rsr 4 has been researched along with alpha-Thalassemia in 1 studies
*alpha-Thalassemia: A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. [MeSH]
| 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 |
|---|---|
| Abraham, DJ; Griffon, N; Kanavakis, E; Kister, J; Marden, MC; Papassotiriou, I; Poyart, C; Stamoulakatou, A; Traeger-Synodinos, J | 1 |
1 trial(s) available for rsr 4 and alpha-Thalassemia
| Article | Year |
|---|---|
Synthesized allosteric effectors of the hemoglobin molecule: a possible mechanism for improved erythrocyte oxygen release capability in hemoglobinopathy H disease.
Topics: Allosteric Regulation; alpha-Thalassemia; Aniline Compounds; Erythrocytes; Hemoglobins; Humans; Molecular Structure; Oxygen; Propionates | 1998 |