fasudil has been researched along with Bruise in 1 studies
fasudil: intracellular calcium antagonist; structure in first source
fasudil : An isoquinoline substituted by a (1,4-diazepan-1-yl)sulfonyl group at position 5. It is a Rho-kinase inhibitor and its hydrochloride hydrate form is approved for the treatment of cerebral vasospasm and cerebral ischemia.
Excerpt | Relevance | Reference |
---|---|---|
"Spinal cord contusion was induced in rats by applying an aneurysm clip extradurally to the spinal cord at T-3 for 1 minute." | 1.31 | Protein kinase inhibition by fasudil hydrochloride promotes neurological recovery after spinal cord injury in rats. ( Hara, M; Noda, A; Suzuki, Y; Takagi, T; Takayasu, M; Watanabe, K; Yoshida, J, 2000) |
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 |
---|---|
Hara, M | 1 |
Takayasu, M | 1 |
Watanabe, K | 1 |
Noda, A | 1 |
Takagi, T | 1 |
Suzuki, Y | 1 |
Yoshida, J | 1 |
1 other study available for fasudil and Bruise
Article | Year |
---|---|
Protein kinase inhibition by fasudil hydrochloride promotes neurological recovery after spinal cord injury in rats.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Analysis of Variance; Animals; Behavior, Animal; Cont | 2000 |