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Nature Communications|August 29, 2014
Structure and mechanism of action of the hydroxy-aryl-aldehyde class of IRE1 endoribonuclease inhibitorsMario Sanches, Nicole M Duffy, Manisha Talukdar, et al.Nature|July 6, 2018
CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesionsMichal Zimmermann, Olga Murina, Martin A M Reijns, et al.Cell|June 21, 2011
An allosteric inhibitor of the human Cdc34 ubiquitin-conjugating enzymeDerek F Ceccarelli, Xiaojing Tang, Benoit Pelletier, et al.Molecular Systems Biology|April 5, 2024
Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stabilityYiQing Lü, Tiffany Cho, Saptaparna Mukherjee, et al.Nature|November 25, 2021
FAM72A antagonizes UNG2 to promote mutagenic repair during antibody maturationYuqing Feng, Conglei Li, Jessica A Stewart, et al.Nature Biotechnology|November 28, 2017
Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR-Cas9 genome-editing efficiencyMarella D Canny, Nathalie Moatti, Leo C K Wan, et al.Nature Communications|November 25, 2025
WEE1 inhibitors trigger GCN2-mediated activation of the integrated stress responseRinskje B Tjeerdsma, Timothy F Ng, Maurits Roorda, et al.Molecular Cell|November 9, 2010
The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombinationLara O'Donnell, Stephanie Panier, Jan Wildenhain, et al.Nature Chemical Biology|August 12, 2020
Functional characterization of a PROTAC directed against BRAF mutant V600EGanna Posternak, Xiaojing Tang, Pierre Maisonneuve, et al.G3 (Bethesda, Md.)|June 29, 2017
Evaluation and Design of Genome-Wide CRISPR/SpCas9 Knockout ScreensTraver Hart, Amy Hin Yan Tong, Katie Chan, et al.Pageof 13