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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 31, 2016
ABBV-399, a c-Met Antibody-Drug Conjugate that Targets Both MET-Amplified and c-Met-Overexpressing Tumors, Irrespective of MET Pathway DependenceJieyi Wang, Mark G Anderson, Anatol Oleksijew, et al.
Conservation Biology : the Journal of the Society for Conservation Biology|April 30, 2015
The theory behind, and the challenges of, conserving nature's stage in a time of rapid changeJoshua J Lawler, David D Ackerly, Christine M Albano, et al.
Cancer Research|February 7, 2007
Influence of Bcl-2 family members on the cellular response of small-cell lung cancer cell lines to ABT-737Stephen K Tahir, Xiufen Yang, Mark G Anderson, et al.
Molecular Cancer Therapeutics|August 28, 2020
Targeting Multiple EGFR-expressing Tumors with a Highly Potent Tumor-selective Antibody-Drug ConjugateMark G Anderson, Hugh D Falls, Michael J Mitten, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2010
Bcl-XL represents a druggable molecular vulnerability during aurora B inhibitor-mediated polyploidizationO Jameel Shah, Xiaoyu Lin, Leiming Li, et al.
Cancer Research|May 3, 2008
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitorChristin Tse, Alexander R Shoemaker, Jessica Adickes, et al.
Anti-Cancer Drugs|October 14, 2005
A highly potent and selective farnesyltransferase inhibitor ABT-100 in preclinical studiesWen-Zhen Gu, Ingrid Joseph, Yi-Chun Wang, et al.
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