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Molecular Cell|December 18, 2018
Interactome Rewiring Following Pharmacological Targeting of BET BromodomainsJean-Philippe Lambert, Sarah Picaud, Takao Fujisawa, et al.Science Translational Medicine|January 29, 2011
Uroporphyrinogen decarboxylase is a radiosensitizing target for head and neck cancerEmma Ito, Shijun Yue, Eduardo H Moriyama, et al.Nature Communications|March 4, 2021
A multiplexed, next generation sequencing platform for high-throughput detection of SARS-CoV-2Marie-Ming Aynaud, J Javier Hernandez, Seda Barutcu, et al.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.Molecular Cell|June 10, 2020
Endogenous DNA 3' Blocks Are Vulnerabilities for BRCA1 and BRCA2 Deficiency and Are Reversed by the APE2 NucleaseAlejandro Álvarez-Quilón, Jessica L Wojtaszek, Marie-Claude Mathieu, 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.Nature|June 3, 2021
A proximity-dependent biotinylation map of a human cellChristopher D Go, James D R Knight, Archita Rajasekharan, 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.Pageof 20