alanine has been researched along with Lipid Metabolism, Inborn Error in 5 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 | 2 (40.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ørngreen, MC | 1 |
| Ejstrup, R | 1 |
| Vissing, J | 1 |
| Martinez, G | 1 |
| Garcia-Lozano, JR | 1 |
| Ribes, A | 1 |
| Maldonado, MD | 1 |
| Baldellou, A | 1 |
| de Pablo, R | 1 |
| Nuñez-Roldan, A | 1 |
| Souri, M | 1 |
| Aoyama, T | 1 |
| Yamaguchi, S | 1 |
| Hashimoto, T | 1 |
| Engel, PC | 1 |
| Boisse, J | 1 |
1 review available for alanine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
[New etiologic approach to periodic ketoacidosis in children].
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Ch | 1971 |
1 trial available for alanine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Effect of diet on exercise tolerance in carnitine palmitoyltransferase II deficiency.
Topics: Alanine; Blood Glucose; Carnitine O-Palmitoyltransferase; Creatine Kinase; Creatine Kinase, MM Form; | 2003 |
3 other studies available for alanine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
High risk of medium chain acyl-coenzyme A dehydrogenase deficiency among gypsies.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Alanine; Alleles; Gene Frequency; Genetic Carrier S | 1998 |
Relationship between structure and substrate-chain-length specificity of mitochondrial very-long-chain acyl-coenzyme A dehydrogenase.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase, Long-Chain; Alanine; Base Sequence; Cells, Cultured; DNA Pr | 1998 |
Possibility of inborn defect in isovalericacidaemia involving altered enzyme specificity rather than total inactivity.
Topics: Alanine; Butyrates; Coenzyme A; Cyclopropanes; Humans; Kinetics; Leucine; Lipid Metabolism, Inborn E | 1974 |