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Volumn 71, Issue 6, 2002, Pages 1395-1412

The founder mutation MSH2*1906G→C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

(33)  Foulkes, William D a,b,c,q   Thiffault, I a,b,c   Gruber, S B d   Horwitz, M e   Hamel, N b,c   Lee, C f   Shia, J f   Markowitz, A f   Figer, A g   Friedman, E h   Farber, D a   Greenwood, C M T b   Bonner, J D d   Nafa, K f   Walsh, T e   Marcus, V b   Tomsho, L d   Gebert, J i   Macrae, F A j   Gaff, C L j,k   more..


Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0036917758     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/345075     Document Type: Article
Times cited : (116)

References (27)
  • 2
    • 0030746291 scopus 로고    scopus 로고
    • Inhibition of nonsense-mediated messenger RNA decay in clinical samples facilitates detection of human MSH2 mutations with an in vivo fusion protein assay and conventional techniques
    • Andreutti-Zaugg C, Scott RJ, Iggo R (1997) Inhibition of nonsense-mediated messenger RNA decay in clinical samples facilitates detection of human MSH2 mutations with an in vivo fusion protein assay and conventional techniques. Cancer Res 57:3288-3293
    • (1997) Cancer Res , vol.57 , pp. 3288-3293
    • Andreutti-Zaugg, C.1    Scott, R.J.2    Iggo, R.3
  • 3
    • 0032534069 scopus 로고    scopus 로고
    • A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
    • Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, Meltzer SJ, Rodriguez-Bigas MA, Fodde R, Ranzani GN, Srivastava S (1998) A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 58:5248-5257
    • (1998) Cancer Res , vol.58 , pp. 5248-5257
    • Boland, C.R.1    Thibodeau, S.N.2    Hamilton, S.R.3    Sidransky, D.4    Eshleman, J.R.5    Burt, R.W.6    Meltzer, S.J.7    Rodriguez-Bigas, M.A.8    Fodde, R.9    Ranzani, G.N.10    Srivastava, S.11
  • 5
    • 0035942495 scopus 로고    scopus 로고
    • A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: A founder mutation in the Chinese population
    • Chan TL, Yuen ST, Ho JW, Chan AS, Kwan K, Chung LP, Lam PW, Tse CW, Leung SY (2001) A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: A founder mutation in the Chinese population. Oncogene 20:2976-2981
    • (2001) Oncogene , vol.20 , pp. 2976-2981
    • Chan, T.L.1    Yuen, S.T.2    Ho, J.W.3    Chan, A.S.4    Kwan, K.5    Chung, L.P.6    Lam, P.W.7    Tse, C.W.8    Leung, S.Y.9
  • 18
    • 0034641938 scopus 로고    scopus 로고
    • Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA
    • Obmolova G, Ban C, Hsieh P, Yang W (2000) Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA. Nature 407:703-710
    • (2000) Nature , vol.407 , pp. 703-710
    • Obmolova, G.1    Ban, C.2    Hsieh, P.3    Yang, W.4
  • 19
    • 0035514049 scopus 로고    scopus 로고
    • A genetic profile of contemporary Jewish populations
    • Ostrer H (2001) A genetic profile of contemporary Jewish populations. Nat Rev Genet 2:891-898
    • (2001) Nat Rev Genet , vol.2 , pp. 891-898
    • Ostrer, H.1
  • 20
    • 0035054387 scopus 로고    scopus 로고
    • Deficient DNA mismatch repair: A common etiologic factor for colon cancer
    • Peltomaki P (2001) Deficient DNA mismatch repair: A common etiologic factor for colon cancer. Hum Mol Genet 10:735-740
    • (2001) Hum Mol Genet , vol.10 , pp. 735-740
    • Peltomaki, P.1
  • 23
    • 0035071957 scopus 로고    scopus 로고
    • A new statistical method for haplotype reconstruction from population data
    • Stephens M, Smith NJ, Donnelly P (2001) A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 68:978-989
    • (2001) Am J Hum Genet , vol.68 , pp. 978-989
    • Stephens, M.1    Smith, N.J.2    Donnelly, P.3
  • 24
    • 0025848680 scopus 로고
    • The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
    • Vasen HF, Mecklin JP, Khan PM, Lynch HT (1991) The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 34:424-425
    • (1991) Dis Colon Rectum , vol.34 , pp. 424-425
    • Vasen, H.F.1    Mecklin, J.P.2    Khan, P.M.3    Lynch, H.T.4
  • 26
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC
    • Vasen HF, Watson P, Mecklin JP, Lynch HT (1999) New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC. Gastroenterology 116:1453-1456
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.