fura-2-am has been researched along with Deafness in 1 studies
| 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 |
|---|---|
| Brini, M; Campeol, M; Carafoli, E; De Mario, A; Giacomello, M; Lopreiato, R; Primerano, S | 1 |
1 other study(ies) available for fura-2-am and Deafness
| Article | Year |
|---|---|
Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect.
Topics: Animals; Blotting, Western; Calcium; Calcium Signaling; Cell Line; Deafness; Endoplasmic Reticulum; Fura-2; HeLa Cells; Humans; Mice; Mutation; Plasma Membrane Calcium-Transporting ATPases | 2011 |