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Items: 1 to 20 of 68

1.
Clinical characteristics and survival analysis of Chinese ovarian cancer patients with RAD51D germline mutations
Hongwen Yao, Ning Li, Hua Yuan
BMC Cancer. 2022; 22: 1337. Published online 2022 Dec 21. doi: 10.1186/s12885-022-10456-z
PMCID:
PMC9768941
AbstractArticlePDF–775K
2.
Identification of new RAD51D-regulating microRNAs that also emerge as potent inhibitors of the Fanconi anemia/homologous recombination pathways
Nina Hater, Katharina M Iwaniuk, Carina Leifeld, Pia Grüten, Constanze Wiek, Katharina Raba, Fan Zhang, Johannes C Fischer, Paul R Andreassen, Helmut Hanenberg, Hans-Ingo Trompeter
Hum Mol Genet. 2022 Dec 15; 31(24): 4241–4254. Published online 2022 Jul 29. doi: 10.1093/hmg/ddac177
PMCID:
PMC9759333
AbstractArticlePDF–1.9M
3.
The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer
Ciyu Yang, Angela G. Arnold, Amanda Catchings, Vikas Rai, Zsofia K. Stadler, Liying Zhang
Breast Cancer Res Treat. Author manuscript; available in PMC 2022 Feb 1.
Published in final edited form as: Breast Cancer Res Treat. 2021 Feb; 185(3): 869–877. Published online 2021 Jan 16. doi: 10.1007/s10549-020-06066-7
PMCID:
PMC8414856
AbstractArticlePDF–1.3M
4.
Association between polymorphisms in MicroRNA target sites of RAD51D genes and risk of hepatocellular carcinoma
Yan‐Ji Jiang, Jian‐Hong Zhong, Zi‐Han Zhou, Mo‐Qin Qiu, Xian‐Guo Zhou, Ying‐Chun Liu, Rong‐Rui Huo, Xiu‐Mei Liang, Zhu Chen, Qiu‐Ling Lin, Xiang‐Yuan Yu, Hong‐Ping Yu
Cancer Med. 2019 May; 8(5): 2545–2552. Published online 2019 Mar 18. doi: 10.1002/cam4.2068
PMCID:
PMC6536933
AbstractArticlePDF–196K
5.
A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer
Liisa M Pelttari, Johanna Kiiski, Riikka Nurminen, Anne Kallioniemi, Johanna Schleutker, Alexandra Gylfe, Lauri A Aaltonen, Arto Leminen, Päivi Heikkilä, Carl Blomqvist, Ralf Bützow, Kristiina Aittomäki, Heli Nevanlinna
J Med Genet. Author manuscript; available in PMC 2017 May 11.
Published in final edited form as: J Med Genet. 2012 Jul; 49(7): 429–432. Published online 2012 May 31. doi: 10.1136/jmedgenet-2012-100852
PMCID:
PMC5426530
AbstractArticlePDF–283K
6.
Germline mutations in RAD51D confer susceptibility to ovarian cancer
Chey Loveday, Clare Turnbull, Emma Ramsay, Deborah Hughes, Elise Ruark, Jessica R Frankum, Georgina Bowden, Bolot Kalmyrzaev, Margaret Warren-Perry, Katie Snape, Julian W Adlard, Julian Barwell, Jonathan Berg, Angela F Brady, Carole Brewer, Glen Brice, Cyril Chapman, Jackie Cook, Rosemarie Davidson, Alan Donaldson, Fiona Douglas, Lynn Greenhalgh, Alex Henderson, Louise Izatt, Ajith Kumar, Fiona Lalloo, Zosia Miedzybrodzka, Patrick J Morrison, Joan Paterson, Mary Porteous, Mark T. Rogers, Susan Shanley, Lisa Walker, Breast Cancer Susceptibility Collaboration (UK), Diana Eccles, D. Gareth Evans, Anthony Renwick, Sheila Seal, Christopher J Lord, Alan Ashworth, Jorge S Reis-Filho, Antonis C Antoniou, Nazneen Rahman
Nat Genet. Author manuscript; available in PMC 2016 Apr 26.
Published in final edited form as: Nat Genet. 2011 Sep; 43(9): 879–882. Published online 2011 Aug 7. doi: 10.1038/ng.893
PMCID:
PMC4845885
AbstractArticlePDF–669K
7.
Loss of function germline mutations in RAD51D in women with ovarian carcinoma
Anneka Wickramanayake, Greta Bernier, Christopher Pennil, Silvia Casadei, Kathy J Agnew, Sunday M. Stray, Jessica Mandell, Rochelle L. Garcia, Tom Walsh, Mary-Claire King, Elizabeth M. Swisher
Gynecol Oncol. Author manuscript; available in PMC 2014 Jan 29.
Published in final edited form as: Gynecol Oncol. 2012 Dec; 127(3): 552–555. Published online 2012 Sep 14. doi: 10.1016/j.ygyno.2012.09.009
Correction in:
volume 132 on page 260
PMCID:
PMC3905744
AbstractArticlePDF–401K
8.
Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer
Ella R. Thompson, Simone M. Rowley, Sarah Sawyer, kConFab, Diana M. Eccles, Alison H. Trainer, Gillian Mitchell, Paul A. James, Ian G. Campbell
PLoS One. 2013; 8(1): e54772. Published online 2013 Jan 25. doi: 10.1371/journal.pone.0054772
PMCID:
PMC3555982
AbstractArticlePDF–386K
9.
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
D J Osher, K De Leeneer, G Michils, N Hamel, E Tomiak, B Poppe, K Leunen, E Legius, A Shuen, E Smith, J Arseneau, P Tonin, G Matthijs, K Claes, M D Tischkowitz, W D Foulkes
Br J Cancer. 2012 Apr 10; 106(8): 1460–1463. Published online 2012 Mar 13. doi: 10.1038/bjc.2012.87
PMCID:
PMC3326673
AbstractArticlePDF–243K
10.
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
Xin Yang, Honglin Song, Goska Leslie, Christoph Engel, Eric Hahnen, Bernd Auber, Judit Horváth, Karin Kast, Dieter Niederacher, Clare Turnbull, Richard Houlston, Helen Hanson, Chey Loveday, Jill S Dolinsky, Holly LaDuca, Susan J Ramus, Usha Menon, Adam N Rosenthal, Ian Jacobs, Simon A Gayther, Ed Dicks, Heli Nevanlinna, Kristiina Aittomäki, Liisa M Pelttari, Hans Ehrencrona, Åke Borg, Anders Kvist, Barbara Rivera, Thomas V O Hansen, Malene Djursby, Andrew Lee, Joe Dennis, David D Bowtell, Nadia Traficante, Orland Diez, Judith Balmaña, Stephen B Gruber, Georgia Chenevix-Trench, kConFab Investigators, Allan Jensen, Susanne K Kjær, Estrid Høgdall, Laurent Castéra, Judy Garber, Ramunas Janavicius, Ana Osorio, Lisa Golmard, Ana Vega, Fergus J Couch, Mark Robson, Jacek Gronwald, Susan M Domchek, Julie O Culver, Miguel de la Hoya, Douglas F Easton, William D Foulkes, Marc Tischkowitz, Alfons Meindl, Rita K Schmutzler, Paul D P Pharoah, Antonis C Antoniou
J Natl Cancer Inst. 2020 Dec; 112(12): 1242–1250. Published online 2020 Feb 28. doi: 10.1093/jnci/djaa030
PMCID:
PMC7735771
AbstractArticlePDF–1.8M
11.
Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic
Marketa Janatova, Jana Soukupova, Jana Stribrna, Petra Kleiblova, Michal Vocka, Petra Boudova, Zdenek Kleibl, Petr Pohlreich
PLoS One. 2015; 10(6): e0127711. Published online 2015 Jun 9. doi: 10.1371/journal.pone.0127711
PMCID:
PMC4461297
AbstractArticlePDF–596K
12.
Enhancing the BOADICEA cancer risk prediction model to incorporate new data on RAD51C, RAD51D, BARD1 updates to tumour pathology and cancer incidence
Andrew Lee, Nasim Mavaddat, Alex Cunningham, Tim Carver, Lorenzo Ficorella, Stephanie Archer, Fiona M Walter, Marc Tischkowitz, Jonathan Roberts, Juliet Usher-Smith, Jacques Simard, Marjanka K Schmidt, Peter Devilee, Vesna Zadnik, Hannes Jürgens, Emmanuelle Mouret-Fourme, Antoine De Pauw, Matti Rookus, Thea M Mooij, Paul PD Pharoah, Douglas F Easton, Antonis C Antoniou
J Med Genet. 2022 Dec; 59(12): 1206–1218. Published online 2022 Sep 26. doi: 10.1136/jmedgenet-2022-108471
PMCID:
PMC9691826
AbstractArticlePDF–3.6M
13.
Sequential role of RAD51 paralog complexes in replication fork remodeling and restart
Matteo Berti, Federico Teloni, Sofija Mijic, Sebastian Ursich, Jevgenij Fuchs, Maria Dilia Palumbieri, Jana Krietsch, Jonas A. Schmid, Edwige B. Garcin, Stéphanie Gon, Mauro Modesti, Matthias Altmeyer, Massimo Lopes
Nat Commun. 2020; 11: 3531. Published online 2020 Jul 15. doi: 10.1038/s41467-020-17324-z
PMCID:
PMC7363682
AbstractArticlePDF–2.1M
14.
BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases
Malwina Suszynska, Magdalena Ratajska, Piotr Kozlowski
J Ovarian Res. 2020; 13: 50. Published online 2020 May 2. doi: 10.1186/s13048-020-00654-3
PMCID:
PMC7196220
AbstractArticlePDF–1024K
15.
Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population
Honglin Song, Ed Dicks, Susan J. Ramus, Jonathan P. Tyrer, Maria P. Intermaggio, Jane Hayward, Christopher K. Edlund, David Conti, Patricia Harrington, Lindsay Fraser, Susan Philpott, Christopher Anderson, Adam Rosenthal, Aleksandra Gentry-Maharaj, David D. Bowtell, Kathryn Alsop, Mine S. Cicek, Julie M. Cunningham, Brooke L. Fridley, Jennifer Alsop, Mercedes Jimenez-Linan, Estrid Høgdall, Claus K. Høgdall, Allan Jensen, Susanne Krüger Kjaer, Jan Lubiński, Tomasz Huzarski, Anna Jakubowska, Jacek Gronwald, Samantha Poblete, Shashi Lele, Lara Sucheston-Campbell, Kirsten B. Moysich, Kunle Odunsi, Ellen L. Goode, Usha Menon, Ian J. Jacobs, Simon A. Gayther, Paul D.P. Pharoah
J Clin Oncol. 2015 Sep 10; 33(26): 2901–2907. Published online 2015 Aug 10. doi: 10.1200/JCO.2015.61.2408
PMCID:
PMC4554751
AbstractArticlePDF–170K
16.
Systematic Screen Identifies miRNAs that Target RAD51 and RAD51D to Enhance Chemosensitivity
Jen-Wei Huang, Yemin Wang, Kiranjit K. Dhillon, Philamer Calses, Emily Villegas, Patrick S. Mitchell, Muneesh Tewari, Christopher J. Kemp, Toshiyasu Taniguchi
Mol Cancer Res. Author manuscript; available in PMC 2014 Jun 1.
Published in final edited form as: Mol Cancer Res. 2013 Dec; 11(12): 10.1158/1541-7786.MCR-13-0292. Published online 2013 Oct 2. doi: 10.1158/1541-7786.MCR-13-0292
PMCID:
PMC3869885
AbstractArticlePDF–788K
17.
Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination
Claudia Wiese, John M. Hinz, Robert S. Tebbs, Peter B. Nham, Salustra S. Urbin, David W. Collins, Larry H. Thompson, David Schild
Nucleic Acids Res. 2006; 34(9): 2833–2843. Published online 2006 May 22. doi: 10.1093/nar/gkl366
PMCID:
PMC1464408
AbstractArticlePDF–458K
18.
Interplay between human DNA repair proteins at a unique double-strand break in vivo
Amélie Rodrigue, Matthieu Lafrance, Marie-Christine Gauthier, Darin McDonald, Michael Hendzel, Stephen C West, Maria Jasin, Jean-Yves Masson
EMBO J. 2006 Jan 11; 25(1): 222–231. Published online 2006 Jan 5. doi: 10.1038/sj.emboj.7600914
PMCID:
PMC1356357
AbstractArticlePDF–279K
19.
Mediator function of the human Rad51B–Rad51C complex in Rad51/RPA-catalyzed DNA strand exchange
Stefan Sigurdsson, Stephen Van Komen, Wendy Bussen, David Schild, Joanna S. Albala, Patrick Sung
Genes Dev. 2001 Dec 15; 15(24): 3308–3318. doi: 10.1101/gad.935501
PMCID:
PMC312844
AbstractArticlePDF–485K
20.
Structural insights into BCDX2 complex function in homologous recombination
Yashpal Rawal, Lijia Jia, Aviv Meir, Shuo Zhou, Hardeep Kaur, Eliza A. Ruben, Youngho Kwon, Kara A. Bernstein, Maria Jasin, Alexander B. Taylor, Sandeep Burma, Robert Hromas, Alexander V. Mazin, Weixing Zhao, Daohong Zhou, Elizabeth V. Wasmuth, Eric C. Greene, Patrick Sung, Shaun K. Olsen
Nature. Author manuscript; available in PMC 2024 Jul 1.
Published in final edited form as: Nature. 2023 Jul; 619(7970): 640–649. Published online 2023 Jun 21. doi: 10.1038/s41586-023-06219-w
PMCID:
PMC10712684
AbstractArticlePDF–9.7M

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