alanine has been researched along with Genetic Diseases, Inborn 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.
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| D'Ari, R | 1 |
| Casadesús, J | 1 |
| Barbetti, F | 1 |
| Gejman, PV | 1 |
| Taylor, SI | 1 |
| Raben, N | 1 |
| Cama, A | 1 |
| Bonora, E | 1 |
| Pizzo, P | 1 |
| Moghetti, P | 1 |
| Muggeo, M | 1 |
| Roth, J | 1 |
2 other studies available for alanine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Underground metabolism.
Topics: Alanine; Biological Evolution; Energy Metabolism; Enzymes; Genetic Diseases, Inborn; Glutamic Acid; | 1998 |
Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis.
Topics: Alanine; Alleles; Arginine; Base Sequence; Child; DNA; Electrophoresis, Polyacrylamide Gel; Exons; F | 1992 |