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Molecular Cancer Research : MCR|June 29, 2017
BRAF-inhibitor Associated MEK Mutations Increase RAF-Dependent and -Independent Enzymatic ActivityCaroline M Emery, Kelli-Ann Monaco, Ping Wang, et al.RNA (New York, N.Y.)|May 15, 2002
Development and characterization of a reconstituted yeast translation initiation systemMikkel A Algire, David Maag, Peter Savio, et al.Biochemistry|April 1, 2016
Structural and Functional Consequences of Three Cancer-Associated Mutations of the Oncogenic Phosphatase SHP2Jonathan R LaRochelle, Michelle Fodor, Xiang Xu, et al.Elife|March 23, 2021
Time-resolved phosphoproteomics reveals scaffolding and catalysis-responsive patterns of SHP2-dependent signalingVidyasiri Vemulapalli, Lily A Chylek, Alison Erickson, et al.Oncotarget|November 17, 2018
The potent and selective cyclin-dependent kinases 4 and 6 inhibitor ribociclib (LEE011) is a versatile combination partner in preclinical cancer modelsSunkyu Kim, Ralph Tiedt, Alice Loo, et al.Oncotarget|April 16, 2020
Correction: The potent and selective cyclin-dependent kinases 4 and 6 inhibitor ribociclib (LEE011) is a versatile combination partner in preclinical cancer modelsSunkyu Kim, Ralph Tiedt, Alice Loo, et al.ACS Chemical Biology|January 6, 2018
Dual Allosteric Inhibition of SHP2 PhosphataseMichelle Fodor, Edmund Price, Ping Wang, et al.Nature|July 1, 2016
Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinasesYing-Nan P Chen, Matthew J LaMarche, Ho Man Chan, et al.Pageof 3