alanine has been researched along with Corneal Dystrophies in 3 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 | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aldave, AJ | 1 |
| Gutmark, JG | 1 |
| Yellore, VS | 1 |
| Affeldt, JA | 1 |
| Meallet, MA | 1 |
| Udar, N | 1 |
| Rao, NA | 1 |
| Small, KW | 1 |
| Klintworth, GK | 2 |
| Liu, NP | 1 |
| Smith, CF | 1 |
| Bowling, BL | 1 |
| Jonasson, F | 1 |
| Correa-Gomez, V | 1 |
| Villalvazo-Cordero, L | 1 |
| Zenteno, JC | 1 |
3 other studies available for alanine and Corneal Dystrophies
| Article | Year |
|---|---|
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
Topics: Adult; Alanine; Amyloid; Amyloidosis; Aspartic Acid; Cornea; Corneal Dystrophies, Hereditary; DNA Mu | 2004 |
Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.
Topics: Alanine; Carbohydrate Sulfotransferases; Corneal Dystrophies, Hereditary; DNA Transposable Elements; | 2006 |
The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
Topics: Adolescent; Adult; Aged; Alanine; Aspartic Acid; Base Sequence; Child; Child, Preschool; Cornea; Cor | 2007 |