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Journal Article
Journal Article
Neurotherapeutics, ISSN 1933-7213, 4/2013, Volume 10, Issue 2, pp. 186 - 198
Mitochondrial DNA (mtDNA) depletion syndromes (MDS) are a genetically and clinically heterogeneous group of autosomal recessive disorders that are... 
Neurology | Neurosciences | Biomedicine | Neurobiology | Mitochondrial encephalomyopathy | Mitochondrial neurogastrointestinal (MNGIE) disease | Mitochondrial myopathy | Neurosurgery | Hepatocerebral syndrome | Alpers-Huttenlocher syndrome | POLYMERASE-GAMMA-A | CORRECTS BIOCHEMICAL DERANGEMENTS | ONSET SPINOCEREBELLAR ATAXIA | NEUROSCIENCES | CLINICAL NEUROLOGY | PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | RESPIRATORY-CHAIN DEFICIENCY | MULTIPLE MTDNA DELETIONS | NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY MNGIE | ALPERS-SYNDROME | PHARMACOLOGY & PHARMACY | DEOXYGUANOSINE KINASE-DEFICIENCY | STEM-CELL TRANSPLANTATION | Mitochondrial Diseases - genetics | Liver Transplantation | DNA, Mitochondrial - metabolism | Humans | Mitochondrial Encephalomyopathies - genetics | DNA, Mitochondrial - physiology | Mutation - genetics | Nervous System Diseases - genetics | Nucleotides - metabolism | Mitochondrial Myopathies - pathology | Mitochondrial Myopathies - therapy | Nervous System Diseases - therapy | Mitochondrial Encephalomyopathies - pathology | Mutation - physiology | Mitochondrial Myopathies - genetics | DNA, Mitochondrial - genetics | Mitochondrial Encephalomyopathies - therapy | DNA Replication - physiology | DNA Replication - genetics | Nervous System Diseases - physiopathology | Mitochondrial Diseases - therapy | Mitochondrial Diseases - physiopathology | Nutritional Support | Thymidine - metabolism | Genetic aspects | Mitochondrial DNA | Health aspects | Genes | Medical genetics | Review
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 7, p. e21779
We have reported that pyrroloquinoline quinone (PQQ) improves reproduction, neonatal development, and mitochondrial function in animals by mechanisms that... 
RESVERATROL | MYOCARDIAL INFARCT SIZE | FATTY-ACID OXIDATION | ANTIOXIDANT | PERFORMANCE | MULTIDISCIPLINARY SCIENCES | GROWTH | GENE-EXPRESSION | SPHINGOLIPIDS | BINDING PROTEIN | SPHINGOSINE 1-PHOSPHATE | Malondialdehyde - metabolism | PQQ Cofactor - therapeutic use | Diabetes Mellitus, Type 2 - prevention & control | Body Weight - drug effects | Rats | Survival Rate | Diabetes Mellitus, Type 2 - metabolism | Mitochondria - drug effects | Myocardial Infarction - metabolism | Rats, Sprague-Dawley | Myocardial Reperfusion Injury - metabolism | Animals | Myocardial Infarction - drug therapy | Lipid Peroxidation - drug effects | Glucose - metabolism | Heart - drug effects | Nutritional Status | Lipids - analysis | Myocardial Reperfusion Injury - drug therapy | Heart Function Tests | Energy Metabolism - drug effects | Disease Models, Animal | Type 2 diabetes | Ischemia | Physiological aspects | Amino acids | Lipids | Cellular signal transduction | Glucose | Dextrose | Heart | Neonates | Plasma | Energy metabolism | Quotients | Liver | Genes | Lipid peroxidation | Mitochondrial DNA | Veterinary medicine | Body composition | Proteins | Ratios | Mitochondria | Pyrroloquinoline quinone | Reperfusion | E coli | Rodents | Lipid metabolism | Cardiology | Heart diseases | Deoxyribonucleic acid--DNA | Nutritional status | Peroxidation | Nutrition | Diabetes mellitus | Quinone | Energy expenditure | Triglycerides | Metabolism | Insulin | Fatty acids | Malondialdehyde | Signaling | Diet | Body size | Diabetes | Deoxyribonucleic acid | DNA
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 11/2016, Volume 119, Issue 3, pp. 187 - 206
Journal Article
Nutrition, ISSN 0899-9007, 03/2018, Volume 47, pp. 56 - 62
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7, p. e40871
Pantothenate kinase (PanK) phosphorylates pantothenic acid (vitamin B-5) and controls the overall rate of coenzyme A (CoA) biosynthesis. Pank1 gene deletion in... 
ENCODES | PANK2 | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | GENE-EXPRESSION | COENZYME-A | IDENTIFICATION | PEROXISOMAL NUDIX HYDROLASE | OXIDATIVE-METABOLISM | BRAIN | IRON ACCUMULATION | Liver - enzymology | Humans | Brain - enzymology | RNA, Messenger - metabolism | Gene Deletion | Germ Cells - metabolism | Fatty Acids - metabolism | NAD - metabolism | Animals, Newborn | Gene Targeting | Oxidation-Reduction | Phosphotransferases (Alcohol Group Acceptor) - deficiency | RNA, Messenger - genetics | Organ Size | Phosphotransferases (Alcohol Group Acceptor) - genetics | Coenzyme A - metabolism | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Triglycerides - metabolism | Phenotype | Animals | Gluconeogenesis - genetics | Stearoyl-CoA Desaturase - metabolism | Mice | Ketones - metabolism | Liver | Physiological aspects | Triglycerides | Genetic aspects | Fatty acids | Phosphotransferases | Brain | Lipids | Iron | Biosynthesis | Gene deletion | Kinases | Inactivation | Accumulation | Proteins | NADH | Neurodegeneration | Rodents | Coenzyme A | Oxidation | Children | Localization | Gluconeogenesis | Pantothenate kinase | Enzymes | Deactivation | Ketones | Hypoglycemia | Metabolism | Mammals | Gene expression | Polymerase chain reaction | Hypotheses | Brain research | Hospitals | Infectious diseases | Insects | Hepatocytes | Isoforms | Stem cells | Nicotinamide adenine dinucleotide | Biomarkers | Scientific imaging | Mutation | Mass spectrometry | Pantothenic acid
Journal Article
Journal Article
Annual Review of Pathology: Mechanisms of Disease, ISSN 1553-4006, 1/2018, Volume 13, Issue 1, pp. 163 - 191
Multisystem metabolic disorders caused by defects in oxidative phosphorylation (OXPHOS) are severe, often lethal, conditions. Inborn errors of OXPHOS function... 
nutritional interventions | electron transport chain | metabolism | primary mitochondrial OXPHOS disorders | Electron transport chain | Nutritional interventions | Primary mitochondrial OXPHOS disorders | Metabolism | OXIDATIVE-PHOSPHORYLATION |