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Yasuhito Uezono

Showing results (51-60 of 183) with videos related to

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Plos One|March 19, 2014
Palliation of bone cancer pain by antagonists of platelet-activating factor receptorsKatsuya Morita, Seiji Shiraishi, Naoyo Motoyama, et al.
Anesthesia and Analgesia|February 22, 2014
The endocannabinoid anandamide inhibits voltage-gated sodium channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 in Xenopus oocytesDan Okura, Takafumi Horishita, Susumu Ueno, et al.
Anesthesia and Analgesia|April 24, 2004
The inhibitory effects of tramadol on 5-hydroxytryptamine type 2C receptors expressed in Xenopus oocytesJunichi Ogata, Kouichiro Minami, Yasuhito Uezono, et al.
Anesthesia and Analgesia|February 28, 2002
Tramadol has no effect on cortical renal blood flow--despite increased serum catecholamine levels--in anesthetized rats: implications for analgesia in renal insufficiencyEtsuko Nagaoka, Kouichiro Minami, Yohsuke Shiga, et al.
Journal of Pharmacological Sciences|November 7, 2009
Presence of GABA(B) receptors forming heterodimers with GABA(B1) and GABA(B2) subunits in human lower esophageal sphincterYasuhiro Torashima, Yasuhito Uezono, Masato Kanaide, et al.
Journal of Pharmacological Sciences|May 31, 2022
Involvement of spinal G-protein inwardly rectifying potassium (GIRK) channels in the enhanced antinociceptive effects of the activation of both μ-opioid and cannabinoid CB<sub>1</sub> receptorsYoshinori Takemura, Yuka Sudo, Tomoya Saeki, et al.
Anesthesia and Analgesia|June 24, 2003
The inhibitory effects of ketamine and pentobarbital on substance p receptors expressed in Xenopus oocytesTakashi Okamoto, Kouichiro Minami, Yasuhito Uezono, et al.
Pharmacology|May 9, 2006
The tramadol metabolite, O-desmethyl tramadol, inhibits 5-hydroxytryptamine type 2C receptors expressed in Xenopus OocytesTakafumi Horishita, Kouichiro Minami, Yasuhito Uezono, et al.
Journal of Clinical Medicine|July 2, 2021
Time-Course of Salivary Metabolomic Profiles during Radiation Therapy for Head and Neck CancerWakako Yatsuoka, Takao Ueno, Kanako Miyano, et al.
Journal of Pharmacological Sciences|August 11, 2012
Inhibition by pregnenolone sulphate, a metabolite of the neurosteroid pregnenolone, of voltage-gated sodium channels expressed in Xenopus oocytesTakafumi Horishita, Susumu Ueno, Nobuyuki Yanagihara, et al.
Pageof 19

Showing results (51-60 of 183) with videos related to

Sort By:
Pageof 19
Plos One|March 19, 2014
Palliation of bone cancer pain by antagonists of platelet-activating factor receptorsKatsuya Morita, Seiji Shiraishi, Naoyo Motoyama, et al.
Anesthesia and Analgesia|February 22, 2014
The endocannabinoid anandamide inhibits voltage-gated sodium channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 in Xenopus oocytesDan Okura, Takafumi Horishita, Susumu Ueno, et al.
Anesthesia and Analgesia|April 24, 2004
The inhibitory effects of tramadol on 5-hydroxytryptamine type 2C receptors expressed in Xenopus oocytesJunichi Ogata, Kouichiro Minami, Yasuhito Uezono, et al.
Anesthesia and Analgesia|February 28, 2002
Tramadol has no effect on cortical renal blood flow--despite increased serum catecholamine levels--in anesthetized rats: implications for analgesia in renal insufficiencyEtsuko Nagaoka, Kouichiro Minami, Yohsuke Shiga, et al.
Journal of Pharmacological Sciences|November 7, 2009
Presence of GABA(B) receptors forming heterodimers with GABA(B1) and GABA(B2) subunits in human lower esophageal sphincterYasuhiro Torashima, Yasuhito Uezono, Masato Kanaide, et al.
Journal of Pharmacological Sciences|May 31, 2022
Involvement of spinal G-protein inwardly rectifying potassium (GIRK) channels in the enhanced antinociceptive effects of the activation of both μ-opioid and cannabinoid CB<sub>1</sub> receptorsYoshinori Takemura, Yuka Sudo, Tomoya Saeki, et al.
Anesthesia and Analgesia|June 24, 2003
The inhibitory effects of ketamine and pentobarbital on substance p receptors expressed in Xenopus oocytesTakashi Okamoto, Kouichiro Minami, Yasuhito Uezono, et al.
Pharmacology|May 9, 2006
The tramadol metabolite, O-desmethyl tramadol, inhibits 5-hydroxytryptamine type 2C receptors expressed in Xenopus OocytesTakafumi Horishita, Kouichiro Minami, Yasuhito Uezono, et al.
Journal of Clinical Medicine|July 2, 2021
Time-Course of Salivary Metabolomic Profiles during Radiation Therapy for Head and Neck CancerWakako Yatsuoka, Takao Ueno, Kanako Miyano, et al.
Journal of Pharmacological Sciences|August 11, 2012
Inhibition by pregnenolone sulphate, a metabolite of the neurosteroid pregnenolone, of voltage-gated sodium channels expressed in Xenopus oocytesTakafumi Horishita, Susumu Ueno, Nobuyuki Yanagihara, et al.
Pageof 19