Compounds > n-caproylglycine

Page last updated: 2024-08-26

n-caproylglycine and carnitine

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

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (25.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	1 (25.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bykov, IL; Shigematsu, E	1
Albers, S; Irons, M; Levy, HL; Marsden, D; Strauss, AW	1
Andresen, BS; Angel, L; Bennetts, B; Carpenter, K; Waddell, L; Wilcken, B; Wiley, V	1
Gavrilov, D; Highsmith, WE; Matern, D; McHugh, D; Oglesbee, D; Raymond, K; Rinaldo, P; Smith, EH; Thomas, C; Tortorelli, S	1

Other Studies

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

Article	Year
[Effect of l-carnitine on the expression of glycine conjugates in rats in experimental B2-hypovitaminosis]. Voprosy pitaniia, 1997, Issue:6 Topics: Animals; Carnitine; Glycine; Rats; Rats, Wistar; Riboflavin Deficiency	1997
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
Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Molecular genetics and metabolism, 2006, Volume: 87, Issue:1 Topics: Acyl-CoA Dehydrogenase; Carnitine; DNA Mutational Analysis; Fibroblasts; Genetic Testing; Genetic Variation; Genotype; Glycine; Homozygote; Humans; Infant, Newborn; Mass Spectrometry; Phenotype; Statistics as Topic	2006
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. Molecular genetics and metabolism, 2010, Volume: 100, Issue:3 Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Alleles; Carnitine; Child; Child, Preschool; DNA Mutational Analysis; Exons; Genetic Association Studies; Genetic Carrier Screening; Genetic Variation; Genotype; Glycine; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Middle Aged; Mutation; Mutation, Missense; Neonatal Screening; Polymorphism, Single Nucleotide; Young Adult	2010