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Volumn 123, Issue 1-4, 2009, Pages 183-187

Chromosome copy number variation and breast cancer risk

Author keywords

[No Author keywords available]

Indexed keywords

BREAST CANCER; CANCER RISK; FAMILIAL CANCER; GENE; GENE COPY NUMBER VARIATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GSTM1 GENE; GSTT1 GENE; HUMAN; MTUS1 GENE; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 62549134474     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000184707     Document Type: Review
Times cited : (19)

References (58)
  • 1
    • 0037370476 scopus 로고    scopus 로고
    • The genetics and genomics of cancer
    • Balmain A, Gray J, Ponder BA: The genetics and genomics of cancer. Nat Genet 33:238-244 (2003).
    • (2003) Nat Genet , vol.33 , pp. 238-244
    • Balmain, A.1    Gray, J.2    Ponder, B.A.3
  • 2
    • 16244403039 scopus 로고    scopus 로고
    • Cancer incidence and mortality in Europe. 2004
    • Boyle P, Ferlay J: Cancer incidence and mortality in Europe. 2004. Ann Oncol 16:481-488 (2005).
    • (2005) Ann Oncol , vol.16 , pp. 481-488
    • Boyle, P.1    Ferlay, J.2
  • 3
    • 34447264706 scopus 로고    scopus 로고
    • Prevalence of BRCA1 and BRCA2 genomic rearrangements in a cohort of consecutive Italian breast and/or ovarian cancer families
    • Buffone A, Capalbo C, Ricevuto E, Sidoni T, Ottini L, et al: Prevalence of BRCA1 and BRCA2 genomic rearrangements in a cohort of consecutive Italian breast and/or ovarian cancer families. Breast Cancer Res Treat 106:289-296 (2007).
    • (2007) Breast Cancer Res Treat , vol.106 , pp. 289-296
    • Buffone, A.1    Capalbo, C.2    Ricevuto, E.3    Sidoni, T.4    Ottini, L.5
  • 4
    • 0036218046 scopus 로고    scopus 로고
    • Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays
    • Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A: Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays. Nat Biotechnol 20:393-396 (2002).
    • (2002) Nat Biotechnol , vol.20 , pp. 393-396
    • Cai, W.W.1    Mao, J.H.2    Chow, C.W.3    Damani, S.4    Balmain, A.5    Bradley, A.6
  • 6
    • 0038207967 scopus 로고    scopus 로고
    • Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors
    • Chaib H, MacDonald JW, Vessella RL, Washburn JG, Quinn JE, et al: Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors. Genes Chromosomes Cancer 37:306-313 (2003).
    • (2003) Genes Chromosomes Cancer , vol.37 , pp. 306-313
    • Chaib, H.1    MacDonald, J.W.2    Vessella, R.L.3    Washburn, J.G.4    Quinn, J.E.5
  • 7
    • 0036835501 scopus 로고    scopus 로고
    • Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells
    • Charafe-Jauffret E, Moulin JF, Ginestier C, Bechlian D, Conte N, et al: Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells. Int J Oncol 21:989-996 (2002).
    • (2002) Int J Oncol , vol.21 , pp. 989-996
    • Charafe-Jauffret, E.1    Moulin, J.F.2    Ginestier, C.3    Bechlian, D.4    Conte, N.5
  • 8
    • 43149125640 scopus 로고    scopus 로고
    • Scanning the human genome at kilobase resolution
    • Chen J, Kim YC, Jung YC, Xuan Z, Dworkin G, et al: Scanning the human genome at kilobase resolution. Genome Res 18:751-762 (2008).
    • (2008) Genome Res , vol.18 , pp. 751-762
    • Chen, J.1    Kim, Y.C.2    Jung, Y.C.3    Xuan, Z.4    Dworkin, G.5
  • 9
    • 34250006413 scopus 로고    scopus 로고
    • Genome-wide association study identifies novel breast cancer susceptibility loci
    • Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, et al: Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447:1087-1093 (2007).
    • (2007) Nature , vol.447 , pp. 1087-1093
    • Easton, D.F.1    Pooley, K.A.2    Dunning, A.M.3    Pharoah, P.D.4    Thompson, D.5
  • 10
    • 46749157576 scopus 로고    scopus 로고
    • MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: Novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases
    • Engert S, Wappenschmidt B, Betz B, Kast K, Kutsche M, et al: MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases. Hum Mutat 29:948-958 (2008).
    • (2008) Hum Mutat , vol.29 , pp. 948-958
    • Engert, S.1    Wappenschmidt, B.2    Betz, B.3    Kast, K.4    Kutsche, M.5
  • 11
  • 12
    • 34547730931 scopus 로고    scopus 로고
    • Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk
    • Frank B, Bermejo JL, Hemminki K, Sutter C, Wappenschmidt B, et al: Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk. Carcinogenesis 28:1442-1445 (2007).
    • (2007) Carcinogenesis , vol.28 , pp. 1442-1445
    • Frank, B.1    Bermejo, J.L.2    Hemminki, K.3    Sutter, C.4    Wappenschmidt, B.5
  • 13
    • 18644382608 scopus 로고    scopus 로고
    • Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families
    • Gad S, Caux-Moncoutier V, Pages-Berhouet S, Gauthier-Villars M, Coupier I, et al: Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families. Oncogene 21:6841-6847 (2002a).
    • (2002) Oncogene , vol.21 , pp. 6841-6847
    • Gad, S.1    Caux-Moncoutier, V.2    Pages-Berhouet, S.3    Gauthier-Villars, M.4    Coupier, I.5
  • 14
    • 0036850003 scopus 로고    scopus 로고
    • Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families
    • Gad S, Klinger M, Caux-Moncoutier V, Pages-Berhouet S, Gauthier-Villars M, et al: Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families. J Med Genet 39:817-821 (2002b).
    • (2002) J Med Genet , vol.39 , pp. 817-821
    • Gad, S.1    Klinger, M.2    Caux-Moncoutier, V.3    Pages-Berhouet, S.4    Gauthier-Villars, M.5
  • 15
    • 34247490187 scopus 로고    scopus 로고
    • Gutierrez-Enriquez S, de la Hoya M, Martinez-Bouzas C, Sanchez de Abajo A, Ramon y Cajal T, et al: Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer. Breast Cancer Res Treat 103:103-107 (2007).
    • Gutierrez-Enriquez S, de la Hoya M, Martinez-Bouzas C, Sanchez de Abajo A, Ramon y Cajal T, et al: Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer. Breast Cancer Res Treat 103:103-107 (2007).
  • 16
    • 28744446802 scopus 로고    scopus 로고
    • Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families
    • Hartmann C, John AL, Klaes R, Hofmann W, Bielen R, et al: Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families. Hum Mutat 24:534 (2004).
    • (2004) Hum Mutat , vol.24 , pp. 534
    • Hartmann, C.1    John, A.L.2    Klaes, R.3    Hofmann, W.4    Bielen, R.5
  • 17
    • 0029561598 scopus 로고
    • The glutathione S-transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance
    • Hayes JD, Pulford DJ: The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance. Crit Rev Biochem Mol Biol 30:445-600 (1995).
    • (1995) Crit Rev Biochem Mol Biol , vol.30 , pp. 445-600
    • Hayes, J.D.1    Pulford, D.J.2
  • 18
    • 0344394343 scopus 로고    scopus 로고
    • Familial breast cancer: Scope for more susceptibility genes?
    • Hemminki K, Granstrom C: Familial breast cancer: scope for more susceptibility genes? Breast Cancer Res Treat 82:17-22 (2003).
    • (2003) Breast Cancer Res Treat , vol.82 , pp. 17-22
    • Hemminki, K.1    Granstrom, C.2
  • 19
    • 0037054932 scopus 로고    scopus 로고
    • Attributable risks for familial breast cancer by proband status and morphology: A nationwide epidemiologic study from Sweden
    • Hemminki K, Granstrom C, Czene K: Attributable risks for familial breast cancer by proband status and morphology: a nationwide epidemiologic study from Sweden. Int J Cancer 100:214-219 (2002).
    • (2002) Int J Cancer , vol.100 , pp. 214-219
    • Hemminki, K.1    Granstrom, C.2    Czene, K.3
  • 20
    • 29444450702 scopus 로고    scopus 로고
    • Common deletions and SNPs are in linkage disequilibrium in the human genome
    • Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA: Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet 38:82-85 (2006).
    • (2006) Nat Genet , vol.38 , pp. 82-85
    • Hinds, D.A.1    Kloek, A.P.2    Jen, M.3    Chen, X.4    Frazer, K.A.5
  • 21
    • 0037380994 scopus 로고    scopus 로고
    • Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
    • Hogervorst FB, Nederlof PM, Gille JJ, McElgunn CJ, Grippeling M, et al: Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method. Cancer Res 63:1449-1453 (2003).
    • (2003) Cancer Res , vol.63 , pp. 1449-1453
    • Hogervorst, F.B.1    Nederlof, P.M.2    Gille, J.J.3    McElgunn, C.J.4    Grippeling, M.5
  • 22
    • 34248525150 scopus 로고    scopus 로고
    • Completing the map of human genetic variation
    • Human Genome Structural Variation Working Group
    • Human Genome Structural Variation Working Group, Eichler EE, Nickerson DA, Altshuler D, Bowcock AM, et al: Completing the map of human genetic variation. Nature 447:161-165 (2007).
    • (2007) Nature , vol.447 , pp. 161-165
    • Eichler, E.E.1    Nickerson, D.A.2    Altshuler, D.3    Bowcock, A.M.4
  • 23
    • 34250001297 scopus 로고    scopus 로고
    • A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
    • Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, et al: A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 39:870-874 (2007).
    • (2007) Nat Genet , vol.39 , pp. 870-874
    • Hunter, D.J.1    Kraft, P.2    Jacobs, K.B.3    Cox, D.G.4    Yeager, M.5
  • 24
    • 36148976077 scopus 로고    scopus 로고
    • Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic, and clinical aspects
    • Ingelman-Sundberg M, Sim SC, Gomez A, Rodriguez-Antona C: Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic, and clinical aspects. Pharmacol Therap 116:496-526 (2007).
    • (2007) Pharmacol Therap , vol.116 , pp. 496-526
    • Ingelman-Sundberg, M.1    Sim, S.C.2    Gomez, A.3    Rodriguez-Antona, C.4
  • 25
    • 0027136288 scopus 로고
    • Inherited amplification of an active gene in cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine
    • Johansson L, Lundquist E, Bertilsson L, Dahl ML, Sjoqvist F, Ingelmann-Sundberg M: Inherited amplification of an active gene in cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine. Proc Natl Acad Sci USA 90:11825-11829 (1993).
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 11825-11829
    • Johansson, L.1    Lundquist, E.2    Bertilsson, L.3    Dahl, M.L.4    Sjoqvist, F.5    Ingelmann-Sundberg, M.6
  • 26
    • 0026495364 scopus 로고
    • Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
    • Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, et al: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821 (1992).
    • (1992) Science , vol.258 , pp. 818-821
    • Kallioniemi, A.1    Kallioniemi, O.P.2    Sudar, D.3    Rutovitz, D.4    Gray, J.W.5
  • 27
    • 15144340686 scopus 로고    scopus 로고
    • Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas
    • Kerangueven F, Noguchi T, Coulier F, Allione F, Wargniez V, et al: Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. Cancer Res 57:5469-5474 (1997).
    • (1997) Cancer Res , vol.57 , pp. 5469-5474
    • Kerangueven, F.1    Noguchi, T.2    Coulier, F.3    Allione, F.4    Wargniez, V.5
  • 29
    • 0034644185 scopus 로고    scopus 로고
    • Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland
    • Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, et al: Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 343:78-85 (2000).
    • (2000) N Engl J Med , vol.343 , pp. 78-85
    • Lichtenstein, P.1    Holm, N.V.2    Verkasalo, P.K.3    Iliadou, A.4    Kaprio, J.5
  • 30
    • 0036466858 scopus 로고    scopus 로고
    • Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population
    • Meindl A: Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. Int J Cancer 97:472-480 (2002).
    • (2002) Int J Cancer , vol.97 , pp. 472-480
    • Meindl, A.1
  • 31
    • 0032878514 scopus 로고    scopus 로고
    • Single amino acids determine specificity of binding of protein kinase A regulatory subunits by protein kinase A anchoring proteins
    • Miki K, Eddy EM: Single amino acids determine specificity of binding of protein kinase A regulatory subunits by protein kinase A anchoring proteins. J Biol Chem 274:29057-29062 (1999).
    • (1999) J Biol Chem , vol.274 , pp. 29057-29062
    • Miki, K.1    Eddy, E.M.2
  • 32
    • 0038364017 scopus 로고    scopus 로고
    • Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families
    • Montagna M, Dalla Palma M, Menin C, Agata S, De Nicolo A, et al: Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families. Hum Mol Genet 12:1055-1061 (2003).
    • (2003) Hum Mol Genet , vol.12 , pp. 1055-1061
    • Montagna, M.1    Dalla Palma, M.2    Menin, C.3    Agata, S.4    De Nicolo, A.5
  • 33
    • 22244453416 scopus 로고    scopus 로고
    • A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
    • Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, et al: A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 65:6071-6079 (2005).
    • (2005) Cancer Res , vol.65 , pp. 6071-6079
    • Nannya, Y.1    Sanada, M.2    Nakazaki, K.3    Hosoya, N.4    Wang, L.5
  • 34
    • 0037181715 scopus 로고    scopus 로고
    • What options for treatment of hereditary breast cancer?
    • Narod S: What options for treatment of hereditary breast cancer? Lancet 359:1451-1452 (2002).
    • (2002) Lancet , vol.359 , pp. 1451-1452
    • Narod, S.1
  • 35
    • 0036178190 scopus 로고    scopus 로고
    • Current understanding of the epidemiology and clinical implications of BRCA1 and BRCA2 mutations for ovarian cancer
    • Narod SA, Boyd J: Current understanding of the epidemiology and clinical implications of BRCA1 and BRCA2 mutations for ovarian cancer. Curr Opin Obstet Gynecol 14:19-26 (2002).
    • (2002) Curr Opin Obstet Gynecol , vol.14 , pp. 19-26
    • Narod, S.A.1    Boyd, J.2
  • 36
    • 0035030368 scopus 로고    scopus 로고
    • Breast cancer genetics: What we know and what we need
    • Nathanson KL, Wooster R, Weber BL: Breast cancer genetics: what we know and what we need. Nat Med 7:552-556 (2001).
    • (2001) Nat Med , vol.7 , pp. 552-556
    • Nathanson, K.L.1    Wooster, R.2    Weber, B.L.3
  • 39
    • 0033516265 scopus 로고    scopus 로고
    • Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
    • Peto J, Collins N, Barfoot R, Seal S, Warren W, et al: Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J Natl Cancer Inst 91:943-949 (1999).
    • (1999) J Natl Cancer Inst , vol.91 , pp. 943-949
    • Peto, J.1    Collins, N.2    Barfoot, R.3    Seal, S.4    Warren, W.5
  • 40
    • 28044442055 scopus 로고    scopus 로고
    • Five genes from chromosomal band 8p22 are significantly down-regulated in ovarian carcinoma: N33 and EFA6R have a potential impact on overall survival
    • Pils D, Horak P, Gleiss A, Sax C, Fabjani G, et al: Five genes from chromosomal band 8p22 are significantly down-regulated in ovarian carcinoma: N33 and EFA6R have a potential impact on overall survival. Cancer 104:2417-2429 (2005).
    • (2005) Cancer , vol.104 , pp. 2417-2429
    • Pils, D.1    Horak, P.2    Gleiss, A.3    Sax, C.4    Fabjani, G.5
  • 41
    • 0033587111 scopus 로고    scopus 로고
    • Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma
    • Pineau P, Nagai H, Prigent S, Wei Y, Gyapay G, et al: Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma. Oncogene 18:3127-3134 (1999).
    • (1999) Oncogene , vol.18 , pp. 3127-3134
    • Pineau, P.1    Nagai, H.2    Prigent, S.3    Wei, Y.4    Gyapay, G.5
  • 42
    • 17344371740 scopus 로고    scopus 로고
    • High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
    • Pinkel D, Segraves R, Sudar D, Clark S, Poole I, et al: High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211 (1998).
    • (1998) Nat Genet , vol.20 , pp. 207-211
    • Pinkel, D.1    Segraves, R.2    Sudar, D.3    Clark, S.4    Poole, I.5
  • 43
    • 33751329250 scopus 로고    scopus 로고
    • Global variation in copy number in the human genome
    • Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, et al: Global variation in copy number in the human genome. Nature 444:444-454 (2006).
    • (2006) Nature , vol.444 , pp. 444-454
    • Redon, R.1    Ishikawa, S.2    Fitch, K.R.3    Feuk, L.4    Perry, G.H.5
  • 44
    • 0035955718 scopus 로고    scopus 로고
    • An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer
    • Reiter R, Wellstein A, Riegel AT: An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer. J Biol Chem 276:39736-39741 (2001).
    • (2001) J Biol Chem , vol.276 , pp. 39736-39741
    • Reiter, R.1    Wellstein, A.2    Riegel, A.T.3
  • 45
    • 1242338795 scopus 로고    scopus 로고
    • Association of homozygous wild-type glutathione S-transferase M1 genotype with increased breast cancer risk
    • Roodi N, Dupont WD, Moore JH, Parl FF: Association of homozygous wild-type glutathione S-transferase M1 genotype with increased breast cancer risk. Cancer Res 64:1233-1236 (2004).
    • (2004) Cancer Res , vol.64 , pp. 1233-1236
    • Roodi, N.1    Dupont, W.D.2    Moore, J.H.3    Parl, F.F.4
  • 47
    • 3242808027 scopus 로고    scopus 로고
    • Large-scale copy number polymorphism in the human genome
    • Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al: Large-scale copy number polymorphism in the human genome. Science 305:525-528 (2004).
    • (2004) Science , vol.305 , pp. 525-528
    • Sebat, J.1    Lakshmi, B.2    Troge, J.3    Alexander, J.4    Young, J.5
  • 48
    • 0037704396 scopus 로고    scopus 로고
    • Identification of a new tumor suppressor gene located at chromosome 8p21.3-22
    • Seibold S, Rudroff C, Weber M, Galle J, Wanner C, Marx M: Identification of a new tumor suppressor gene located at chromosome 8p21.3-22. FASEB J 17:1180-1182 (2003).
    • (2003) FASEB J , vol.17 , pp. 1180-1182
    • Seibold, S.1    Rudroff, C.2    Weber, M.3    Galle, J.4    Wanner, C.5    Marx, M.6
  • 50
    • 0033816360 scopus 로고    scopus 로고
    • Characterization of the glutathione S-transferase GSTT1 deletion: Discrimination of all genotypes by polymerase chain reaction indicates a trimodular genotype-phenotype correlation
    • Sprenger R, Schlagenhaufer R, Kerb R, Bruhn C, Brockmöller J, et al: Characterization of the glutathione S-transferase GSTT1 deletion: discrimination of all genotypes by polymerase chain reaction indicates a trimodular genotype-phenotype correlation. Pharmacogenetics 10:557-565 (2000).
    • (2000) Pharmacogenetics , vol.10 , pp. 557-565
    • Sprenger, R.1    Schlagenhaufer, R.2    Kerb, R.3    Bruhn, C.4    Brockmöller, J.5
  • 51
    • 0037169354 scopus 로고    scopus 로고
    • Cancer susceptibility and the functions of BRCA1 and BRCA2
    • Venkitaraman AR: Cancer susceptibility and the functions of BRCA1 and BRCA2 . Cell 108:171-182 (2002).
    • (2002) Cell , vol.108 , pp. 171-182
    • Venkitaraman, A.R.1
  • 53
    • 33645084562 scopus 로고    scopus 로고
    • Spectrum of mutations in BRCA1 , BRCA2, CHEK2 and TP53 in families at high risk of breast cancer
    • Walsh T, Casadei S, Coats KH, Swisher E, Stray SM, et al: Spectrum of mutations in BRCA1 , BRCA2, CHEK2 and TP53 in families at high risk of breast cancer. JAMA 295:1379-1388 (2006).
    • (2006) JAMA , vol.295 , pp. 1379-1388
    • Walsh, T.1    Casadei, S.2    Coats, K.H.3    Swisher, E.4    Stray, S.M.5
  • 54
    • 34548076029 scopus 로고    scopus 로고
    • Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families
    • Weitzel JN, Lagos VI, Herzog JS, Judkins T, Hendrickson B, et al: Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families. Cancer Epidemiol Biomarkers Prev 16:1615-1620 (2007).
    • (2007) Cancer Epidemiol Biomarkers Prev , vol.16 , pp. 1615-1620
    • Weitzel, J.N.1    Lagos, V.I.2    Herzog, J.S.3    Judkins, T.4    Hendrickson, B.5
  • 55
    • 0038054378 scopus 로고    scopus 로고
    • Transfer of chromosome 8 into two breast cancer cell lines: Total exclusion of three regions indicates location of putative in vitro growth suppressor genes
    • Wilson P, Cuthbert A, Marsh A, Arnold J, Flanagan J, et al: Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes. Cancer Genet Cytogenet 143:100-112 (2003).
    • (2003) Cancer Genet Cytogenet , vol.143 , pp. 100-112
    • Wilson, P.1    Cuthbert, A.2    Marsh, A.3    Arnold, J.4    Flanagan, J.5
  • 56
    • 33344469939 scopus 로고    scopus 로고
    • Identification of frequent chromosome copy number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays
    • Wirtenberger M, Hemminki K, Burwinkel B: Identification of frequent chromosome copy number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays. Am J Hum Genet 78:520-522 (2006).
    • (2006) Am J Hum Genet , vol.78 , pp. 520-522
    • Wirtenberger, M.1    Hemminki, K.2    Burwinkel, B.3
  • 57
    • 0037685164 scopus 로고    scopus 로고
    • Breast and ovarian cancer
    • Wooster R, Weber BL: Breast and ovarian cancer. N Engl J Med 348:2339-2347 (2003).
    • (2003) N Engl J Med , vol.348 , pp. 2339-2347
    • Wooster, R.1    Weber, B.L.2
  • 58
    • 0032917458 scopus 로고    scopus 로고
    • Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1
    • Yokota T, Yoshimoto M, Akiyama F, Sakamoto G, Kasumi F, et al: Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1. Cancer 85:447-452 (1999).
    • (1999) Cancer , vol.85 , pp. 447-452
    • Yokota, T.1    Yoshimoto, M.2    Akiyama, F.3    Sakamoto, G.4    Kasumi, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.