These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
175 related articles for article (PubMed ID: 19728081)
1. Genetic contribution of GADD45A to susceptibility to sporadic and non-BRCA1/2 familial breast cancers: a systematic evaluation in Chinese populations. Yu KD; Di GH; Li WF; Rao NY; Fan L; Yuan WT; Hu Z; Wu J; Shen ZZ; Huang W; Shao ZM Breast Cancer Res Treat; 2010 May; 121(1):157-67. PubMed ID: 19728081 [TBL] [Abstract][Full Text] [Related]
2. Analysis of GADD45A sequence variations in French Canadian families with high risk of breast cancer. Desjardins S; Ouellette G; Labrie Y; Simard J; ; Durocher F J Hum Genet; 2008; 53(6):490-498. PubMed ID: 18350249 [TBL] [Abstract][Full Text] [Related]
3. Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from India. Hedau S; Jain N; Husain SA; Mandal AK; Ray G; Shahid M; Kant R; Gupta V; Shukla NK; Deo SS; Das BC Breast Cancer Res Treat; 2004 Nov; 88(2):177-86. PubMed ID: 15564800 [TBL] [Abstract][Full Text] [Related]
4. Germline RAP80 mutations and susceptibility to breast cancer. Akbari MR; Ghadirian P; Robidoux A; Foumani M; Sun Y; Royer R; Zandvakili I; Lynch H; Narod SA Breast Cancer Res Treat; 2009 Jan; 113(2):377-81. PubMed ID: 18306035 [TBL] [Abstract][Full Text] [Related]
5. Common non-synonymous polymorphisms in the BRCA1 Associated RING Domain (BARD1) gene are associated with breast cancer susceptibility: a case-control analysis. Huo X; Hu Z; Zhai X; Wang Y; Wang S; Wang X; Qin J; Chen W; Jin G; Liu J; Gao J; Wei Q; Wang X; Shen H Breast Cancer Res Treat; 2007 May; 102(3):329-37. PubMed ID: 17028982 [TBL] [Abstract][Full Text] [Related]
6. RAD50 and NBS1 are not likely to be susceptibility genes in Chinese non-BRCA1/2 hereditary breast cancer. He M; Di GH; Cao AY; Hu Z; Jin W; Shen ZZ; Shao ZM Breast Cancer Res Treat; 2012 May; 133(1):111-6. PubMed ID: 21811815 [TBL] [Abstract][Full Text] [Related]
7. Genetic polymorphims of estrogen receptor alpha -397 PvuII (T>C) and -351 XbaI (A>G) in a portuguese population: prevalence and relation with breast cancer susceptibility. Ramalhinho AC; Marques J; Fonseca-Moutinho JA; Breitenfeld L Mol Biol Rep; 2013 Aug; 40(8):5093-103. PubMed ID: 23666105 [TBL] [Abstract][Full Text] [Related]
8. Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals. Kuusisto KM; Bebel A; Vihinen M; Schleutker J; Sallinen SL Breast Cancer Res; 2011 Feb; 13(1):R20. PubMed ID: 21356067 [TBL] [Abstract][Full Text] [Related]
9. Association of common ATM variants with familial breast cancer in a South American population. González-Hormazábal P; Bravo T; Blanco R; Valenzuela CY; Gómez F; Waugh E; Peralta O; Ortuzar W; Reyes JM; Jara L BMC Cancer; 2008 Apr; 8():117. PubMed ID: 18433505 [TBL] [Abstract][Full Text] [Related]
10. Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent. Cavallone L; Arcand SL; Maugard C; Ghadirian P; Mes-Masson AM; Provencher D; Tonin PN BMC Cancer; 2008 Apr; 8():96. PubMed ID: 18402691 [TBL] [Abstract][Full Text] [Related]
11. Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population. Loizidou MA; Cariolou MA; Neuhausen SL; Newbold RF; Bashiardes E; Marcou Y; Michael T; Daniel M; Kakouri E; Papadopoulos P; Malas S; Hadjisavvas A; Kyriacou K Breast Cancer Res Treat; 2010 May; 121(1):147-56. PubMed ID: 19714462 [TBL] [Abstract][Full Text] [Related]
12. Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing. Li G; Guo X; Tang L; Chen M; Luo X; Peng L; Xu X; Wang S; Xiao Z; Yi W; Dai L; Wang J J Cancer Res Clin Oncol; 2017 Oct; 143(10):2011-2024. PubMed ID: 28664449 [TBL] [Abstract][Full Text] [Related]
13. Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk. Ricks-Santi LJ; Sucheston LE; Yang Y; Freudenheim JL; Isaacs CJ; Schwartz MD; Dumitrescu RG; Marian C; Nie J; Vito D; Edge SB; Shields PG BMC Cancer; 2011 Jun; 11():278. PubMed ID: 21708019 [TBL] [Abstract][Full Text] [Related]
14. Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex. Hsu HM; Wang HC; Chen ST; Hsu GC; Shen CY; Yu JC Cancer Epidemiol Biomarkers Prev; 2007 Oct; 16(10):2024-32. PubMed ID: 17932350 [TBL] [Abstract][Full Text] [Related]
15. Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2 deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age. Turkovic L; Gurrin LC; Bahlo M; Dite GS; Southey MC; Hopper JL BMC Cancer; 2010 Sep; 10():466. PubMed ID: 20807450 [TBL] [Abstract][Full Text] [Related]
17. Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families. Durocher F; Labrie Y; Soucy P; Sinilnikova O; Labuda D; Bessette P; Chiquette J; Laframboise R; Lépine J; Lespérance B; Ouellette G; Pichette R; Plante M; Tavtigian SV; Simard J BMC Cancer; 2006 Sep; 6():230. PubMed ID: 17010193 [TBL] [Abstract][Full Text] [Related]
18. BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity. Juwle A; Saranath D Med Oncol; 2012 Dec; 29(5):3272-81. PubMed ID: 22752604 [TBL] [Abstract][Full Text] [Related]
19. Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women Lu J; Wei Q; Bondy ML; Li D; Brewster A; Shete S; Yu TK; Sahin A; Meric-Bernstam F; Hunt KK; Singletary SE; Ross MI; Wang LE Carcinogenesis; 2006 Nov; 27(11):2209-16. PubMed ID: 16714331 [TBL] [Abstract][Full Text] [Related]
20. Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent. Yarden RI; Friedman E; Metsuyanim S; Olender T; Ben-Asher E; Papa MZ Mol Carcinog; 2010 Jun; 49(6):545-55. PubMed ID: 20306497 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]