alanine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia in 1 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Roxburgh, RH | 1 |
| Marquis-Nicholson, R | 1 |
| Ashton, F | 1 |
| George, AM | 1 |
| Lea, RA | 1 |
| Eccles, D | 1 |
| Mossman, S | 1 |
| Bird, T | 1 |
| van Gassen, KL | 1 |
| Kamsteeg, EJ | 1 |
| Love, DR | 1 |
1 other study available for alanine and Autosomal Dominant Hereditary Spastic Paraplegia
| Article | Year |
|---|---|
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry.
Topics: Adult; Age of Onset; Alanine; ATPases Associated with Diverse Cellular Activities; Female; Genetic P | 2013 |