Compounds > acetyl coenzyme a

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acetyl coenzyme a and Electron Transport Chain Deficiencies, Mitochondrial

acetyl coenzyme a has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (33.33)	29.6817
2010's	3 (50.00)	24.3611
2020's	1 (16.67)	2.80

Authors

Authors	Studies
Alberici, LC; Araujo, JS; Escarso, SHA; Espreafico, EM; Sobreira, CFDR; Zuccolotto-Dos-Reis, FH	1
Abramov, AY; Angelova, PR; Arber, C; Bhatia, KP; Duce, JA; Gout, I; Hardy, J; Houlden, H; Mazzacuva, F; Mills, K; Preza, E; Tsuchiya, Y; Wiethoff, S; Wray, S	1
Campbell, H; Campbell, I	1
Ikon, N; Ryan, RO	1
Gunay-Aygun, M	1
Brandt, U; Dröse, S; Hoffmann, GF; Kölker, S; Nijtmans, LG; Okun, JG; Rodenburg, RJ; Sauer, SW; Schwab, MA; Smeitink, JA; Ter Laak, H; van den Heuvel, LP	1

Reviews

1 review(s) available for acetyl coenzyme a and Electron Transport Chain Deficiencies, Mitochondrial

Article	Year
3-Methylglutaconic aciduria: a common biochemical marker in various syndromes with diverse clinical features. Molecular genetics and metabolism, 2005, Volume: 84, Issue:1 Topics: Abnormalities, Multiple; Acetyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Glutarates; Humans; Hydro-Lyases; Leucine; Mitochondrial Diseases; Sterols	2005

Other Studies

5 other study(ies) available for acetyl coenzyme a and Electron Transport Chain Deficiencies, Mitochondrial

Article	Year
Acetyl-CoA-driven respiration in frozen muscle contributes to the diagnosis of mitochondrial disease. European journal of clinical investigation, 2021, Volume: 51, Issue:9 Topics: Acetyl Coenzyme A; Adolescent; Adult; Biopsy; Cell Respiration; Child; Clinical Laboratory Techniques; Cryopreservation; Electron Transport; Female; Humans; Male; MELAS Syndrome; Membrane Potential, Mitochondrial; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Membranes; Muscle, Skeletal; Ophthalmoplegia, Chronic Progressive External; Oxidative Phosphorylation; Oxygen Consumption; Permeability; Specimen Handling; Young Adult	2021
iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease. PloS one, 2017, Volume: 12, Issue:9 Topics: Acetyl Coenzyme A; Adolescent; Biopsy; Brain; Cell Differentiation; Child; Coenzyme A; Female; Fibroblasts; Humans; Induced Pluripotent Stem Cells; Iron; Karyotyping; Lipid Peroxidation; Male; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial Diseases; Mutation; NAD; Neurons; Pantothenate Kinase-Associated Neurodegeneration; Pantothenic Acid; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Plasmids; Reactive Oxygen Species	2017
A pyruvate dehydrogenase complex disorder hypothesis for bipolar disorder. Medical hypotheses, 2019, Volume: 130 Topics: Acetyl Coenzyme A; Action Potentials; Adenosine Triphosphate; Affect; Bipolar Disorder; Diet, Ketogenic; Epilepsy; Humans; Ketones; Ketosis; Mitochondria; Mitochondrial Diseases; Models, Biological; Neurons; Oxidative Phosphorylation; Pyruvate Dehydrogenase Complex	2019
On the origin of 3-methylglutaconic acid in disorders of mitochondrial energy metabolism. Journal of inherited metabolic disease, 2016, Volume: 39, Issue:5 Topics: Acetyl Coenzyme A; Energy Metabolism; Glutarates; Humans; Mitochondria; Mitochondrial Diseases	2016
Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins. The Biochemical journal, 2006, Aug-15, Volume: 398, Issue:1 Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Cattle; Energy Metabolism; Fatty Acids; Female; Fibroblasts; Humans; Infant, Newborn; Male; Mitochondrial Diseases; Oxidative Phosphorylation; Propionates; Pyruvate Dehydrogenase Complex; Quadriceps Muscle; Skin; Swine; Toxins, Biological	2006