Citations for
1RAD51C, XRCC3
Hot on RAD51C: structure and functions of RAD51C-XRCC3.
Szakal B, Branzei D.
Mol Oncol. Oct;17(10):1950-1952. doi: 10.1002/1878-0261.13518. Epub 2023 Sep 11. 2023
2RAD51C, XRCC3
RAD51 paralogs synergize with RAD51 to protect reversed forks from cellular nucleases
Guh CL, Lei KH, Chen YA, Jiang YZ, Chang HY, Liaw H, Li HW, Yen HY, Chi P.
Nucleic Acids Res. Nov 27;51(21):11717-11731. doi: 10.1093/nar/gkad856. 2023
3RAD51B, RAD51D, RAD51c, XRCC2, XRCC3
Sequential role of RAD51 paralog complexes in replication fork remodeling and restart
Berti M, Teloni F, Mijic S, Ursich S, Fuchs J, Palumbieri MD, Krietsch J, Schmid JA, Garcin EB, Gon S, Modesti M, Altmeyer M, Lopes M.
Nat Commun. Jul 15;11(1):3531. doi: 10.1038/s41467-020-17324-z. 2020
4RAD51B, RAD51D, RAD51c, XRCC2, XRCC3
Differential Requirements for the RAD51 Paralogs in Genome Repair and Maintenance in Human Cells
Garcin EB, Gon S, Sullivan MR, Brunette GJ, Cian A, Concordet JP, Giovannangeli C, Dirks WG, Eberth S, Bernstein KA, Prakash R, Jasin M, Modesti M
PLoS Genet. Oct 4;15(10):e1008355. doi: 10.1371/journal.pgen.1008355. 2019
5RAD51C, XRCC3
RAD51C/XRCC3 Facilitates Mitochondrial DNA Replication and Maintains Integrity of the Mitochondrial Genome
Mishra A, Saxena S, Kaushal A, Nagaraju G.
Mol Cell Biol. Jan 16;38(3):e00489-17. doi: 10.1128/MCB.00489-17. 2018
6RAD51B, RAD51D, RAD51c, XRCC2, XRCC3
Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers
Golmard L, Castéra L, Krieger S, Moncoutier V, Abidallah K, Tenreiro H, Laugé A, Tarabeux J, Millot GA, Nicolas A, Laé M, Abadie C, Berthet P, Polycarpe F, Frébourg T, Elan C, de Pauw A, Gauthier-Villars M, Buecher B, Stern MH, Stoppa-Lyonnet D, Vaur D, Houdayer C.
Eur J Hum Genet Dec;25(12):1345-1353. doi: 10.1038/s41431-017-0021-2. Epub 2017 Nov 8. 2017
7BRCA1, FANCR, FANCS, FANCT, FANCU, FANCV, MAD2L2, RAD51, RAD51B, RAD51C, RAD51D, REV3L, UBE2T, XRCC2
Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia.
Mamrak NE, Shimamura A, Howlett NG.
Blood Rev lood Rev. 2016 Oct 13. pii: S0268-960X(16)30054-6. doi: 10.1016/j.blre.2016.10.002. Review. 2016
8RAD51B, RAD51C, RAD51D, XRCC2, XRCC3
The RAD51 paralogs ensure cellular protection against mitotic defects and aneuploidy.
Rodrigue A, Coulombe Y, Jacquet K, Gagné JP, Roques C, Gobeil S, Poirier G, Masson JY.
J Cell Sci 126(Pt 1):348-59. doi: 10.1242/jcs.114595. Epub 2012 Oct 29. 2013
9ATR, HELQ, RAD51A, RAD51B, RAD51C, XRCC2
Human DNA helicase HELQ participates in DNA interstrand crosslink tolerance with ATR and RAD51 paralogs.
Takata K, Reh S, Tomida J, Person MD, Wood RD.
Nat Commun 4:2338. doi: 10.1038/ncomms3338. 2013
10RAD51C, XRCC3
ATM- and ATR-mediated phosphorylation of XRCC3 regulates DNA double-strand break-induced checkpoint activation and repair.
Somyajit K, Basavaraju S, Scully R, Nagaraju G.
Mol Cell Biol. May;33(9):1830-44. doi: 10.1128/MCB.01521-12. Epub 2013 Feb 25 2013
11RAD51C
Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.
Somyajit K, Subramanya S, Nagaraju G.
J Biol Chem 287(5):3366-80. Epub 2011 Dec 13. 2012
12RAD51C
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
Thompson ER, Boyle SE, Johnson J, Ryland GL, Sawyer S, Choong DY, kConFab, Chenevix-Trench G, Trainer AH, Lindeman GJ, Mitchell G, James PA, Campbell IG.
Hum Mutat 33(1):95-9. doi: 10.1002/humu.21625. Epub 2011 Nov 4. 2012
13RAD51C
Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.
Osorio A, Endt D, Fernández F, Eirich K, de la Hoya M, Schmutzler R, Caldés T, Meindl A, Schindler D, Benitez J.
Hum Mol Genet 21(13):2889-98. doi: 10.1093/hmg/dds115. Epub 2012 Mar 26. 2012
14RAD51C, RAD51D
Germline RAD51C mutations confer susceptibility to ovarian cancer.
Loveday C, Turnbull C, Ruark E, Xicola RM, Ramsay E, Hughes D, Warren-Perry M, Snape K; Breast Cancer Susceptibility Collaboration (UK), Eccles D, Evans DG, Gore M, Renwick A, Seal S, Antoniou AC, Rahman N.
Nat Genet 44(5):475-6; author reply 476. doi: 10.1038/ng.2224. No abstract available. 2012
15RAD51C
RAD51C is a susceptibility gene for ovarian cancer.
Pelttari LM, Heikkinen T, Thompson D, Kallioniemi A, Schleutker J, Holli K, Blomqvist C, Aittomäki K, Bützow R, Nevanlinna H.
Hum Mol Genet 20(16):3278-88. Epub 2011 May 25. 2011
16RAD51C
RAD51C germline mutations in breast and ovarian cancer cases from high-risk families.
Clague J, Wilhoite G, Adamson A, Bailis A, Weitzel JN, Neuhausen SL.
PLoS One 6(9):e25632. Epub 2011 Sep 28. 2011
17BARD1, BRCA1, BRCA2, BRIP1, CHEK2, MRE11A, MSH6, NBN, PALB2, RAD50, RAD51c, TP53
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
Walsh T, Casadei S, Lee MK, Pennil CC, Nord AS, Thornton AM, Roeb W, Agnew KJ, Stray SM, Wickramanayake A, Norquist B, Pennington KP, Garcia RL, King MC, Swisher EM.
Proc Natl Acad Sci U S A 108(44):18032-7. doi: 10.1073/pnas.1115052108. Epub 2011 Oct 17. 2011
18RAD51B, RAD51C, RAD51D, XRCC2, XRCC3
RAD51 paralogs: roles in DNA damage signalling, recombinational repair and tumorigenesis.
Suwaki N, Klare K, Tarsounas M.
Semin Cell Dev Biol 22(8):898-905. doi: 10.1016/j.semcdb.2011.07.019. Epub 2011 Jul 28. Review. 2011
19FANCO, RAD51C
Mutation of the RAD51C gene in a Fanconi anemia-like disorder.
Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V, Neveling K, Endt D, Kesterton I, Autore F, Fraternali F, Freund M, Hartmann L, Grimwade D, Roberts RG, Schaal H, Mohammed S, Rahman N, Schindler D, Mathew CG.
Nat Genet 42(5):406-9. Epub 2010 Apr 18. 2010
20FANCO, RAD51C
Fanconi anemia and breast cancer susceptibility meet again.
Levy-Lahad E.
Nat Genet 42(5):368-9. 2010
21FANCO, RAD51C
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Meindl A, Hellebrand H, Wiek C, Erven V, Wappenschmidt B, Niederacher D, Freund M, Lichtner P, Hartmann L, Schaal H, Ramser J, Honisch E, Kubisch C, Wichmann HE, Kast K, Deissler H, Engel C, Müller-Myhsok B, Neveling K, Kiechle M, Mathew CG, Schindler D, Schmutzler RK, Hanenberg H.
Nat Genet 42(5):410-4. Epub 2010 Apr 18.PMID: 20400964 2010
22RAD51, RAD51C, XRCC3
Discovery of a novel function for human Rad51: maintenance of the mitochondrial genome.
Sage JM, Gildemeister OS, Knight KL.
J Biol Chem 285(25):18984-90. Epub 2010 Apr 22.PMID: 20413593 2010
23FACM, FAN1, RAD51C
Expanded roles of the Fanconi anemia pathway in preserving genomic stability.
Kee Y, D'Andrea AD.
Genes Dev 24(16):1680-94. Review.PMID: 20713514 2010
24RAD51C
Rad51C is essential for embryonic development and haploinsufficiency causes increased DNA damage sensitivity and genomic instability.
Smeenk G, de Groot AJ, Romeijn RJ, van Buul PP, Zdzienicka MZ, Mullenders LH, Pastink A, Godthelp BC.
Mutat Res 689(1-2):50-8. Epub 2010 May 13. 2010
25RAD51C
The ATR-Chk1 pathway plays a role in the generation of centrosome aberrations induced by Rad51C dysfunction.
Katsura M, Tsuruga T, Date O, Yoshihara T, Ishida M, Tomoda Y, Okajima M, Takaku M, Kurumizaka H, Kinomura A, Mishima HK, Miyagawa K.
Nucleic Acids Res 37(12):3959-68. Epub 2009 Apr 29. 2009
26RAD51C, RAD51D
The interaction profile of homologous recombination repair proteins RAD51C, RAD51D and XRCC2 as determined by proteomic analysis.
Rajesh C, Gruver AM, Basrur V, Pittman DL.
Proteomics 9(16):4071-86. 2009
27RAD51C
Common single-nucleotide polymorphisms in DNA double-strand break repair genes and breast cancer risk.
Pooley KA, Baynes C, Driver KE, Tyrer J, Azzato EM, Pharoah PD, Easton DF, Ponder BA, Dunning AM.
Cancer Epidemiol Biomarkers Prev. ooley KA, Baynes C, Driver KE, Tyrer J, Azzato EM, Pharoah Dec;17(12):3482-9. doi: 10.1158/1055-9965.EPI-08-0594. 2008
28RAD51C, XRCC3
Role of RAD51C and XRCC3 in genetic recombination and DNA repair.
Liu Y, Tarsounas M, O'regan P, West SC.
J Biol Chem 282(3):1973-9. Epub 2006 Nov 17. 2007
29RAD51C
RAD51C (RAD51L2) is involved in maintaining centrosome number in mitosis.
Renglin Lindh A, Schultz N, Saleh-Gohari N, Helleday T.
Cytogenet Genome Res 116(1-2):38-45. 2007
30RAD51B, RAD51C, RAD51D, XRCC2, XRCC3
The RAD51 gene family, genetic instability and cancer.
Thacker J.
Cancer Lett 219(2):125-35. Review. 2005
31RAD51C
RAD51C is required for Holliday junction processing in mammalian cells.
Liu Y, Masson JY, Shah R, O'Regan P, West SC.
Science 303(5655):243-6. 2004
32RAD51C
Identification of functional domains in the RAD51L2 (RAD51C) protein and its requirement for gene conversion.
French CA, Tambini CE, Thacker J.
J Biol Chem 278(46):45445-50. Epub 2003 Sep 8. 2003
33RAD51C
Sequence, chromosomal location and expression analysis of the murine homologue of human RAD51L2/RAD51C.
Leasure CS, Chandler J, Gilbert DJ, Householder DB, Stephens R, Copeland NG, Jenkins NA, Sharan SK.
Gene 271(1):59-67. 2001
34MKS1, TRIM37, RAD51C
High-resolution physical and genetic mapping of the critical region for meckel syndrome and mulibrey nanism on chromosome 17q22-q23.
Paavola P, et al.
Genome Res 9(3):267-76. 1999
35RAD51B, RAD51C
Isolation of novel human and mouse genes of the recA/RAD51 recombination-repair gene family.
Cartwright R, et al.
Nucleic Acids Res 26 : 1653-1659. 1998
36RAD51C
Isolation and characterization of RAD51C, a new human member of the RAD51 family of related genes.
Dosanjh MK, Collins DW, Fan W, Lennon GG, Albala JS, Shen Z, Schild D.
Nucleic Acids Res 26(5):1179-84. 1998