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Volumn 33, Issue 6, 2011, Pages

Is the NBN gene mutation I171V a potential risk factor for malignant solid tumors in children?

Author keywords

I171V mutation; NBN; solid tumors in children

Indexed keywords

ISOLEUCINE; VALINE;

EID: 80051787595     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e3181faf886     Document Type: Article
Times cited : (5)

References (15)
  • 1
    • 0035328489 scopus 로고    scopus 로고
    • Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)
    • Varon R, Reis A, Henze G, et al. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Cancer Res. 2001;61:3570-3572. (Pubitemid 32694962)
    • (2001) Cancer Research , vol.61 , Issue.9 , pp. 3570-3572
    • Varon, R.1    Reis, A.2    Henze, G.3    Einsiedel, H.G.V.4    Sperling, K.5    Seeger, K.6
  • 3
    • 33745225487 scopus 로고    scopus 로고
    • Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland
    • Steffen J, Nowakowska D, Niwinska A, et al. Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland. Int J Cancer. 2006;119:472-475.
    • (2006) Int J Cancer. , vol.119 , pp. 472-475
    • Steffen, J.1    Nowakowska, D.2    Niwinska, A.3
  • 7
    • 40449131773 scopus 로고    scopus 로고
    • Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours
    • Nowak J, Mosor M, Ziókowska I, et al. Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours. Eur J Cancer. 2008;44:627-630.
    • (2008) Eur J Cancer. , vol.44 , pp. 627-630
    • Nowak, J.1    Mosor, M.2    Zióowska, I.3
  • 8
    • 34748906012 scopus 로고    scopus 로고
    • Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene
    • DOI 10.1111/j.1349-7006.2007.00594.x
    • Ziókowska I, Mosor M, Wierzbicka M, et al. Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene. Cancer Sci. 2007;98:1701-1705. (Pubitemid 47487904)
    • (2007) Cancer Science , vol.98 , Issue.11 , pp. 1701-1705
    • Ziolkowska, I.1    Mosor, M.2    Wierzbicka, M.3    Rydzanicz, M.4    Pernak-Schwarz, M.5    Nowak, J.6
  • 9
    • 33746130359 scopus 로고    scopus 로고
    • Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia [9]
    • DOI 10.1038/sj.leu.2404285, PII 2404285
    • Mosor M, Ziókowska I, Pernak-Schwarz M, et al. Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia. Leukemia. 2006;20:1454-1456. (Pubitemid 44084066)
    • (2006) Leukemia , vol.20 , Issue.8 , pp. 1454-1456
    • Mosor, M.1    Ziolkowska, I.2    Pernak-Schwarz, M.3    Januszkiewicz-Lewandowska, D.4    Nowak, J.5
  • 10
    • 45749123993 scopus 로고    scopus 로고
    • NBS1 heterozygosity and cancer risk
    • DOI 10.2174/138920208784533610
    • Di Masi A, Antoccia A. NBS1 Heterozygosity and Cancer Risk. Curr Genomics. 2008; 9:275-281. (Pubitemid 351864253)
    • (2008) Current Genomics , vol.9 , Issue.4 , pp. 275-281
    • Di Masi, A.1    Antoccia, A.2
  • 11
    • 34547816215 scopus 로고    scopus 로고
    • Germline NBS1 mutations in families with aggregation of breast and/or ovarian cancer from North-East Poland
    • Kanka C, Brozek I, Skalska B, et al. Germline NBS1 mutations in families with aggregation of breast and/or ovarian cancer from north-east Poland. Anticancer Res. 2007;27:3015-3018. (Pubitemid 47228039)
    • (2007) Anticancer Research , vol.27 , Issue.4 C , pp. 3015-3018
    • Kanka, C.1    Brozek, I.2    Skalska, B.3    Siemiatkowska, A.4    Limon, J.5
  • 12
    • 70350366189 scopus 로고    scopus 로고
    • Ganglioglioma associated with alterations of NBN gene. A case report
    • Grajkowska W, Piekutowska-Abramczuk D, Ciara E, et al. Ganglioglioma associated with alterations of NBN gene. A case report. Folia Neuropathol. 2009;47:278-283.
    • (2009) Folia Neuropathol. , vol.47 , pp. 278-283
    • Grajkowska, W.1    Piekutowska-Abramczuk, D.2    Ciara, E.3
  • 13
    • 48249134779 scopus 로고    scopus 로고
    • Mutations in the Nijmegen breakage syndrome gene in medulloblastomas
    • Huang J, Grotzer MA, Watanabe T, et al. Mutations in the Nijmegen breakage syndrome gene in medulloblastomas. Clin Cancer Res. 2008;14:4053-4058.
    • (2008) Clin Cancer Res. , vol.14 , pp. 4053-4058
    • Huang, J.1    Grotzer, M.A.2    Watanabe, T.3
  • 14
    • 0141918879 scopus 로고    scopus 로고
    • Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukaemia
    • Taylor GM, O'Brien HP, Greaves MF, et al. Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukaemia. Cancer Res. 2003;63:6563-6564.
    • (2003) Cancer Res. , vol.63 , pp. 6563-6564
    • Taylor, G.M.1    O'Brien, H.P.2    Greaves, M.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.