1
|
Ergul E and Sazci A: Molecular genetics of
breast cancer. Turk J Med Sci. 31:1–14. 2001.
|
2
|
Ergul E, Sazci A, Utkan Z and Canturk NZ:
Polymorphisms in the MTHFR gene are associated with breast cancer.
Tumour Biol. 24:286–290. 2003. View Article : Google Scholar : PubMed/NCBI
|
3
|
Siegel R, Naishadham D and Jemal A: Cancer
statistics, 2012. CA Cancer J Clin. 62:10–29. 2012. View Article : Google Scholar : PubMed/NCBI
|
4
|
Lu J, Wei Q, Bondy ML, Yu TK, Li D,
Brewster A, Shete S, Sahin A, Meric-Bernstam F and Wang LE:
Promoter polymorphism (−786t>C) in the endothelial nitric oxide
synthase gene is associated with risk of sporadic breast cancer in
non-Hispanic white women age younger than 55 years. Cancer.
107:2245–2253. 2006. View Article : Google Scholar : PubMed/NCBI
|
5
|
Wang Z, Cui D and Lu W: NBS1 8360G > C
polymorphism is associated with breast cancer risk: A
meta-analysis. Breast Cancer Res Treat. 123:557–561. 2010.
View Article : Google Scholar : PubMed/NCBI
|
6
|
Bogdanova N, Feshchenko S, Schürmann P,
Waltes R, Wieland B, Hillemanns P, Rogov YI, Dammann O, Bremer M,
Karstens JH, et al: Nijmegen Breakage Syndrome mutations and risk
of breast cancer. Int J Cancer. 122:802–806. 2008. View Article : Google Scholar : PubMed/NCBI
|
7
|
di Masi A and Antoccia A: NBS1
heterozygosity and cancer risk. Curr Genomics. 9:275–281. 2008.
View Article : Google Scholar : PubMed/NCBI
|
8
|
Tessitore A, Biordi L, Flati V, Toniato E,
Marchetti P, Ricevuto E, Ficorella C, Scotto L, Giannini G, Frati
L, et al: New mutations and protein variants of NBS1 are identified
in cancer cell lines. Genes Chromosomes Cancer. 36:198–204. 2003.
View Article : Google Scholar : PubMed/NCBI
|
9
|
Hsu HMWH, Wang HC, Chen ST, Hsu GC, Shen
CY and Yu JC: Breast cancer risk is associated with the genes
encoding the DNA double-strand break repair Mre11/Rad50/Nbs1
complex. Cancer Epidemiol Biomarkers Prev. 16:2024–2032. 2007.
View Article : Google Scholar : PubMed/NCBI
|
10
|
Damiola F, Pertesi M, Oliver J, Le
Calvez-Kelm F, Voegele C, Young EL, Robinot N, Forey N, Durand G,
Vallée MP, et al: Rare key functional domain missense substitutions
in MRE11A, RAD50, and NBN contribute to breast cancer
susceptibility: Results from a Breast Cancer Family Registry
case-control mutation-screening study. Breast Cancer Res.
16:R582014. View
Article : Google Scholar : PubMed/NCBI
|
11
|
The International Nijmegen Breakage
Syndrome Study Group: Nijmegen breakage syndrome. Arch Dis Child.
82:400–406. 2000. View Article : Google Scholar : PubMed/NCBI
|
12
|
International HapMap Consortium: The
International HapMap Project. Nature. 426:789–796. 2003. View Article : Google Scholar : PubMed/NCBI
|
13
|
Reference SNP (refSNP) Cluster Report:
rs1805787. http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=1805787Accessed.
July 06–2015
|
14
|
Goricar K, Erculj N, Zadel M and Dolzan V:
Genetic polymorphisms in homologous recombination repair genes in
healthy Slovenian population and their influence on DNA damage.
Radiol Oncol. 46:46–53. 2012. View Article : Google Scholar : PubMed/NCBI
|
15
|
Lu M, Lu J, Yang X, Yang M, Tan H, Yun B
and Shi L: Association between the NBS1 E185Q polymorphism and
cancer risk: A meta-analysis. BMC Cancer. 9:1242009. View Article : Google Scholar : PubMed/NCBI
|
16
|
Smith TR, Levine EA, Freimanis RI, Akman
SA, Allen GO, Hoang KN, Liu-Mares W and Hu JJ: Polygenic model of
DNA repair genetic polymorphisms in human breast cancer risk.
Carcinogenesis. 29:2132–2138. 2008. View Article : Google Scholar : PubMed/NCBI
|
17
|
Mavaddat N, Dunning AM, Ponder BA, Easton
DF and Pharoah PD: Common genetic variation in candidate genes and
susceptibility to subtypes of breast cancer. Cancer Epidemiol
Biomarkers Prev. 18:255–259. 2009. View Article : Google Scholar : PubMed/NCBI
|
18
|
Miller SA, Dykes DD and Polesky HF: A
simple salting out procedure for extracting DNA from human
nucleated cells. Nucleic Acids Res. 16:12151988. View Article : Google Scholar : PubMed/NCBI
|
19
|
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 and Wang LE: Polymorphisms and haplotypes of the NBS1 gene
are associated with risk of sporadic breast cancer in non-Hispanic
white women <or=55 years. Carcinogenesis. 27:2209–2216. 2006.
View Article : Google Scholar : PubMed/NCBI
|
20
|
Ergul E, Ozel MD, Sazci A and Idrisoglu
HA: TP53 Arg72Pro polymorphism in Turkish patients with sporadic
amyotrophic lateral sclerosis. Neurobiol Aging. 32:2107.e2101–2102.
2011. View Article : Google Scholar
|
21
|
Heikkinen K, Rapakko K, Karppinen SM,
Erkko H, Knuutila S, Lundán T, Mannermaa A, Børresen-Dale AL, Borg
A, Barkardottir RB, et al: RAD50 and NBS1 are breast cancer
susceptibility genes associated with genomic instability.
Carcinogenesis. 27:1593–1599. 2006. View Article : Google Scholar : PubMed/NCBI
|
22
|
Xiong P, Bondy ML, Li D, Shen H, Wang LE,
Singletary SE, Spitz MR and Wei Q: Sensitivity to benzo(a)pyrene
diol-epoxide associated with risk of breast cancer in young women
and modulation by glutathione S-transferase polymorphisms: A
case-control study. Cancer Res. 61:8465–8469. 2001.PubMed/NCBI
|
23
|
Shi Q, Wang LE, Bondy ML, Brewster A,
Singletary SE and Wei Q: Reduced DNA repair of benzo[a]pyrene diol
epoxide-induced adducts and common XPD polymorphisms in breast
cancer patients. Carcinogenesis. 25:1695–1700. 2004. View Article : Google Scholar : PubMed/NCBI
|
24
|
Desjardins S, Beauparlant JC, Labrie Y,
Ouellette G and Durocher F: INHERIT BRCAs: Variations in the
NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French
Canadian families with high risk of breast cancer. BMC Cancer.
9:1812009. View Article : Google Scholar : PubMed/NCBI
|