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Items: 1 to 20 of 24

1.
Suppression of retroviral infection by the RAD52 DNA repair protein
Alan Lau, Roland Kanaar, Stephen P Jackson, Mark J O'Connor
EMBO J. 2004 Aug 18; 23(16): 3421–3429. Published online 2004 Aug 5. doi: 10.1038/sj.emboj.7600348
PMCID:
PMC514521
ArticlePDF–226K
2.
Nucleotide sequence of small polyadenylated B2 RNA.
D A Kramerov, S V Tillib, A P Ryskov, G P Georgiev
Nucleic Acids Res. 1985 Sep 25; 13(18): 6423–6437. doi: 10.1093/nar/13.18.6423
PMCID:
PMC321968
SummaryPage BrowsePDF–1.8M
3.
Targeted Inactivation of Mouse RAD52 Reduces Homologous Recombination but Not Resistance to Ionizing Radiation
Tonnie Rijkers, Jody Van Den Ouweland, Bruno Morolli, Anton G. Rolink, Willy M. Baarends, Petra P. H. Van Sloun, Paul H. M. Lohman, Albert Pastink
Mol Cell Biol. 1998 Nov; 18(11): 6423–6429. doi: 10.1128/mcb.18.11.6423
PMCID:
PMC109228
ArticlePDF–274K
4.
RAD52 Adjusts Repair of Single-Strand Breaks via Reducing DNA-Damage-Promoted XRCC1/LIG3α Co-localization
Jian Wang, You-Take Oh, Zhentian Li, Juan Dou, Siyuan Tang, Xiang Wang, Hongyan Wang, Shunichi Takeda, Ya Wang
Cell Rep. Author manuscript; available in PMC 2021 Feb 9.
Published in final edited form as: Cell Rep. 2021 Jan 12; 34(2): 108625. doi: 10.1016/j.celrep.2020.108625
PMCID:
PMC7872142
ArticlePDF–1.5M
5.
Simultaneous Targeting of PARP1 and RAD52 Triggers Dual Synthetic Lethality in BRCA-Deficient Tumor Cells
Katherine Sullivan-Reed, Elisabeth Bolton-Gillespie, Yashodhara Dasgupta, Samantha Langer, Micheal Siciliano, Margaret Nieborowska-Skorska, Kritika Hanamshet, Elizaveta A. Belyaeva, Andrea J. Bernhardy, Jaewong Lee, Morgan Moore, Huaqing Zhao, Peter Valent, Ksenia Matlawska-Wasowska, Markus Müschen, Smita Bhatia, Ravi Bhatia, Neil Johnson, Mariusz A. Wasik, Alexander V. Mazin, Tomasz Skorski
Cell Rep. Author manuscript; available in PMC 2018 Aug 8.
Published in final edited form as: Cell Rep. 2018 Jun 12; 23(11): 3127–3136. doi: 10.1016/j.celrep.2018.05.034
PMCID:
PMC6082171
ArticlePDF–1.3M
6.
The concerted roles of FANCM and Rad52 in the protection of common fragile sites
Hailong Wang, Shibo Li, Joshua Oaks, Jianping Ren, Lei Li, Xiaohua Wu
Nat Commun. 2018; 9: 2791. Published online 2018 Jul 18. doi: 10.1038/s41467-018-05066-y
PMCID:
PMC6052092
ArticlePDF–1.2M
7.
Rad52 deficiency decreases development of lung squamous cell carcinomas by enhancing immuno-surveillance
Rachel Lieberman, Jing Pan, Qi Zhang, Ming You
Oncotarget. 2017 May 23; 8(21): 34032–34044. Published online 2017 Mar 18. doi: 10.18632/oncotarget.16371
PMCID:
PMC5470949
ArticlePDF–1.2M
8.
The HSV-1 Exonuclease, UL12, Stimulates Recombination by a Single Strand Annealing Mechanism
April J. Schumacher, Kareem N. Mohni, Yinan Kan, Eric A. Hendrickson, Jeremy M. Stark, Sandra K. Weller
PLoS Pathog. 2012 Aug; 8(8): e1002862. Published online 2012 Aug 9. doi: 10.1371/journal.ppat.1002862
PMCID:
PMC3415443
ArticlePDF–908K
9.
Mammalian RAD52 Functions in Break-Induced Replication Repair of Collapsed DNA Replication Forks
Sotirios K. Sotiriou, Irene Kamileri, Natalia Lugli, Konstantinos Evangelou, Caterina Da-Ré, Florian Huber, Laura Padayachy, Sebastien Tardy, Noemie L. Nicati, Samia Barriot, Fena Ochs, Claudia Lukas, Jiri Lukas, Vassilis G. Gorgoulis, Leonardo Scapozza, Thanos D. Halazonetis
Mol Cell. 2016 Dec 15; 64(6): 1127–1134. doi: 10.1016/j.molcel.2016.10.038
PMCID:
PMC5179496
Article
10.
Rad54 is required for the normal development of male and female germ cells and contributes to the maintainance of their genome integrity after genotoxic stress
S Messiaen, A Le Bras, C Duquenne, V Barroca, D Moison, N Déchamps, M Doussau, A-L Bauchet, M-J Guerquin, G Livera, J Essers, R Kanaar, R Habert, J Bernardino-Sgherri
Cell Death Dis. 2013 Aug; 4(8): e774. Published online 2013 Aug 15. doi: 10.1038/cddis.2013.281
PMCID:
PMC3763443
ArticlePDF–2.9M
11.
Cells Expressing Murine RAD52 Splice Variants Favor Sister Chromatid Repair
Peter H. Thorpe, Vanessa A. Marrero, Margaret H. Savitzky, Ivana Sunjevaric, Tom C. Freeman, Rodney Rothstein
Mol Cell Biol. 2006 May; 26(10): 3752–3763. doi: 10.1128/MCB.26.10.3752-3763.2006
PMCID:
PMC1488992
ArticlePDF–515K
12.
Rad52 mediates class-switch DNA recombination to IgD
Yijiang Xu, Hang Zhou, Ginell Post, Hong Zan, Paolo Casali
Nat Commun. 2022; 13: 980. Published online 2022 Feb 21. doi: 10.1038/s41467-022-28576-2
PMCID:
PMC8861003
ArticlePDF–5.6M
13.
Rad52 competes with Ku70/Ku86 for binding to S-region DSB ends to modulate antibody class-switch DNA recombination
Hong Zan, Connie Tat, Zhifang Qiu, Julia R. Taylor, Justin A. Guerrero, Tian Shen, Paolo Casali
Nat Commun. 2017; 8: 14244. Published online 2017 Feb 8. doi: 10.1038/ncomms14244
PMCID:
PMC5309807
ArticlePDF–5.2M
14.
Timeless Maintains Genomic Stability and Suppresses Sister Chromatid Exchange during Unperturbed DNA Replication
Karen A. Urtishak, Kevin D. Smith, Rebecca A. Chanoux, Roger A. Greenberg, F. Brad Johnson, Eric J. Brown
J Biol Chem. 2009 Mar 27; 284(13): 8777–8785. doi: 10.1074/jbc.M806103200
PMCID:
PMC2659236
ArticlePDF–670K
15.
The Recombination Protein RAD52 Cooperates with the Excision Repair Protein OGG1 for the Repair of Oxidative Lesions in Mammalian Cells
Nadja C. de Souza-Pinto, Scott Maynard, Kazunari Hashiguchi, Jingping Hu, Meltem Muftuoglu, Vilhelm A. Bohr
Mol Cell Biol. 2009 Aug; 29(16): 4441–4454. Published online 2009 Jun 8. doi: 10.1128/MCB.00265-09
PMCID:
PMC2725742
ArticlePDF–2.4M
16.
A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome
Jens Hansen, Thomas Floss, Petra Van Sloun, Ernst-Martin Füchtbauer, Franz Vauti, Hans-Hennig Arnold, Frank Schnütgen, Wolfgang Wurst, Harald von Melchner, Patricia Ruiz
Proc Natl Acad Sci U S A. 2003 Aug 19; 100(17): 9918–9922. Published online 2003 Aug 6. doi: 10.1073/pnas.1633296100
PMCID:
PMC187885
ArticlePDF–287K
17.
BayGenomics: a resource of insertional mutations in mouse embryonic stem cells
Doug Stryke, Michiko Kawamoto, Conrad C. Huang, Susan J. Johns, Leslie A. King, Courtney A. Harper, Elaine C. Meng, Roy E. Lee, Alice Yee, Larry L'Italien, Pao-Tien Chuang, Stephen G. Young, William C. Skarnes, Patricia C. Babbitt, Thomas E. Ferrin
Nucleic Acids Res. 2003 Jan 1; 31(1): 278–281. doi: 10.1093/nar/gkg064
PMCID:
PMC165511
ArticlePDF–217K
18.
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
Gwenn M. Hansen, Diane C. Markesich, Michael B. Burnett, Qichao Zhu, Karen M. Dionne, Lizabeth J. Richter, Richard H. Finnell, Arthur T. Sands, Brian P. Zambrowicz, Alejandro Abuin
Genome Res. 2008 Oct; 18(10): 1670–1679. doi: 10.1101/gr.078352.108
PMCID:
PMC2556270
ArticlePDF–493K
19.
Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention
Brian P. Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, Lizabeth J. Richter, James Piggott, Hector BeltrandelRio, Eric C. Buxton, Joel Edwards, Rick A. Finch, Carl J. Friddle, Anupma Gupta, Gwenn Hansen, Yi Hu, Wenhu Huang, Crystal Jaing, Billie Wayne Key, Jr., Peter Kipp, Buckley Kohlhauff, Zhi-Qing Ma, Diane Markesich, Robert Payne, David G. Potter, Ny Qian, Joseph Shaw, Jeff Schrick, Zheng-Zheng Shi, Mary Jean Sparks, Isaac Van Sligtenhorst, Peter Vogel, Wade Walke, Nianhua Xu, Qichao Zhu, Christophe Person, Arthur T. Sands
Proc Natl Acad Sci U S A. 2003 Nov 25; 100(24): 14109–14114. Published online 2003 Nov 10. doi: 10.1073/pnas.2336103100
Correction in:
Proc Natl Acad Sci U S A. 2004 Mar 23; 101(12): 4332.
PMCID:
PMC283554
ArticlePDF–481K
20.
A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo
Graciana Diez-Roux, Sandro Banfi, Marc Sultan, Lars Geffers, Santosh Anand, David Rozado, Alon Magen, Elena Canidio, Massimiliano Pagani, Ivana Peluso, Nathalie Lin-Marq, Muriel Koch, Marchesa Bilio, Immacolata Cantiello, Roberta Verde, Cristian De Masi, Salvatore A. Bianchi, Juliette Cicchini, Elodie Perroud, Shprese Mehmeti, Emilie Dagand, Sabine Schrinner, Asja Nürnberger, Katja Schmidt, Katja Metz, Christina Zwingmann, Norbert Brieske, Cindy Springer, Ana Martinez Hernandez, Sarah Herzog, Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel Garcia-Lopez, Diego Echevarria, Eduardo Puelles, Elena Garcia-Calero, Stefan Kruse, Markus Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan R. Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie-Laure Yaspo, Salvador Martinez, Richard A. Baldock, Gregor Eichele, Andrea Ballabio
PLoS Biol. 2011 Jan; 9(1): e1000582. Published online 2011 Jan 18. doi: 10.1371/journal.pbio.1000582
PMCID:
PMC3022534
ArticlePDF–3.8M

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