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Nature Reviews. Drug Discovery
|
October 21, 2020
Author Correction: RAS-targeted therapies: is the undruggable drugged?
Amanda R Moore, Scott C Rosenberg, Frank McCormick, et al.
The Journal of Biological Chemistry
|
April 11, 2003
X-ray crystal structure of an IkappaBbeta x NF-kappaB p65 homodimer complex
Shiva Malek, De-Bin Huang, Tom Huxford, et al.
Assay and Drug Development Technologies
|
May 21, 2010
A plate-based assay to measure cellular ERK substrate phosphorylation: utility for drug discovery of the MAPK-signaling cascade
Sreemathy Ramaswamy, Ivana Yen, Steve Sideris, et al.
Biochemistry
|
September 24, 2020
Dimerization Induced by C-Terminal 14-3-3 Binding Is Sufficient for BRAF Kinase Activation
Nicholas P D Liau, Avinashnarayan Venkatanarayan, John G Quinn, et al.
Molecular Cancer Therapeutics
|
September 17, 2013
Identification of preferred chemotherapeutics for combining with a CHK1 inhibitor
Yang Xiao, Judi Ramiscal, Kaska Kowanetz, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2013
A hit to lead discovery of novel N-methylated imidazolo-, pyrrolo-, and pyrazolo-pyrimidines as potent and selective mTOR inhibitors
Wendy Lee, Daniel F Ortwine, Philippe Bergeron, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 3, 2014
Discovery of the 1,7-diazacarbazole class of inhibitors of checkpoint kinase 1
Lewis Gazzard, Brent Appleton, Kerry Chapman, et al.
Cancer Discovery
|
December 12, 2012
Noncovalent wild-type-sparing inhibitors of EGFR T790M
Ho-June Lee, Gabriele Schaefer, Timothy P Heffron, et al.
Nature Structural & Molecular Biology
|
January 29, 2020
Negative regulation of RAF kinase activity by ATP is overcome by 14-3-3-induced dimerization
Nicholas P D Liau, Timothy J Wendorff, John G Quinn, et al.
Cancer Cell
|
August 27, 2014
Structure of the BRAF-MEK complex reveals a kinase activity independent role for BRAF in MAPK signaling
Jacob R Haling, Jawahar Sudhamsu, Ivana Yen, et al.
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Search research articles
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Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
Nature Reviews. Drug Discovery
|
October 21, 2020
Author Correction: RAS-targeted therapies: is the undruggable drugged?
Amanda R Moore, Scott C Rosenberg, Frank McCormick, et al.
The Journal of Biological Chemistry
|
April 11, 2003
X-ray crystal structure of an IkappaBbeta x NF-kappaB p65 homodimer complex
Shiva Malek, De-Bin Huang, Tom Huxford, et al.
Assay and Drug Development Technologies
|
May 21, 2010
A plate-based assay to measure cellular ERK substrate phosphorylation: utility for drug discovery of the MAPK-signaling cascade
Sreemathy Ramaswamy, Ivana Yen, Steve Sideris, et al.
Biochemistry
|
September 24, 2020
Dimerization Induced by C-Terminal 14-3-3 Binding Is Sufficient for BRAF Kinase Activation
Nicholas P D Liau, Avinashnarayan Venkatanarayan, John G Quinn, et al.
Molecular Cancer Therapeutics
|
September 17, 2013
Identification of preferred chemotherapeutics for combining with a CHK1 inhibitor
Yang Xiao, Judi Ramiscal, Kaska Kowanetz, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2013
A hit to lead discovery of novel N-methylated imidazolo-, pyrrolo-, and pyrazolo-pyrimidines as potent and selective mTOR inhibitors
Wendy Lee, Daniel F Ortwine, Philippe Bergeron, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 3, 2014
Discovery of the 1,7-diazacarbazole class of inhibitors of checkpoint kinase 1
Lewis Gazzard, Brent Appleton, Kerry Chapman, et al.
Cancer Discovery
|
December 12, 2012
Noncovalent wild-type-sparing inhibitors of EGFR T790M
Ho-June Lee, Gabriele Schaefer, Timothy P Heffron, et al.
Nature Structural & Molecular Biology
|
January 29, 2020
Negative regulation of RAF kinase activity by ATP is overcome by 14-3-3-induced dimerization
Nicholas P D Liau, Timothy J Wendorff, John G Quinn, et al.
Cancer Cell
|
August 27, 2014
Structure of the BRAF-MEK complex reveals a kinase activity independent role for BRAF in MAPK signaling
Jacob R Haling, Jawahar Sudhamsu, Ivana Yen, et al.
Page
of 6