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Shin-ichi Satoh

Pharmaceuticals Research Center

Asahi Kasei Pharma Corporation

Izunokuni-shi

Shizuoka 410-2321

Japan

[email]@om.asahi-kasei.co.jp

Name/email consistency: medium

 
 
 
 
 
 
 

Affiliations

  • Pharmaceuticals Research Center, Asahi Kasei Pharma Corporation, Izunokuni-shi, Shizuoka 410-2321, Japan. 2007 - 2011
  • Institute for Life Science Research, Asahi Kasei Corporation, Tagata-Gun, Japan. 2001 - 2002

References

  1. Fasudil protects cultured N1E-115 cells against lysophosphatidic acid-induced neurite retraction through inhibition of Rho-kinase. Satoh, S., Kawasaki, K., Hitomi, A., Ikegaki, I., Asano, T. Brain Res. Bull. (2011) [Pubmed]
  2. Amelioration of endothelial damage/dysfunction is a possible mechanism for the neuroprotective effects of Rho-kinase inhibitors against ischemic brain damage. Satoh, S., Hitomi, A., Ikegaki, I., Kawasaki, K., Nakazono, O., Iwasaki, M., Mohri, M., Asano, T. Brain Res. Bull. (2010) [Pubmed]
  3. Wide therapeutic time window for Rho-kinase inhibition therapy in ischemic brain damage in a rat cerebral thrombosis model. Satoh, S., Toshima, Y., Hitomi, A., Ikegaki, I., Seto, M., Asano, T. Brain Res. (2008) [Pubmed]
  4. Wide therapeutic time window for fasudil neuroprotection against ischemia-induced delayed neuronal death in gerbils. Satoh, S., Toshima, Y., Ikegaki, I., Iwasaki, M., Asano, T. Brain Res. (2007) [Pubmed]
  5. Fasudil attenuates interstitial fibrosis in rat kidneys with unilateral ureteral obstruction. Satoh, S., Yamaguchi, T., Hitomi, A., Sato, N., Shiraiwa, K., Ikegaki, I., Asano, T., Shimokawa, H. Eur. J. Pharmacol. (2002) [Pubmed]
  6. Pharmacological profile of hydroxy fasudil as a selective rho kinase inhibitor on ischemic brain damage. Satoh, S., Utsunomiya, T., Tsurui, K., Kobayashi, T., Ikegaki, I., Sasaki, Y., Asano, T. Life Sci. (2001) [Pubmed]
  7. Antiischemic properties of fasudil in experimental models of vasospastic angina. Sato, S., Ikegaki, I., Asano, T., Shimokawa, H. Jpn. J. Pharmacol. (2001) [Pubmed]
 
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