glycine has been researched along with Acquired Nephrogenic Diabetes Insipidus in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mutations in AQP2 cause autosomal nephrogenic diabetes insipidus (NDI), a disease that renders the kidney unresponsive to vasopressin, resulting in polyuria and polydipsia." | 1.35 | Repulsion between Lys258 and upstream arginines explains the missorting of the AQP2 mutant p.Glu258Lys in nephrogenic diabetes insipidus. ( Deen, PM; Kamsteeg, EJ; Konings, IB; Stoffels, M; Tamma, G, 2009) |
| 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 |
|---|---|
| Kamsteeg, EJ | 1 |
| Stoffels, M | 1 |
| Tamma, G | 1 |
| Konings, IB | 1 |
| Deen, PM | 1 |
1 other study available for glycine and Acquired Nephrogenic Diabetes Insipidus
| Article | Year |
|---|---|
Repulsion between Lys258 and upstream arginines explains the missorting of the AQP2 mutant p.Glu258Lys in nephrogenic diabetes insipidus.
Topics: Amino Acid Sequence; Aquaporin 2; Arginine; Cell Compartmentation; Diabetes Insipidus, Nephrogenic; | 2009 |