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Neuropharmacology|November 23, 2013
Bladder pain relief by HMGB1 neutralization and soluble thrombomodulin in mice with cyclophosphamide-induced cystitisJunichi Tanaka, Kaoru Yamaguchi, Hiroyasu Ishikura, et al.Toxicology|July 31, 2016
Involvement of high mobility group box 1 in the development and maintenance of chemotherapy-induced peripheral neuropathy in ratsTakeshi Nishida, Maho Tsubota, Yudai Kawaishi, et al.Journal of Neurochemistry|December 5, 2008
Hydrogen sulfide evokes neurite outgrowth and expression of high-voltage-activated Ca2+ currents in NG108-15 cells: involvement of T-type Ca2+ channelsKeita Nagasawa, Takeshi Tarui, Shigeru Yoshida, et al.Toxicology|August 4, 2009
Rhodanese, but not cystathionine-gamma-lyase, is associated with dextran sulfate sodium-evoked colitis in mice: a sign of impaired colonic sulfide detoxification?Eiichi Taniguchi, Maho Matsunami, Takeshi Kimura, et al.Biological & Pharmaceutical Bulletin|June 10, 2004
Neutralizing antibody evasion ability of adenovirus vector induced by the bioconjugation of methoxypolyethylene glycol succinimidyl propionate (MPEG-SPA)Yusuke Eto, Jian-Qing Gao, Fumiko Sekiguchi, et al.Journal of Pharmacological Sciences|February 18, 2016
Peripheral HMGB1-induced hyperalgesia in mice: Redox state-dependent distinct roles of RAGE and TLR4Daichi Yamasoba, Maho Tsubota, Risa Domoto, et al.British Journal of Pharmacology|June 1, 2012
Involvement of the endogenous hydrogen sulfide/Ca(v) 3.2 T-type Ca2+ channel pathway in cystitis-related bladder pain in miceMaho Matsunami, Takahiro Miki, Kanae Nishiura, et al.Pain|March 30, 2016
Therapeutic potential of RQ-00311651, a novel T-type Ca2+ channel blocker, in distinct rodent models for neuropathic and visceral painFumiko Sekiguchi, Yuma Kawara, Maho Tsubota, et al.Toxicology|December 16, 2018
Critical role of Cav3.2 T-type calcium channels in the peripheral neuropathy induced by bortezomib, a proteasome-inhibiting chemotherapeutic agent, in miceShiori Tomita, Fumiko Sekiguchi, Tomoyo Deguchi, et al.The Journal of Pharmacology and Experimental Therapeutics|February 21, 2004
Potent and metabolically stable agonists for protease-activated receptor-2: evaluation of activity in multiple assay systems in vitro and in vivoAtsufumi Kawabata, Toru Kanke, Daiki Yonezawa, et al.Pageof 13