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    Results: 5

    1.

    Differing clinical impact of BRCA1 and BRCA2 mutations in serous ovarian cancer.

    Liu G, Yang D, Sun Y, Shmulevich I, Xue F, Sood AK, Zhang W.

    Pharmacogenomics. 2012 Oct;13(13):1523-35. doi: 10.2217/pgs.12.137. Review.

    PMID:
    23057551
    [PubMed - indexed for MEDLINE]

    Related citations

    2.

    Genetics of breast cancer: contribution of BRCA1/2 genes alterations to hereditary predisposition.

    Branković-Magić M, Dobricić J, Krivokuća A.

    Vojnosanit Pregl. 2012 Aug;69(8):700-6. Review. No abstract available.

    PMID:
    22924267
    [PubMed - indexed for MEDLINE]

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    3.

    Mechanisms of BRCA1 tumor suppression.

    Silver DP, Livingston DM.

    Cancer Discov. 2012 Aug;2(8):679-84. doi: 10.1158/2159-8290.CD-12-0221. Epub 2012 Jul 27. Review.

    PMID:
    22843421
    [PubMed - indexed for MEDLINE]

    Related citations

    4.

    BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.

    Tammaro C, Raponi M, Wilson DI, Baralle D.

    Biochem Soc Trans. 2012 Aug;40(4):768-72. doi: 10.1042/BST20120140. Review.

    PMID:
    22817731
    [PubMed - indexed for MEDLINE]

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    5.

    A guide for functional analysis of BRCA1 variants of uncertain significance.

    Millot GA, Carvalho MA, Caputo SM, Vreeswijk MP, Brown MA, Webb M, Rouleau E, Neuhausen SL, Hansen Tv, Galli A, Brandão RD, Blok MJ, Velkova A, Couch FJ, Monteiro AN; ENIGMA Consortium Functional Assay Working Group.

    Hum Mutat. 2012 Nov;33(11):1526-37. doi: 10.1002/humu.22150. Epub 2012 Jul 16. Review.

    PMID:
    22753008
    [PubMed - indexed for MEDLINE]

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