Showing results (71-80 of 77) with videos related to
Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Bioorganic & Medicinal Chemistry Letters|August 28, 2003
Synthesis and evaluation of 4-anilino-6,7-dialkoxy-3-quinolinecarbonitriles as inhibitors of kinases of the Ras-MAPK signaling cascadeDan Berger, Minu Dutia, Dennis Powell, et al.Cancer Research|June 3, 2004
Antitumor activity of HKI-272, an orally active, irreversible inhibitor of the HER-2 tyrosine kinaseSridhar K Rabindran, Carolyn M Discafani, Edward C Rosfjord, et al.Journal of Medicinal Chemistry|February 18, 2005
Optimization of 6,7-disubstituted-4-(arylamino)quinoline-3-carbonitriles as orally active, irreversible inhibitors of human epidermal growth factor receptor-2 kinase activityHwei-Ru Tsou, Elsebe G Overbeek-Klumpers, William A Hallett, et al.Journal of Racial and Ethnic Health Disparities|October 31, 2020
Vital Voices: HIV Prevention and Care Interventions Developed for Disproportionately Affected Communities by Historically Underrepresented, Early-Career ScientistsMadeline Y Sutton, Omar Martinez, Bridgette M Brawner, et al.The Journal of Biological Chemistry|June 27, 1997
Cloning, in vitro expression, and functional characterization of a novel human CC chemokine of the monocyte chemotactic protein (MCP) family (MCP-4) that binds and signals through the CC chemokine receptor 2BT A Berkhout, H M Sarau, K Moores, et al.Journal of Medicinal Chemistry|December 28, 2002
Synthesis and structure-activity relationships of 6,7-disubstituted 4-anilinoquinoline-3-carbonitriles. The design of an orally active, irreversible inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor-2 (HER-2)Allan Wissner, Elsebe Overbeek, Marvin F Reich, et al.Journal of Leukocyte Biology|November 19, 1997
Cloning and functional characterization of a novel human CC chemokine that binds to the CCR3 receptor and activates human eosinophilsJ R White, C Imburgia, E Dul, et al.Pageof 8