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Science (New York, N.Y.)
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August 8, 2009
Glucose deprivation contributes to the development of KRAS pathway mutations in tumor cells
Jihye Yun, Carlo Rago, Ian Cheong, et al.
Nature
|
August 12, 2005
Colorectal cancer: mutations in a signalling pathway
D Williams Parsons, Tian-Li Wang, Yardena Samuels, et al.
Oncotarget
|
May 17, 2014
Combination of PIM and JAK2 inhibitors synergistically suppresses MPN cell proliferation and overcomes drug resistance
Shih-Min A Huang, Anlai Wang, Rita Greco, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 25, 2014
Preparation and optimization of new 4-(2-(indolin-1-yl)-2-oxoethyl)-2-morpholinothiazole-5-carboxylic acid and amide derivatives as potent and selective PI3Kβ inhibitors
Victor Certal, Frank Halley, Angela Virone-Oddos, et al.
Cancer Discovery
|
October 3, 2019
Acquired On-Target Clinical Resistance Validates FGFR4 as a Driver of Hepatocellular Carcinoma
Megan A Hatlen, Oleg Schmidt-Kittler, Cori Ann Sherwin, et al.
Gastro Hep Advances
|
August 12, 2024
Evaluation of Protein Kinase cAMP-Activated Catalytic Subunit Alpha as a Therapeutic Target for Fibrolamellar Carcinoma
Stefanie S Schalm, Erin O'Hearn, Kevin Wilson, et al.
Blood
|
July 10, 2014
PIM inhibitors target CD25-positive AML cells through concomitant suppression of STAT5 activation and degradation of MYC oncogene
Zhuyan Guo, Anlai Wang, Weidong Zhang, et al.
Cancer Research
|
May 6, 2004
Three classes of genes mutated in colorectal cancers with chromosomal instability
Zhenghe Wang, Jordan M Cummins, Dong Shen, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 18, 2012
Preparation and optimization of new 4-(morpholin-4-yl)-(6-oxo-1,6-dihydropyrimidin-2-yl)amide derivatives as PI3Kβ inhibitors
Victor Certal, Frank Halley, Angela Virone-Oddos, et al.
The Journal of Biological Chemistry
|
September 5, 2013
Evaluation of cancer dependence and druggability of PRP4 kinase using cellular, biochemical, and structural approaches
Qiang Gao, Ingrid Mechin, Nayantara Kothari, et al.
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Search research articles
Search
Showing results (61-70 of 79) with videos related to
Sort By:
Page
of 8
Science (New York, N.Y.)
|
August 8, 2009
Glucose deprivation contributes to the development of KRAS pathway mutations in tumor cells
Jihye Yun, Carlo Rago, Ian Cheong, et al.
Nature
|
August 12, 2005
Colorectal cancer: mutations in a signalling pathway
D Williams Parsons, Tian-Li Wang, Yardena Samuels, et al.
Oncotarget
|
May 17, 2014
Combination of PIM and JAK2 inhibitors synergistically suppresses MPN cell proliferation and overcomes drug resistance
Shih-Min A Huang, Anlai Wang, Rita Greco, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 25, 2014
Preparation and optimization of new 4-(2-(indolin-1-yl)-2-oxoethyl)-2-morpholinothiazole-5-carboxylic acid and amide derivatives as potent and selective PI3Kβ inhibitors
Victor Certal, Frank Halley, Angela Virone-Oddos, et al.
Cancer Discovery
|
October 3, 2019
Acquired On-Target Clinical Resistance Validates FGFR4 as a Driver of Hepatocellular Carcinoma
Megan A Hatlen, Oleg Schmidt-Kittler, Cori Ann Sherwin, et al.
Gastro Hep Advances
|
August 12, 2024
Evaluation of Protein Kinase cAMP-Activated Catalytic Subunit Alpha as a Therapeutic Target for Fibrolamellar Carcinoma
Stefanie S Schalm, Erin O'Hearn, Kevin Wilson, et al.
Blood
|
July 10, 2014
PIM inhibitors target CD25-positive AML cells through concomitant suppression of STAT5 activation and degradation of MYC oncogene
Zhuyan Guo, Anlai Wang, Weidong Zhang, et al.
Cancer Research
|
May 6, 2004
Three classes of genes mutated in colorectal cancers with chromosomal instability
Zhenghe Wang, Jordan M Cummins, Dong Shen, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 18, 2012
Preparation and optimization of new 4-(morpholin-4-yl)-(6-oxo-1,6-dihydropyrimidin-2-yl)amide derivatives as PI3Kβ inhibitors
Victor Certal, Frank Halley, Angela Virone-Oddos, et al.
The Journal of Biological Chemistry
|
September 5, 2013
Evaluation of cancer dependence and druggability of PRP4 kinase using cellular, biochemical, and structural approaches
Qiang Gao, Ingrid Mechin, Nayantara Kothari, et al.
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of 8