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Volumn 118, Issue 2, 2009, Pages 407-413

Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk

Author keywords

BRCA1; BRCA2; Breast cancer risk; Case control study; Codon usage

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

EID: 70350218734     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-009-0348-7     Document Type: Article
Times cited : (5)

References (50)
  • 1
    • 14944385553 scopus 로고    scopus 로고
    • Global cancer statistics, 2002
    • 10.3322/canjclin.55.2.74 10.3322/canjclin.55.2.74 15761078
    • DM Parkin F Bray J Ferlay P Pisani 2005 Global cancer statistics, 2002 CA Cancer J Clin 55 74 108 10.3322/canjclin.55.2.74 10.3322/canjclin.55.2.74 15761078
    • (2005) CA Cancer J Clin , vol.55 , pp. 74-108
    • Parkin, D.M.1    Bray, F.2    Ferlay, J.3    Pisani, P.4
  • 2
    • 0034749873 scopus 로고    scopus 로고
    • Genetic epidemiology of female breast cancer
    • DOI 10.1006/scbi.2001.0392
    • JL Hopper 2001 Genetic epidemiology of female breast cancer Semin Cancer Biol 11 367 374 10.1006/scbi.2001.0392 10.1006/scbi.2001.0392 1:CAS:528:DC%2BD3MXmvVGgtrk%3D 11562179 (Pubitemid 33016032)
    • (2001) Seminars in Cancer Biology , vol.11 , Issue.5 , pp. 367-374
    • Hopper, J.L.1
  • 3
    • 0036488497 scopus 로고    scopus 로고
    • Modifiers of risk of hereditary breast and ovarian cancer
    • 10.1038/nrc726 10.1038/nrc726 12635174
    • SA Narod 2002 Modifiers of risk of hereditary breast and ovarian cancer Nat Rev Cancer 2 113 123 10.1038/nrc726 10.1038/nrc726 12635174
    • (2002) Nat Rev Cancer , vol.2 , pp. 113-123
    • Narod, S.A.1
  • 4
    • 0037052644 scopus 로고    scopus 로고
    • Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish Family-Cancer Database
    • DOI 10.1002/ijc.10332
    • K Czene P Lichtenstein K Hemminki 2002 Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish family-cancer database Int J Cancer 99 260 266 10.1002/ijc.10332 10.1002/ijc.10332 1:CAS:528: DC%2BD38XivFyrs7o%3D 11979442 (Pubitemid 34309484)
    • (2002) International Journal of Cancer , vol.99 , Issue.2 , pp. 260-266
    • Czene, K.1    Lichtenstein, P.2    Hemminki, K.3
  • 5
    • 0034644185 scopus 로고    scopus 로고
    • Environmental and heritable factors in the causation of cancer: Analyses of cohorts of twins from Sweden, Denmark, and Finland
    • DOI 10.1056/NEJM200007133430201
    • P Lichtenstein NV Holm PK Verkasalo A Iliadou J Kaprio M Koskenvuo E Pukkala A Skytthe K Hemminki 2000 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 10.1056/NEJM200007133430201 10.1056/ NEJM200007133430201 1:STN:280:DC%2BD3czjtFCiug%3D%3D 10891514 (Pubitemid 30451850)
    • (2000) New England Journal of Medicine , vol.343 , Issue.2 , pp. 78-85
    • Lichtenstein, P.1    Holm, N.V.2    Verkasalo, P.K.3    Iliadou, A.4    Kaprio, J.5    Koskenvuo, M.6    Pukkala, E.7    Skytthe, A.8    Hemminki, K.9
  • 6
    • 4143133373 scopus 로고    scopus 로고
    • Genetic epidemiology of cancer: From families to heritable genes
    • DOI 10.1002/ijc.20355
    • K Hemminki R Rawal B Chen JL Bermejo 2004 Genetic epidemiology of cancer: from families to heritable genes Int J Cancer 111 944 950 10.1002/ijc.20355 10.1002/ijc.20355 1:CAS:528:DC%2BD2cXntVant7c%3D 15300808 (Pubitemid 39096245)
    • (2004) International Journal of Cancer , vol.111 , Issue.6 , pp. 944-950
    • Hemminki, K.1    Rawal, R.2    Chen, B.3    Bermejo, J.L.4
  • 7
    • 0030914999 scopus 로고    scopus 로고
    • Family history and the risk of breast cancer: A systematic review and meta-analysis
    • DOI 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.0.CO;2-B
    • PD Pharoah NE Day S Duffy DF Easton BA Ponder 1997 Family history and the risk of breast cancer: a systematic review and meta-analysis Int J Cancer 7 800 809 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.0.CO;2-B 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.0.CO;2-B (Pubitemid 27237202)
    • (1997) International Journal of Cancer , vol.71 , Issue.5 , pp. 800-809
    • Pharoah, P.D.P.1    Day, N.E.2    Duffy, S.3    Easton, D.F.4    Ponder, B.A.J.5
  • 8
    • 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
    • DOI 10.1002/ijc.1626
    • A Meindl 2002 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 10.1002/ijc.1626 10.1002/ijc.1626 1:CAS:528:DC%2BD38XkvFegtg%3D%3D 11802209 (Pubitemid 34027806)
    • (2002) International Journal of Cancer , vol.97 , Issue.4 , pp. 472-480
    • Meindl, A.1
  • 12
    • 0037685164 scopus 로고    scopus 로고
    • Breast and ovarian cancer
    • DOI 10.1056/NEJMra012284
    • R Wooster BL Weber 2003 Breast and ovarian cancer N Engl J Med 348 2339 2347 10.1056/NEJMra012284 10.1056/NEJMra012284 1:CAS:528:DC%2BD3sXkt1Kktrc%3D 12788999 (Pubitemid 36638109)
    • (2003) New England Journal of Medicine , vol.348 , Issue.23 , pp. 2339-2347
    • Wooster, R.1    Weber, B.L.2
  • 13
    • 0037130889 scopus 로고    scopus 로고
    • Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program
    • 1:CAS:528:DC%2BD38Xnt1Gnurg%3D 12237282
    • MS Brose TR Rebbeck KA Calzone JE Stopfer KL Nathanson BL Weber 2002 Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program J Natl Cancer Inst 94 1365 1372 1:CAS:528: DC%2BD38Xnt1Gnurg%3D 12237282
    • (2002) J Natl Cancer Inst , vol.94 , pp. 1365-1372
    • Brose, M.S.1    Rebbeck, T.R.2    Calzone, K.A.3    Stopfer, J.E.4    Nathanson, K.L.5    Weber, B.L.6
  • 14
    • 0037130887 scopus 로고    scopus 로고
    • Cancer incidence in BRCA1 mutation carriers
    • D Thompson DF Easton 2002 Cancer Incidence in BRCA1 mutation carriers J Natl Cancer Inst 94 1358 1365 1:CAS:528:DC%2BD38Xnt1Gnurs%3D 12237281 (Pubitemid 35154140)
    • (2002) Journal of the National Cancer Institute , vol.94 , Issue.18 , pp. 1358-1365
    • Thompson, D.1    Easton, D.F.2
  • 15
    • 48349120930 scopus 로고    scopus 로고
    • Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers
    • 10.1007/s10689-008-9181-0 10.1007/s10689-008-9181-0 1:CAS:528: DC%2BD1cXptVKksbs%3D 18283561
    • DJ Hughes 2008 Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers Fam Cancer 7 233 244 10.1007/s10689-008-9181-0 10.1007/s10689-008-9181-0 1:CAS:528: DC%2BD1cXptVKksbs%3D 18283561
    • (2008) Fam Cancer , vol.7 , pp. 233-244
    • Hughes, D.J.1
  • 16
    • 15844373362 scopus 로고    scopus 로고
    • CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair
    • DOI 10.1038/nature03404
    • F Esashi N Christ J Gannon Y Liu T Hunt M Jasin SC West 2005 CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair Nature 434 598 604 10.1038/nature03404 10.1038/nature03404 1:CAS:528:DC%2BD2MXislCmsr0%3D 15800615 (Pubitemid 40488546)
    • (2005) Nature , vol.434 , Issue.7033 , pp. 598-604
    • Esashi, F.1    Christ, N.2    Cannon, J.3    Liu, Y.4    Hunt, T.5    Jasin, M.6    West, S.C.7
  • 18
    • 41649097333 scopus 로고    scopus 로고
    • Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
    • 10.1016/j.ajhg.2008.02.008 10.1016/j.ajhg.2008.02.008 1:CAS:528:DC%2BD1cXltVKrsbc%3D 18355772
    • AC Antoniou AB Spurdle OM Sinilnikova S Healey KA Pooley RK Schmutzler B Versmold C Engel A Meindl N Arnold, et al. 2008 Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers Am J Hum Genet 82 937 948 10.1016/j.ajhg.2008.02.008 10.1016/j.ajhg.2008.02.008 1:CAS:528:DC%2BD1cXltVKrsbc%3D 18355772
    • (2008) Am J Hum Genet , vol.82 , pp. 937-948
    • Antoniou, A.C.1    Spurdle, A.B.2    Sinilnikova, O.M.3    Healey, S.4    Pooley, K.A.5    Schmutzler, R.K.6    Versmold, B.7    Engel, C.8    Meindl, A.9    Arnold, N.10
  • 19
    • 34447319406 scopus 로고    scopus 로고
    • Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA
    • DOI 10.1093/hmg/ddm062
    • R Duan C Pak P Jin 2007 Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA Hum Mol Genet 16 1124 1131 10.1093/hmg/ddm062 10.1093/hmg/ddm062 1:CAS:528:DC%2BD2sXntVKqsb8%3D 17400653 (Pubitemid 47062732)
    • (2007) Human Molecular Genetics , vol.16 , Issue.9 , pp. 1124-1131
    • Duan, R.1    Pak, C.H.2    Jin, P.3
  • 20
    • 24644466927 scopus 로고    scopus 로고
    • Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes
    • DOI 10.1016/j.taap.2004.09.024, PII S0041008X05003510
    • X Wang DJ Tomso X Liu DA Bell 2005 Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes Toxicol Appl Pharmacol 207 84 90 10.1016/j.taap.2004.09.024 10.1016/j.taap.2004.09.024 16002116 (Pubitemid 41265500)
    • (2005) Toxicology and Applied Pharmacology , vol.207 , Issue.2 SUPPL.
    • Wang, X.1    Tomso, D.J.2    Liu, X.3    Bell, D.A.4
  • 21
    • 33750200729 scopus 로고    scopus 로고
    • Cis-regulatory variations: A study of SNPs around genes showing cis-linkage in segregating mouse populations
    • DOI 10.1186/1471-2164-7-235
    • D GuhaThakurta T Xie M Anand SW Edwards G Li SS Wang EE Schadt 2006 Cis-regulatory variations: a study of SNPs around genes showing cis-linkage in segregating mouse populations BMC Genomics 7 235 10.1186/1471-2164-7-235 10.1186/1471-2164-7-235 16978413 (Pubitemid 44604583)
    • (2006) BMC Genomics , vol.7 , pp. 235
    • GuhaThakurta, D.1    Xie, T.2    Anand, M.3    Edwards, S.W.4    Li, G.5    Wang, S.S.6    Schadt, E.E.7
  • 23
    • 33746266617 scopus 로고    scopus 로고
    • Highly parallel genomic assays
    • DOI 10.1038/nrg1901, PII NRG1901
    • JB Fan MS Chee KL Gunderson 2006 Highly parallel genomic assays Nat Rev Genet 7 632 644 10.1038/nrg1901 10.1038/nrg1901 1:CAS:528:DC%2BD28XmvFCnu7c%3D 16847463 (Pubitemid 44100520)
    • (2006) Nature Reviews Genetics , vol.7 , Issue.8 , pp. 632-644
    • Fan, J.-B.1    Chee, M.S.2    Gunderson, K.L.3
  • 24
    • 33846923410 scopus 로고    scopus 로고
    • Genetic polymorphisms in the nucleotide excision repair pathway and lung cancer risk: A meta-analysis
    • 1:CAS:528:DC%2BD2sXms1KrsrY%3D 17299578
    • C Kiyohara K Yoshimasu 2007 Genetic polymorphisms in the nucleotide excision repair pathway and lung cancer risk: a meta-analysis Int J Med Sci 4 59 71 1:CAS:528:DC%2BD2sXms1KrsrY%3D 17299578
    • (2007) Int J Med Sci , vol.4 , pp. 59-71
    • Kiyohara, C.1    Yoshimasu, K.2
  • 25
    • 33846504706 scopus 로고    scopus 로고
    • A "silent" polymorphism in the MDR1 gene changes substrate specificity
    • DOI 10.1126/science.1135308
    • C Kimchi-Sarfaty JM Oh IW Kim ZE Sauna AM Calcagno SV Ambudkar MM Gottesman 2007 A "silent" polymorphism in the MDR1 gene changes substrate specificity Science 315 525 528 10.1126/science.1135308 10.1126/science.1135308 1:CAS:528:DC%2BD2sXotFCitA%3D%3D 17185560 (Pubitemid 46175758)
    • (2007) Science , vol.315 , Issue.5811 , pp. 525-528
    • Kimchi-Sarfaty, C.1    Oh, J.M.2    Kim, I.-W.3    Sauna, Z.E.4    Calcagno, A.M.5    Ambudkar, S.V.6    Gottesman, M.M.7
  • 26
    • 35448992847 scopus 로고    scopus 로고
    • Silent polymorphisms speak: How they affect pharmacogenomics and the treatment of cancer
    • DOI 10.1158/0008-5472.CAN-07-2377
    • ZE Sauna C Kimchi-Sarfaty SV Ambudkar MM Gottesman 2007 Silent polymorphisms speak: how they affect pharmacogenomics and the treatment of cancer Cancer Res 67 9609 9612 10.1158/0008-5472.CAN-07-2377 10.1158/0008-5472.CAN-07-2377 1:CAS:528:DC%2BD2sXhtFOnsLnO 17942888 (Pubitemid 47621204)
    • (2007) Cancer Research , vol.67 , Issue.20 , pp. 9609-9612
    • Sauna, Z.E.1    Kimchi-Sarfaty, C.2    Ambudkar, S.V.3    Gottesman, M.M.4
  • 28
    • 56049113262 scopus 로고    scopus 로고
    • The coding-synonymous polymorphism rs1045280 (Ser280Ser) in beta-arrestin 2 (ARRB2) gene is associated with tardive dyskinesia in Chinese patients with schizophrenia
    • 10.1111/j.1468-1331.2008.02316.x 10.1111/j.1468-1331.2008.02316.x 19049562
    • YJ Liou YC Wang JY Chen ML Chen TT Chen YM Bai CC Lin DL Liao IC Lai 2008 The coding-synonymous polymorphism rs1045280 (Ser280Ser) in beta-arrestin 2 (ARRB2) gene is associated with tardive dyskinesia in Chinese patients with schizophrenia Eur J Neurol 15 1406 1408 10.1111/j.1468-1331.2008.02316.x 10.1111/j.1468-1331.2008.02316.x 19049562
    • (2008) Eur J Neurol , vol.15 , pp. 1406-1408
    • Liou, Y.J.1    Wang, Y.C.2    Chen, J.Y.3    Chen, M.L.4    Chen, T.T.5    Bai, Y.M.6    Lin, C.C.7    Liao, D.L.8    Lai, I.C.9
  • 29
    • 47649093907 scopus 로고    scopus 로고
    • Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families?
    • DOI 10.1111/j.1365-2516.2008.01753.x
    • KE Knobe E Sjorin RC Ljung 2008 Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families? Haemophilia 14 723 728 10.1111/j.1365-2516.2008.01753.x 10.1111/j.1365-2516. 2008.01753.x 1:CAS:528:DC%2BD1cXps1Glsbo%3D 18459950 (Pubitemid 352016027)
    • (2008) Haemophilia , vol.14 , Issue.4 , pp. 723-728
    • Knobe, K.E.1    Sjorin, E.2    Ljung, R.C.R.3
  • 30
    • 33846588874 scopus 로고    scopus 로고
    • SNPs, silent but not invisible
    • DOI 10.1126/science.1138239
    • AA Komar 2007 Genetics SNPs, silent but not invisible Science 315 466 467 10.1126/science.1138239 10.1126/science.1138239 1:CAS:528:DC%2BD2sXhtFOqsLs%3D 17185559 (Pubitemid 46178389)
    • (2007) Science , vol.315 , Issue.5811 , pp. 466-467
    • Komar, A.A.1
  • 31
    • 0029902243 scopus 로고    scopus 로고
    • Protein structure and the sequential structure of mRNA: Alpha-helix and beta-sheet signals at the nucleotide level
    • 10.1002/(SICI)1097-0134(199606)25:2<237::AID-PROT9>3.3.CO;2-Y 10.1002/(SICI)1097-0134(199606)25:2<237::AID-PROT9>3.3.CO;2-Y 1:CAS:528:DyaK28XktlShu7o%3D 8811739
    • S Brunak J Engelbrecht 1996 Protein structure and the sequential structure of mRNA: alpha-helix and beta-sheet signals at the nucleotide level Proteins 25 237 252 10.1002/(SICI)1097-0134(199606)25:2<237::AID-PROT9>3. 3.CO;2-Y 10.1002/(SICI)1097-0134(199606)25:2<237::AID-PROT9>3.3.CO;2-Y 1:CAS:528:DyaK28XktlShu7o%3D 8811739
    • (1996) Proteins , vol.25 , pp. 237-252
    • Brunak, S.1    Engelbrecht, J.2
  • 32
    • 0034708361 scopus 로고    scopus 로고
    • Studies on the relationships between the synonymous codon usage and protein secondary structural units
    • DOI 10.1006/bbrc.2000.2351
    • SK Gupta S Majumdar TK Bhattacharya TC Ghosh 2000 Studies on the relationships between the synonymous codon usage and protein secondary structural units Biochem Biophys Res Commun 269 692 696 10.1006/bbrc.2000.2351 10.1006/bbrc.2000.2351 1:CAS:528:DC%2BD3cXhslequrk%3D 10720478 (Pubitemid 30440363)
    • (2000) Biochemical and Biophysical Research Communications , vol.269 , Issue.3 , pp. 692-696
    • Gupta, S.K.1    Majumdar, S.2    Bhattacharya, T.K.3    Ghosh, T.C.4
  • 33
    • 0036295371 scopus 로고    scopus 로고
    • Silent mutations affect in vivo protein folding in Escherichia coli
    • DOI 10.1016/S0006-291X(02)00226-7, PII S0006291X02002267
    • P Cortazzo C Cervenansky M Marin C Reiss R Ehrlich A Deana 2002 Silent mutations affect in vivo protein folding in Escherichia coli Biochem Biophys Res Commun 293 537 541 10.1016/S0006-291X(02)00226-7 10.1016/S0006-291X(02)00226-7 1:CAS:528:DC%2BD38XksVGhs7w%3D 12054634 (Pubitemid 34694241)
    • (2002) Biochemical and Biophysical Research Communications , vol.293 , Issue.1 , pp. 537-541
    • Cortazzo, P.1    Cerveansky, C.2    Marin, M.3    Reiss, C.4    Ehrlich, R.5    Deana, A.6
  • 34
    • 0034696628 scopus 로고    scopus 로고
    • A functional significance for codon third bases
    • DOI 10.1016/S0378-1119(00)00042-1, PII S0378111900000421
    • RJ Epstein K Lin TW Tan 2000 A functional significance for codon third bases Gene 245 291 298 10.1016/S0378-1119(00)00042-1 10.1016/S0378-1119(00) 00042-1 1:CAS:528:DC%2BD3cXhs12isbo%3D 10717480 (Pubitemid 30136434)
    • (2000) Gene , vol.245 , Issue.2 , pp. 291-298
    • Epstein, R.J.1    Lin, K.2    Tan, T.W.3
  • 36
    • 19544391975 scopus 로고    scopus 로고
    • A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups
    • DOI 10.1093/hmg/ddh273
    • F Capon MH Allen M Ameen AD Burden D Tillman JN Barker RC Trembath 2004 A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups Hum Mol Genet 13 2361 2368 10.1093/hmg/ddh273 10.1093/hmg/ddh273 1:CAS:528: DC%2BD2cXnvVOku70%3D 15333584 (Pubitemid 39377840)
    • (2004) Human Molecular Genetics , vol.13 , Issue.20 , pp. 2361-2368
    • Capon, F.1    Allen, M.H.2    Ameen, M.3    Burden, A.D.4    Tillman, D.5    Barker, J.N.6    Trembath, R.C.7
  • 39
    • 0032430986 scopus 로고    scopus 로고
    • Power and sample size calculations for studies involving linear regression
    • DOI 10.1016/S0197-2456(98)00037-3, PII S0197245698000373
    • WD Dupont WD Plummer Jr 1998 Power and sample size calculations for studies involving linear regression Control Clin Trials 19 589 601 10.1016/S0197-2456(98)00037-3 10.1016/S0197-2456(98)00037-3 1:STN:280: DyaK1M%2FptFSnsA%3D%3D 9875838 (Pubitemid 29057724)
    • (1998) Controlled Clinical Trials , vol.19 , Issue.6 , pp. 589-601
    • Dupont, W.D.1    Plummer Jr., W.D.2
  • 40
    • 33846676140 scopus 로고    scopus 로고
    • Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus
    • DOI 10.1111/j.1399-0004.2007.00747.x
    • M Loizidou Y Marcou V Anastasiadou R Newbold A Hadjisavvas K Kyriacou 2007 Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus Clin Genet 71 165 170 10.1111/j.1399-0004. 2007.00747.x 10.1111/j.1399-0004.2007.00747.x 1:STN:280:DC%2BD2s%2FkslClsA%3D%3D 17250666 (Pubitemid 46189221)
    • (2007) Clinical Genetics , vol.71 , Issue.2 , pp. 165-170
    • Loizidou, M.1    Marcou, B.2    Anastasiadou, V.3    Newbold, R.4    Hadjisavvas, A.5    Kyriacou, K.6
  • 41
    • 36448996703 scopus 로고    scopus 로고
    • Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations
    • DOI 10.1038/nrc2054, PII NRC2054
    • JD Fackenthal OI Olopade 2007 Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations Nat Rev Cancer 7 937 948 10.1038/nrc2054 10.1038/nrc2054 1:CAS:528:DC%2BD2sXhtlCrsLbK 18034184 (Pubitemid 350165853)
    • (2007) Nature Reviews Cancer , vol.7 , Issue.12 , pp. 937-948
    • Fackenthal, J.D.1    Olopade, O.I.2
  • 43
    • 0033740880 scopus 로고    scopus 로고
    • Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases
    • Anglian Breast Cancer Study Group. 10.1054/bjoc.2000.1407 10.1054/bjoc.2000.1407
    • Anglian Breast Cancer Study Group 2000 Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases Br J Cancer 83 1301 1308 10.1054/bjoc.2000.1407 10.1054/bjoc.2000.1407
    • (2000) Br J Cancer , vol.83 , pp. 1301-1308
  • 44
    • 0029794992 scopus 로고    scopus 로고
    • Ashkenazi jewish population frequencies for common mutations in BRCA1 and BRCA2
    • DOI 10.1038/ng1096-185
    • BB Roa AA Boyd K Volcik CS Richards 1996 Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2 Nat Genet 14 185 187 10.1038/ng1096-185 10.1038/ng1096-185 1:CAS:528:DyaK28XmtVKntLs%3D 8841191 (Pubitemid 26338801)
    • (1996) Nature Genetics , vol.14 , Issue.2 , pp. 185-187
    • Roa, B.B.1    Boyd, A.A.2    Volcik, K.3    Richards, C.S.4
  • 45
    • 36048929748 scopus 로고    scopus 로고
    • Association between the BRCA2 N372H variant and male breast cancer risk: A population-based case-control study in Tuscany Central Italy
    • 10.1186/1471-2407-7-170 10.1186/1471-2407-7-170 17767707
    • D Palli M Falchetti G Masala R Lupi F Sera C Saieva C D'Amico M Ceroti P Rizzolo MA Caligo, et al. 2007 Association between the BRCA2 N372H variant and male breast cancer risk: a population-based case-control study in Tuscany Central Italy BMC Cancer 7 170 10.1186/1471-2407-7-170 10.1186/1471-2407-7-170 17767707
    • (2007) BMC Cancer , vol.7 , pp. 170
    • Palli, D.1    Falchetti, M.2    Masala, G.3    Lupi, R.4    Sera, F.5    Saieva, C.6    D'Amico, C.7    Ceroti, M.8    Rizzolo, P.9    Caligo, M.A.10
  • 48
    • 0038823932 scopus 로고    scopus 로고
    • The future of association studies of common cancers
    • 12574941
    • RS Houlston J Peto 2003 The future of association studies of common cancers Hum Genet 112 434 435 12574941
    • (2003) Hum Genet , vol.112 , pp. 434-435
    • Houlston, R.S.1    Peto, J.2
  • 49
    • 0142063079 scopus 로고    scopus 로고
    • Polygenic Inheritance of Breast Cancer: Implications for Design of Association Studies
    • DOI 10.1002/gepi.10261
    • AC Antoniou DF Easton 2003 Polygenic inheritance of breast cancer: implications for design of association studies Genet Epidemiol 25 190 202 10.1002/gepi.10261 10.1002/gepi.10261 14557987 (Pubitemid 37296594)
    • (2003) Genetic Epidemiology , vol.25 , Issue.3 , pp. 190-202
    • Antoniou, A.C.1    Easton, D.F.2
  • 50
    • 33645508511 scopus 로고    scopus 로고
    • Regions of extreme synonymous codon selection in mammalian genes
    • 10.1093/nar/gkl095 10.1093/nar/gkl095 1:CAS:528:DC%2BD28XjslKqtLk%3D 16556911
    • P Schattner M Diekhans 2006 Regions of extreme synonymous codon selection in mammalian genes Nucleic Acids Res 34 1700 1710 10.1093/nar/gkl095 10.1093/nar/gkl095 1:CAS:528:DC%2BD28XjslKqtLk%3D 16556911
    • (2006) Nucleic Acids Res , vol.34 , pp. 1700-1710
    • Schattner, P.1    Diekhans, M.2


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