Citations for
1RAD51B, 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
2RAD51B, 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
3RAD51B, 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
4BRCA1, 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
5RAD51B, 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
6RAD51D
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families.
Osher DJ, De Leeneer K, Michils G, Hamel N, Tomiak E, Poppe B, Leunen K, Legius E, Shuen A, Smith E, Arseneau J, Tonin P, Matthijs G, Claes K, Tischkowitz MD, Foulkes WD.
Br J Cancer 106(8):1460-3. doi: 10.1038/bjc.2012.87. Epub 2012 Mar 13. 2012
7RAD51C, 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
8RAD51D
Germline mutations in RAD51D confer susceptibility to ovarian cancer.
Loveday C, Turnbull C, Ramsay E, Hughes D, Ruark E, Frankum JR, Bowden G, Kalmyrzaev B, Warren-Perry M, Snape K, Adlard JW, Barwell J, Berg J, Brady AF, Brewer C, Brice G, Chapman C, Cook J, Davidson R, Donaldson A, Douglas F, Greenhalgh L, Henderson A, Izatt L, Kumar A, Lalloo F, Miedzybrodzka Z, Morrison PJ, Paterson J, Porteous M, Rogers MT, Shanley S, Walker L; Breast Cancer Susceptibility Collaboration (UK), Eccles D, Evans DG, Renwick A, Seal S, Lord CJ, Ashworth A, Reis-Filho JS, Antoniou AC, Rahman N.
Nat Genet 43(9):879-82. doi: 10.1038/ng.893. 2011
9RAD51D
Structural and functional characterization of the N-terminal domain of human Rad51D.
Kim YM, Choi BS.
Int J Biochem Cell Biol 43(3):416-22. Epub 2010 Nov 24. 2011
10RAD51B, 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
11RAD51C, 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
12RAD51D
The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women.
Dowty JG, Lose F, Jenkins MA, Chang JH, Chen X, Beesley J, Dite GS, Southey MC, Byrnes GB, Tesoriero A, Giles GG, Hopper JL, Spurdle AB; kConFab Investigators; Australian Breast Cancer Family Study (ABCFS).
Breast Cancer Res Treat 112(1):35-9. Epub 2007 Dec 4. 2008
13RAD51D
Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination.
Wiese C, Hinz JM, Tebbs RS, Nham PB, Urbin SS, Collins DW, Thompson LH, Schild D.
Nucleic Acids Res 34(9):2833-43. Print 2006. 2006
14RAD51B, RAD51C, RAD51D, XRCC2, XRCC3
The RAD51 gene family, genetic instability and cancer.
Thacker J.
Cancer Lett 219(2):125-35. Review. 2005
15RAD51D
Telomere maintenance requires the RAD51D recombination/repair protein.
Tarsounas M, Munoz P, Claas A, Smiraldo PG, Pittman DL, Blasco MA, West SC.
Cell 117(3):337-47. 2004
16BLM, RAD51D
Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D).
Braybrooke JP, Li JL, Wu L, Caple F, Benson FE, Hickson ID.
J Biol Chem 278(48):48357-66. Epub 2003 Sep 15. 2003
17RAD51D
The RAD51 family member, RAD51L3, is a DNA-stimulated ATPase that forms a complex with XRCC2.
Braybrooke JP, Spink KG, Thacker J, Hickson ID.
J Biol Chem 275(37):29100-6. 2000
18RAD51D
Identification, characterization, and genetic mapping of Rad51d, a new mouse and human RAD51/RecA-related gene.
Pittman DL, et al.
Genomics 49 : 103-111. 1998