Zobrazeno 1 - 10
of 222
pro vyhledávání: '"Satoh, Masamichi"'
Autor:
Deyama, Satoshi 1, 2, Takishita, Azusa 2, Tanimoto, Sachi 2, Ide, Soichiro 1, Nakagawa, Takayuki 2, Satoh, Masamichi 3, Minami, Masabumi 1, *
Publikováno v:
In Journal of Pharmacological Sciences 2010 114(1):123-126
Autor:
Ueda, Hiroshi, Harada, Hitoshi, Nozaki, Masakatsu, Katada, Toshiaki, Ui, Michio, Satoh, Masamichi, Takagi, Hiroshi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1988 Sep . 85(18), 7013-7017.
Externí odkaz:
https://www.jstor.org/stable/32513
Publikováno v:
In Journal of Pharmacological Sciences 2006 100(5):461-470
Autor:
Fujio, Mayumi 1, Nakagawa, Takayuki 1, *, Suzuki, Yuichi 1, Satoh, Masamichi 2, Kaneko, Shuji 1
Publikováno v:
In Journal of Pharmacological Sciences 2005 99(4):415-418
Autor:
Fukui, Masato 1, Takishita, Azusa 1, Zhang, Nannan 1, Nakagawa, Takayuki 1, Minami, Masabumi 1, Satoh, Masamichi 1, *
Publikováno v:
In Journal of Pharmacological Sciences 2004 94(2):153-160
Publikováno v:
Molecular Pain, Vol 7, Iss 1, p 23 (2011)
Abstract Background (-)-Pentazocine has been hypothesized to induce analgesia via the κ-opioid (KOP) receptor, although the involvement of other opioid receptor subtypes in the effects of pentazocine remains unknown. In this study, we investigated t
Externí odkaz:
https://doaj.org/article/43822bc3ec0c449dbbe968e4dc1adab6
Publikováno v:
Molecular Pain, Vol 2, Iss 1, p 19 (2006)
Abstract Extracellular ATP is known to mediate synaptic transmission as a neurotransmitter or a neuromodulator via ionotropic P2X and metabotropic P2Y receptors. Several lines of evidence have suggested that ATP facilitates pain transmission at perip
Externí odkaz:
https://doaj.org/article/ee97098688044a75b3047adac29533f3
Publikováno v:
In European Journal of Pharmacology 2001 433(1):29-36
Autor:
Nakagawa, Takayuki, Ozawa, Tohru, Shige, Kaori, Yamamoto, Rie, Minami, Masabumi, Satoh, Masamichi *
Publikováno v:
In European Journal of Pharmacology 2001 419(1):39-45
Publikováno v:
In European Journal of Pharmacology 2001 419(1):25-31