Page last updated: 2024-10-18

glycocyamine and Inborn Urea Cycle Disorder

glycocyamine has been researched along with Inborn Urea Cycle Disorder in 3 studies

glycocyamine: RN given refers to parent cpd; structure
guanidinoacetate : A monocarboxylic acid anion that is the conjugate base of guanidinoacetic acid, obtained by deprotonation of the carboxy group.
guanidinoacetic acid : The N-amidino derivative of glycine.

Research Excerpts

ExcerptRelevanceReference
"Creatine synthesis is a major component of arginine metabolism, amounting to more than 20% of the dietary intake of this amino acid."1.36Creatine metabolism and the urea cycle. ( Brosnan, JT; Brosnan, ME, 2010)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Auray-Blais, C1
Maranda, B1
Lavoie, P1
Huemer, M1
Carvalho, DR1
Brum, JM1
Ünal, Ö1
Coskun, T1
Weisfeld-Adams, JD1
Schrager, NL1
Scholl-Bürgi, S1
Schlune, A1
Donner, MG1
Hersberger, M1
Gemperle, C1
Riesner, B1
Ulmer, H1
Häberle, J1
Karall, D1
Brosnan, JT1
Brosnan, ME1

Other Studies

3 other studies available for glycocyamine and Inborn Urea Cycle Disorder

ArticleYear
High-throughput tandem mass spectrometry multiplex analysis for newborn urinary screening of creatine synthesis and transport disorders, Triple H syndrome and OTC deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 2014, Sep-25, Volume: 436

    Topics: Biomarkers; Creatine; Creatinine; Filtration; Glycine; Humans; Hyperammonemia; Infant, Newborn; Orni

2014
Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency.
    Journal of inherited metabolic disease, 2016, Volume: 39, Issue:3

    Topics: Adolescent; Adult; Amino Acids; Arginase; Arginine; Case-Control Studies; Child; Child, Preschool; F

2016
Creatine metabolism and the urea cycle.
    Molecular genetics and metabolism, 2010, Volume: 100 Suppl 1

    Topics: Animals; Creatine; Glycine; Humans; Kidney; Urea; Urea Cycle Disorders, Inborn

2010