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Volumn 133, Issue 2, 2012, Pages 809-811

Germline mutations 657del5 and 643C>T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 84863716568     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-012-2049-x     Document Type: Letter
Times cited : (13)

References (11)
  • 3
    • 77952821315 scopus 로고    scopus 로고
    • High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany
    • Maurer MH, Hoffmann K, Sperling K, Varon R (2010) High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany. J Appl Genet 51:211-214
    • (2010) J Appl Genet , vol.51 , pp. 211-214
    • Maurer, M.H.1    Hoffmann, K.2    Sperling, K.3    Varon, R.4
  • 4
    • 45749123993 scopus 로고    scopus 로고
    • NBS1 heterozygosity and cancer risk
    • di Masi A, Antoccia A (2008) NBS1 heterozygosity and cancer risk. Curr Genomics 9:275-281
    • (2008) Curr Genomics , vol.9 , pp. 275-281
    • Di Masi, A.1    Antoccia, A.2
  • 8
    • 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 AM, Ponder BA (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
  • 9
    • 84860333452 scopus 로고    scopus 로고
    • RAD50 and NBS1 are not likely to be susceptibility genes in Chinese non-BRCA1/2 hereditary breast cancer
    • doi:10.1007/s10549-011-1700-2
    • He M, Di GH, Cao AY, Hu Z, Jin W, Shen ZZ, Shao ZM (2011) RAD50 and NBS1 are not likely to be susceptibility genes in Chinese non-BRCA1/2 hereditary breast cancer. Breast Cancer Res Treat. doi:10.1007/s10549-011-1700-2
    • (2011) Breast Cancer Res Treat
    • He, M.1    Di, G.H.2    Cao, A.Y.3    Hu, Z.4    Jin, W.5    Shen, Z.Z.6    Shao, Z.M.7
  • 11
    • 52949100992 scopus 로고    scopus 로고
    • Analysis of CHEK2 FHA domain in Czech patients with sporadic breast cancer revealed distinct rare genetic alterations
    • Kleibl Z, Havranek O, Novotny J, Kleiblova P, Soucek P, Pohlreich P (2008) Analysis of CHEK2 FHA domain in Czech patients with sporadic breast cancer revealed distinct rare genetic alterations. Breast Cancer Res Treat 112:159-164
    • (2008) Breast Cancer Res Treat , vol.112 , pp. 159-164
    • Kleibl, Z.1    Havranek, O.2    Novotny, J.3    Kleiblova, P.4    Soucek, P.5    Pohlreich, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.