메뉴 건너뛰기




Volumn 65, Issue 2, 2005, Pages 383-386

Germ line fanconi anemia complementation group C mutations and pancreatic cancer

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 12544255089     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (122)

References (20)
  • 1
    • 0026784163 scopus 로고
    • Familial pancreatic cancer: A family study
    • Lynch HT, Fusaro L, Lynch JF. Familial pancreatic cancer: a family study. Pancreas 1992;7:511-5.
    • (1992) Pancreas , vol.7 , pp. 511-515
    • Lynch, H.T.1    Fusaro, L.2    Lynch, J.F.3
  • 3
    • 12644253827 scopus 로고    scopus 로고
    • Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas
    • Goggins M, Schutte M, Lu J, et al. Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. Cancer Res 1996;56:5360-4.
    • (1996) Cancer Res , vol.56 , pp. 5360-5364
    • Goggins, M.1    Schutte, M.2    Lu, J.3
  • 4
    • 0033523268 scopus 로고    scopus 로고
    • Cancer risks in BRCA2 mutation carriers
    • Breast Cancer Linkage Consortium. Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst 1999;91:1310-6.
    • (1999) J Natl Cancer Inst , vol.91 , pp. 1310-1316
  • 5
    • 0036644884 scopus 로고    scopus 로고
    • Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%
    • Murphy KM, Brune KA, Griffin C, et al. Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%. Cancer Res 2002;62:3789-93.
    • (2002) Cancer Res , vol.62 , pp. 3789-3793
    • Murphy, K.M.1    Brune, K.A.2    Griffin, C.3
  • 6
    • 0037420026 scopus 로고    scopus 로고
    • BRCA2 germline mutations in familial pancreatic carcinoma
    • Hahn SA, Greenhalf B, Ellis I, et al. BRCA2 germline mutations in familial pancreatic carcinoma. J Natl Cancer Inst 2003;95:214-21.
    • (2003) J Natl Cancer Inst , vol.95 , pp. 214-221
    • Hahn, S.A.1    Greenhalf, B.2    Ellis, I.3
  • 7
    • 18444362122 scopus 로고    scopus 로고
    • Biallelic inactivation of BRCA2 in Fanconi anemia
    • Howlett NG, Taniguchi T, Olson S, et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 2002;297:606-9.
    • (2002) Science , vol.297 , pp. 606-609
    • Howlett, N.G.1    Taniguchi, T.2    Olson, S.3
  • 8
  • 9
    • 0037441757 scopus 로고    scopus 로고
    • A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
    • Kutler DI, Singh B, Satagopan J, et al. A 20-year perspective on the International Fanconi Anemia Registry (IFAR). Blood 2003;101:1249-56.
    • (2003) Blood , vol.101 , pp. 1249-1256
    • Kutler, D.I.1    Singh, B.2    Satagopan, J.3
  • 10
    • 0033710326 scopus 로고    scopus 로고
    • Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9
    • Demuth I, Wlodarski M, Tipping AJ, et al. Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. Eur J Hum Genet 2000;8:861-8.
    • (2000) Eur J Hum Genet , vol.8 , pp. 861-868
    • Demuth, I.1    Wlodarski, M.2    Tipping, A.J.3
  • 11
    • 0034672154 scopus 로고    scopus 로고
    • Association of complementation group and mutation type with clinical outcome in Fanconi anemia
    • Faivre L, Guardiola P, Lewis C, et al. Association of complementation group and mutation type with clinical outcome in Fanconi anemia. Blood 2000;96:4064-70.
    • (2000) Blood , vol.96 , pp. 4064-4070
    • Faivre, L.1    Guardiola, P.2    Lewis, C.3
  • 13
    • 0030023770 scopus 로고    scopus 로고
    • Fanconi anaemia complementation groups in Germany and the Netherlands
    • Joenje H. Fanconi anaemia complementation groups in Germany and the Netherlands. Hum Genet 1996;97:280-2.
    • (1996) Hum Genet , vol.97 , pp. 280-282
    • Joenje, H.1
  • 14
    • 0027288907 scopus 로고
    • A common mutation in the Facc gene causes Fanconi-anemia in Ashkenazi Jews
    • Whitney MA, Saito H, Jakobs PM, et al. A common mutation in the Facc gene causes Fanconi-anemia in Ashkenazi Jews. Nat Genet 1993;4:202-5.
    • (1993) Nat Genet , vol.4 , pp. 202-205
    • Whitney, M.A.1    Saito, H.2    Jakobs, P.M.3
  • 15
    • 0037439356 scopus 로고    scopus 로고
    • Cancer in Fanconi anemia, 1927-2001
    • Alter BP. Cancer in Fanconi anemia, 1927-2001. Cancer 2003;97:425-40.
    • (2003) Cancer , vol.97 , pp. 425-440
    • Alter, B.P.1
  • 16
    • 3042581455 scopus 로고    scopus 로고
    • The genetics of FANCC and FANCG in familial pancreatic cancer
    • Rogers CD, van der Heijden MS, Brune K, et al. The genetics of FANCC and FANCG in familial pancreatic cancer. Cancer Biol Ther 2004;3:167-9.
    • (2004) Cancer Biol Ther , vol.3 , pp. 167-169
    • Rogers, C.D.1    Van Der Heijden, M.S.2    Brune, K.3
  • 17
    • 3242789247 scopus 로고    scopus 로고
    • Functional defects in the Fanconi anemia pathway in pancreatic cancer cells
    • van der Heijden MS, Brody JR, Gallmeier E, et al. Functional defects in the Fanconi anemia pathway in pancreatic cancer cells. Am J Pathol 2004;165:651-7.
    • (2004) Am J Pathol , vol.165 , pp. 651-657
    • Van Der Heijden, M.S.1    Brody, J.R.2    Gallmeier, E.3
  • 18
    • 0028231738 scopus 로고
    • Mutation analysis of the Fanconi-anemia gene Facc
    • Verlander PC, Lin JD, Udono MU, et al. Mutation analysis of the Fanconi-anemia gene Facc. Am J Hum Genet 1994;54:595-601.
    • (1994) Am J Hum Genet , vol.54 , pp. 595-601
    • Verlander, P.C.1    Lin, J.D.2    Udono, M.U.3
  • 19
    • 9144268932 scopus 로고    scopus 로고
    • Evaluation of Fanconi anemia genes in familial breast cancer predisposition
    • Seal S, Barfoot R, Jayatilake H, et al. Evaluation of Fanconi anemia genes in familial breast cancer predisposition. Cancer Res 2003;63:8596-9.
    • (2003) Cancer Res , vol.63 , pp. 8596-8599
    • Seal, S.1    Barfoot, R.2    Jayatilake, H.3
  • 20
    • 0037393869 scopus 로고    scopus 로고
    • Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia
    • Barber LM, Mcgrath HEN, Meyer S, et al. Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia. Br J Haematol 2003;121:57-62.
    • (2003) Br J Haematol , vol.121 , pp. 57-62
    • Barber, L.M.1    Mcgrath, H.E.N.2    Meyer, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.