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Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe.
Bogdanova N, Togo AV, Ratajska M, Kluźniak W, Takhirova Z, Tarp T, Prokofyeva D, Bermisheva M, Yanus GA, Gorodnova TV, Sokolenko AP, Kuźniacka A, Podolak A, Stukan M, Wokołorczyk D, Gronwald J, Vasilevska D, Rudaitis V, Runnebaum IB, Dürst M, Park-Simon TW, Hillemanns P, Antonenkova N, Khusnutdinova E, Limon J, Lubinski J, Cybulski C, Imyanitov E, Dörk T. Bogdanova N, et al. Fam Cancer. 2015 Mar;14(1):145-9. doi: 10.1007/s10689-014-9748-x. Fam Cancer. 2015. PMID: 25182961
Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.
Landwehr R, Bogdanova NV, Antonenkova N, Meyer A, Bremer M, Park-Simon TW, Hillemanns P, Karstens JH, Schindler D, Dörk T. Landwehr R, et al. Breast Cancer Res Treat. 2011 Dec;130(3):1021-8. doi: 10.1007/s10549-011-1681-1. Epub 2011 Jul 31. Breast Cancer Res Treat. 2011. PMID: 21805310
Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome.
Jamshidi M, Schmidt MK, Dörk T, Garcia-Closas M, Heikkinen T, Cornelissen S, van den Broek AJ, Schürmann P, Meyer A, Park-Simon TW, Figueroa J, Sherman M, Lissowska J, Keong GT, Irwanto A, Laakso M, Hautaniemi S, Aittomäki K, Blomqvist C, Liu J, Nevanlinna H. Jamshidi M, et al. Int J Cancer. 2013 May 1;132(9):2044-55. doi: 10.1002/ijc.27884. Epub 2012 Oct 25. Int J Cancer. 2013. PMID: 23034890 Free PMC article.
Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations.
Prokofyeva D, Bogdanova N, Dubrowinskaja N, Bermisheva M, Takhirova Z, Antonenkova N, Turmanov N, Datsyuk I, Gantsev S, Christiansen H, Park-Simon TW, Hillemanns P, Khusnutdinova E, Dörk T. Prokofyeva D, et al. Breast Cancer Res Treat. 2013 Jan;137(2):533-9. doi: 10.1007/s10549-012-2357-1. Epub 2012 Dec 6. Breast Cancer Res Treat. 2013. PMID: 23225144
CYP2B6*6 is associated with increased breast cancer risk.
Justenhoven C, Pentimalli D, Rabstein S, Harth V, Lotz A, Pesch B, Brüning T, Dörk T, Schürmann P, Bogdanova N, Park-Simon TW, Couch FJ, Olson JE, Fasching PA, Beckmann MW, Häberle L, Ekici A, Hall P, Czene K, Liu J, Li J, Baisch C, Hamann U, Ko YD, Brauch H. Justenhoven C, et al. Int J Cancer. 2014 Jan 15;134(2):426-30. doi: 10.1002/ijc.28356. Epub 2013 Jul 30. Int J Cancer. 2014. PMID: 23824676 Free PMC article.
Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer.
Kohlhase S, Bogdanova NV, Schürmann P, Bermisheva M, Khusnutdinova E, Antonenkova N, Park-Simon TW, Hillemanns P, Meyer A, Christiansen H, Schindler D, Dörk T. Kohlhase S, et al. PLoS One. 2014 Jan 21;9(1):e85334. doi: 10.1371/journal.pone.0085334. eCollection 2014. PLoS One. 2014. PMID: 24465539 Free PMC article.
123 results