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Volumn 12, Issue 16, 2006, Pages 4832-4835

CHEK2-positive breast cancers in young Polish women

Author keywords

[No Author keywords available]

Indexed keywords

CHECKPOINT KINASE 2;

EID: 33748347521     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-06-0158     Document Type: Article
Times cited : (34)

References (28)
  • 2
    • 0033566082 scopus 로고    scopus 로고
    • Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway
    • Chaturvedi P, Eng WK, Zhu Y, et al. Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway. Oncogene 1999;18:4047-54.
    • (1999) Oncogene , vol.18 , pp. 4047-4054
    • Chaturvedi, P.1    Eng, W.K.2    Zhu, Y.3
  • 3
    • 18544389716 scopus 로고    scopus 로고
    • Low-penetrance susceptibility to breast cancer due to CHEK2*1100-delC in noncarriers of BRCA1 or BRCA2 mutations
    • CHEK2 Breast Cancer Consortium. Low-penetrance susceptibility to breast cancer due to CHEK2*1100-delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 2002;31:55-9.
    • (2002) Nat Genet , vol.31 , pp. 55-59
  • 4
    • 0347626108 scopus 로고    scopus 로고
    • The CHEK2 1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families
    • Oldenburg RA, Kroeze-Jansema K, Kraan J, et al. The CHEK2 1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families. Cancer Res 2003;63:8153-7.
    • (2003) Cancer Res , vol.63 , pp. 8153-8157
    • Oldenburg, R.A.1    Kroeze-Jansema, K.2    Kraan, J.3
  • 5
    • 18444379055 scopus 로고    scopus 로고
    • A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
    • Vahteristo P, Bartkova J, Eerola H, et al. A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet 2002;71:432-8.
    • (2002) Am J Hum Genet , vol.71 , pp. 432-438
    • Vahteristo, P.1    Bartkova, J.2    Eerola, H.3
  • 6
    • 3042582651 scopus 로고    scopus 로고
    • CHEK2 1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
    • CHEK2 Breast Cancer Case-Control consortium. CHEK2 1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet 2004;74:1175-82.
    • (2004) Am J Hum Genet , vol.74 , pp. 1175-1182
  • 7
    • 8844220451 scopus 로고    scopus 로고
    • CHEK2 is a multiorgan cancer susceptibility gene
    • Cybulski C, Gorski B, Huzarski T, et al. CHEK2 is a multiorgan cancer susceptibility gene. Am J Hum Genet 2004;75:1131-5.
    • (2004) Am J Hum Genet , vol.75 , pp. 1131-1135
    • Cybulski, C.1    Gorski, B.2    Huzarski, T.3
  • 8
    • 3843071233 scopus 로고    scopus 로고
    • CHEK2 variant I157T may be associated with increased breast cancer risk
    • Kilpivaara O, Vahteristo P, Falck J, et al. CHEK2 variant I157T may be associated with increased breast cancer risk. Int J Cancer 2004;111:543-7.
    • (2004) Int J Cancer , vol.111 , pp. 543-547
    • Kilpivaara, O.1    Vahteristo, P.2    Falck, J.3
  • 9
    • 14044272193 scopus 로고    scopus 로고
    • CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population
    • Shaag A, Walsh T, Renbaum P, et al. CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population. Hum Mol Genet 2005;14:555-63.
    • (2005) Hum Mol Genet , vol.14 , pp. 555-563
    • Shaag, A.1    Walsh, T.2    Renbaum, P.3
  • 11
    • 8844283535 scopus 로고    scopus 로고
    • A novel founder CHEK2 mutation is associated with increased prostate cancer risk
    • Cybulski C, Huzarski T, Górski B, et al. A novel founder CHEK2 mutation is associated with increased prostate cancer risk. Cancer Res 2004;64:2677-9.
    • (2004) Cancer Res , vol.64 , pp. 2677-2679
    • Cybulski, C.1    Huzarski, T.2    Górski, B.3
  • 13
    • 0033281609 scopus 로고    scopus 로고
    • The pathology of familial breast cancer: Morphological aspects
    • Lakhani SR. The pathology of familial breast cancer: Morphological aspects. Breast Cancer Res 1999;1:31-5.
    • (1999) Breast Cancer Res , vol.1 , pp. 31-35
    • Lakhani, S.R.1
  • 14
    • 12944286550 scopus 로고    scopus 로고
    • The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
    • Lakhani SR, Gusterson BA, Jacquemier J, et al. The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2. Clin Cancer Res 2000;6:782-9.
    • (2000) Clin Cancer Res , vol.6 , pp. 782-789
    • Lakhani, S.R.1    Gusterson, B.A.2    Jacquemier, J.3
  • 15
    • 6344261987 scopus 로고    scopus 로고
    • Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant
    • de Bock GH, Schutte M, Krol-Warmerdam EM, et al. Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant. J Med Genet 2004;41:731-5.
    • (2004) J Med Genet , vol.41 , pp. 731-735
    • De Bock, G.H.1    Schutte, M.2    Krol-Warmerdam, E.M.3
  • 16
    • 0942279575 scopus 로고    scopus 로고
    • Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers
    • Broeks A, de Witte L, Nooijen A, et al. Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers. Breast Cancer Res Treat 2004;83:91-3.
    • (2004) Breast Cancer Res Treat , vol.83 , pp. 91-93
    • Broeks, A.1    De Witte, L.2    Nooijen, A.3
  • 17
    • 27544515629 scopus 로고    scopus 로고
    • Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: A familial study
    • Johnson N, Fletcher O, Naceur-Lombardelli C, dos Santos Silva I, Ashworth A, Peto J. Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: a familial study. Lancet 2005;366:1554-7.
    • (2005) Lancet , vol.366 , pp. 1554-1557
    • Johnson, N.1    Fletcher, O.2    Naceur-Lombardelli, C.3    Dos Santos Silva, I.4    Ashworth, A.5    Peto, J.6
  • 18
    • 0038406108 scopus 로고    scopus 로고
    • The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype
    • Meijers-Heijboer H, Wijnen J, Vasen H, et al. The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype. Am J Hum Genet 2003;72:1308-14.
    • (2003) Am J Hum Genet , vol.72 , pp. 1308-1314
    • Meijers-Heijboer, H.1    Wijnen, J.2    Vasen, H.3
  • 19
    • 0034940858 scopus 로고    scopus 로고
    • Mutation analysis of the CHK2 gene in families with hereditary breast cancer
    • Allinen M, Huusko P, Mantyniemi S, Launonen V, Winqvist R. Mutation analysis of the CHK2 gene in families with hereditary breast cancer. Br J Cancer 2001;85:209-12.
    • (2001) Br J Cancer , vol.85 , pp. 209-212
    • Allinen, M.1    Huusko, P.2    Mantyniemi, S.3    Launonen, V.4    Winqvist, R.5
  • 20
    • 0345669750 scopus 로고    scopus 로고
    • Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility
    • Schutte M, Seal S, Barfoot R, et al. Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility. Am J Hum Genet 2003;72:1023-8.
    • (2003) Am J Hum Genet , vol.72 , pp. 1023-1028
    • Schutte, M.1    Seal, S.2    Barfoot, R.3
  • 21
    • 0035951809 scopus 로고    scopus 로고
    • Characterization of tumor-associated Chk2 mutations
    • Wu X, Webster SR, Chen J. Characterization of tumor-associated Chk2 mutations. J Biol Chem 2001;276:2971-4.
    • (2001) J Biol Chem , vol.276 , pp. 2971-2974
    • Wu, X.1    Webster, S.R.2    Chen, J.3
  • 22
    • 0035817764 scopus 로고    scopus 로고
    • Functional impact on concomitant versus alternative defects in the Chk2-53 tumour suppressor pathway
    • Falck J, Lukas C, Protopopova M, Lukas J, Selinanova G, Bartek J. Functional impact on concomitant versus alternative defects in the Chk2-53 tumour suppressor pathway. Oncogene 2001;20:5503-10.
    • (2001) Oncogene , vol.20 , pp. 5503-5510
    • Falck, J.1    Lukas, C.2    Protopopova, M.3    Lukas, J.4    Selinanova, G.5    Bartek, J.6
  • 23
    • 0035848819 scopus 로고    scopus 로고
    • The ATM-Chk2-25A checkpoint pathway guards against radioresistant DNA synthesis
    • Falck J, Mailand N, Syljuåsen RG, Bartek J, Lukas J. The ATM-Chk2-25A checkpoint pathway guards against radioresistant DNA synthesis. Nature 2001;410:842-7.
    • (2001) Nature , vol.410 , pp. 842-847
    • Falck, J.1    Mailand, N.2    Syljuåsen, R.G.3    Bartek, J.4    Lukas, J.5
  • 24
    • 0036285705 scopus 로고    scopus 로고
    • Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2
    • Li J, Williams BL, Haire LF, et al. Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2. Mol Cell 2002;9:1045-54.
    • (2002) Mol Cell , vol.9 , pp. 1045-1054
    • Li, J.1    Williams, B.L.2    Haire, L.F.3
  • 25
    • 22044445244 scopus 로고    scopus 로고
    • Association of two mutations in the CHEK2 gene with breast cancer
    • Bogdanova N, Enssen-Dubrowinskaja N, Feshchenko S, et al. Association of two mutations in the CHEK2 gene with breast cancer. Int J Cancer 2005;116:263-6.
    • (2005) Int J Cancer , vol.116 , pp. 263-266
    • Bogdanova, N.1    Enssen-Dubrowinskaja, N.2    Feshchenko, S.3
  • 26
    • 0347382813 scopus 로고    scopus 로고
    • CHEK2 variants associate with hereditary prostate cancer
    • Seppala EH, Ikonen T, Mononen N, et al. CHEK2 variants associate with hereditary prostate cancer. Br J Cancer 2003;89:1966-70.
    • (2003) Br J Cancer , vol.89 , pp. 1966-1970
    • Seppala, E.H.1    Ikonen, T.2    Mononen, N.3
  • 28
    • 33745952966 scopus 로고    scopus 로고
    • Variants in the ATM-BRCA2-2 axis predispose to chronic lymphocytic leukaemia
    • Rudd MF, Sellick GS, Webb EL, Catovsky D, Houlston RS. Variants in the ATM-BRCA2-2 axis predispose to chronic lymphocytic leukaemia. Blood 2006;108:638-44.
    • (2006) Blood , vol.108 , pp. 638-644
    • Rudd, M.F.1    Sellick, G.S.2    Webb, E.L.3    Catovsky, D.4    Houlston, R.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.