alanine has been researched along with Hereditary Optic Atrophy 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 | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kalinin, VN | 1 |
| Schmidt, W | 1 |
| Poller, W | 1 |
| Olek, K | 1 |
| Zickermann, V | 1 |
| Barquera, B | 1 |
| Wikström, M | 1 |
| Finel, M | 1 |
| Batandier, C | 1 |
| Picard, A | 1 |
| Tessier, N | 1 |
| Lunardi, J | 1 |
3 other studies available for alanine and Hereditary Optic Atrophy
| Article | Year |
|---|---|
[A new point mutation in the mitochondrial gene ND1, detected in a patient with type II diabetes].
Topics: Alanine; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Humans; NADH Dehydrogenase; Optic Atrophies, | 1995 |
Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans.
Topics: Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Conserved Sequence; DNA, Mitochondrial; Electr | 1998 |
Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.
Topics: Alanine; Amino Acid Substitution; DNA, Mitochondrial; Electron Transport Complex I; Female; Humans; | 2000 |