysis | Heart diseases | 3-Hydroxyacyl-CoA dehydrogenase | Channeling | Polypeptides | Cardiac muscle | Muscles | Cytochrome c1 | Metabolism | Gene expression | Children & youth | Medicine | Hospitals | Oxidative phosphorylation | Nicotinamide adenine dinucleotide | Metabolic pathways | Mutation | Laboratory animals | Homocysteine | Index Medicus
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 08/2017, Volume 136, Issue 13, pp. e200 - e231
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of morbidity and mortality. The management of cardiac disease in NMDs is made... 
Neuromuscular disease | Pediatrics | Cardiomyopathy | Muscular dystrophy | AHA Scientific Statements | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | MECHANICAL CIRCULATORY SUPPORT | neuromuscular disease | CONVERTING ENZYME-INHIBITORS | LUNG TRANSPLANTATION GUIDELINES | LEFT-VENTRICULAR NONCOMPACTION | muscular dystrophy | pediatrics | CHEYNE-STOKES RESPIRATION | LAMIN A/C GENE | PERIPHERAL VASCULAR DISEASE | DUCHENNE MUSCULAR-DYSTROPHY | MYOCARDIAL DELAYED ENHANCEMENT | cardiomyopathy | CARDIOSELECTIVE BETA-BLOCKERS | Myotonic Dystrophy - metabolism | Barth Syndrome - metabolism | Friedreich Ataxia - pathology | Myotonic Dystrophy - diagnosis | United States | Humans | Myopathies, Structural, Congenital - genetics | Neuromuscular Diseases - pathology | Barth Syndrome - pathology | Myotonic Dystrophy - pathology | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Cardiomyopathies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Friedreich Ataxia - metabolism | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Diseases - metabolism | Risk Factors | Friedreich Ataxia - diagnosis | Muscular Dystrophy, Emery-Dreifuss - pathology | Cardiomyopathies - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Diseases - pathology | Barth Syndrome - diagnosis | American Heart Association | Muscular Diseases - diagnosis | Muscular Dystrophy, Emery-Dreifuss - metabolism | Muscular Dystrophies, Limb-Girdle - metabolism | Barth Syndrome - genetics | Neuromuscular Diseases - complications | Myopathies, Structural, Congenital - pathology | Cardiomyopathies - complications | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - metabolism | Myopathies, Structural, Congenital - metabolism | Muscular Dystrophy, Duchenne - diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2014, Volume 289, Issue 4, pp. 2250 - 2259
Journal Article
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