alanine has been researched along with ACY2 Deficiency in 2 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Janson, CG | 1 |
| Kolodny, EH | 1 |
| Zeng, BJ | 1 |
| Raghavan, S | 1 |
| Pastores, G | 1 |
| Torres, P | 1 |
| Assadi, M | 1 |
| McPhee, S | 1 |
| Goldfarb, O | 1 |
| Saslow, B | 1 |
| Freese, A | 1 |
| Wang, DJ | 1 |
| Bilaniuk, L | 1 |
| Shera, D | 1 |
| Leone, P | 1 |
| Velinov, M | 1 |
| Zellers, N | 1 |
| Styles, J | 1 |
| Wisniewski, K | 1 |
2 other studies available for alanine and ACY2 Deficiency
| Article | Year |
|---|---|
Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene.
Topics: Adult; Alanine; Amidohydrolases; Aspartic Acid; Canavan Disease; DNA Mutational Analysis; Female; Gl | 2006 |
Homozygosity for mutation G212A of the gene for aspartoacylase is associated with atypical form of Canavan's disease.
Topics: Alanine; Amidohydrolases; Amino Acid Substitution; Aspartic Acid; Canavan Disease; Child, Preschool; | 2008 |