glycine has been researched along with Inborn Urea Cycle Disorder in 5 studies
| 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 | 5 (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 |
| Jung, CW | 1 |
| Lee, BH | 1 |
| Kim, JH | 1 |
| Kim, GH | 1 |
| Lee, J | 1 |
| Choi, JH | 1 |
| Yoo, HW | 1 |
| Morscher, RJ | 1 |
| Grünert, SC | 1 |
| Bürer, C | 1 |
| Burda, P | 1 |
| Suormala, T | 1 |
| Fowler, B | 1 |
| Baumgartner, MR | 1 |
5 other studies available for glycine 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 |
Uneventful clinical courses of Korean patients with methylcrotonylglycinuria and their common mutations.
Topics: Asian People; Carbon-Carbon Ligases; Child; Child, Preschool; Disease Progression; Female; Glycine; | 2012 |
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency.
Topics: Acyl Coenzyme A; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child; Child, Preschool; DNA Mut | 2012 |