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2018, ISBN 3038972401
Mitochondrial disease constitutes a complex and heterogeneous group of disorders resulting from a defect in mitochondrial respiratory chain (MRC) enzyme... 
diagnosis | mitochondrial respiratory chain (MRC) | mitochondrial disorders | biochemical parameters/markers | oxidative stress | biomarks
eBook
American Journal of Clinical Nutrition, ISSN 0002-9165, 02/2016, Volume 103, Issue 2, pp. 579 - 588
Journal Article
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 04/2018, Volume 7, Issue 4, p. 66
Mitochondrial respiratory chain (MRC) disorders have a multifaceted clinical presentation and genetic origin[...]. 
BIOMARKER | MEDICINE, GENERAL & INTERNAL | DISORDERS | n/a
Journal Article
01/2015, ISBN 9781634828222
Book
Neuroscience Letters, ISSN 0304-3940, 12/2008, Volume 447, Issue 1, pp. 17 - 19
There is increasing evidence that impairment of mitochondrial function and oxidative damage are contributing factors to the pathophysiology of Parkinson's... 
Cerebellum | Electron transport chain | Brain | Oxidative stress | Striatum | Parkinson's disease | Substantia nigra | Cortex | Coenzyme Q | Antioxidant | Parkinson Disease - pathology | Humans | Ubiquinone - analogs & derivatives | Brain - enzymology | Brain - pathology | Ubiquinone - metabolism | Female | Male | Aged | Case-Control Studies | Index Medicus
Journal Article
Molecular Metabolism, ISSN 2212-8778, 11/2013, Volume 2, Issue 4, pp. 480 - 490
Studies in human and animals have demonstrated that nutritionally induced low birth-weight followed by rapid postnatal growth increases the risk of metabolic... 
Oxidative-stress | Ubiquinone | DNA damage | Cellular senescence | Developmental programming | Telomere length
Journal Article
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2014, Volume 35, Issue 5, pp. 1111 - 1115
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 15676 - 13
Isolated Complex I (CI) deficiency is the most commonly observed mitochondrial respiratory chain biochemical defect, affecting the largest OXPHOS component. CI... 
LEIGH-LIKE-SYNDROME | ASSEMBLY FACTOR | DNA MUTATION | G13513A MUTATION | MULTIDISCIPLINARY SCIENCES | DISEASE | SUBUNITS | MELAS | IDENTIFICATION | CLINICAL PHENOTYPE | ND5 GENE | Electron transport chain | NADH-ubiquinone oxidoreductase | Mitochondrial DNA | Genomes | Immunoreactivity | Mutation | Spectrophotometry | Electron transport | Skeletal muscle
Journal Article
Neuroscience Letters, ISSN 0304-3940, 12/2008, Volume 447, Issue 1, p. 17
There is increasing evidence that impairment of mitochondrial function and oxidative damage are contributing factors to the pathophysiology of Parkinson's... 
Antioxidants | Brain | Neurosciences | Coenzymes | Questions and answers
Journal Article
Biophysical Journal, ISSN 0006-3495, 02/2016, Volume 110, Issue 3, pp. 474a - 474a
Journal Article
Mitochondrion, ISSN 1567-7249, 06/2007, Volume 7, p. S175-S180
Mevalonic aciduria (MVA) and phenylketonuria (PKU) are inborn errors of metabolism caused by deficiencies in the enzymes mevalonate kinase and phenylalanine... 
Enzymes | Phenylketonuria | Physiological aspects | Blood lipids
Journal Article
AMERICAN JOURNAL OF CLINICAL NUTRITION, ISSN 0002-9165, 02/2016, Volume 103, Issue 2, pp. 579 - 588
Journal Article
Mitochondrion, ISSN 1567-7249, 2007, Volume 7, pp. S175 - S180
Mevalonic aciduria (MVA) and phenylketonuria (PKU) are inborn errors of metabolism caused by deficiencies in the enzymes mevalonate kinase and phenylalanine... 
Phenylketonuria | Phenylalanine | Coenzyme Q10 | Mevalonic aciduria
Journal Article
American Journal of Physiology - Regulatory, Integrative and Comparative Physiology, ISSN 0363-6119, 09/2009, Volume 297, Issue 3, pp. 675 - 681
We recently reported insulin resistance in adult offspring of obese C57BL/6J mice. We have now evaluated whether parameters of skeletal muscle structure and... 
Electron transport chain | Developmental programming | Maternal obesity | Muscle metabolism | Insulin signaling | electron transport chain | muscle metabolism | PHYSIOLOGY | FIBER NUMBER | maternal obesity | RATS | BIRTH-WEIGHT | GLUCOSE-TRANSPORT | BODY-COMPOSITION | DIET-INDUCED OBESITY | PREGNANCY | insulin signaling | TYPE-2 DIABETIC-PATIENTS | GENE-EXPRESSION | developmental programming | Electron Transport Complex III - metabolism | Phosphorylation | Prenatal Exposure Delayed Effects | Body Weight | Maternal Nutritional Physiological Phenomena | Glucose Transporter Type 4 - metabolism | Mitochondria, Muscle - metabolism | Ubiquinone - metabolism | Male | Phosphatidylinositol 3-Kinases - metabolism | Insulin Receptor Substrate Proteins - metabolism | Muscle Fibers, Skeletal - metabolism | Quadriceps Muscle - enzymology | Protein Kinase C - metabolism | Female | Proto-Oncogene Proteins c-akt - metabolism | Quadriceps Muscle - pathology | Disease Models, Animal | Mitochondria, Muscle - enzymology | Signal Transduction | Mice, Inbred C57BL | Insulin Resistance | Obesity - physiopathology | Obesity - metabolism | Obesity - pathology | Pregnancy | Insulin - metabolism | Animals | Class I Phosphatidylinositol 3-Kinases | Animal Nutritional Physiological Phenomena | Electron Transport Complex II - metabolism | Sex Factors | Receptor, Insulin - metabolism | Mice | Quadriceps Muscle - metabolism | Proteins | Musculoskeletal system | Obesity | Models | Insulin | Rodents | Index Medicus
Journal Article
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