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Volumn 121, Issue 2, 2011, Pages 353-357

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

Author keywords

BRCA1; BRCA2; Ovarian cancer

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

EID: 79955478110     PISSN: 00908258     EISSN: 10956859     Source Type: Journal    
DOI: 10.1016/j.ygyno.2011.01.020     Document Type: Article
Times cited : (338)

References (24)
  • 5
    • 0033799478 scopus 로고    scopus 로고
    • Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing
    • M.A. Unger, K.L. Nathanson, K. Calzone, D. Antin-Ozerkis, H.A. Shih, A.M. Martin, G.M. Lenoir, S. Mazoyer, and B.L. Weber Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing Am. J. Hum. Genet. 67 2000 841 850
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 841-850
    • Unger, M.A.1    Nathanson, K.L.2    Calzone, K.3    Antin-Ozerkis, D.4    Shih, H.A.5    Martin, A.M.6    Lenoir, G.M.7    Mazoyer, S.8    Weber, B.L.9
  • 7
    • 0033028701 scopus 로고    scopus 로고
    • Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history
    • DOI 10.1034/j.1399-0004.1999.550504.x
    • P.N. Tonin, A.-M. Mes-Masson, S.A. Narod, P. Ghadirian, and D. Provencher Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history Clin. Genet. 55 1999 318 324 (Pubitemid 29295324)
    • (1999) Clinical Genetics , vol.55 , Issue.5 , pp. 318-324
    • Tonin, P.N.1    Mes-Masson, A.-M.2    Narod, S.A.3    Ghadirian, P.4    Provencher, D.5
  • 8
    • 0034125402 scopus 로고    scopus 로고
    • A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes
    • DOI 10.1034/j.1399-0004.2000.570307.x
    • G. Kuperstein, W.D. Foulkes, P. Ghadirian, J. Hakimi, and S.A. Narod A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes Clin. Genet. 57 2000 213 220 (Pubitemid 30168749)
    • (2000) Clinical Genetics , vol.57 , Issue.3 , pp. 213-220
    • Kuperstein, G.1    Foulkes, W.D.2    Ghadirian, P.3    Hakimi, J.4    Narod, S.A.5
  • 9
    • 0033909581 scopus 로고    scopus 로고
    • The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations
    • BRCA1 Exon 13 Duplication Screening Group
    • BRCA1 Exon 13 Duplication Screening Group The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations Am. J. Hum. Genet. 67 2000 207 212
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 207-212
  • 10
    • 34548864078 scopus 로고    scopus 로고
    • Mutation screening using fluorescence multiplex denaturing gradient gel electrophoresis (FMD): Detecting mutations in the BRCA1 gene
    • S. Zhang, G. Kuperstein, and S.A. Narod Mutation screening using fluorescence multiplex denaturing gradient gel electrophoresis (FMD): detecting mutations in the BRCA1 gene Nat. Protoc. 1 2007 3101 3110
    • (2007) Nat. Protoc. , vol.1 , pp. 3101-3110
    • Zhang, S.1    Kuperstein, G.2    Narod, S.A.3
  • 11
    • 0033805671 scopus 로고    scopus 로고
    • Identification of specific BRCA1 and BRCA2 variants by DHPLC
    • E. Gross, N. Arnold, K. Pfeifer, K. Bandick, and M. Kiechle Identification of specific BRCA1 and BRCA2 variants by DHPLC Hum. Mutat. 16 2000 345 353
    • (2000) Hum. Mutat. , vol.16 , pp. 345-353
    • Gross, E.1    Arnold, N.2    Pfeifer, K.3    Bandick, K.4    Kiechle, M.5
  • 20
    • 33745881036 scopus 로고    scopus 로고
    • Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation 2
    • Hereditary Ovarian Cancer Clinical Study Group
    • A. Finch, M. Beiner, J. Lubinski, H.T. Lynch, P. Moller, B. Rosen, J. Murphy, P. Ghadirian, E. Friedman, W.D. Foulkes, C. Kim-Sing, and T. Wagner Hereditary Ovarian Cancer Clinical Study Group. Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation 2 JAMA 296 2006 Jul 12 185 192
    • (2006) JAMA , vol.296 , pp. 185-192
    • Finch, A.1    Beiner, M.2    Lubinski, J.3    Lynch, H.T.4    Moller, P.5    Rosen, B.6    Murphy, J.7    Ghadirian, P.8    Friedman, E.9    Foulkes, W.D.10    Kim-Sing, C.11    Wagner, T.12
  • 22
    • 0037403380 scopus 로고    scopus 로고
    • Improved survival in women with BRCA-associated ovarian carcinoma
    • DOI 10.1002/cncr.11310
    • I. Cass, R.L. Baldwin, T. Varkey, R. Moslehi, S.A. Narod, and B.Y. Karlan Improved survival in women with BRCA-associated ovarian carcinoma Cancer 97 2003 2187 2195 (Pubitemid 36444059)
    • (2003) Cancer , vol.97 , Issue.9 , pp. 2187-2195
    • Cass, I.1    Baldwin, R.L.2    Varkey, T.3    Moslehi, R.4    Narod, S.A.5    Karlan, B.Y.6
  • 23
    • 57149093237 scopus 로고    scopus 로고
    • BRCAness″ syndrome in ovarian cancer: A case-control study describing the clinical features and outcome of patients with epithelial ovarian cancer associated with BRCA1 and BRCA2 mutations
    • D.S. Tan, C. Rothermundt, K. Thomas, E. Bancroft, R. Eeles, S. Shanley, A. Ardern-Jones, A. Norman, S.B. Kaye, and M.E. Gore BRCAness″ syndrome in ovarian cancer: a case-control study describing the clinical features and outcome of patients with epithelial ovarian cancer associated with BRCA1 and BRCA2 mutations J. Clin. Oncol. 26 34 2008 Dec 1 5530 5536
    • (2008) J. Clin. Oncol. , vol.26 , Issue.34 , pp. 5530-5536
    • Tan, D.S.1    Rothermundt, C.2    Thomas, K.3    Bancroft, E.4    Eeles, R.5    Shanley, S.6    Ardern-Jones, A.7    Norman, A.8    Kaye, S.B.9    Gore, M.E.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.