aurin has been researched along with Cystic Fibrosis in 1 studies
aurin: structure
Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
| 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 |
|---|---|
| Marzaro, G | 1 |
| Guiotto, A | 1 |
| Borgatti, M | 1 |
| Finotti, A | 1 |
| Gambari, R | 1 |
| Breveglieri, G | 1 |
| Chilin, A | 1 |
1 other study available for aurin and Cystic Fibrosis
| Article | Year |
|---|---|
Psoralen derivatives as inhibitors of NF-κB/DNA interaction: synthesis, molecular modeling, 3D-QSAR, and biological evaluation.
Topics: Anti-Inflammatory Agents; Binding Sites; Cystic Fibrosis; DNA; Furocoumarins; Inhibitory Concentrati | 2013 |