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Molecular Cancer Therapeutics
|
September 15, 2011
The Bcl-2/Bcl-X(L)/Bcl-w inhibitor, navitoclax, enhances the activity of chemotherapeutic agents in vitro and in vivo
Jun Chen, Sha Jin, Vivek Abraham, et al.
Leukemia
|
December 13, 2019
A novel CDK9 inhibitor increases the efficacy of venetoclax (ABT-199) in multiple models of hematologic malignancies
Darren C Phillips, Sha Jin, Gareth P Gregory, et al.
Chemical Biology & Drug Design
|
July 17, 2007
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategies
Jeffrey R Huth, Chang Park, Andrew M Petros, et al.
Journal of Medicinal Chemistry
|
May 2, 2015
Correction to Structure-Guided Design of a Series of MCL-1 Inhibitors with High Affinity and Selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Journal of Medicinal Chemistry
|
February 14, 2015
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Science Translational Medicine
|
March 20, 2015
Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy
Joel D Leverson, Darren C Phillips, Michael J Mitten, et al.
ACS Medicinal Chemistry Letters
|
October 15, 2014
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity
Zhi-Fu Tao, Lisa Hasvold, Le Wang, et al.
Nature Medicine
|
January 8, 2013
ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets
Andrew J Souers, Joel D Leverson, Erwin R Boghaert, et al.
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Search research articles
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Showing results (141-150 of 148) with videos related to
Sort By:
Page
of 15
You have reached the last page of results.
This site can display upto 148 results.
Molecular Cancer Therapeutics
|
September 15, 2011
The Bcl-2/Bcl-X(L)/Bcl-w inhibitor, navitoclax, enhances the activity of chemotherapeutic agents in vitro and in vivo
Jun Chen, Sha Jin, Vivek Abraham, et al.
Leukemia
|
December 13, 2019
A novel CDK9 inhibitor increases the efficacy of venetoclax (ABT-199) in multiple models of hematologic malignancies
Darren C Phillips, Sha Jin, Gareth P Gregory, et al.
Chemical Biology & Drug Design
|
July 17, 2007
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategies
Jeffrey R Huth, Chang Park, Andrew M Petros, et al.
Journal of Medicinal Chemistry
|
May 2, 2015
Correction to Structure-Guided Design of a Series of MCL-1 Inhibitors with High Affinity and Selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Journal of Medicinal Chemistry
|
February 14, 2015
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Science Translational Medicine
|
March 20, 2015
Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy
Joel D Leverson, Darren C Phillips, Michael J Mitten, et al.
ACS Medicinal Chemistry Letters
|
October 15, 2014
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity
Zhi-Fu Tao, Lisa Hasvold, Le Wang, et al.
Nature Medicine
|
January 8, 2013
ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets
Andrew J Souers, Joel D Leverson, Erwin R Boghaert, et al.
Page
of 15