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Journal of Medicinal Chemistry|April 19, 2011
Potent, selective, and orally bioavailable inhibitors of mammalian target of rapamycin (mTOR) kinase based on a quaternary substituted dihydrofuropyrimidineFrederick Cohen, Philippe Bergeron, Elizabeth Blackwood, et al.International Journal of Medical Informatics|July 16, 1999
The Regenstrief Medical Record System: a quarter century experienceC J McDonald, J M Overhage, W M Tierney, et al.Cancer Cell|December 8, 2009
Somatic mutations in p85alpha promote tumorigenesis through class IA PI3K activationBijay S Jaiswal, Vasantharajan Janakiraman, Noelyn M Kljavin, et al.Proceedings of the National Academy of Sciences of the United States of America|November 9, 2012
Disruption of PH-kinase domain interactions leads to oncogenic activation of AKT in human cancersChaitali Parikh, Vasantharajan Janakiraman, Wen-I Wu, et al.Journal of Medicinal Chemistry|October 13, 2015
Noncovalent Mutant Selective Epidermal Growth Factor Receptor Inhibitors: A Lead Optimization Case StudyRobert Heald, Krista K Bowman, Marian C Bryan, et al.Journal of Medicinal Chemistry|August 27, 2016
Discovery of a Noncovalent, Mutant-Selective Epidermal Growth Factor Receptor InhibitorBryan K Chan, Emily J Hanan, Krista K Bowman, et al.Cancer Cell|May 18, 2013
Oncogenic ERBB3 mutations in human cancersBijay S Jaiswal, Noelyn M Kljavin, Eric W Stawiski, et al.JAMA Network Open|July 8, 2024
A Hospice Transitions Program for Patients in the Emergency DepartmentChristopher W Baugh, Kei Ouchi, Jason K Bowman, et al.Science (New York, N.Y.)|December 19, 2015
Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonistShivani Ahuja, Susmith Mukund, Lunbin Deng, et al.Bioorganic & Medicinal Chemistry Letters|September 12, 2013
Identification of amides derived from 1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT)Xiaozhang Zheng, Kenneth W Bair, Paul Bauer, et al.Pageof 39