ibuprofen has been researched along with Muscular Dystrophy, Oculopharyngeal in 1 studies
Midol: combination of cinnamedrine, phenacetin, aspirin & caffeine
Muscular Dystrophy, Oculopharyngeal: An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.
| 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 |
|---|---|
| Wang, Q | 1 |
| Mosser, DD | 1 |
| Bag, J | 1 |
1 other study available for ibuprofen and Muscular Dystrophy, Oculopharyngeal
| Article | Year |
|---|---|
Induction of HSP70 expression and recruitment of HSC70 and HSP70 in the nucleus reduce aggregation of a polyalanine expansion mutant of PABPN1 in HeLa cells.
Topics: Active Transport, Cell Nucleus; Cell Nucleus; Green Fluorescent Proteins; HeLa Cells; HSC70 Heat-Sho | 2005 |