alanine has been researched along with Deficiency, Factor II in 1 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Prothrombin deficiency is a rare (1:200 000) autosomal recessive disorder caused by diverse mutations in prothrombin gene." | 1.33 | Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation. ( Baidya, S; Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A; Viswabandya, A, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jayandharan, G | 1 |
| Viswabandya, A | 1 |
| Baidya, S | 1 |
| Nair, SC | 1 |
| Shaji, RV | 1 |
| Chandy, M | 1 |
| Srivastava, A | 1 |
1 other study available for alanine and Deficiency, Factor II
| Article | Year |
|---|---|
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.
Topics: Adult; Alanine; Alternative Splicing; Child, Preschool; Codon; DNA; DNA Mutational Analysis; DNA Pri | 2005 |