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Molecular Cancer Therapeutics|July 26, 2013
Synthetic lethal targeting of PTEN-deficient cancer cells using selective disruption of polynucleotide kinase/phosphataseTodd R Mereniuk, Mohamed A M El Gendy, Ana M Mendes-Pereira, et al.
Metallomics : Integrated Biometal Science|October 31, 2014
Therapeutic and analytical applications of arsenic binding to proteinsBeibei Chen, Qingqing Liu, Aleksandra Popowich, et al.
Advances in Experimental Medicine and Biology|October 1, 2015
Biobanking in the Twenty-First Century: Driving Population Metrics into Biobanking QualityJoseph N Roberts, Charlene Karvonen, Kathryn Graham, et al.
The Journal of Biological Chemistry|November 27, 2009
Mechanism of action of an imidopiperidine inhibitor of human polynucleotide kinase/phosphataseGary K Freschauf, Rajam S Mani, Todd R Mereniuk, et al.
Cancer Chemotherapy and Pharmacology|January 5, 2021
Enhancing the activity of platinum-based drugs by improved inhibitors of ERCC1-XPF-mediated DNA repairGloria Ciniero, Ahmed H Elmenoufy, Francesco Gentile, et al.
Cell Discovery|January 20, 2017
ATPase activity tightly regulates RecA nucleofilaments to promote homologous recombinationBailin Zhao, Dapeng Zhang, Chengmin Li, et al.
International Journal of Molecular Sciences|July 18, 2019
RUNX3 Promotes the Tumorigenic Phenotype in KGN, a Human Granulosa Cell Tumor-Derived Cell LineHuachen Chen, Powel Crosley, Abul K Azad, et al.
The Journal of Investigative Dermatology|May 14, 2004
Keratinocyte-releasable stratifin functions as a potent collagenase-stimulating factor in fibroblastsAziz Ghahary, Feridoun Karimi-Busheri, Yvonne Marcoux, et al.
Fundamental & Clinical Pharmacology|November 9, 2024
The synergy between alkylating agents and ERCC1-XPF inhibitors is p53 dependentGloria Ciniero, Tiago Marques Pedro, Charles Dumontet, et al.
The Journal of Biological Chemistry|September 21, 2010
Dual modes of interaction between XRCC4 and polynucleotide kinase/phosphatase: implications for nonhomologous end joiningRajam S Mani, Yaping Yu, Shujuan Fang, et al.
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