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Volumn 63, Issue 7, 2003, Pages 1449-1453

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN;

EID: 0037380994     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (280)

References (14)
  • 1
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    • Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions
    • Puget, N., Stoppa-Lyonnet, D., Sinilnikova, O. M., Pages, S., Lynch, H. T., Lenoir, G. M., and Mazoyer, S. Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions. Cancer Res., 59: 455-461, 1999.
    • (1999) Cancer Res. , vol.59 , pp. 455-461
    • Puget, N.1    Stoppa-Lyonnet, D.2    Sinilnikova, O.M.3    Pages, S.4    Lynch, H.T.5    Lenoir, G.M.6    Mazoyer, S.7
  • 2
    • 0036024851 scopus 로고    scopus 로고
    • Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments
    • Casilli, F., Di Rocco, Z. C., Gad, S., Tournier, I., Stoppa-Lyonnet, D., Frebourg, T., and Tosi, M. Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments. Hum. Mutat., 20: 218-226, 2002.
    • (2002) Hum. Mutat. , vol.20 , pp. 218-226
    • Casilli, F.1    Di Rocco, Z.C.2    Gad, S.3    Tournier, I.4    Stoppa-Lyonnet, D.5    Frebourg, T.6    Tosi, M.7
  • 3
    • 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
    • Unger, M. A., Nathanson, K. L., Calzone, K., Antin-Ozerkis, D., Shih, H. A., Martin, A. M., Lenoir, G. M., Mazoyer, S., and L. W. B. 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: 841-850, 2000.
    • (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
  • 6
    • 0030869406 scopus 로고    scopus 로고
    • Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family
    • Swensen, J., Hoffman, M., Skolnick, M. H., and Neuhausen, S. L. Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family. Hum. Mol. Genet., 6: 1513-1517, 1997.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1513-1517
    • Swensen, J.1    Hoffman, M.2    Skolnick, M.H.3    Neuhausen, S.L.4
  • 8
    • 0033566173 scopus 로고    scopus 로고
    • Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families
    • Montagna, M., Santacatterina, M., Torri, A., Menin, C., Zullato, D., Chieco-Bianchi, L., and D'Andrea. E. Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families. Oncogene, 18: 4160-4165, 1999.
    • (1999) Oncogene , vol.18 , pp. 4160-4165
    • Montagna, M.1    Santacatterina, M.2    Torri, A.3    Menin, C.4    Zullato, D.5    Chieco-Bianchi, L.6    D'Andrea, E.7
  • 9
    • 3543023204 scopus 로고    scopus 로고
    • Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
    • Schouten, J. P., McElgunn, C. J., Waaijer, R., Zwijnenburg, D., Diepvens, F., and Pals, G. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. Nucleic Acids Res., 30: e57, 1-13, 2002.
    • (2002) Nucleic Acids Res , vol.30 , Issue.E57 , pp. 1-13
    • Schouten, J.P.1    McElgunn, C.J.2    Waaijer, R.3    Zwijnenburg, D.4    Diepvens, F.5    Pals, G.6
  • 11
    • 0028834145 scopus 로고
    • A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening
    • Shattuck-Eidens, D., McClure, M., Simard, J., Labrie, F., Narod, S., Couch, F., Hoskins, K., Weber, B., Castilla, L., Erdos, M., and et al. A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening. JAMA, 273: 535-541, 1995.
    • (1995) JAMA , vol.273 , pp. 535-541
    • Shattuck-Eidens, D.1    McClure, M.2    Simard, J.3    Labrie, F.4    Narod, S.5    Couch, F.6    Hoskins, K.7    Weber, B.8    Castilla, L.9    Erdos, M.10
  • 12
    • 0029934489 scopus 로고    scopus 로고
    • The 5′ end of the BRCA1 gene lies within a duplicated region of human chromosome 17q21
    • Brown, M. A., Xu, C. F., Nicolai, H., Griffiths, B., Chambers, J. A., Black, D., and Solomon, E. The 5′ end of the BRCA1 gene lies within a duplicated region of human chromosome 17q21. Oncogene, 12: 2507-2513, 1996.
    • (1996) Oncogene , vol.12 , pp. 2507-2513
    • Brown, M.A.1    Xu, C.F.2    Nicolai, H.3    Griffiths, B.4    Chambers, J.A.5    Black, D.6    Solomon, E.7
  • 14
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    • Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1
    • Smith, T. M., Lee, M. K., Szabo, C. I., Jerome, N., McEuen, M., Taylor, M., Hood, L., and King, M. C. Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. Genome Res., 6: 1029-1049, 1996.
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    • Smith, T.M.1    Lee, M.K.2    Szabo, C.I.3    Jerome, N.4    McEuen, M.5    Taylor, M.6    Hood, L.7    King, M.C.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.