| 1 | GID4, RAD51B
|
| A pan-sarcoma landscape of telomeric content shows that alterations in RAD51B and GID4 are associated with higher telomeric content. 2023 PMID:
|
| Sharaf R, Jin DX, Grady J, Napier C, Ebot E, Frampton GM, Albacker LA, Thomas DM, Montesion M.
|
| NPJ Genom Med. Sep 14;8(1):26. doi: 10.1038/s41525-023-00369-6. 2023
|
| 2 | RAD51B, 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
|
| 3 | RAD51B, 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
|
| 4 | RAD51B, 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
|
| 5 | BRCA1, 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
|
| 6 | RAD51B, 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
|
| 7 | ATR, 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
|
| 8 | RAD51B
|
| Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
|
| Orr N, Lemnrau A, Cooke R, Fletcher O, Tomczyk K, Jones M, Johnson N, Lord CJ, Mitsopoulos C, Zvelebil M, McDade SS, Buck G, Blancher C; KConFab Consortium, Trainer AH, James PA, Bojesen SE, Bokmand S, Nevanlinna H, Mattson J, Friedman E, Laitman Y, Palli D, Masala G, Zanna I, Ottini L, Giannini G, Hollestelle A, Ouweland AM, Novaković S, Krajc M, Gago-Dominguez M, Castelao JE, Olsson H, Hedenfalk I, Easton DF, Pharoah PD, Dunning AM, Bishop DT, Neuhausen SL, Steele L, Houlston RS, Garcia-Closas M, Ashworth A, Swerdlow AJ.
|
| Nat Genet 44(11):1182-4. doi: 10.1038/ng.2417. Epub 2012 Sep 23.
2012
|
| 9 | RAD51B, 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
|
| 10 | RAD51B
|
| Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families.
|
| Johnson J, Healey S, Khanna KK; kConFab, Chenevix-Trench G.
|
| Breast Cancer Res Treat 129(1):255-63. doi: 10.1007/s10549-011-1539-6. Epub 2011 Apr 28.
2011
|
| 11 | RAD51B
|
| Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.
|
| Figueroa JD, Garcia-Closas M, Humphreys M, Platte R, Hopper JL, Southey MC, Apicella C, Hammet F, Schmidt MK, Broeks A, Tollenaar RA, Van't Veer LJ, Fasching PA, Beckmann MW, Ekici AB, Strick R, Peto J, dos Santos Silva I, Fletcher O, Johnson N, Sawyer E, Tomlinson I, Kerin M, Burwinkel B, Marme F, Schneeweiss A, Sohn C, Bojesen S, Flyger H, Nordestgaard BG, Benítez J, Milne RL, Ignacio Arias J, Zamora MP, Brenner H, Müller H, Arndt V, Rahman N, Turnbull C, Seal S, Renwick A, Brauch H, Justenhoven C, Brüning T; GENICA Network, Chang-Claude J, Hein R, Wang-Gohrke S, Dörk T, Schürmann P, Bremer M, Hillemanns P, Nevanlinna H, Heikkinen T, Aittomäki K, Blomqvist C, Bogdanova N, Antonenkova N, Rogov YI, Karstens JH, Bermisheva M, Prokofieva D, Gantcev SH, Khusnutdinova E, Lindblom A, Margolin S, Chenevix-Trench G, Beesley J, Chen X; kConFab AOCS Management Group, Mannermaa A, Kosma VM, Soini Y, Kataja V, Lambrechts D, Yesilyurt BT, Chrisiaens MR, Peeters S, Radice P, Peterlongo P, Manoukian S, Barile M, Couch F, Lee AM, Diasio R, Wang X, Giles GG, Severi G, Baglietto L, Maclean C, Offit K, Robson M, Joseph V, Gaudet M, John EM, Winqvist R, Pylkäs K, Jukkola-Vuorinen A, Grip M, Andrulis I, Knight JA, Mulligan AM, O'Malley FP, Brinton LA, Sherman ME, Lissowska J, Chanock SJ, Hooning M, Martens JW, van den Ouweland AM, Collée JM, Hall P, Czene K, Cox A, Brock IW, Reed MW, Cross SS, Pharoah P, Dunning AM, Kang D, Yoo KY, Noh DY, Ahn SH, Jakubowska A, Lubinski J, Jaworska K, Durda K, Sangrajrang S, Gaborieau V, Brennan P, McKay J, Shen CY, Ding SL, Hsu HM, Yu JC, Anton-Culver H, Ziogas A, Ashworth A, Swerdlow A, Jones M, Orr N, Trentham-Dietz A, Egan K, Newcomb P, Titus-Ernstoff L, Easton D, Spurdle AB.
|
| Hum Mol Genet 20(23):4693-706. doi: 10.1093/hmg/ddr368. Epub 2011 Aug 18.
2011
|
| 12 | EDA, HMGA2, HOXB2, IGF2BP1, KCNJ2, MSRB3, RAD51B
|
| Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.
|
| Pillas D, Hoggart CJ, Evans DM, O'Reilly PF, Sipilä K, Lähdesmäki R, Millwood IY, Kaakinen M, Netuveli G, Blane D, Charoen P, Sovio U, Pouta A, Freimer N, Hartikainen AL, Laitinen J, Vaara S, Glaser B, Crawford P, Timpson NJ, Ring SM, Deng G, Zhang W, McCarthy MI, Deloukas P, Peltonen L, Elliott P, Coin LJ, Smith GD, Jarvelin MR.
|
| PLoS Genet 6(2):e1000856. 2010
|
| 13 | RAD51B
|
| A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
|
| Thomas G, Jacobs KB, Kraft P, Yeager M, Wacholder S, Cox DG, Hankinson SE, Hutchinson A, Wang Z, Yu K, Chatterjee N, Garcia-Closas M, Gonzalez-Bosquet J, Prokunina-Olsson L, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Diver R, Prentice R, Jackson R, Kooperberg C, Chlebowski R, Lissowska J, Peplonska B, Brinton LA, Sigurdson A, Doody M, Bhatti P, Alexander BH, Buring J, Lee IM, Vatten LJ, Hveem K, Kumle M, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF Jr, Hoover RN, Chanock SJ, Hunter DJ.
|
| Nat Genet 41(5):579-84. Epub 2009 Mar 29. 2009
|
| 14 | EVL, RAD51, RAD51B
|
| Recombination activator function of the novel RAD51- and RAD51B-binding protein, human EVL.
|
| Takaku M, Machida S, Hosoya N, Nakayama S, Takizawa Y, Sakane I, Shibata T, Miyagawa K, Kurumizaka H.
|
| J Biol Chem 284(21):14326-36. Epub 2009 Mar 26. 2009
|
| 15 | RAD51B
|
| Haploinsufficiency of RAD51B causes centrosome fragmentation and aneuploidy in human cells.
|
| Date O, Katsura M, Ishida M, Yoshihara T, Kinomura A, Sueda T, Miyagawa K.
|
| Cancer Res 66(12):6018-24. 2006
|
| 16 | RAD51B
|
| Nuclear localization of Rad51B is independent of Rad51C and BRCA2.
|
| Miller KA, Hinz JM, Yamada NA, Thompson LH, Albala JS.
|
| Mutagenesis 20(1):57-63. Epub 2005 Feb 8. 2005
|
| 17 | RAD51B, RAD51C, RAD51D, XRCC2, XRCC3
|
| The RAD51 gene family, genetic instability and cancer.
|
| Thacker J.
|
| Cancer Lett 219(2):125-35. Review. 2005
|
| 18 | RAD51B
|
| Holliday junction binding activity of the human Rad51B protein.
|
| Yokoyama H, Kurumizaka H, Ikawa S, Yokoyama S, Shibata T.
|
| J Biol Chem 278(4):2767-72. Epub 2002 Nov 18. 2003
|
| 19 | HMGA2, RAD51B
|
| Evidence for RAD51L1/HMGIC fusion in the pathogenesis of uterine leiomyoma.
|
| Takahashi T, Nagai N, Oda H, Ohama K, Kamada N, Miyagawa K.
|
| Genes Chromosomes Cancer 30(2):196-201. 2001
|
| 20 | HMGA2, RAD51B
|
| Cumulative dosage effect of a RAD51L1/HMGA2 fusion and RAD51L1 loss in a case of pseudo-Meigs' syndrome.
|
| Amant F, Debiec-Rychter M, Schoenmakers EF, Hagemeijer-Hausman A, Vergote I.
|
| Genes Chromosomes Cancer 32(4):324-9. 2001
|
| 21 | RAD51B
|
| Intragenic breakpoint within RAD51L1 in a t(6;14)(p21.3;q24) of a pulmonary chondroid hamartoma.
|
| Blank C, Schoenmakers EF, Rogalla P, Huys EH, Van Rijk AA, Drieschner N, Bullerdiek J.
|
| Cytogenet Cell Genet 95(1-2):17-9. 2001
|
| 22 | RAD51B, 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
|
| 23 | ACTN1, BANF1, RAD51B, ULCR14, WDR22
|
| Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
|
| Lynch RA, et al.
|
| Genomics 52 : 17-26. 1998
|
| 24 | RAD51B
|
| Analysis of the human RAD51L1 promoter region and its activation by UV light.
|
| Peng L, Rice MC, Kmiec EB.
|
| Genomics 54 : 529-541. 1998
|
| 25 | RAD51B
|
| Isolation of human and mouse genes based on homology to REC2, a recombinational repair gene from the fungus Ustilago maydis.
|
| Rice MC, Smith ST, Bullrich F, Havre P, Kmiec EB.
|
| Proc Natl Acad Sci U S A 94(14):7417-22. 1997
|
| 26 | RAD51B
|
| Identification of a novel human RAD51 homolog, RAD51B.
|
| Albala JS, Thelen MP, Prange C, Fan W, Christensen M, Thompson LH, Lennon GG.
|
| Genomics 46(3):476-9. Erratum in: Genomics 1998 Aug 1;51(3):480. 1997
|