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Journal of Molecular Biology|January 4, 2017
Compound Selectivity and Target Residence Time of Kinase Inhibitors Studied with Surface Plasmon ResonanceNicole Willemsen-Seegers, Joost C M Uitdehaag, Martine B W Prinsen, et al.
Bioorganic & Medicinal Chemistry|January 9, 2003
Synthesis and structure-activity relationships of 5,6,7,8-tetrahydropyrido[3,4-b]pyrazine-based hydroxamic acids as HB-EGF shedding inhibitorsKazuya Yoshiizumi, Minoru Yamamoto, Tomohiro Miyasaka, et al.
Clinical and Translational Science|November 11, 2024
Safety, pharmacokinetics, and pharmacodynamics of sofnobrutinib, a novel non-covalent BTK inhibitor, in healthy subjects: First-in-human phase I studyKyoko Miyamoto, Robert M Miller, Christine Voors-Pette, et al.
British Journal of Cancer|November 27, 2020
Pharmacological blockage of transforming growth factor-β signalling by a Traf2- and Nck-interacting kinase inhibitor, NCB-0846Teppei Sugano, Mari Masuda, Fumitaka Takeshita, et al.
Cancers|May 21, 2020
Feasibility of Targeting Traf2-and-Nck-Interacting Kinase in Synovial SarcomaTetsuya Sekita, Tesshi Yamada, Eisuke Kobayashi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 20, 2023
BCL6B Contributes to Ocular Vascular Diseases via Notch Signal SilencingMiruto Tanaka, Shinsuke Nakamura, Tomohisa Sakaue, et al.
Journal of Medicinal Chemistry|February 8, 2002
New type of metalloproteinase inhibitor: design and synthesis of new phosphonamide-based hydroxamic acidsMasaaki Sawa, Takao Kiyoi, Kiriko Kurokawa, et al.
JCI Insight|January 5, 2021
Direct conversion of osteosarcoma to adipocytes by targeting TNIKToru Hirozane, Mari Masuda, Teppei Sugano, et al.
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