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International Journal of Biological Sciences|January 14, 2020
Soluble CD83 alleviates experimental allergic rhinitis through modulating antigen-specific Th2 cell propertyYong-Jin Wu, Yan-Nan Song, Xiao-Rui Geng, et al.Archives of Biochemistry and Biophysics|September 16, 2018
Bcl2L12 mediates effects of protease-activated receptor-2 on the pathogenesis of Th2-dominated responses of patients with ulcerative colitisBai-Sui Feng, Yong-Jin Wu, Xian-Hai Zeng, et al.Journal of the American Chemical Society|June 26, 2024
Cu-Catalyzed Amination of Base-Sensitive Aryl Bromides and the Chemoselective N- and O-Arylation of Amino AlcoholsMichael J Strauss, Kaylee X Liu, Megan E Greaves, et al.Bioorganic & Medicinal Chemistry Letters|November 7, 2016
Discovery of furo[2,3-d][1,3]thiazinamines as beta amyloid cleaving enzyme-1 (BACE1) inhibitorsYong-Jin Wu, Jason Guernon, Ramkumar Rajamani, et al.Journal of Medicinal Chemistry|May 14, 2004
Synthesis and structure-activity relationship of acrylamides as KCNQ2 potassium channel openersYong-Jin Wu, Huan He, Li-Qiang Sun, et al.Journal of Medicinal Chemistry|October 31, 2003
Identification of a potent and selective 5-HT(6) antagonist: one-step synthesis of (E)-3-(benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from 2-(benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrileYong-Jin Wu, Huan He, Shuanghua Hu, et al.Bioorganic & Medicinal Chemistry Letters|February 11, 2014
Discovery of a cyclopentylamine as an orally active dual NK1 receptor antagonist-serotonin reuptake transporter inhibitorYong-Jin Wu, Huan He, Qi Gao, et al.International Forum of Allergy & Rhinology|July 15, 2018
Histone deacetylase 11 inhibits interleukin 10 in B cells of subjects with allergic rhinitisJian-Bo Shao, Xiang-Qian Luo, Yong-Jin Wu, et al.Bioorganic & Medicinal Chemistry|February 6, 2014
Structure activity relationship studies of 3-arylsulfonyl-pyrido[1,2-a]pyrimidin-4-imines as potent 5-HT₆ antagonistsShuanghua Hu, Yazhong Huang, Yong-Jin Wu, et al.Bioorganic & Medicinal Chemistry Letters|December 18, 2004
(S,E)-N-[1-(3-heteroarylphenyl)ethyl]-3-(2-fluorophenyl)acrylamides: synthesis and KCNQ2 potassium channel opener activityAlexandre L'Heureux, Alain Martel, Huan He, et al.Pageof 4