Compounds > n-caproylglycine
Page last updated: 2024-08-26

n-caproylglycine and suberylglycine

n-caproylglycine has been researched along with suberylglycine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
O'Shea, JJ; Rinaldo, P; Tanaka, K; Welch, RD1
Coates, PM; Hale, DE; O'Shea, JJ; Rinaldo, P; Stanley, CA; Tanaka, K1
Kimura, M; Yamaguchi, S1
Albers, S; Irons, M; Levy, HL; Marsden, D; Strauss, AW1

Other Studies

4 other study(ies) available for n-caproylglycine and suberylglycine

ArticleYear
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring.
    Biomedical & environmental mass spectrometry, 1989, Volume: 18, Issue:7

    Topics: Chemical Phenomena; Chemistry; Child; Chromatography, Ion Exchange; Dicarboxylic Acids; Gas Chromatography-Mass Spectrometry; Glycine; Humans

1989
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
    The New England journal of medicine, 1988, Nov-17, Volume: 319, Issue:20

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Child; Child, Preschool; Diagnosis, Differential; Dicarboxylic Acids; Glycine; Humans; Infant; Infant, Newborn; Methods; Radioisotope Dilution Technique; Retrospective Studies; Reye Syndrome; Sudden Infant Death

1988
Screening for fatty acid beta oxidation disorders. Acylglycine analysis by electron impact ionization gas chromatography-mass spectrometry.
    Journal of chromatography. B, Biomedical sciences and applications, 1999, Aug-06, Volume: 731, Issue:1

    Topics: Dicarboxylic Acids; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Lipid Metabolism, Inborn Errors; Reference Standards

1999
Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.
    Journal of inherited metabolic disease, 2001, Volume: 24, Issue:3

    Topics: Acyl-CoA Dehydrogenases; Caprylates; Carnitine; Child; Child, Preschool; Dicarboxylic Acids; DNA Mutational Analysis; Female; Glycine; Heterozygote; Humans; Infant, Newborn; Male; Mutation; Neonatal Screening

2001