C1QBP Promotes Homologous Recombination by Stabilizing MRE11 and Controlling the Assembly and Activation of MRE11/RAD50/NBS1 Complex - Bai, Yongtai; Wang, Weibin; Li, Siyu; Zhan, Jun; Li, Hanxiao; Zhao, Meimei; Zhou, Xiao Albert; Li, Shiwei; Li, Xiaoman; Huo, Yanfei; Shen, Qinjian; Zhou, Mei; et al. (Molecular cell, 2019)
Keywords: Acid Anhydride Hydrolases - genetics; Acid Anhydride Hydrolases - metabolism; Animals; breast neoplasms; C1QBP; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cell Cycle Proteins - genetics; Cell Cycle Proteins - metabolism; chromatin; DNA; DNA damage; DNA damage repair; DNA double-strand breaks; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; drug therapy; enzyme activity; enzymes; genetic instability; HEK293 Cells; HeLa Cells; Homologous Recombination; Humans; Mitochondrial Proteins - genetics; Mitochondrial Proteins - metabolism; MRE11; MRE11 Homologue Protein - genetics; MRE11 Homologue Protein - metabolism; MRN complex; Multiprotein Complexes - genetics; Multiprotein Complexes - metabolism; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Protein Stability; remission; resection; Sf9 Cells; Spodoptera; DNA damage repair; MRE11; homologous recombination; DNA double-strand breaks; C1QBP; MRN complex