alanine has been researched along with Sphingolipid Storage Diseases 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 |
|---|---|
| Baenziger, JU | 1 |
| Dierks, T | 2 |
| Schmidt, B | 2 |
| Borissenko, LV | 1 |
| Peng, J | 1 |
| Preusser, A | 1 |
| Mariappan, M | 2 |
| von Figura, K | 2 |
| Dickmanns, A | 1 |
| Preusser-Kunze, A | 1 |
| Ficner, R | 1 |
| Rudolph, MG | 1 |
1 review available for alanine and Sphingolipid Storage Diseases
| Article | Year |
|---|---|
A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease.
Topics: Alanine; Animals; Catalytic Domain; Gene Expression Regulation, Enzymologic; Glycine; Humans; Mutati | 2003 |
2 other studies available for alanine and Sphingolipid Storage Diseases
| Article | Year |
|---|---|
Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme.
Topics: Alanine; Amino Acid Sequence; Animals; Base Sequence; Biological Assay; Cattle; CHO Cells; Chromosom | 2003 |
Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.
Topics: Alanine; Amino Acid Sequence; Binding Sites; Calcium; Catalytic Domain; Crystallography, X-Ray; Cyst | 2005 |