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Volumn 199, Issue 2, 2008, Pages 148.e1-148.e3

Gynecologic malignancies in Ashkenazi families with the MSH2 A636P founder mutation

Author keywords

Ashkenazi Jews; colorectal cancer; endometrial cancer; HNFCC; MSH2 A636P founder mutation

Indexed keywords

PROTEIN MSH2;

EID: 48149095196     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajog.2008.02.018     Document Type: Article
Times cited : (7)

References (13)
  • 1
    • 0036917758 scopus 로고    scopus 로고
    • The founder mutation MSH2*1906G→C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
    • Foulkes W.D., Thiffault I., Gruber S.B., et al. The founder mutation MSH2*1906G→C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population. Am J Hum Genet 71 (2002) 1395-1412
    • (2002) Am J Hum Genet , vol.71 , pp. 1395-1412
    • Foulkes, W.D.1    Thiffault, I.2    Gruber, S.B.3
  • 2
    • 23444452690 scopus 로고    scopus 로고
    • Clinical and genetic findings in an Ashkenazi Jewish population with colorectal neoplasms
    • Zauber N.P., Sabbath-Solitare M., Marotta S., et al. Clinical and genetic findings in an Ashkenazi Jewish population with colorectal neoplasms. Cancer 104 (2005) 719-729
    • (2005) Cancer , vol.104 , pp. 719-729
    • Zauber, N.P.1    Sabbath-Solitare, M.2    Marotta, S.3
  • 3
    • 26944479284 scopus 로고    scopus 로고
    • The HNPCC associated MSH2*1906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population
    • Sun S., Greenwood C.M., Thiffault I., Hamel N., Chong G., and Foulkes W.D. The HNPCC associated MSH2*1906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population. J Med Genet 42 (2005) 766-768
    • (2005) J Med Genet , vol.42 , pp. 766-768
    • Sun, S.1    Greenwood, C.M.2    Thiffault, I.3    Hamel, N.4    Chong, G.5    Foulkes, W.D.6
  • 5
    • 28944442873 scopus 로고    scopus 로고
    • Cancer characteristics in Swedish families fulfilling criteria for hereditary nonpolyposis colorectal cancer
    • Bermejo J.L., Eng C., and Hemminki K. Cancer characteristics in Swedish families fulfilling criteria for hereditary nonpolyposis colorectal cancer. Gastroenterology 129 (2005) 1889-1899
    • (2005) Gastroenterology , vol.129 , pp. 1889-1899
    • Bermejo, J.L.1    Eng, C.2    Hemminki, K.3
  • 6
    • 20544467125 scopus 로고    scopus 로고
    • Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment
    • Quehenberger F., Vasen H.F., and van Houwelingen H.C. Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment. J Med Genet 42 (2005) 491-496
    • (2005) J Med Genet , vol.42 , pp. 491-496
    • Quehenberger, F.1    Vasen, H.F.2    van Houwelingen, H.C.3
  • 7
    • 3142660643 scopus 로고    scopus 로고
    • Frequency of extra-colonic tumors in hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) Brazilian families: an analysis by a Brazilian Hereditary Colorectal Cancer Institutional Registry
    • Oliveira Ferreira F., Napoli Ferreira C.C., Rossi B.M., et al. Frequency of extra-colonic tumors in hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) Brazilian families: an analysis by a Brazilian Hereditary Colorectal Cancer Institutional Registry. Fam Cancer 3 (2004) 41-47
    • (2004) Fam Cancer , vol.3 , pp. 41-47
    • Oliveira Ferreira, F.1    Napoli Ferreira, C.C.2    Rossi, B.M.3
  • 8
    • 1342309591 scopus 로고    scopus 로고
    • Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden
    • Cederquist K., Emanuelsson M., Goransson I., et al. Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. Int J Cancer 109 (2004) 370-376
    • (2004) Int J Cancer , vol.109 , pp. 370-376
    • Cederquist, K.1    Emanuelsson, M.2    Goransson, I.3
  • 9
    • 33745094646 scopus 로고    scopus 로고
    • MSH2 splice site mutation and endometrial cancer
    • Bianchi F., Rosati S., Belvederesi L., et al. MSH2 splice site mutation and endometrial cancer. Int J Gynecol Cancer 16 (2006) 1419-1423
    • (2006) Int J Gynecol Cancer , vol.16 , pp. 1419-1423
    • Bianchi, F.1    Rosati, S.2    Belvederesi, L.3
  • 10
    • 21344471434 scopus 로고    scopus 로고
    • Genetic analyses in consecutive Israeli Jewish colorectal cancer patients
    • Fidder H.H., Figer A., Geva R., et al. Genetic analyses in consecutive Israeli Jewish colorectal cancer patients. Am J Gastroenterol 100 (2005) 1376-1380
    • (2005) Am J Gastroenterol , vol.100 , pp. 1376-1380
    • Fidder, H.H.1    Figer, A.2    Geva, R.3
  • 11
    • 8544276607 scopus 로고    scopus 로고
    • A636P testing in Ashkenazi Jews
    • Guillem J.G., Moore H.G., Palmer C., et al. A636P testing in Ashkenazi Jews. Fam Cancer 3 (2004) 223-227
    • (2004) Fam Cancer , vol.3 , pp. 223-227
    • Guillem, J.G.1    Moore, H.G.2    Palmer, C.3
  • 12
    • 0032941343 scopus 로고    scopus 로고
    • Cancer risk in mutation carriers of DNA-mismatch-repair genes
    • Aarnio M., Sankila R., Pukkala E., et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 81 (1999) 214-218
    • (1999) Int J Cancer , vol.81 , pp. 214-218
    • Aarnio, M.1    Sankila, R.2    Pukkala, E.3
  • 13
    • 0032870177 scopus 로고    scopus 로고
    • hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
    • Planck M., Koul A., Fernebro E., et al. hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden. Int J Cancer 83 (1999) 197-202
    • (1999) Int J Cancer , vol.83 , pp. 197-202
    • Planck, M.1    Koul, A.2    Fernebro, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.