Lauren M. Congdon, Ph.D.
Affiliations: | 2012 | Genetic, Molecular, and Cell Biology | University of Southern California, Los Angeles, CA, United States |
Area:
Molecular Biology, BiochemistryGoogle:
"Lauren Congdon"Parents
Sign in to add mentor| Judd C. Rice | grad student | 2012 | USC | |
| (Multiple functions of the PR-Set7 histone methyltransferase: From transcription to the cell cycle.) | ||||
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| Tuzon CT, Spektor T, Kong X, et al. (2014) Concerted activities of distinct H4K20 methyltransferases at DNA double-strand breaks regulate 53BP1 nucleation and NHEJ-directed repair. Cell Reports. 8: 430-8 |
| Congdon LM, Sims JK, Tuzon CT, et al. (2014) The PR-Set7 binding domain of Riz1 is required for the H4K20me1-H3K9me1 trans-tail 'histone code' and Riz1 tumor suppressor function. Nucleic Acids Research. 42: 3580-9 |
| Tuzon CT, Spektor TM, Congdon LM, et al. (2014) Abstract LB-133: Orchestrated recruitment of histone methyltransferases to DNA double strand breaks facilitates 53BP1 binding and proficient repair Cancer Research. 74 |
| Spektor TM, Congdon LM, Veerappan CS, et al. (2011) The UBC9 E2 SUMO conjugating enzyme binds the PR-Set7 histone methyltransferase to facilitate target gene repression. Plos One. 6: e22785 |
| Wu S, Wang W, Kong X, et al. (2010) Dynamic regulation of the PR-Set7 histone methyltransferase is required for normal cell cycle progression. Genes & Development. 24: 2531-42 |
| Congdon LM, Houston SI, Veerappan CS, et al. (2010) PR-Set7-mediated monomethylation of histone H4 lysine 20 at specific genomic regions induces transcriptional repression. Journal of Cellular Biochemistry. 110: 609-19 |