glycine has been researched along with Pseudohypoaldosteronism in 1 studies
Pseudohypoaldosteronism: A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pseudohypoaldosteronism type 1 (PHA-1) is an inherited disease characterized by severe neonatal salt-wasting and caused by mutations in subunits of the amiloride-sensitive epithelial sodium channel (ENaC)." | 7.69 | A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel. ( Chang, SS; Firsov, D; Gautschi, I; Gründer, S; Jaeger, NF; Lifton, RP; Rossier, BC; Schild, L, 1997) |
| "Pseudohypoaldosteronism type 1 (PHA-1) is an inherited disease characterized by severe neonatal salt-wasting and caused by mutations in subunits of the amiloride-sensitive epithelial sodium channel (ENaC)." | 3.69 | A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel. ( Chang, SS; Firsov, D; Gautschi, I; Gründer, S; Jaeger, NF; Lifton, RP; Rossier, BC; Schild, L, 1997) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Gründer, S | 1 |
| Firsov, D | 1 |
| Chang, SS | 1 |
| Jaeger, NF | 1 |
| Gautschi, I | 1 |
| Schild, L | 1 |
| Lifton, RP | 1 |
| Rossier, BC | 1 |
1 other study available for glycine and Pseudohypoaldosteronism
| Article | Year |
|---|---|
A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel.
Topics: Amiloride; Amino Acid Sequence; Animals; Conserved Sequence; Epithelial Sodium Channels; Glycine; Hu | 1997 |