Works matching DE "ACYL-CoA dehydrogenases"
Results: 47
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Correspondence.
- Published in:
- Indian Pediatrics, 2016, v. 53, n. 3, p. 262, doi. 10.1007/s13312-016-0833-0
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- Publication type:
- Article
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation.
- Published in:
- 2017
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- Publication type:
- Case Study
Myocardial energy shortage and unmet anaplerotic needs in the fasted long-chain acyl-CoA dehydrogenase knockout mouse.
- Published in:
- Cardiovascular Research, 2013, v. 100, n. 3, p. 441, doi. 10.1093/cvr/cvt212
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- Publication type:
- Article
Activation of PPARα by Fatty Acid Accumulation Enhances Fatty Acid Degradation and Sulfatide Synthesis.
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- Tohoku Journal of Experimental Medicine, 2016, v. 240, n. 2, p. 113, doi. 10.1620/tjem.240.113
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- Publication type:
- Article
A Heterozygous Missense Mutation in Adolescent-Onset Very Long-Chain Acyl-CoA Dehydrogenase Deficiency with Exercise-Induced Rhabdomyolysis.
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- Tohoku Journal of Experimental Medicine, 2015, v. 235, n. 4, p. 305, doi. 10.1620/tjem.235.305
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- Publication type:
- Article
Identification of the Catalytic Residue of Rat Acyl-CoA Dehydrogenase 9 by Site-Directed Mutagenesis.
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- Applied Biochemistry & Biotechnology, 2017, v. 182, n. 3, p. 1198, doi. 10.1007/s12010-016-2392-1
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- Publication type:
- Article
"It's Just Always Eating": The Experiences of Young People Growing up Medium Chain Acyl-coA Dehydrogenase Deficiency.
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- Global Qualitative Nursing Research, 2021, v. 8, p. 1, doi. 10.1177/23333936211032203
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- Publication type:
- Article
Ethylmalonic Acid Induces Permeability Transition in Isolated Brain Mitochondria.
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- Neurotoxicity Research, 2014, v. 26, n. 2, p. 168, doi. 10.1007/s12640-014-9460-5
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- Publication type:
- Article
Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients.
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- Journal of Human Genetics, 2014, v. 59, n. 5, p. 256, doi. 10.1038/jhg.2014.10
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- Publication type:
- Article
Medium chain acyl-CoA dehydrogenase deficiency in a premature infant.
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- Pediatric Reports, 2017, v. 9, n. 4, p. 33, doi. 10.4081/pr.2017.7045
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- Publication type:
- Article
Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report.
- Published in:
- 2018
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- Publication type:
- journal article
Identification of leptospiral 3-hydroxyacyl-CoA dehydrogenase released in the urine of infected hamsters.
- Published in:
- BMC Microbiology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2180-14-132
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- Publication type:
- Article
Escherichia coli ydiO and ydiQRST genes encode components of acyl-CoA dehydrogenase complex of anaerobic fatty acid β-oxidation pathway.
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- Russian Journal of Genetics, 2016, v. 52, n. 10, p. 1101, doi. 10.1134/S1022795416100021
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- Publication type:
- Article
The effect of short/branched chain acyl-coenzyme A dehydrogenase gene on triglyceride synthesis of bovine mammary epithelial cells.
- Published in:
- Archives Animal Breeding / Archiv Tierzucht, 2018, v. 61, n. 1, p. 115, doi. 10.5194/aab-61-115-2018
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- Publication type:
- Article
A novel ACAD8 mutation in asymptomatic patients with isobutyryl- CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum.
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- Clinical Genetics, 2015, v. 87, n. 2, p. 196, doi. 10.1111/cge.12350
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- Publication type:
- Article
Long-chain 3-hydroxy fatty acids accumulating in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies uncouple oxidative phosphorylation in heart mitochondria.
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- Journal of Bioenergetics & Biomembranes, 2013, v. 45, n. 1/2, p. 47, doi. 10.1007/s10863-012-9481-9
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- Publication type:
- Article
Insights into Medium-chain Acyl-CoA Dehydrogenase Structure by Molecular Dynamics Simulations.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 2, p. 281, doi. 10.1111/cbdd.12755
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- Publication type:
- Article
Disruption of redox homeostasis in cerebral cortex of developing rats by acylcarnitines accumulating in medium-chain acyl-CoA dehydrogenase deficiency
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- International Journal of Developmental Neuroscience, 2012, v. 30, n. 5, p. 383, doi. 10.1016/j.ijdevneu.2012.03.238
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- Publication type:
- Article
Combined HIIT and Resistance Training in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: A Case Report.
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- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00650
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- Publication type:
- Article
Fimasartan Ameliorates Nonalcoholic Fatty Liver Disease through PPARδ Regulation in Hyperlipidemic and Hypertensive Conditions.
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- PPAR Research, 2017, p. 1, doi. 10.1155/2017/8048720
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- Publication type:
- Article
Bacterial Production, Characterization and Protein Modeling of a Novel Monofuctional Isoform of FAD Synthase in Humans: An Emergency Protein?
- Published in:
- Molecules, 2018, v. 23, n. 1, p. 116, doi. 10.3390/molecules23010116
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- Publication type:
- Article
Molecular Basis for Converting (2S)-Methylsuccinyl-CoA Dehydrogenase into an Oxidase.
- Published in:
- Molecules, 2018, v. 23, n. 1, p. 68, doi. 10.3390/molecules23010068
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- Publication type:
- Article
The Story of Equine Atypical Myopathy: A Review from the Beginning to a Possible End.
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- ISRN Veterinary Science, 2012, p. 1, doi. 10.5402/2012/281018
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- Publication type:
- Article
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.
- Published in:
- 2016
- By:
- Publication type:
- journal article
In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-43
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- Publication type:
- Article
Bent spine syndrome as an initial manifestation of late-onset multiple acyl-CoA dehydrogenase deficiency: a case report and literature review.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Upstream sequence of fatty acyl- CoA reductase ( FAR6) of Arabidopsis thaliana drives wound-inducible and stem-specific expression.
- Published in:
- Plant Cell Reports, 2012, v. 31, n. 5, p. 839, doi. 10.1007/s00299-011-1205-9
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- Publication type:
- Article
ACADL plays a tumor-suppressor role by targeting Hippo/YAP signaling in hepatocellular carcinoma.
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- NPJ Precision Oncology, 2020, v. 4, n. 1, p. 1, doi. 10.1038/s41698-020-0111-4
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- Publication type:
- Article
Analysis of plasma ghrelin in patients with medium-chain acyl-CoA dehydrogenase deficiency and glutaric aciduria type II.
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- European Journal of Endocrinology, 2012, v. 166, n. 2, p. 235, doi. 10.1530/EJE-11-0785
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- Publication type:
- Article
Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Biochemical phenotyping of multiple myeloma patients at diagnosis reveals a disorder of mitochondrial complexes I and II and a Hartnup-like disturbance as underlying conditions, also influencing different stages of the disease.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-75862-4
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- Publication type:
- Article
Detection of equine atypical myopathy-associated hypoglycin A in plant material: Optimisation and validation of a novel LC-MS based method without derivatisation.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0199521
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- Publication type:
- Article
Effect of temperature on fatty acid metabolism in skeletal muscle mitochondria of untrained and endurance-trained rats.
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- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189456
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- Publication type:
- Article
Transcriptional control of lipid metabolism by the MarR-like regulator FamR and the global regulator GlxR in the lipophilic axilla isolate Corynebacterium jeikeium K411.
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- Microbial Biotechnology, 2013, v. 6, n. 2, p. 118, doi. 10.1111/1751-7915.12004
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- Publication type:
- Article
Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Erratum.
- Published in:
- 2016
- Publication type:
- Correction Notice
Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Adulthood: A Potential Diagnosis in a Patient with Mental Status Changes Suspected of Drug Toxicity.
- Published in:
- Journal of Forensic Sciences, 2015, v. 60, n. 4, p. 1101, doi. 10.1111/1556-4029.12808
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- Publication type:
- Article
Dimerization Interface of 3-Hydroxyacyl-CoA Dehydrogenase Tunes the Formation of Its Catalytic Intermediate.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0095965
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- Publication type:
- Article
Diet-Sensitive Sources of Reactive Oxygen Species in Liver Mitochondria: Role of Very Long Chain Acyl-CoA Dehydrogenases.
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0077088
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- Publication type:
- Article
Tissue-Specific Strategies of the Very-Long Chain Acyl-CoA Dehydrogenase-Deficient (VLCAD<sup>-/-</sup>) Mouse to Compensate a Defective Fatty Acid β-Oxidation.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045429
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- Publication type:
- Article
Functional Effects of Different Medium-Chain Acyl-CoA Dehydrogenase Genotypes and Identification of Asymptomatic Variants.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045110
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- Publication type:
- Article
Equine Multiple Acyl-CoA Dehydrogenase Deficiency ( MADD) Associated with Seasonal Pasture Myopathy in the Midwestern United States.
- Published in:
- Journal of Veterinary Internal Medicine, 2012, v. 26, n. 4, p. 1012, doi. 10.1111/j.1939-1676.2012.00957.x
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- Publication type:
- Article
Turkish case of ethylmalonic encephalopathy misdiagnosed as short chain acyl-CoA dehydrogenase deficiency.
- Published in:
- Metabolic Brain Disease, 2018, v. 33, n. 3, p. 977, doi. 10.1007/s11011-017-0152-8
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- Publication type:
- Article
Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency.
- Published in:
- 2017
- By:
- Publication type:
- Erratum
The value of fasting in the diagnosis of medium-chain acyl-CoA dehydrogenase deficiency.
- Published in:
- Jornal Brasileiro de Patologia e Medicina Laboratorial, 2020, v. 56, p. 1, doi. 10.5935/1676-2444.20200011
- By:
- Publication type:
- Article
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening.
- Published in:
- 2015
- By:
- Publication type:
- Case Study