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Acta Neuropathologica Communications|March 18, 2017
A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosisJohnathan Cooper-Knock, Claire Green, Gabriel Altschuler, et al.ACS Medicinal Chemistry Letters|May 20, 2017
Discovery of GSK2193874: An Orally Active, Potent, and Selective Blocker of Transient Receptor Potential Vanilloid 4Mui Cheung, Weike Bao, David J Behm, et al.Breast Cancer Research and Treatment|December 28, 2014
Weekly paclitaxel and concurrent pazopanib following doxorubicin and cyclophosphamide as neoadjuvant therapy for HER-negative locally advanced breast cancer: NSABP Foundation FB-6, a phase II studyA R Tan, H Johannes, P Rastogi, et al.Bioorganic & Medicinal Chemistry Letters|December 9, 2008
Discovery of potent, selective sulfonylfuran urea endothelial lipase inhibitorsKrista B Goodman, Michael J Bury, Mui Cheung, et al.Journal of Medicinal Chemistry|July 3, 2019
Discovery of a First-in-Class Receptor Interacting Protein 2 (RIP2) Kinase Specific Clinical Candidate, 2-((4-(Benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl Dihydrogen Phosphate, for the Treatment of Inflammatory DiseasesPamela A Haile, Linda N Casillas, Bartholomew J Votta, et al.Journal of Medicinal Chemistry|April 26, 2016
The Identification and Pharmacological Characterization of 6-(tert-Butylsulfonyl)-N-(5-fluoro-1H-indazol-3-yl)quinolin-4-amine (GSK583), a Highly Potent and Selective Inhibitor of RIP2 KinasePamela A Haile, Bartholomew J Votta, Robert W Marquis, et al.Scientific Data|April 14, 2025
Establishing a comprehensive host-parasite stable isotope database to unravel trophic relationshipsAmandine J M Sabadel, Philip Riekenberg, Monica Ayala-Diaz, et al.ACS Medicinal Chemistry Letters|June 20, 2020
Correction to Identification of Quinoline-Based RIP2 Kinase Inhibitors with an Improved Therapeutic Index to the hERG Ion ChannelPamela A Haile, Linda N Casillas, Michael J Bury, et al.ACS Medicinal Chemistry Letters|October 23, 2018
Identification of Quinoline-Based RIP2 Kinase Inhibitors with an Improved Therapeutic Index to the hERG Ion ChannelPamela A Haile, Linda N Casillas, Michael J Bury, et al.Pageof 26