Compounds > octanoyl-coenzyme a
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octanoyl-coenzyme a and Lipid Metabolism, Inborn Error

octanoyl-coenzyme a has been researched along with Lipid Metabolism, Inborn Error in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Herebian, D; Koster, KL; Smits, SH; Spiekerkoetter, U; Sturm, M1
Herebian, D; Laryea, MD; Mueller, M; Spiekerkoetter, U; Sturm, M1
Amendt, BA; Rhead, WJ2

Other Studies

4 other study(ies) available for octanoyl-coenzyme a and Lipid Metabolism, Inborn Error

ArticleYear
Functional studies of 18 heterologously expressed medium-chain acyl-CoA dehydrogenase (MCAD) variants.
    Journal of inherited metabolic disease, 2014, Volume: 37, Issue:6

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; DNA Mutational Analysis; Escherichia coli; Flavin-Adenine Dinucleotide; Genotype; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Mutation; Neonatal Screening; Oxidation-Reduction; Protein Structure, Tertiary; Substrate Specificity

2014
Functional effects of different medium-chain acyl-CoA dehydrogenase genotypes and identification of asymptomatic variants.
    PloS one, 2012, Volume: 7, Issue:9

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Carnitine; Chromatography, High Pressure Liquid; Genotype; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Lymphocytes; Mutation; Neonatal Screening; Oxidation-Reduction; Spectrometry, Mass, Electrospray Ionization

2012
The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
    The Journal of clinical investigation, 1986, Volume: 78, Issue:1

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Adipates; Animals; Caprylates; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Fibroblasts; Flavin-Adenine Dinucleotide; Flavoproteins; Glutarates; Lipid Metabolism, Inborn Errors; Liver; Malonates; Mitochondria; Palmitoyl Coenzyme A; Succinates; Succinic Acid; Swine

1986
Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.
    The Journal of clinical investigation, 1985, Volume: 76, Issue:3

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Adult; Fibroblasts; Flavin-Adenine Dinucleotide; Hemiterpenes; Humans; Infant; Isovaleryl-CoA Dehydrogenase; Lipid Metabolism, Inborn Errors; Male; Methylphenazonium Methosulfate; Mitochondria, Liver; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pentanoic Acids; Subcellular Fractions

1985