Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yasuhito Uezono

Showing results (131-140 of 183) with videos related to

Pageof 19
Sort By:
Biological & Pharmaceutical Bulletin|December 5, 2017
Active Ingredients of Hange-shashin-to, Baicalelin and 6-Gingerol, Inhibit 5-Fluorouracil-Induced Upregulation of CXCL1 in the Colon to Attenuate Diarrhea DevelopmentHiroyasu Sakai, Shoko Tabata, Minami Kimura, et al.
Peptides|November 8, 2022
The first structure-activity relationship study of oxytocin as a positive allosteric modulator for the µ opioid receptorTakaaki Mizuguchi, Kanako Miyano, Risa Yamauchi, et al.
Molecular Pain|June 19, 2016
Characterization of methadone as a β-arrestin-biased μ-opioid receptor agonistSeira Doi, Tomohisa Mori, Naoki Uzawa, et al.
Biomolecules|March 25, 2022
Ketamine Improves Desensitization of µ-Opioid Receptors Induced by Repeated Treatment with Fentanyl but Not with MorphineYusuke Mizobuchi, Kanako Miyano, Sei Manabe, et al.
Anesthesia and Analgesia|April 15, 2021
Local Anesthetics Inhibit Transient Receptor Potential Vanilloid Subtype 3 Channel Function in Xenopus OocytesReiko Horishita, Yuichi Ogata, Ryo Fukui, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 15, 2017
Antidepressants inhibit Na<sub>v</sub>1.3, Na<sub>v</sub>1.7, and Na<sub>v</sub>1.8 neuronal voltage-gated sodium channels more potently than Na<sub>v</sub>1.2 and Na<sub>v</sub>1.6 channels expressed in Xenopus oocytesTakafumi Horishita, Nobuyuki Yanagihara, Susumu Ueno, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 6, 2023
G protein-biased LPAR1 agonism of prototypic antidepressants: Implication in the identification of novel therapeutic target for depressionNaoto Kajitani, Mami Okada-Tsuchioka, Asuka Inoue, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 26, 2017
Relief from neuropathic pain by blocking of the platelet-activating factor-pain loopHideo Shindou, Seiji Shiraishi, Suzumi M Tokuoka, et al.
The Journal of Toxicological Sciences|August 7, 2012
Increased expression of aquaporin-4 with methylmercury exposure in the brain of the common marmosetMegumi Yamamoto, Motohiro Takeya, Hiroko Ikeshima-Kataoka, et al.
Synapse (New York, N.Y.)|March 26, 2011
Possible involvement of β-endorphin in a loss of the coordinated balance of μ-opioid receptors trafficking processes by fentanylSatoshi Imai, Yuka Sudo, Atsushi Nakamura, et al.
Pageof 19

Showing results (131-140 of 183) with videos related to

Sort By:
Pageof 19
Biological & Pharmaceutical Bulletin|December 5, 2017
Active Ingredients of Hange-shashin-to, Baicalelin and 6-Gingerol, Inhibit 5-Fluorouracil-Induced Upregulation of CXCL1 in the Colon to Attenuate Diarrhea DevelopmentHiroyasu Sakai, Shoko Tabata, Minami Kimura, et al.
Peptides|November 8, 2022
The first structure-activity relationship study of oxytocin as a positive allosteric modulator for the µ opioid receptorTakaaki Mizuguchi, Kanako Miyano, Risa Yamauchi, et al.
Molecular Pain|June 19, 2016
Characterization of methadone as a β-arrestin-biased μ-opioid receptor agonistSeira Doi, Tomohisa Mori, Naoki Uzawa, et al.
Biomolecules|March 25, 2022
Ketamine Improves Desensitization of µ-Opioid Receptors Induced by Repeated Treatment with Fentanyl but Not with MorphineYusuke Mizobuchi, Kanako Miyano, Sei Manabe, et al.
Anesthesia and Analgesia|April 15, 2021
Local Anesthetics Inhibit Transient Receptor Potential Vanilloid Subtype 3 Channel Function in Xenopus OocytesReiko Horishita, Yuichi Ogata, Ryo Fukui, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 15, 2017
Antidepressants inhibit Na<sub>v</sub>1.3, Na<sub>v</sub>1.7, and Na<sub>v</sub>1.8 neuronal voltage-gated sodium channels more potently than Na<sub>v</sub>1.2 and Na<sub>v</sub>1.6 channels expressed in Xenopus oocytesTakafumi Horishita, Nobuyuki Yanagihara, Susumu Ueno, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 6, 2023
G protein-biased LPAR1 agonism of prototypic antidepressants: Implication in the identification of novel therapeutic target for depressionNaoto Kajitani, Mami Okada-Tsuchioka, Asuka Inoue, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 26, 2017
Relief from neuropathic pain by blocking of the platelet-activating factor-pain loopHideo Shindou, Seiji Shiraishi, Suzumi M Tokuoka, et al.
The Journal of Toxicological Sciences|August 7, 2012
Increased expression of aquaporin-4 with methylmercury exposure in the brain of the common marmosetMegumi Yamamoto, Motohiro Takeya, Hiroko Ikeshima-Kataoka, et al.
Synapse (New York, N.Y.)|March 26, 2011
Possible involvement of β-endorphin in a loss of the coordinated balance of μ-opioid receptors trafficking processes by fentanylSatoshi Imai, Yuka Sudo, Atsushi Nakamura, et al.
Pageof 19