Publications
Current Bielinsky-Hendrickson Publications
RNF4 prevents genomic instability caused by chronic DNA under-replication
DNA Repair (Amst). 2024 Mar;135:103646. doi: 10.1016/j.dnarep.2024.103646. Epub 2024 Feb 7.ABSTRACTEukaryotic genome stability is maintained by a complex and diverse set of molecular processes. One class of enzymes that promotes…FANCD2-dependent mitotic DNA synthesis relies on PCNA K164 ubiquitination
Cell Rep. 2023 Dec 26;42(12):113523. doi: 10.1016/j.celrep.2023.113523. Epub 2023 Dec 5.ABSTRACTUbiquitination of proliferating cell nuclear antigen (PCNA) at lysine 164 (K164) activates DNA damage tolerance pathways. Currently, we lack a…RNF4 and USP7 cooperate in ubiquitin-regulated steps of DNA replication
Open Biol. 2023 Aug;13(8):230068. doi: 10.1098/rsob.230068. Epub 2023 Aug 23.ABSTRACTDNA replication requires precise regulation achieved through post-translational modifications, including ubiquitination and SUMOylation. These modifications are linked by the SUMO-targeted E3…Publications (10 years) Prior to 2023
(For a complete list of publications)
https://pubmed.ncbi.nlm.nih.gov/?term=Bielinsky+AK&sort=date
2022
Lin, K., Chang, Y. -C., de Velasco, E. M. F., Wickman, K., Myers, C. L., & Bielinsky, A. -K. (2022). Scalable CRISPR-Cas9 chemical genetic screens in non-transformed human cells. STAR PROTOCOLS, 3(4). doi:10.1016/j.xpro.2022.101675
Grange, L. J., Reynolds, J. J., Ullah, F., Isidor, B., Shearer, R. F., Latypova, X., . . . Stewart, G. S. (2022). Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy. NATURE COMMUNICATIONS, 13(1). doi:10.1038/s41467-022-34349-8
2021
Okamoto, Y., Abe, M., Mu, A., Tempaku, Y., Rogers, C. B., Mochizuki, A. L., . . . Takata, M. (2021). SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells. BLOOD, 137(3), 336-348. doi:10.1182/blood.2019003782
Baxley, R. M., Leung, W., Schmit, M. M., Matson, J. P., Yin, L., Oram, M. K., . . . Bielinsky, A. -K. (2021). Bi-allelic MCM10 variants associated with immune dysfunction and cardiomyopathy cause telomere shortening. NATURE COMMUNICATIONS, 12(1). doi:10.1038/s41467-021-21878-x
Kang, Z., Fu, P., Alcivar, A. L., Fu, H., Redon, C., Foo, T. K., . . . Xia, B. (2021). BRCA2 associates with MCM10 to suppress PRIMPOL-mediated repriming and single-stranded gap formation after DNA damage. NATURE COMMUNICATIONS, 12(1). doi:10.1038/s41467-021-26227-6
Schmit, M., & Bielinsky, A. -K. (2021). Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 22(2). doi:10.3390/ijms22020911
Chang, Y. -C., Oram, M. K., & Bielinsky, A. -K. (2021). SUMO-Targeted Ubiquitin Ligases and Their Functions in Maintaining Genome Stability. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 22(10). doi:10.3390/ijms22105391
2020
Mace, E. M., Paust, S., Conte, M. I., Baxley, R. M., Schmit, M. M., Patil, S. L., . . . Orange, J. S. (2020). Human NK cell deficiency as a result of biallelic mutations in MCM10. JOURNAL OF CLINICAL INVESTIGATION, 130(10), 5272-5286. doi:10.1172/JCI134966
Raghunandan, M., Yeo, J. E., Walter, R., Saito, K., Harvey, A. J., Ittershagen, S., . . . Sobeck, A. (2020). Functional cross talk between the Fanconi anemia and ATRX/DAXX histone chaperone pathways promotes replication fork recovery. HUMAN MOLECULAR GENETICS, 29(7), 1083-1095. doi:10.1093/hmg/ddz250
Thakar, T., Leung, W., Nicolae, C. M., Clements, K. E., Shen, B., Bielinsky, A. -K., & Moldovan, G. -L. (2020). Ubiquitinated-PCNA protects replication forks from DNA2-mediated degradation by regulating Okazaki fragment maturation and chromatin assembly. NATURE COMMUNICATIONS, 11(1). doi:10.1038/s41467-020-16096-w
Stroik, S., Kurtz, K., Lin, K., Karachenets, S., Myers, C. L., Bielinsky, A. -K., & Hendrickson, E. A. (2020). EXO1 resection at G-quadruplex structures facilitates resolution and replication. NUCLEIC ACIDS RESEARCH, 48(9), 4960-4975. doi:10.1093/nar/gkaa199
2019
Matson, J. P., Dumitru, R., Coryell, P., Baxley, R. M., Chen, W., Twaroski, K., . . . Cook, J. G. (2019). Correction: Rapid DNA replication origin licensing protects stem cell pluripotency.. eLife, 8, e49040. doi:10.7554/elife.49040
Leung, W., Baxley, R. M., Moldovan, G. -L., & Bielinsky, A. -K. (2019). Mechanisms of DNA Damage Tolerance: Post-Translational Regulation of PCNA. GENES, 10(1). doi:10.3390/genes10010010
Paulson, C. N., John, K., Baxley, R. M., Kurniawan, F., Orellana, K., Francis, R., . . . Bielinsky, A. -K. (2019). The anti-parasitic agent suramin and several of its analogues are inhibitors of the DNA binding protein Mcm10. OPEN BIOLOGY, 9(8). doi:10.1098/rsob.190117
2018
Becker, J. R., Gallo, D., Leung, W., Croissant, T., Thu, Y. M., Hai, D. N., . . . Bielinsky, A. -K. (2018). Flap endonuclease overexpression drives genome instability and DNA damage hypersensitivity in a PCNA-dependent manner. NUCLEIC ACIDS RESEARCH, 46(11), 5634-5650. doi:10.1093/nar/gky313
Kurniawan, F., Shi, K., Kurahashi, K., Bielinsky, A. -K., & Aihara, H. (2018). Crystal Structure of Entamoeba histolytica Cdc45 Suggests a Conformational Switch that May Regulate DNA Replication. ISCIENCE, 3, 102-+. doi:10.1016/j.isci.2018.04.011
2017
Matson, J. P., Dumitru, R., Coryell, P., Baxley, R. M., Chen, W., Twaroski, K., . . . Cook, J. G. (2017). Rapid DNA replication origin licensing protects stem cell pluripotency. ELIFE, 6. doi:10.7554/eLife.30473
Baxley, R. M., & Bielinsky, A. -K. (2017). Mcm10: A Dynamic Scaffold at Eukaryotic Replication Forks. GENES, 8(2). doi:10.3390/genes8020073
2016
Zhang, T., Fultz, B. L., Das-Bradoo, S., & Bielinsky, A. -K. (2016). Mapping ubiquitination sites of S. cerevisiae Mcm10.. Biochemistry and biophysics reports, 8, 212-218. doi:10.1016/j.bbrep.2016.09.003
Bielinsky, A. -K. (2016). Mcm10: The glue at replication forks. CELL CYCLE, 15(22), 3024-3025. doi:10.1080/15384101.2016.1216925
Thu, Y. M., Van Riper, S. K., Higgins, L., Zhang, T., Becker, J. R., Markowski, T. W., . . . Bielinsky, A. K. (2016). Slx5/Slx8 Promotes Replication Stress Tolerance by Facilitating Mitotic Progression. CELL REPORTS, 15(6), 1254-1265. doi:10.1016/j.celrep.2016.04.017
Bielinsky, A. -K., & Leung, W. (2016). Not just for coding: a new role for histone tails in replication enzyme activation. FEBS Journal, 283(23), 4244-4246. doi:10.1111/febs.13958
2015
Avdulov, S., Herrera, J., Smith, K., Peterson, M., Gomez-Garcia, J. R., Beadnell, T. C., . . . Polunovsky, V. A. (2015). eIF4E Threshold Levels Differ in Governing Normal and Neoplastic Expansion of Mammary Stem and Luminal Progenitor Cells. CANCER RESEARCH, 75(4), 687-697. doi:10.1158/0008-5472.CAN-14-2571
Becker, J. R., Pons, C., Hai, D. N., Costanzo, M., Boone, C., Myers, C. L., & Bielinsky, A. -K. (2015). Genetic Interactions Implicating Postreplicative Repair in Okazaki Fragment Processing. PLOS GENETICS, 11(11). doi:10.1371/journal.pgen.1005659
Bielinsky, A. -K. (2015). Penetrating enemy territory: Soluble PCNA-peptides stress out MYCN-overexpressing neuroblastomas. EBIOMEDICINE, 2(12), 1844-1845. doi:10.1016/j.ebiom.2015.12.012
2014
Thu, Y. M., & Bielinsky, A. -K. (2014). MCM10: One tool for all-Integrity, maintenance and damage control. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 30, 121-130. doi:10.1016/j.semcdb.2014.03.017
Alver, R. C., Zhang, T., Josephrajan, A., Fultz, B. L., Hendrix, C. J., Das-Bradoo, S., & Bielinsky, A. -K. (2014). The N-terminus of Mcm10 is important for interaction with the 9-1-1 clamp and in resistance to DNA damage. NUCLEIC ACIDS RESEARCH, 42(13), 8389-8404. doi:10.1093/nar/gku479
Becker, J. R., Hai, D. N., Wang, X., & Bielinsky, A. -K. (2014). Mcm10 deficiency causes defective-replisome-induced mutagenesis and a dependency on error-free postreplicative repair. CELL CYCLE, 13(11). doi:10.4161/cc.28652
2013
Du, W., Josephrajan, A., Adhikary, S., Bowles, T., Bielinsky, A. -K., & Eichman, B. F. (2013). Mcm10 Self-Association Is Mediated by an N-Terminal Coiled-Coil Domain. PLOS ONE, 8(7). doi:10.1371/journal.pone.0070518
Nguyen, H. D., Becker, J., Thu, Y. M., Costanzo, M., Koch, E. N., Smith, S., . . . Bielinsky, A. -K. (2013). Unligated Okazaki Fragments Induce PCNA Ubiquitination and a Requirement for Rad59-Dependent Replication Fork Progression. PLOS ONE, 8(6). doi:10.1371/journal.pone.0066379
Ragland, R. L., Patel, S., Rivard, R. S., Smith, K., Peters, A. A., Bielinsky, A. -K., & Brown, E. J. (2013). RNF4 and PLK1 are required for replication fork collapse in ATR-deficient cells. GENES & DEVELOPMENT, 27(20), 2259-2273. doi:10.1101/gad.223180.113
Thu, Y. M., & Bielinsky, A. -K. (2013). Enigmatic roles of Mcm10 in DNA replication. TRENDS IN BIOCHEMICAL SCIENCES, 38(4), 184-194. doi:10.1016/j.tibs.2012.12.003
(For a complete list of publications)
https://pubmed.ncbi.nlm.nih.gov/?term=Hendrickson+EA&sort=date
2022
Liddiard, K., Aston-Evans, A. N., Cleal, K., Hendrickson, E. A., & Baird, D. M. (2022). POLQ suppresses genome instability and alterations in DNA repeat tract lengths. NAR CANCER, 4(3). doi:10.1093/narcan/zcac020
Geiller, H. E. B., Harvey, A., Jones, R. E., Grimstead, J. W., Cleal, K., Hendrickson, E. A., & Baird, D. M. (2022). ATRX modulates the escape from a telomere crisis. PLOS GENETICS, 18(11). doi:10.1371/journal.pgen.1010485
2021
Baxley, R. M., Leung, W., Schmit, M. M., Matson, J. P., Yin, L., Oram, M. K., . . . Bielinsky, A. -K. (2021). Bi-allelic MCM10 variants associated with immune dysfunction and cardiomyopathy cause telomere shortening. NATURE COMMUNICATIONS, 12(1). doi:10.1038/s41467-021-21878-x
2020
Stroik, S., & Hendrickson, E. A. (2020). Telomere fusions and translocations: a bridge too far?. CURRENT OPINION IN GENETICS & DEVELOPMENT, 60, 85-91. doi:10.1016/j.gde.2020.02.010
Hendrickson, E. A. (2020). RAD52: Viral Friend or Foe?. CANCERS, 12(2). doi:10.3390/cancers12020399
Ruis, B., Molan, A., Takasugi, T., & Hendrickson, E. A. (2020). Absence of XRCC4 and its paralogs in human cells reveal differences in outcomes for DNA repair and V(D)J recombination. DNA REPAIR, 85. doi:10.1016/j.dnarep.2019.102738
Ferrer, A., Mangaonkar, A. A., Stroik, S., Zimmermann, M. T., Sigafoos, A. N., Kamath, P. S., . . . Patnaik, M. M. (2020). Functional validation of TERT and TERC variants of uncertain significance in patients with short telomere syndromes. BLOOD CANCER JOURNAL, 10(11). doi:10.1038/s41408-020-00386-z
Stroik, S., & Hendrickson, E. A. (2020). Telomere replication-When the going gets tough. DNA REPAIR, 94. doi:10.1016/j.dnarep.2020.102875
Raghunandan, M., Yeo, J. E., Walter, R., Saito, K., Harvey, A. J., Ittershagen, S., . . . Sobeck, A. (2020). Functional cross talk between the Fanconi anemia and ATRX/DAXX histone chaperone pathways promotes replication fork recovery. HUMAN MOLECULAR GENETICS, 29(7), 1083-1095. doi:10.1093/hmg/ddz250
Stroik, S., Kurtz, K., Lin, K., Karachenets, S., Myers, C. L., Bielinsky, A. -K., & Hendrickson, E. A. (2020). EXO1 resection at G-quadruplex structures facilitates resolution and replication. NUCLEIC ACIDS RESEARCH, 48(9), 4960-4975. doi:10.1093/nar/gkaa199
2019
Liddiard, K., Ruis, B., Kan, Y., Cleal, K., Ashelford, K. E., Hendrickson, E. A., & Baird, D. M. (2019). DNA Ligase 1 is an essential mediator of sister chromatid telomere fusions in G2 cell cycle phase. NUCLEIC ACIDS RESEARCH, 47(5), 2402-2424. doi:10.1093/nar/gky1279
Cleal, K., Jones, R. E., Grimstead, J. W., Hendrickson, E. A., & Baird, D. M. (2019). Chromothripsis during telomere crisis is independent of NHEJ, and consistent with a replicative origin. GENOME RESEARCH, 29(5), 737-749. doi:10.1101/gr.240705.118
Nera, B., Huang, H. -S., Hendrickson, E. A., & Xu, L. (2019). Both the classical and alternative non-homologous end joining pathways contribute to the fusion of drastically shortened telomeres induced by TRF2 overexpression. CELL CYCLE, 18(8), 880-888. doi:10.1080/15384101.2019.1598724
Kan, Y., & Hendrickson, E. A. (2019). Conversion Tract Analysis of Homology-Directed Genome Editing Using Oligonucleotide Donors. DNA REPAIR: METHODS AND PROTOCOLS, 1999, 131-144. doi:10.1007/978-1-4939-9500-4_7
Lu, H., Saha, J., Beckmann, P. J., Hendrickson, E. A., & Davis, A. J. (2019). DNA-PKcs promotes chromatin decondensation to facilitate initiation of the DNA damage response. NUCLEIC ACIDS RESEARCH, 47(18), 9467-9479. doi:10.1093/nar/gkz694
Stroik, S., Kurtz, K., & Hendrickson, E. A. (2019). NAR Breakthrough Article CtIP is essential for telomere replication. NUCLEIC ACIDS RESEARCH, 47(17), 8927-8940. doi:10.1093/nar/gkz652
2018
Ngo, G., Hyatt, S., Grimstead, J., Jones, R., Hendrickson, E., Pepper, C., & Baird, D. (2018). PARP inhibition prevents escape from a telomere-driven crisis and inhibits cell immortalisation.. Oncotarget, 9(101), 37549-37563. doi:10.18632/oncotarget.26499
Harvey, A., Mielke, N., Grimstead, J. W., Jones, R. E., Nguyen, T., Mueller, M., . . . Hendrickson, E. A. (2018). PARP1 is required for preserving telomeric integrity but is dispensable for A-NHEJ.. Oncotarget, 9(78), 34821-34837. doi:10.18632/oncotarget.26201
Baird, D. M., & Hendrickson, E. A. (2018). Telomeres and Chromosomal Translocations There’s a Ligase at the End of the Translocation. CHROMOSOME TRANSLOCATION, 1044, 89-112. doi:10.1007/978-981-13-0593-1_7
Li, G., Martinez-Bonet, M., Wu, D., Yang, Y., Cui, J., Nguyen, H. N., . . . Nigrovic, P. A. (2018). High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction. NATURE GENETICS, 50(8), 1180-+. doi:10.1038/s41588-018-0159-z
Gu, P., Jia, S., Takasugi, T., Smith, E., Nandakumar, J., Hendrickson, E., & Chang, S. (2018). CTC1-STN1 coordinates G- and C-strand synthesis to regulate telomere length. AGING CELL, 17(4). doi:10.1111/acel.12783
Kawale, A. S., Akopiants, K., Valerie, K., Ruis, B., Hendrickson, E. A., Huang, S. -Y. N., . . . Povirk, L. F. (2018). TDP1 suppresses mis-joining of radiomimetic DNA double-strand breaks and cooperates with Artemis to promote optimal nonhomologous end joining. NUCLEIC ACIDS RESEARCH, 46(17), 8926-8939. doi:10.1093/nar/gky694
2017
Kan, Y., Batada, N. N., & Hendrickson, E. A. (2017). Human somatic cells deficient for RAD52 are impaired for viral integration and compromised for most aspects of homology-directed repair. DNA REPAIR, 55, 64-75. doi:10.1016/j.dnarep.2017.04.006
Kan, Y., Ruis, B., Takasugi, T., & Hendrickson, E. A. (2017). Mechanisms of precise genome editing using oligonucleotide donors. GENOME RESEARCH, 27(7), 1099-1111. doi:10.1101/gr.214775.116
Thompson, E. L., Yeo, J. E., Lee, E. -A., Kan, Y., Raghunandan, M., Wiek, C., . . . Sobeck, A. (2017). FANCI and FANCD2 have common as well as independent functions during the cellular replication stress response. NUCLEIC ACIDS RESEARCH, 45(20), 11837-11857. doi:10.1093/nar/gkx847
2016
Liddiard, K., Ruis, B., Takasugi, T., Harvey, A., Ashelford, K. E., Hendrickson, E. A., & Baird, D. M. (2016). Sister chromatid telomere fusions, but not NHEJ-mediated inter-chromosomal telomere fusions, occur independently of DNA ligases 3 and 4. GENOME RESEARCH, 26(5), 588-600. doi:10.1101/gr.200840.115
Neal, J. A., Xu, Y., Abe, M., Hendrickson, E., & Meek, K. (2016). Restoration of ATM Expression in DNA-PKcs-Deficient Cells Inhibits Signal End Joining. JOURNAL OF IMMUNOLOGY, 196(7), 3032-3042. doi:10.4049/jimmunol.1501654
Alotaibi, M., Sharma, K., Saleh, T., Povirk, L. F., Hendrickson, E. A., & Gewirtz, D. A. (2016). Radiosensitization by PARP Inhibition in DNA Repair Proficient and Deficient Tumor Cells: Proliferative Recovery in Senescent Cells. RADIATION RESEARCH, 185(3), 229-245. doi:10.1667/RR14202.1
2015
Thangavel, S., Berti, M., Levikova, M., Pinto, C., Gomathinayagam, S., Vujanovic, M., . . . Vindigni, A. (2015). DNA2 drives processing and restart of reversed replication forks in human cells.. The Journal of cell biology, 208(5), 545-562. doi:10.1083/jcb.201406100
Hendrickson, E. A., & Baird, D. M. (2015). Alternative end joining, clonal evolution, and escape from a telomere-driven crisis. MOLECULAR & CELLULAR ONCOLOGY, 2(1). doi:10.4161/23723556.2014.975623
Batenburg, N. L., Thompson, E. L., Hendrickson, E. A., & Zhu, X. -D. (2015). Cockayne syndrome group B protein regulates DNA double-strand break repair and checkpoint activation. EMBO JOURNAL, 34(10), 1399-1416. doi:10.15252/embj.201490041
Li, Y., Park, A. I., Mou, H., Colpan, C., Bizhanova, A., Akama-Garren, E., . . . Xue, W. (2015). A versatile reporter system for CRISPR-mediated chromosomal rearrangements. GENOME BIOLOGY, 16. doi:10.1186/s13059-015-0680-7
Napier, C. E., Huschtscha, L. I., Harvey, A., Bower, K., Noble, J. R., Hendrickson, E. A., & Reddel, R. R. (2015). ATRX represses alternative lengthening of telomeres. ONCOTARGET, 6(18), 16543-16558. doi:10.18632/oncotarget.3846
Castella, M., Jacquemont, C., Thompson, E. L., Yeo, J. E., Cheung, R. S., Huang, J. -W., . . . Taniguchi, T. (2015). FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2. PLoS Genetics, 11(10). doi:10.1371/journal.pgen.1005563
Roy, S., de Melo, A. J., Xu, Y., Tadi, S. K., Negrel, A., Hendrickson, E., . . . Meek, K. (2015). XRCC4/XLF Interaction Is Variably Required for DNA Repair and Is Not Required for Ligase IV Stimulation. MOLECULAR AND CELLULAR BIOLOGY, 35(17), 3017-3028. doi:10.1128/MCB.01503-14
2014
Smith, S., Fox, J., Mejia, M., Ruangpradit, W., Saberi, A., Kim, S., . . . Myung, K. (2014). Histone Deacetylase Inhibitors Selectively Target Homology Dependent DNA Repair Defective Cells and Elevate Non-Homologous Endjoining Activity. PLOS ONE, 9(1). doi:10.1371/journal.pone.0087203
Fattah, F. J., Kweon, J., Wang, Y., Lee, E. H., Kan, Y., Lichter, N., . . . Hendrickson, E. A. (2014). A role for XLF in DNA repair and recombination in human somatic cells. DNA REPAIR, 15, 39-53. doi:10.1016/j.dnarep.2013.12.006
Yeo, J. E., Lee, E. H., Hendrickson, E. A., & Sobeck, A. (2014). CtIP mediates replication fork recovery in a FANCD2-regulated manner. HUMAN MOLECULAR GENETICS, 23(14), 3695-3705. doi:10.1093/hmg/ddu078
Karanja, K. K., Lee, E. H., Hendrickson, E. A., & Campbell, J. L. (2014). Preventing over-resection by DNA2 helicase/nuclease suppresses repair defects in Fanconi anemia cells. CELL CYCLE, 13(10), 1540-1550. doi:10.4161/cc.28476
Oh, S., Harvey, A., Zimbric, J., Wang, Y., Thanh, N., Jackson, P. J., & Hendrickson, E. A. (2014). DNA ligase III and DNA ligase IV carry out genetically distinct forms of end joining in human somatic cells. DNA REPAIR, 21, 97-110. doi:10.1016/j.dnarep.2014.04.015
Kan, Y., Ruis, B., Lin, S., & Hendrickson, E. A. (2014). The Mechanism of Gene Targeting in Human Somatic Cells. PLOS GENETICS, 10(4). doi:10.1371/journal.pgen.1004251
Waters, C. A., Strande, N. T., Pryor, J. M., Strom, C. N., Mieczkowski, P., Burkhalter, M. D., . . . Ramsden, D. A. (2014). The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining. NATURE COMMUNICATIONS, 5. doi:10.1038/ncomms5286
Ghezraoui, H., Piganeau, M., Renouf, B., Renaud, J. -B., Sallmyr, A., Ruis, B., . . . Brunet, E. (2014). Chromosomal Translocations in Human Cells Are Generated by Canonical Nonhomologous End-Joining. MOLECULAR CELL, 55(6), 829-842. doi:10.1016/j.molcel.2014.08.002
Jones, R. E., Oh, S., Grimstead, J. W., Zimbric, J., Roger, L., Heppel, N. H., . . . Baird, D. M. (2014). Escape from Telomere-Driven Crisis Is DNA Ligase III Dependent. CELL REPORTS, 8(4), 1063-1076. doi:10.1016/j.celrep.2014.07.007
2013
Yang, Y., Durando, M., Smith-Roe, S. L., Sproul, C., Greenwalt, A. M., Kaufmann, W., . . . Vaziri, C. (2013). Cell cycle stage-specific roles of Rad18 in tolerance and repair of oxidative DNA damage. NUCLEIC ACIDS RESEARCH, 41(4), 2296-2312. doi:10.1093/nar/gks1325
Oh, S., Wang, Y., Zimbric, J., & Hendrickson, E. A. (2013). Human LIGIV is synthetically lethal with the loss of Rad54B-dependent recombination and is required for certain chromosome fusion events induced by telomere dysfunction. NUCLEIC ACIDS RESEARCH, 41(3), 1734-1749. doi:10.1093/nar/gks1326