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Volumn 91, Issue 6, 2004, Pages 1155-1159

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

Author keywords

APC; BRCA1; BRCA2; hMLH1; hMSH2; MLPA

Indexed keywords

APC PROTEIN; BRCA1 PROTEIN; BRCA2 PROTEIN; DNA;

EID: 5044227573     PISSN: 00070920     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bjc.6602121     Document Type: Article
Times cited : (158)

References (14)
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    • MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer
    • Charbonnier F, Olschwang S, Wang Q, Boisson C, Martin C, Buisine MP, Puisieux A, Frebourg T (2002) MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer. Cancer Res 62: 848-853
    • (2002) Cancer Res , vol.62 , pp. 848-853
    • Charbonnier, F.1    Olschwang, S.2    Wang, Q.3    Boisson, C.4    Martin, C.5    Buisine, M.P.6    Puisieux, A.7    Frebourg, T.8
  • 3
    • 2942726188 scopus 로고    scopus 로고
    • A new scoring system for the chances of identifying a BRCA1/2 mutation, outperforms existing models including BRCAPRO
    • Evans G, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F (2004) A new scoring system for the chances of identifying a BRCA1/2 mutation, outperforms existing models including BRCAPRO. J Med Genet 41: 474-480
    • (2004) J Med Genet , vol.41 , pp. 474-480
    • Evans, G.1    Eccles, D.M.2    Rahman, N.3    Young, K.4    Bulman, M.5    Amir, E.6    Shenton, A.7    Howell, A.8    Lalloo, F.9
  • 6
    • 0038364017 scopus 로고    scopus 로고
    • Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families
    • Montagna M, Palma MD, Menin C, Agata S, De Nicolo A, Chieco-Bianchi L, D'Andrea E (2003) Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families. Hum Mol Genet 12: 1055-1061
    • (2003) Hum Mol Genet , vol.12 , pp. 1055-1061
    • Montagna, M.1    Palma, M.D.2    Menin, C.3    Agata, S.4    De Nicolo, A.5    Chieco-Bianchi, L.6    D'Andrea, E.7
  • 7
    • 0142124795 scopus 로고    scopus 로고
    • Identification and characterisation of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques
    • Nakagawa H, Hampel H, de la Chapelle A (2003) Identification and characterisation of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques. Hum Mutat 22: 258
    • (2003) Hum Mutat , vol.22 , pp. 258
    • Nakagawa, H.1    Hampel, H.2    De La Chapelle, A.3
  • 12
    • 0346363771 scopus 로고    scopus 로고
    • Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary nonpolyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA
    • Taylor F, Charlton RS, Burn J, Sheridan E, Taylor GR (2003) Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary nonpolyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. Hum Mutat 22: 428-433
    • (2003) Hum Mutat , vol.22 , pp. 428-433
    • Taylor, F.1    Charlton, R.S.2    Burn, J.3    Sheridan, E.4    Taylor, G.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.