n-caproylglycine has been researched along with glycine in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (27.78) | 18.7374 |
| 1990's | 6 (33.33) | 18.2507 |
| 2000's | 5 (27.78) | 29.6817 |
| 2010's | 2 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baretz, BH; Ramsdell, HS; Tanaka, K | 1 |
| Bennett, MJ; Bhala, A; Hale, DE; Poirier, SF; Ragni, MC; Willi, SM | 1 |
| O'Shea, JJ; Rinaldo, P; Tanaka, K; Welch, RD | 1 |
| Coates, PM; Hale, DE; O'Shea, JJ; Rinaldo, P; Stanley, CA; Tanaka, K | 1 |
| David, M; Divry, P; Gregersen, N; Hobolth, N; Kølvraa, S; Mortensen, PB; Rasmussen, K | 1 |
| Gregersen, N; Hobolth, N; Kølvraa, S; Lauritzen, R; Rasmussen, K; Rosleff, F | 1 |
| Bennett, MJ; Ostfeld, RJ; Ragni, MC; Santer, R; Schmidt-Sommerfeld, E | 1 |
| Bennett, MJ; Bhala, A; Hale, DE; McGowan, KL | 1 |
| Bykov, IL; Shigematsu, E | 1 |
| Kimura, M; Yamaguchi, S | 1 |
| Baumgart, LE; DeBlassio, JL; Glufke, U; King, L; Merkler, DJ; Merkler, KA; Ritenour-Rodgers, K; Vederas, JC; Wilcox, BJ | 1 |
| Albers, S; Irons, M; Levy, HL; Marsden, D; Strauss, AW | 1 |
| García Conca, V; García Sánchez, J; Hueso Abancens, JR; Mengual Verdú, E; Placeres Daban, J; Schargel Palacios, K; Zorraquino Marti, A | 1 |
| Andresen, BS; Angel, L; Bennetts, B; Carpenter, K; Waddell, L; Wilcken, B; Wiley, V | 1 |
| Dogru, M; Goto, E; Inoue, H; Matsumoto, Y; Saito, I; Sasaki, Y; Shimazaki, J; Tsubota, K | 1 |
| Dalton, RN; Downing, M; Krywawych, S; Manning, NJ; Oerton, J | 1 |
| Gavrilov, D; Highsmith, WE; Matern, D; McHugh, D; Oglesbee, D; Raymond, K; Rinaldo, P; Smith, EH; Thomas, C; Tortorelli, S | 1 |
| Kawasaki, Y; Tanuma, N; Yamada, H; Yui, K | 1 |
1 trial(s) available for n-caproylglycine and glycine
| Article | Year |
|---|---|
[Modification of the conjuntival flora with cleaning palpebral solutions].
Topics: Adult; Aged; Aged, 80 and over; Conjunctiva; Female; Glycine; Humans; Male; Middle Aged; Ophthalmic Solutions; Prospective Studies | 2004 |
17 other study(ies) available for n-caproylglycine and glycine
| Article | Year |
|---|---|
Identification of n-hexanoylglycine in urines from two patients with Jamaican vomiting sickness.
Topics: Gas Chromatography-Mass Spectrometry; Glycine; Humans; Hypoglycins; Jamaica; Plant Poisoning; Vomiting | 1976 |
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenases; Enterobacteriaceae; Feces; Female; Glycine; Humans; Infant; Infant, Newborn; Intestines; Neonatal Screening; Phenylpropionates | 1992 |
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring.
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.
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 |
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Adipates; Caproates; Caprylates; Carboxylic Acids; Child, Preschool; Decanoic Acids; Dicarboxylic Acids; Female; Glycine; Humans; Hydroxy Acids; Hydroxybutyrates; Infant; Male | 1983 |
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases.
Topics: Adipates; Caproates; Caprylates; Child, Preschool; Chromatography, Gas; Decanoic Acids; Dicarboxylic Acids; Fatty Acid Desaturases; Fatty Acids; Glycine; Humans; Hydroxy Acids; Hydroxybutyrates; Hypoglycemia; Infant; Lipid Metabolism, Inborn Errors; Male; Mass Spectrometry; Valerates | 1980 |
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Child, Preschool; Decanoic Acids; Fatty Acids; Fatty Acids, Monounsaturated; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Infant; Infant, Newborn; Neonatal Screening; Reference Values; Sensitivity and Specificity | 1994 |
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Adult; Anti-Bacterial Agents; Bacteria, Anaerobic; Caproates; Child; Clostridium; Fatty Acid Desaturases; Glycine; Humans; Infant; Phenylalanine; Phenylpropionates | 1993 |
[Effect of l-carnitine on the expression of glycine conjugates in rats in experimental B2-hypovitaminosis].
Topics: Animals; Carnitine; Glycine; Rats; Rats, Wistar; Riboflavin Deficiency | 1997 |
Screening for fatty acid beta oxidation disorders. Acylglycine analysis by electron impact ionization gas chromatography-mass spectrometry.
Topics: Dicarboxylic Acids; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Lipid Metabolism, Inborn Errors; Reference Standards | 1999 |
A pathway for the biosynthesis of fatty acid amides.
Topics: Adult; Amides; Animals; CHO Cells; Cricetinae; Enzyme Inhibitors; Fatty Acids; Female; Glycine; Glyoxylates; Humans; In Vitro Techniques; Mixed Function Oxygenases; Models, Biological; Multienzyme Complexes; Rats; Recombinant Proteins; Substrate Specificity | 1999 |
Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.
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.
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 |
Alterations of the tear film and ocular surface health in chronic smokers.
Topics: Adult; Breath Tests; Capnography; Carbon Dioxide; Case-Control Studies; Conjunctiva; Enzyme-Linked Immunosorbent Assay; Eye Diseases; Female; Glycine; Humans; Lipid Metabolism; Male; Middle Aged; Neutrophils; Smoking; Specimen Handling; Tears | 2008 |
Detection of urinary hexanoylglycine in the diagnosis of MCAD deficiency from newborn screening.
Topics: Acyl-CoA Dehydrogenase; Clinical Laboratory Techniques; Glycine; Humans; Infant, Newborn; Metabolic Diseases; Multicenter Studies as Topic; Neonatal Screening; Pilot Projects; Sensitivity and Specificity; United Kingdom | 2008 |
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing.
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 |
Reduced endogenous urinary total antioxidant power and its relation of plasma antioxidant activity of superoxide dismutase in individuals with autism spectrum disorder.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Adolescent; Antioxidants; Autism Spectrum Disorder; Biomarkers; Child; Child, Preschool; Deoxyguanosine; Enzyme Activation; Female; Glycine; Humans; Male; Reproducibility of Results; Sensitivity and Specificity; Superoxide Dismutase; Young Adult | 2017 |