fura-2 has been researched along with Spastic Paraplegia, Hereditary 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 |
|---|---|
| Ho, PW; Ho, SL; Kung, MH; Li, M; Pang, SY; Sham, PC; Tse, ZH | 1 |
1 other study(ies) available for fura-2 and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion.
Topics: Asian People; Blotting, Western; Calcium; Fluorescent Dyes; Fura-2; Humans; Microscopy, Confocal; Mutation, Missense; Plasma Membrane Calcium-Transporting ATPases; Real-Time Polymerase Chain Reaction; Spastic Paraplegia, Hereditary | 2015 |