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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Creatine synthesis is a major component of arginine metabolism, amounting to more than 20% of the dietary intake of this amino acid." | 1.36 | Creatine metabolism and the urea cycle. ( Brosnan, JT; Brosnan, ME, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auray-Blais, C | 1 |
| Maranda, B | 1 |
| Lavoie, P | 1 |
| Huemer, M | 1 |
| Carvalho, DR | 1 |
| Brum, JM | 1 |
| Ünal, Ö | 1 |
| Coskun, T | 1 |
| Weisfeld-Adams, JD | 1 |
| Schrager, NL | 1 |
| Scholl-Bürgi, S | 1 |
| Schlune, A | 1 |
| Donner, MG | 1 |
| Hersberger, M | 1 |
| Gemperle, C | 1 |
| Riesner, B | 1 |
| Ulmer, H | 1 |
| Häberle, J | 1 |
| Karall, D | 1 |
| Brosnan, JT | 1 |
| Brosnan, ME | 1 |
3 other studies available for glycocyamine and Inborn Urea Cycle Disorder
| Article | Year |
|---|---|
High-throughput tandem mass spectrometry multiplex analysis for newborn urinary screening of creatine synthesis and transport disorders, Triple H syndrome and OTC deficiency.
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.
Topics: Adolescent; Adult; Amino Acids; Arginase; Arginine; Case-Control Studies; Child; Child, Preschool; F | 2016 |
Creatine metabolism and the urea cycle.
Topics: Animals; Creatine; Glycine; Humans; Kidney; Urea; Urea Cycle Disorders, Inborn | 2010 |