메뉴 건너뛰기




Volumn 28, Issue 6, 2013, Pages 683-697

Functional variants in NBS1 and cancer risk: Evidence from a meta-analysis of 60 publications with 111 individual studies

Author keywords

[No Author keywords available]

Indexed keywords

NIBRIN;

EID: 84888599972     PISSN: 02678357     EISSN: 14643804     Source Type: Journal    
DOI: 10.1093/mutage/get048     Document Type: Article
Times cited : (41)

References (100)
  • 1
    • 0035093737 scopus 로고    scopus 로고
    • DNA double-strand breaks: Signaling, repair and the cancer connection
    • Khanna, K. K. and Jackson, S. P. (2001) DNA double-strand breaks: signaling, repair and the cancer connection. Nat. Genet., 27, 247-254.
    • (2001) Nat. Genet , vol.27 , pp. 247-254
    • Khanna, K.K.1    Jackson, S.P.2
  • 2
    • 0033590179 scopus 로고    scopus 로고
    • DNA damage-induced cell cycle checkpoints and DNA strand break repair in development and tumorigenesis
    • Dasika, G. K., Lin, S. C., Zhao, S., Sung, P., Tomkinson, A. and Lee, E. Y. (1999) DNA damage-induced cell cycle checkpoints and DNA strand break repair in development and tumorigenesis. Oncogene, 18, 7883-7899.
    • (1999) Oncogene , vol.18 , pp. 7883-7899
    • Dasika, G.K.1    Lin, S.C.2    Zhao, S.3    Sung, P.4    Tomkinson, A.5    Lee, E.Y.6
  • 3
    • 0035839840 scopus 로고    scopus 로고
    • DNA double strand break repair and chromosomal translocation: Lessons from animal models
    • Ferguson, D. O. and Alt, F. W. (2001) DNA double strand break repair and chromosomal translocation: lessons from animal models. Oncogene, 20, 5572-5579.
    • (2001) Oncogene , vol.20 , pp. 5572-5579
    • Ferguson, D.O.1    Alt, F.W.2
  • 4
    • 31144471460 scopus 로고    scopus 로고
    • The role of NBS1 in DNA double strand break repair, telomere stability, and cell cycle checkpoint control
    • Zhang, Y., Zhou, J. and Lim, C. U. (2006) The role of NBS1 in DNA double strand break repair, telomere stability, and cell cycle checkpoint control. Cell Res., 16, 45-54.
    • (2006) Cell Res , vol.16 , pp. 45-54
    • Zhang, Y.1    Zhou, J.2    Lim, C.U.3
  • 5
    • 26444479826 scopus 로고    scopus 로고
    • Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk
    • Millikan, R. C., Player, J. S., Decotret, A. R., Tse, C. K. and Keku, T. (2005) Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk. Cancer Epidemiol. Biomarkers Prev., 14, 2326-2334.
    • (2005) Cancer Epidemiol. Biomarkers Prev , vol.14 , pp. 2326-2334
    • Millikan, R.C.1    Player, J.S.2    Decotret, A.R.3    Tse, C.K.4    Keku, T.5
  • 6
    • 33747875848 scopus 로고    scopus 로고
    • Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin
    • Thirumaran, R. K., Bermejo, J. L., Rudnai, P., et al. (2006) Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin. Carcinogenesis, 27, 1676-1681.
    • (2006) Carcinogenesis , vol.27 , pp. 1676-1681
    • Thirumaran, R.K.1    Bermejo, J.L.2    Rudnai, P.3
  • 8
    • 65649138379 scopus 로고    scopus 로고
    • Association between the NBS1 E185Q polymorphism and cancer risk: A meta-analysis
    • Lu, M., Lu, J., Yang, X., Yang, M., Tan, H., Yun, B. and Shi, L. (2009) Association between the NBS1 E185Q polymorphism and cancer risk: A meta-analysis. BMC Cancer, 9, 124.
    • (2009) BMC Cancer , vol.9 , pp. 124
    • Lu, M.1    Lu, J.2    Yang, X.3    Yang, M.4    Tan, H.5    Yun, B.6    Shi, L.7
  • 9
    • 84877108475 scopus 로고    scopus 로고
    • Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: A meta-analysis
    • Yao, F., Fang, Y., Chen, B., Jin, F. and Wang, S. (2013) Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: A meta-analysis. Tumour Biol., 34, 1255-1262.
    • (2013) Tumour Biol , vol.34 , pp. 1255-1262
    • Yao, F.1    Fang, Y.2    Chen, B.3    Jin, F.4    Wang, S.5
  • 10
    • 17844365867 scopus 로고    scopus 로고
    • A method for meta-analysis of molecular association studies
    • Thakkinstian, A., McElduff, P., D'Este, C., Duffy, D. and Attia, J. (2005) A method for meta-analysis of molecular association studies. Stat. Med., 24, 1291-1306.
    • (2005) Stat. Med , vol.24 , pp. 1291-1306
    • Thakkinstian, A.1    McElduff, P.2    D'Este, C.3    Duffy, D.4    Attia, J.5
  • 11
    • 29244445375 scopus 로고    scopus 로고
    • The choice of a genetic model in the meta-analysis of molecular association studies
    • Minelli, C., Thompson, J. R., Abrams, K. R., Thakkinstian, A. and Attia, J. (2005) The choice of a genetic model in the meta-analysis of molecular association studies. Int. J. Epidemiol., 34, 1319-1328.
    • (2005) Int. J. Epidemiol , vol.34 , pp. 1319-1328
    • Minelli, C.1    Thompson, J.R.2    Abrams, K.R.3    Thakkinstian, A.4    Attia, J.5
  • 12
    • 0030922816 scopus 로고    scopus 로고
    • Bias in meta-analysis detected by a simple, graphical test
    • Egger, M., Davey Smith, G., Schneider, M. and Minder, C. (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ, 315, 629-634.
    • (1997) BMJ , vol.315 , pp. 629-634
    • Egger, M.1    Davey Smith, G.2    Schneider, M.3    Minder, C.4
  • 13
    • 33744729997 scopus 로고    scopus 로고
    • Genetic polymorphisms in the DNA double-strand break repair genes XRCC3, XRCC2, and NBS1 are not associated with acute side effects of radiotherapy in breast cancer patients. Cancer Epidemiol
    • Popanda, O., Tan, X. L., Ambrosone, C. B., et al. (2006) Genetic polymorphisms in the DNA double-strand break repair genes XRCC3, XRCC2, and NBS1 are not associated with acute side effects of radiotherapy in breast cancer patients. Cancer Epidemiol. Biomarkers Prev., 15, 1048-1050.
    • (2006) Biomarkers Prev , vol.15 , pp. 1048-1050
    • Popanda, O.1    Tan, X.L.2    Ambrosone, C.B.3
  • 14
    • 0034085362 scopus 로고    scopus 로고
    • No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence
    • Stanulla, M., Stumm, M., Dieckvoss, B. O., Seidemann, K., Schemmel, V., Muller Brechlin, A., Schrappe, M., Welte, K. and Reiter, A. (2000) No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence. Br. J. Haematol., 109, 117-120.
    • (2000) Br. J. Haematol , vol.109 , pp. 117-120
    • Stanulla, M.1    Stumm, M.2    Dieckvoss, B.O.3    Seidemann, K.4    Schemmel, V.5    Muller Brechlin, A.6    Schrappe, M.7    Welte, K.8    Reiter, A.9
  • 15
    • 34547442363 scopus 로고    scopus 로고
    • Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia
    • Sokolenko, A. P., Rozanov, M. E., Mitiushkina, N. V., et al. (2007) Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia. Fam. Cancer, 6, 281-286.
    • (2007) Fam. Cancer , vol.6 , pp. 281-286
    • Sokolenko, A.P.1    Rozanov, M.E.2    Mitiushkina, N.V.3
  • 17
    • 33748852526 scopus 로고    scopus 로고
    • Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland)
    • Ziołkowska, I., Mosor, M. and Nowak, J. (2006) Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland). J. Appl. Genet., 47, 269-272.
    • (2006) J. Appl. Genet , vol.47 , pp. 269-272
    • Ziołkowska, I.1    Mosor, M.2    Nowak, J.3
  • 19
    • 0033869097 scopus 로고    scopus 로고
    • Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients
    • Hama, S., Matsuura, S., Tauchi, H., et al. (2000) Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients. Anticancer Res., 20, 1897-1900.
    • (2000) Anticancer Res. , vol.20 , pp. 1897-1900
    • Hama, S.1    Matsuura, S.2    Tauchi, H.3
  • 20
    • 0042026468 scopus 로고    scopus 로고
    • Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations. Cancer Epidemiol
    • Medina, P. P., Ahrendt, S. A., Pollan, M., Fernandez, P., Sidransky, D. and Sanchez-Cespedes, M. (2003) Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations. Cancer Epidemiol. Biomarkers Prev., 12, 699-704.
    • (2003) Biomarkers Prev , vol.12 , pp. 699-704
    • Medina, P.P.1    Ahrendt, S.A.2    Pollan, M.3    Fernandez, P.4    Sidransky, D.5    Sanchez-Cespedes, M.6
  • 21
    • 0036802287 scopus 로고    scopus 로고
    • Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans. Cancer Epidemiol
    • Mohrenweiser, H. W., Xi, T., Vazquez-Matias, J. and Jones, I. M. (2002) Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans. Cancer Epidemiol. Biomarkers Prev., 11, 1054-1064.
    • (2002) Biomarkers Prev , vol.11 , pp. 1054-1064
    • Mohrenweiser, H.W.1    Xi, T.2    Vazquez-Matias, J.3    Jones, I.M.4
  • 22
    • 0033902941 scopus 로고    scopus 로고
    • The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T cell non-Hodgkin lymphoma in a pediatric population
    • Rischewski, J., Bismarck, P., Kabisch, H., Janka-Schaub, G., Obser, T. and Schneppenheim, R. (2000) The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T cell non-Hodgkin lymphoma in a pediatric population. Leukemia, 14, 1528-1529.
    • (2000) Leukemia , vol.14 , pp. 1528-1529
    • Rischewski, J.1    Bismarck, P.2    Kabisch, H.3    Janka-Schaub, G.4    Obser, T.5    Schneppenheim, R.6
  • 23
    • 77951297126 scopus 로고    scopus 로고
    • Some common mutations of RAD50 and NBS1 in western populations do not contribute significantly to Chinese non-BRCA1/2 hereditary breast cancer
    • Cao, A. Y., Hu, Z., Yin, W. J., Jin, W. and Shao, Z. M. (2010) Some common mutations of RAD50 and NBS1 in western populations do not contribute significantly to Chinese non-BRCA1/2 hereditary breast cancer. Breast Cancer Res. Treat., 121, 247-249.
    • (2010) Breast Cancer Res. Treat , vol.121 , pp. 247-249
    • Cao, A.Y.1    Hu, Z.2    Yin, W.J.3    Jin, W.4    Shao, Z.M.5
  • 25
    • 33747884830 scopus 로고    scopus 로고
    • RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
    • Heikkinen, K., Rapakko, K., Karppinen, S. M., et al. (2006) RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. Carcinogenesis, 27, 1593-1599.
    • (2006) Carcinogenesis , vol.27 , pp. 1593-1599
    • Heikkinen, K.1    Rapakko, K.2    Karppinen, S.M.3
  • 26
    • 84863070560 scopus 로고    scopus 로고
    • A functional polymorphism at microRNA-629-binding site in the 3'-untranslated region of NBS1 gene confers an increased risk of lung cancer in Southern and Eastern Chinese population
    • Yang, L., Li, Y., Cheng, M., et al. (2012) A functional polymorphism at microRNA-629-binding site in the 3'-untranslated region of NBS1 gene confers an increased risk of lung cancer in Southern and Eastern Chinese population. Carcinogenesis, 33, 338-347.
    • (2012) Carcinogenesis , vol.33 , pp. 338-347
    • Yang, L.1    Li, Y.2    Cheng, M.3
  • 27
    • 84861394579 scopus 로고    scopus 로고
    • Genetic variation in the NBS1 gene is associated with hepatic cancer risk in a Chinese population
    • Huang, M. D., Chen, X. F., Xu, G., Wu, Q. Q., Zhang, J. H., Chen, G. F., Cai, Y. and Qi, F. Z. (2012) Genetic variation in the NBS1 gene is associated with hepatic cancer risk in a Chinese population. DNA Cell Biol., 31, 678-682.
    • (2012) DNA Cell Biol , vol.31 , pp. 678-682
    • Huang, M.D.1    Chen, X.F.2    Xu, G.3    Wu, Q.Q.4    Zhang, J.H.5    Chen, G.F.6    Cai, Y.7    Qi, F.Z.8
  • 28
    • 79960650252 scopus 로고    scopus 로고
    • Functional NBS1 polymorphism is associated with occurrence and advanced disease status of nasopharyngeal carcinoma
    • Zheng, J., Zhang, C., Jiang, L., You, Y., Liu, Y., Lu, J. and Zhou, Y. (2011) Functional NBS1 polymorphism is associated with occurrence and advanced disease status of nasopharyngeal carcinoma. Mol. Carcinog., 50, 689-696.
    • (2011) Mol. Carcinog , vol.50 , pp. 689-696
    • Zheng, J.1    Zhang, C.2    Jiang, L.3    You, Y.4    Liu, Y.5    Lu, J.6    Zhou, Y.7
  • 29
    • 84855192961 scopus 로고    scopus 로고
    • The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer
    • Gil, J., Ramsey, D., Stembalska, A., Karpinski, P., Pesz, K. A., Laczmanska, I., Leszczynski, P., Grzebieniak, Z. and Sasiadek, M. M. (2012) The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer. Mol. Biol. Rep., 39, 527-534.
    • (2012) Mol. Biol. Rep , vol.39 , pp. 527-534
    • Gil, J.1    Ramsey, D.2    Stembalska, A.3    Karpinski, P.4    Pesz, K.A.5    Laczmanska, I.6    Leszczynski, P.7    Grzebieniak, Z.8    Sasiadek, M.M.9
  • 30
    • 79951670633 scopus 로고    scopus 로고
    • Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population
    • Jiang, L., Liang, J., Jiang, M., Yu, X., Zheng, J., Liu, H., Wu, D. and Zhou, Y. (2011) Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population. Eur. J. Haematol., 86, 199-205.
    • (2011) Eur. J. Haematol , vol.86 , pp. 199-205
    • Jiang, L.1    Liang, J.2    Jiang, M.3    Yu, X.4    Zheng, J.5    Liu, H.6    Wu, D.7    Zhou, Y.8
  • 31
    • 77956311219 scopus 로고    scopus 로고
    • Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population
    • Jelonek, K., Gdowicz-Klosok, A., Pietrowska, M., Borkowska, M., Korfanty, J., Rzeszowska-Wolny, J. and Widlak, P. (2010) Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population. J. Appl. Genet., 51, 343-352.
    • (2010) J. Appl. Genet , vol.51 , pp. 343-352
    • Jelonek, K.1    Gdowicz-Klosok, A.2    Pietrowska, M.3    Borkowska, M.4    Korfanty, J.5    Rzeszowska-Wolny, J.6    Widlak, P.7
  • 32
    • 77954355121 scopus 로고    scopus 로고
    • Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers
    • Park, S. L., Bastani, D., Goldstein, B. Y., et al. (2010) Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers. Carcinogenesis, 31, 1264-1271.
    • (2010) Carcinogenesis , vol.31 , pp. 1264-1271
    • Park, S.L.1    Bastani, D.2    Goldstein, B.Y.3
  • 33
    • 76449084869 scopus 로고    scopus 로고
    • Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51
    • Silva, S. N., Tomar, M., Paulo, C., Gomes, B. C., Azevedo, A. P., Teixeira, V., Pina, J. E., Rueff, J. and Gaspar, J. F. (2010) Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51. Cancer Epidemiol., 34, 85-92.
    • (2010) Cancer Epidemiol , vol.34 , pp. 85-92
    • Silva, S.N.1    Tomar, M.2    Paulo, C.3    Gomes, B.C.4    Azevedo, A.P.5    Teixeira, V.6    Pina, J.E.7    Rueff, J.8    Gaspar, J.F.9
  • 34
    • 77953020607 scopus 로고    scopus 로고
    • Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients
    • Ciara, E., Piekutowska-Abramczuk, D., Popowska, E., et al. (2010) Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta Neuropathol., 119, 325-334.
    • (2010) Acta Neuropathol , vol.119 , pp. 325-334
    • Ciara, E.1    Piekutowska-Abramczuk, D.2    Popowska, E.3
  • 35
    • 70350650666 scopus 로고    scopus 로고
    • Association of polymorphisms in genes of the homologous recombination DNA repair pathway and thyroid cancer risk
    • Bastos, H. N., Antao, M. R., Silva, S. N., et al. (2009) Association of polymorphisms in genes of the homologous recombination DNA repair pathway and thyroid cancer risk. Thyroid, 19, 1067-1075.
    • (2009) Thyroid , vol.19 , pp. 1067-1075
    • Bastos, H.N.1    Antao, M.R.2    Silva, S.N.3
  • 36
    • 77951298296 scopus 로고    scopus 로고
    • Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population
    • Loizidou, M. A., Cariolou, M. A., Neuhausen, S. L., et al. (2010) Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population. Breast Cancer Res. Treat., 121, 147-156.
    • (2010) Breast Cancer Res. Treat , vol.121 , pp. 147-156
    • Loizidou, M.A.1    Cariolou, M.A.2    Neuhausen, S.L.3
  • 37
    • 67650090387 scopus 로고    scopus 로고
    • INHERIT BRCAs(2009) 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
    • Desjardins, S., Beauparlant, J. C., Labrie, Y., Ouellette, G. and Durocher, F.; INHERIT BRCAs. (2009) 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, 181.
    • BMC Cancer , vol.9 , pp. 181
    • Desjardins, S.1    Beauparlant, J.C.2    Labrie, Y.3    Ouellette, G.4    Durocher, F.5
  • 38
    • 53349153181 scopus 로고    scopus 로고
    • Genetic susceptibility to renal cell carcinoma: The role of DNA doublestrand break repair pathway
    • Margulis, V., Lin, J., Yang, H., Wang, W., Wood, C. G. and Wu, X. (2008) Genetic susceptibility to renal cell carcinoma: The role of DNA doublestrand break repair pathway. Cancer Epidemiol. Biomarkers Prev., 17, 2366-2373.
    • (2008) Cancer Epidemiol. Biomarkers Prev , vol.17 , pp. 2366-2373
    • Margulis, V.1    Lin, J.2    Yang, H.3    Wang, W.4    Wood, C.G.5    Wu, X.6
  • 42
    • 34748906012 scopus 로고    scopus 로고
    • Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene
    • Ziolkowska, I., Mosor, M., Wierzbicka, M., Rydzanicz, M., Pernak- Schwarz, M. and Nowak, J. (2007) Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene. Cancer Sci., 98, 1701-1705.
    • (2007) Cancer Sci. , vol.98 , pp. 1701-1705
    • Ziolkowska, I.1    Mosor, M.2    Wierzbicka, M.3    Rydzanicz, M.4    Pernak-Schwarz, M.5    Nowak, J.6
  • 43
    • 34548056355 scopus 로고    scopus 로고
    • Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk
    • Figueroa, J. D., Malats, N., Rothman, N., et al. (2007) Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. Carcinogenesis, 28, 1788-1793.
    • (2007) Carcinogenesis , vol.28 , pp. 1788-1793
    • Figueroa, J.D.1    Malats, N.2    Rothman, N.3
  • 44
    • 33750476354 scopus 로고    scopus 로고
    • 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, M. L., et al. (2006) Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non- Hispanic white women
    • (2006) Carcinogenesis , vol.27 , pp. 2209-2216
    • Lu, J.1    Wei, Q.2    Bondy, M.L.3
  • 45
    • 33744718463 scopus 로고    scopus 로고
    • Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer
    • Hebbring, S. J., Fredriksson, H., White, K. A., et al. (2006) Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer. Cancer Epidemiol. Biomarkers Prev., 15, 935-938.
    • (2006) Cancer Epidemiol. Biomarkers Prev , vol.15 , pp. 935-938
    • Hebbring, S.J.1    Fredriksson, H.2    White, K.A.3
  • 46
    • 23644459841 scopus 로고    scopus 로고
    • Single nucleotide polymorphisms for DNA repair genes in breast cancer patients
    • Zhang, L., Zhang, Z. and Yan, W. (2005) Single nucleotide polymorphisms for DNA repair genes in breast cancer patients. Clin. Chim. Acta., 359, 150-155.
    • (2005) Clin. Chim. Acta , vol.359 , pp. 150-155
    • Zhang, L.1    Zhang, Z.2    Yan, W.3
  • 47
    • 27144475439 scopus 로고    scopus 로고
    • Polymorphisms in DNA repair genes and epithelial ovarian cancer risk
    • Auranen, A., Song, H., Waterfall, C., et al. (2005) Polymorphisms in DNA repair genes and epithelial ovarian cancer risk. Int. J. Cancer, 117, 611-618.
    • (2005) Int. J. Cancer , vol.117 , pp. 611-618
    • Auranen, A.1    Song, H.2    Waterfall, C.3
  • 48
    • 23744443341 scopus 로고    scopus 로고
    • Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China
    • Lan, Q., Shen, M., Berndt, S. I., et al. (2005) Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. Lung Cancer, 49, 317-323.
    • (2005) Lung Cancer , vol.49 , pp. 317-323
    • Lan, Q.1    Shen, M.2    Berndt, S.I.3
  • 49
    • 21144438855 scopus 로고    scopus 로고
    • Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism
    • Festa, F., Kumar, R., Sanyal, S., et al. (2005) Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism. Mutat. Res., 574, 105-111.
    • (2005) Mutat. Res , vol.574 , pp. 105-111
    • Festa, F.1    Kumar, R.2    Sanyal, S.3
  • 50
    • 2442453654 scopus 로고    scopus 로고
    • Polymorphisms in DNA repair and metabolic genes in bladder cancer
    • Sanyal, S., Festa, F., Sakano, S., et al. (2004) Polymorphisms in DNA repair and metabolic genes in bladder cancer. Carcinogenesis, 25, 729-734.
    • (2004) Carcinogenesis , vol.25 , pp. 729-734
    • Sanyal, S.1    Festa, F.2    Sakano, S.3
  • 51
    • 71749090715 scopus 로고    scopus 로고
    • Variants in DNA double- strand break repair genes and breast cancer susceptibility
    • Kuschel, B., Auranen, A., McBride, S., et al. (2002) Variants in DNA double- strand break repair genes and breast cancer susceptibility. Hum. Mol. Genet., 11, 1399-1407.
    • (2002) Hum. Mol. Genet , vol.11 , pp. 1399-1407
    • Kuschel, B.1    Auranen, A.2    McBride, S.3
  • 52
    • 38349052915 scopus 로고    scopus 로고
    • Nijmegen Breakage Syndrome mutations and risk of breast cancer
    • Bogdanova, N., Feshchenko, S., Schurmann, P., et al. (2008) Nijmegen Breakage Syndrome mutations and risk of breast cancer. Int. J. Cancer, 122, 802-806.
    • (2008) Int. J. Cancer , vol.122 , pp. 802-806
    • Bogdanova, N.1    Feshchenko, S.2    Schurmann, P.3
  • 53
    • 33745225487 scopus 로고    scopus 로고
    • Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland
    • Steffen, J., Nowakowska, D., Niwinska, A., Czapczak, D., Kluska, A., Piatkowska, M., Wisniewska, A. and Paszko, Z. (2006) Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland. Int. J. Cancer, 119, 472-475.
    • (2006) Int. J. Cancer , vol.119 , pp. 472-475
    • Steffen, J.1    Nowakowska, D.2    Niwinska, A.3    Czapczak, D.4    Kluska, A.5    Piatkowska, M.6    Wisniewska, A.7    Paszko, Z.8
  • 54
    • 3042818662 scopus 로고    scopus 로고
    • Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland
    • Steffen, J., Varon, R., Mosor, M., et al. (2004) Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. Int. J. Cancer, 111, 67-71.
    • (2004) Int. J. Cancer , vol.111 , pp. 67-71
    • Steffen, J.1    Varon, R.2    Mosor, M.3
  • 55
    • 0038505600 scopus 로고    scopus 로고
    • Germline 657del5 mutation in the NBS1 gene in breast cancer patients
    • Gorski, B., Debniak, T., Masojć, B., et al. (2003) Germline 657del5 mutation in the NBS1 gene in breast cancer patients. Int. J. Cancer, 106, 379-381.
    • (2003) Int. J. Cancer , vol.106 , pp. 379-381
    • Gorski, B.1    Debniak, T.2    Masojc, B.3
  • 57
    • 20044366887 scopus 로고    scopus 로고
    • NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia
    • Buslov, K. G., Iyevleva, A. G., Chekmariova, E. V., et al. (2005) NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia. Int. J. Cancer, 114, 585-589.
    • (2005) Int. J. Cancer , vol.114 , pp. 585-589
    • Buslov, K.G.1    Iyevleva, A.G.2    Chekmariova, E.V.3
  • 58
    • 0032792820 scopus 로고    scopus 로고
    • Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: No association with risk of breast cancer
    • Carlomagno, F., Chang-Claude, J., Dunning, A. M. and Ponder, B. A. (1999) Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer. Genes. Chromosomes Cancer, 25, 393-395.
    • (1999) Genes. Chromosomes Cancer , vol.25 , pp. 393-395
    • Carlomagno, F.1    Chang-Claude, J.2    Dunning, A.M.3    Ponder, B.A.4
  • 60
    • 22844444113 scopus 로고    scopus 로고
    • Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer
    • Broberg, K., Bjork, J., Paulsson, K., Hoglund, M. and Albin, M. (2005) Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer. Carcinogenesis, 26, 1263-1271.
    • (2005) Carcinogenesis , vol.26 , pp. 1263-1271
    • Broberg, K.1    Bjork, J.2    Paulsson, K.3    Hoglund, M.4    Albin, M.5
  • 61
    • 38049082619 scopus 로고    scopus 로고
    • DNA repair genetic polymorphisms and risk of colorectal cancer in the Czech Republic
    • Pardini, B., Naccarati, A., Novotny, J., et al. (2008) DNA repair genetic polymorphisms and risk of colorectal cancer in the Czech Republic. Mutat. Res. 638, 146-153.
    • (2008) Mutat. Res. , vol.638 , pp. 146-153
    • Pardini, B.1    Naccarati, A.2    Novotny, J.3
  • 62
    • 84878422343 scopus 로고    scopus 로고
    • NBS1 rs1805794G>C polymorphism is associated with decreased risk of acute myeloid leukemia in a Chinese population
    • Li, N., Xu, Y., Zheng, J., Jiang, L., You, Y., Wu, H., Li, W., Wu, D. and Zhou, Y. (2013) NBS1 rs1805794G>C polymorphism is associated with decreased risk of acute myeloid leukemia in a Chinese population. Mol. Biol. Rep., 40, 3749-3756.
    • (2013) Mol. Biol. Rep , vol.40 , pp. 3749-3756
    • Li, N.1    Xu, Y.2    Zheng, J.3    Jiang, L.4    You, Y.5    Wu, H.6    Li, W.7    Wu, D.8    Zhou, Y.9
  • 63
    • 33344464252 scopus 로고    scopus 로고
    • Bladder cancer predisposition: A multigenic approach to DNA-repair and cell-cycle-control genes
    • Wu, X., Gu, J., Grossman, H. B., et al. (2006) Bladder cancer predisposition: A multigenic approach to DNA-repair and cell-cycle-control genes. Am. J. Hum. Genet., 78, 464-479.
    • (2006) Am. J. Hum. Genet , vol.78 , pp. 464-479
    • Wu, X.1    Gu, J.2    Grossman, H.B.3
  • 64
    • 31844434470 scopus 로고    scopus 로고
    • Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies
    • Chrzanowska, K. H., Piekutowska-Abramczuk, D., Popowska, E., et al. (2006) Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies. Int. J. Cancer, 118, 1269-1274.
    • (2006) Int. J. Cancer , vol.118 , pp. 1269-1274
    • Chrzanowska, K.H.1    Piekutowska-Abramczuk, D.2    Popowska, E.3
  • 65
    • 0038074370 scopus 로고    scopus 로고
    • Multiplex single-tube screening for mutations in the nijmegen breakage syndrome (NBS1) gene in Hodgkin's and non-hodgkin's lymphoma patients of Slavic origin
    • Soucek, P., Gut, I., Trneny, M., Skovlund, E., Grenaker Alnaes, G., Kristensen, T., Borresen-Dale, A. L. and Kristensen, V. N. (2003) Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin. Eur. J. Hum. Genet., 11, 416-419.
    • (2003) Eur. J. Hum. Genet , vol.11 , pp. 416-419
    • Soucek, P.1    Gut, I.2    Trneny, M.3    Skovlund, E.4    Grenaker Alnaes, G.5    Kristensen, T.6    Borresen-Dale, A.L.7    Kristensen, V.N.8
  • 66
    • 10744226677 scopus 로고    scopus 로고
    • 657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls
    • Resnick, I. B., Kondratenko, I., Pashanov, E., et al. (2003) 657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls. Am. J. Med. Genet. A, 120A, 174-179.
    • (2003) Am. J. Med. Genet. A , vol.120 A , pp. 174-179
    • Resnick, I.B.1    Kondratenko, I.2    Pashanov, E.3
  • 67
    • 33746130359 scopus 로고    scopus 로고
    • Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia
    • Mosor, M., Ziołkowska, I., Pernak-Schwarz, M., Januszkiewicz- Lewandowska, D. and Nowak, J. (2006) Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia. Leukemia, 20, 1454-1456.
    • (2006) Leukemia , vol.20 , pp. 1454-1456
    • Mosor, M.1    Ziołkowska, I.2    Pernak-Schwarz, M.3    Januszkiewicz- Lewandowska, D.4    Nowak, J.5
  • 68
    • 33845564143 scopus 로고    scopus 로고
    • Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma. Leuk
    • Rollinson, S., Kesby, H. and Morgan, G. J. (2006) Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma. Leuk. Lymphoma, 47, 2567-2583.
    • (2006) Lymphoma , vol.47 , pp. 2567-2583
    • Rollinson, S.1    Kesby, H.2    Morgan, G.J.3
  • 69
    • 0035328489 scopus 로고    scopus 로고
    • Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)
    • Varon, R., Reis, A., Henze, G., von Einsiedel, H. G., Sperling, K. and Seeger, K. (2001) Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Cancer Res., 61, 3570-3572.
    • (2001) Cancer Res. , vol.61 , pp. 3570-3572
    • Varon, R.1    Reis, A.2    Henze, G.3    Von Einsiedel, H.G.4    Sperling, K.5    Seeger, K.6
  • 70
    • 10744233070 scopus 로고    scopus 로고
    • NBS1 is a prostate cancer susceptibility gene
    • Cybulski, C., Gorski, B., Debniak, T., et al. (2004) NBS1 is a prostate cancer susceptibility gene. Cancer Res., 64, 1215-1219.
    • (2004) Cancer Res , vol.64 , pp. 1215-1219
    • Cybulski, C.1    Gorski, B.2    Debniak, T.3
  • 71
    • 34547816215 scopus 로고    scopus 로고
    • Germline NBS1 mutations in families with aggregation of breast and/or ovarian cancer from north-east Poland
    • Kanka, C., Brozek, I., Skalska, B., Siemiatkowska, A. and Limon, J. (2007) Germline NBS1 mutations in families with aggregation of breast and/or ovarian cancer from north-east Poland. Anticancer Res 27, 3015-3018.
    • (2007) Anticancer Res , vol.27 , pp. 3015-3018
    • Kanka, C.1    Brozek, I.2    Skalska, B.3    Siemiatkowska, A.4    Limon, J.5
  • 72
    • 40449131773 scopus 로고    scopus 로고
    • Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours
    • Nowak, J., Mosor, M., Ziołkowska, I., et al. (2008) Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours. Eur. J. Cancer, 44, 627-630.
    • (2008) Eur. J. Cancer , vol.44 , pp. 627-630
    • Nowak, J.1    Mosor, M.2    Ziołkowska, I.3
  • 73
    • 75049083168 scopus 로고    scopus 로고
    • The frequency of NBN molecular variants in pediatric astrocytic tumors
    • Piekutowska-Abramczuk, D., Ciara, E., Popowska, E., et al. (2010) The frequency of NBN molecular variants in pediatric astrocytic tumors. J. Neurooncol., 96, 161-168.
    • (2010) J. Neurooncol , vol.96 , pp. 161-168
    • Piekutowska-Abramczuk, D.1    Ciara, E.2    Popowska, E.3
  • 75
    • 84857926657 scopus 로고    scopus 로고
    • The role of microRNAbinding site polymorphisms in DNA repair genes as risk factors for bladder cancer and breast cancer and their impact on radiotherapy outcomes
    • Teo, M. T., Landi, D., Taylor, C. F., et al. (2012) The role of microRNAbinding site polymorphisms in DNA repair genes as risk factors for bladder cancer and breast cancer and their impact on radiotherapy outcomes. Carcinogenesis, 33, 581-586.
    • (2012) Carcinogenesis , vol.33 , pp. 581-586
    • Teo, M.T.1    Landi, D.2    Taylor, C.F.3
  • 76
    • 17144442945 scopus 로고    scopus 로고
    • Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin
    • Debniak, T., Gorski, B., Cybulski, C., et al. (2003) Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin. Melanoma Res., 13, 365-370.
    • (2003) Melanoma, Res. , vol.13 , pp. 365-370
    • Debniak, T.1    Gorski, B.2    Cybulski, C.3
  • 77
    • 33751581029 scopus 로고    scopus 로고
    • Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation
    • Steffen, J., Maneva, G., Popławska, L., Varon, R., Mioduszewska, O. and Sperling, K. (2006) Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation. Int. J. Cancer, 119, 2970-2973.
    • (2006) Int. J. Cancer , vol.119 , pp. 2970-2973
    • Steffen, J.1    Maneva, G.2    Popławska, L.3    Varon, R.4    Mioduszewska, O.5    Sperling, K.6
  • 78
    • 53049107194 scopus 로고    scopus 로고
    • Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia
    • Mosor, M., Ziołkowska, I., Januszkiewicz-Lewandowska, D. and Nowak, J. (2008) Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia. Eur. J. Cancer, 44, 2226-2232.
    • (2008) Eur. J. Cancer , vol.44 , pp. 2226-2232
    • Mosor, M.1    Ziołkowska, I.2    Januszkiewicz-Lewandowska, D.3    Nowak, J.4
  • 79
    • 84863716568 scopus 로고    scopus 로고
    • Germline mutations 657del5 and 643C>T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women
    • Mateju, M., Kleiblova, P., Kleibl, Z., Janatova, M., Soukupova, J., Ticha, I., Novotny, J. and Pohlreich, P. (2012) Germline mutations 657del5 and 643C>T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women. Breast Cancer Res. Treat., 133, 809-811.
    • (2012) Breast Cancer Res. Treat , vol.133 , pp. 809-811
    • Mateju, M.1    Kleiblova, P.2    Kleibl, Z.3    Janatova, M.4    Soukupova, J.5    Ticha, I.6    Novotny, J.7    Pohlreich, P.8
  • 80
    • 84867083547 scopus 로고    scopus 로고
    • Association of single nucleotide polymorphisms of NBS1 gene with genetic susceptibility to primary liver cancer in a Chinese Han Population
    • Huang, J., Zhao, Y., Li, Q., Zhang, J., Wang, Y. and Zhang, B. (2012) Association of single nucleotide polymorphisms of NBS1 gene with genetic susceptibility to primary liver cancer in a Chinese Han Population. Prog. Biochem. Biophys., 39, 678-686.
    • (2012) Prog. Biochem. Biophys , vol.39 , pp. 678-686
    • Huang, J.1    Zhao, Y.2    Li, Q.3    Zhang, J.4    Wang, Y.5    Zhang, B.6
  • 81
    • 84929297896 scopus 로고    scopus 로고
    • Association of smoking, residential environment and polymorphisms with lung cancer
    • Qiu, Y., Lin, Y., Huang, M., Chen, X., He, F., Fan, L., Chen, B. and Cai, L. (2011) Association of smoking, residential environment and polymorphisms with lung cancer. J. Environ. Occup. Med. 28, 133-136-140.
    • (2011) J. Environ. Occup. Med. , vol.28 , pp. 140
    • Qiu, Y.1    Lin, Y.2    Huang, M.3    Chen, X.4    He, F.5    Fan, L.6    Chen, B.7    Cai, L.8
  • 82
    • 80054117419 scopus 로고    scopus 로고
    • Study on the association between DNA double-strand break repair gene NBS1 polymorphisms and susceptibility on lung cancer
    • Fan, L. H., Chen, J. L. and Cai, L. (2010) [Study on the association between DNA double-strand break repair gene NBS1 polymorphisms and susceptibility on lung cancer]. Zhonghua Liu Xing Bing Xue Za Zhi, 31, 213-217.
    • (2010) Zhonghua Liu Xing Bing Xue Za Zhi , vol.31 , pp. 213-217
    • Fan, L.H.1    Chen, J.L.2    Cai, L.3
  • 83
    • 0038290163 scopus 로고    scopus 로고
    • Meta-analyses of molecular association studies: Methodologic lessons for genetic epidemiology
    • Attia, J., Thakkinstian, A. and D'Este, C. (2003) Meta-analyses of molecular association studies: methodologic lessons for genetic epidemiology. J. Clin. Epidemiol., 56, 297-303.
    • (2003) J. Clin. Epidemiol , vol.56 , pp. 297-303
    • Attia, J.1    Thakkinstian, A.2    D'Este, C.3
  • 84
    • 0035049158 scopus 로고    scopus 로고
    • Adjusting for multiple testing-when and how?
    • Bender, R. and Lange, S. (2001) Adjusting for multiple testing-when and how? J. Clin. Epidemiol., 54, 343-349.
    • (2001) J. Clin. Epidemiol , vol.54 , pp. 343-349
    • Bender, R.1    Lange, S.2
  • 85
    • 0028931857 scopus 로고
    • Multiple significance tests: The Bonferroni method
    • Bland, J. M. and Altman, D. G. (1995) Multiple significance tests: The Bonferroni method. BMJ, 310, 170.
    • (1995) BMJ , vol.310 , pp. 170
    • Bland, J.M.1    Altman, D.G.2
  • 86
    • 0030670944 scopus 로고    scopus 로고
    • Some comments on frequently used multiple endpoint adjustment methods in clinical trials
    • Sankoh, A. J., Huque, M. F. and Dubey, S. D. (1997) Some comments on frequently used multiple endpoint adjustment methods in clinical trials. Stat. Med., 16, 2529-2542.
    • (1997) Stat. Med , vol.16 , pp. 2529-2542
    • Sankoh, A.J.1    Huque, M.F.2    Dubey, S.D.3
  • 88
    • 0030932869 scopus 로고    scopus 로고
    • Cancer-susceptibility genes. Gatekeepers and caretakers
    • Kinzler, K. W. and Vogelstein, B. (1997) Cancer-susceptibility genes. Gatekeepers and caretakers. Nature, 386, 761, 763.
    • (1997) Nature , vol.386 , pp. 761-763
    • Kinzler, K.W.1    Vogelstein, B.2
  • 89
    • 11844259424 scopus 로고    scopus 로고
    • Functional interaction of H2AX, NBS1, and p53 in ATM-dependent DNA damage responses and tumor suppression
    • Kang, J., Ferguson, D., Song, H., Bassing, C., Eckersdorff, M., Alt, F. W. and Xu, Y. (2005) Functional interaction of H2AX, NBS1, and p53 in ATM-dependent DNA damage responses and tumor suppression. Mol. Cell. Biol., 25, 661-670.
    • (2005) Mol. Cell. Biol , vol.25 , pp. 661-670
    • Kang, J.1    Ferguson, D.2    Song, H.3    Bassing, C.4    Eckersdorff, M.5    Alt, F.W.6    Xu, Y.7
  • 91
    • 22144462810 scopus 로고    scopus 로고
    • Role of Nbs1 in the activation of the Atm kinase revealed in humanized mouse models
    • Difilippantonio, S., Celeste, A., Fernandez-Capetillo, O., et al. (2005) Role of Nbs1 in the activation of the Atm kinase revealed in humanized mouse models. Nat. Cell Biol., 7, 675-685.
    • (2005) Nat. Cell Biol , vol.7 , pp. 675-685
    • Difilippantonio, S.1    Celeste, A.2    Fernandez-Capetillo, O.3
  • 92
    • 84874083026 scopus 로고    scopus 로고
    • Current evidence on the relationship between two polymorphisms in the NBS1 gene and breast cancer risk: A meta-analysis
    • Zhang, Z. H., Yang, L. S., Huang, F., Hao, J. H., Su, P. Y. and Sun, Y. H. (2012) Current evidence on the relationship between two polymorphisms in the NBS1 gene and breast cancer risk: A meta-analysis. Asian Pac. J. Cancer Prev., 13, 5375-5379.
    • (2012) Asian Pac. J. Cancer Prev , vol.13 , pp. 5375-5379
    • Zhang, Z.H.1    Yang, L.S.2    Huang, F.3    Hao, J.H.4    Su, P.Y.5    Sun, Y.H.6
  • 93
    • 41149127607 scopus 로고    scopus 로고
    • The R215W mutation in NBS1 impairs gamma- H2AX binding and affects DNA repair: Molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients
    • di Masi, A., Viganotti, M., Polticelli, F., Ascenzi, P., Tanzarella, C. and Antoccia, A. (2008) The R215W mutation in NBS1 impairs gamma- H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients. Biochem. Biophys. Res. Commun., 369, 835-840.
    • (2008) Biochem. Biophys. Res. Commun , vol.369 , pp. 835-840
    • Di Masi, A.1    Viganotti, M.2    Polticelli, F.3    Ascenzi, P.4    Tanzarella, C.5    Antoccia, A.6
  • 96
    • 0033655698 scopus 로고    scopus 로고
    • Endogenous estrogens as carcinogens through metabolic activation
    • Yager, J. D. (2000) Endogenous estrogens as carcinogens through metabolic activation. J. Natl Cancer Inst., 27, 67-73.
    • (2000) J. Natl Cancer Inst , vol.27 , pp. 67-73
    • Yager, J.D.1
  • 97
    • 35448952908 scopus 로고    scopus 로고
    • Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex
    • Hsu, H. M., Wang, H. C., Chen, S. T., Hsu, G. C., Shen, C. Y. and Yu, J. C. (2007) 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) Cancer Epidemiol. Biomarkers Prev , vol.16 , pp. 2024-2032
    • Hsu, H.M.1    Wang, H.C.2    Chen, S.T.3    Hsu, G.C.4    Shen, C.Y.5    Yu, J.C.6
  • 98
    • 0035866332 scopus 로고    scopus 로고
    • Chromosomal alterations in lung adenocarcinoma from smokers and nonsmokers
    • Sanchez-Cespedes, M., Ahrendt, S. A., Piantadosi, S., et al. (2001) Chromosomal alterations in lung adenocarcinoma from smokers and nonsmokers. Cancer Res., 61, 1309-1313.
    • (2001) Cancer Res , vol.61 , pp. 1309-1313
    • Sanchez-Cespedes, M.1    Ahrendt, S.A.2    Piantadosi, S.3
  • 99
    • 0034796812 scopus 로고    scopus 로고
    • Persistent increase in chromosome instability in lung cancer: Possible indirect involvement of p53 inactivation
    • Haruki, N., Harano, T., Masuda, A., et al. (2001) Persistent increase in chromosome instability in lung cancer: possible indirect involvement of p53 inactivation. Am. J. Pathol., 159, 1345-1352.
    • (2001) Am. J. Pathol , vol.159 , pp. 1345-1352
    • Haruki, N.1    Harano, T.2    Masuda, A.3
  • 100
    • 0028152471 scopus 로고
    • Why sources of heterogeneity in meta-analysis should be investigated
    • Thompson, S. G. (1994) Why sources of heterogeneity in meta-analysis should be investigated. BMJ, 309, 1351-1355.
    • (1994) BMJ , vol.309 , pp. 1351-1355
    • Thompson, S.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.