메뉴 건너뛰기




Volumn 27, Issue 4 C, 2007, Pages 3015-3018

Germline NBS1 mutations in families with aggregation of breast and/or ovarian cancer from North-East Poland

Author keywords

657del5 mutation; Breast cancer; Cancer predisposition; I171V mutation; NBS1 gene; Ovarian cancer

Indexed keywords

NIBRIN;

EID: 34547816215     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (19)

References (22)
  • 1
    • 0035960431 scopus 로고    scopus 로고
    • Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease
    • Collaborative Group on Hormonal Factors in Breast Cancer
    • Collaborative Group on Hormonal Factors in Breast Cancer: Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease. Lancet 358: 1389-1399, 2001.
    • (2001) Lancet , vol.358 , pp. 1389-1399
  • 4
    • 28244478365 scopus 로고    scopus 로고
    • Genomic instability and cancer: Networks involved in response to DNA damage
    • Eyfjord JE and Bodvarsdottir SK: Genomic instability and cancer: Networks involved in response to DNA damage. Mutat Res 592: 18-28, 2005.
    • (2005) Mutat Res , vol.592 , pp. 18-28
    • Eyfjord, J.E.1    Bodvarsdottir, S.K.2
  • 8
    • 0035328489 scopus 로고    scopus 로고
    • Mutations in the Nijmegen Breakage Syndrome Gene (NBS1) in childhood acute lymphoblastic leukaemia (ALL)
    • Varon R, Reis A, Henze G, Graf v. Einsiedl H, Sperling K and Seeger K: Mutations in the Nijmegen Breakage Syndrome Gene (NBS1) in childhood acute lymphoblastic leukaemia (ALL). Cancer Res 61: 3570-3572, 2001.
    • (2001) Cancer Res , vol.61 , pp. 3570-3572
    • Varon, R.1    Reis, A.2    Henze, G.3    Graf4    Einsiedl, H.5    Sperling, K.6    Seeger, K.7
  • 10
    • 31844434470 scopus 로고    scopus 로고
    • Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, Koltan A, Kuzmicz M, Luszawska-Kutrzeba T, Maciejka-Kapuscinska L, Stolarska M, Stefanska K, Sznurkowska K, Wakulinska A, Wieczorek M, Szczepanski T and Kowalczyk J: Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish paediatric patients with sporadic lymphoid malignancies. Int J Cancer 18: 1269-1274, 2006.
    • Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, Koltan A, Kuzmicz M, Luszawska-Kutrzeba T, Maciejka-Kapuscinska L, Stolarska M, Stefanska K, Sznurkowska K, Wakulinska A, Wieczorek M, Szczepanski T and Kowalczyk J: Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish paediatric patients with sporadic lymphoid malignancies. Int J Cancer 18: 1269-1274, 2006.
  • 15
    • 33746130359 scopus 로고    scopus 로고
    • Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukaemia
    • Mosor M, Ziolkowska I, Pernak-Schwarz M, Januszkiewicz-Lewandowska D and Nowak J: Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukaemia. Leukemia 8: 1454-1456, 2006.
    • (2006) Leukemia , vol.8 , pp. 1454-1456
    • Mosor, M.1    Ziolkowska, I.2    Pernak-Schwarz, M.3    Januszkiewicz-Lewandowska, D.4    Nowak, J.5
  • 16
    • 5044248651 scopus 로고    scopus 로고
    • First case of aplastic anaemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability
    • Shimada H, Shimizu K, Mimaki S, Sakiyama T, Mori T, Shimasaki N, Yokota J, Nakachi K, Ohta T and Ohki M: First case of aplastic anaemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability. Hum Genet 115: 372-376, 2004.
    • (2004) Hum Genet , vol.115 , pp. 372-376
    • Shimada, H.1    Shimizu, K.2    Mimaki, S.3    Sakiyama, T.4    Mori, T.5    Shimasaki, N.6    Yokota, J.7    Nakachi, K.8    Ohta, T.9    Ohki, M.10
  • 18
    • 33748852526 scopus 로고    scopus 로고
    • Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland)
    • Ziolkowska I, Mosor M and Nowak J: Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland). J Appl Genet 47: 269-272, 2006.
    • (2006) J Appl Genet , vol.47 , pp. 269-272
    • Ziolkowska, I.1    Mosor, M.2    Nowak, J.3
  • 22
    • 0032792820 scopus 로고    scopus 로고
    • Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: No association with risk of breast cancer
    • Carlomagno F, Chang-Claude J, Dunning AM and Ponder BA: Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer. Genes Chromosomes Cancer 25: 393-395, 1999.
    • (1999) Genes Chromosomes Cancer , vol.25 , pp. 393-395
    • Carlomagno, F.1    Chang-Claude, J.2    Dunning, A.M.3    Ponder, B.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.