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Journal of Medicinal Chemistry|July 25, 2023
Exploration of Tetrahydroisoquinoline- and Benzo[<i>c</i>]azepine-Based Sphingosine 1-Phosphate Receptor 1 Agonists for the Treatment of Multiple SclerosisEunji Cha, Jushin Kim, Lizaveta Gotina, et al.Angewandte Chemie (International Ed. in English)|November 22, 2013
Therapeutic targeting of oncogenic K-Ras by a covalent catalytic site inhibitorSang Min Lim, Kenneth D Westover, Scott B Ficarro, et al.European Journal of Medicinal Chemistry|August 14, 2018
Identification of crizotinib derivatives as potent SHIP2 inhibitors for the treatment of Alzheimer's diseaseJi Woong Lim, Seok Kyu Kim, Seo Yun Choi, et al.Experimental & Molecular Medicine|March 14, 2023
Levosimendan inhibits disulfide tau oligomerization and ameliorates tau pathology in Tau<sup>P301L</sup>-BiFC miceSungsu Lim, Seulgi Shin, Yoonsik Sung, et al.Glycoconjugate Journal|May 15, 2015
Glycan structure and serum half-life of recombinant CTLA4Ig, an immunosuppressive agent, expressed in suspension-cultured rice cells with coexpression of human β1,4-galactosyltransferase and human CTLA4IgSeung Hoon Kang, Hahn Sun Jung, Song Jae Lee, et al.Cancer Discovery|February 14, 2012
Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancerPeter S Hammerman, Martin L Sos, Alex H Ramos, et al.Pageof 7