alloxan has been researched along with Heritable Pulmonary Arterial Hypertension in 1 studies
Alloxan: Acidic compound formed by oxidation of URIC ACID. It is isolated as an efflorescent crystalline hydrate.
alloxan : A member of the class of pyrimidones, the structure of which is that of perhydropyrimidine substituted at C-2, -4, -5 and -6 by oxo groups.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Barnes, JW | 1 |
| Tian, L | 1 |
| Heresi, GA | 1 |
| Farver, CF | 1 |
| Asosingh, K | 1 |
| Comhair, SA | 1 |
| Aulak, KS | 1 |
| Dweik, RA | 1 |
1 other study available for alloxan and Heritable Pulmonary Arterial Hypertension
| Article | Year |
|---|---|
O-linked β-N-acetylglucosamine transferase directs cell proliferation in idiopathic pulmonary arterial hypertension.
Topics: Adult; Alloxan; Cell Division; Cells, Cultured; Disease Progression; Familial Primary Pulmonary Hype | 2015 |