-
2
-
-
33747829208
-
-
American Cancer Society Atlanta, GA: American Cancer Society
-
American Cancer Society. Breast Cancer Facts & Figures, 2011-2012. Atlanta, GA: American Cancer Society; 2012.
-
(2012)
Breast Cancer Facts & Figures, 2011-2012
-
-
-
3
-
-
42149134292
-
Epidemiology of basal-like breast cancer
-
Millikan RC, Newman B, Tse CK, Moorman PG, Conway K, Dressler LG, et al. Epidemiology of basal-like breast cancer. Breast Cancer Res Treat 2008;109:123-39.
-
(2008)
Breast Cancer Res Treat
, vol.109
, pp. 123-139
-
-
Millikan, R.C.1
Newman, B.2
Tse, C.K.3
Moorman, P.G.4
Conway, K.5
Dressler, L.G.6
-
4
-
-
70349932822
-
Patterns of recurrence in the basal and non-basal subtypes of triplenegative breast cancers
-
Nofech-Mozes S, Trudeau M, Kahn HK, Dent R, Rawlinson E, Sun P, et al. Patterns of recurrence in the basal and non-basal subtypes of triplenegative breast cancers. Breast Cancer Res Treat 2009;118:131-7.
-
(2009)
Breast Cancer Res Treat
, vol.118
, pp. 131-137
-
-
Nofech-Mozes, S.1
Trudeau, M.2
Kahn, H.K.3
Dent, R.4
Rawlinson, E.5
Sun, P.6
-
5
-
-
34247569300
-
Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the socalled triple-negative phenotype: A population-based study from the California cancer Registry
-
Bauer KR, Brown M, Cress RD, Parise CA, Caggiano V. Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the socalled triple-negative phenotype: a population-based study from the California cancer Registry. Cancer 2007;109:1721-8.
-
(2007)
Cancer
, vol.109
, pp. 1721-1728
-
-
Bauer, K.R.1
Brown, M.2
Cress, R.D.3
Parise, C.A.4
Caggiano, V.5
-
6
-
-
0037478605
-
Repeated observation of breast tumor subtypes in independent gene expression data sets
-
Sorlie T, Tibshirani R, Parker J, Hastie T, Marron JS, Nobel A, et al. Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci U S A 2003;100: 8418-23.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 8418-8423
-
-
Sorlie, T.1
Tibshirani, R.2
Parker, J.3
Hastie, T.4
Marron, J.S.5
Nobel, A.6
-
7
-
-
78049308800
-
Phenotypic and molecular characterization of the claudin-low intrinsic subtype of breast cancer
-
Prat A, Parker JS, Karginova O, Fan C, Livasy C, Herschkowitz JI, et al. Phenotypic and molecular characterization of the claudin-low intrinsic subtype of breast cancer. Breast Cancer Res 2010;12: R68.
-
(2010)
Breast Cancer Res
, vol.12
-
-
Prat, A.1
Parker, J.S.2
Karginova, O.3
Fan, C.4
Livasy, C.5
Herschkowitz, J.I.6
-
8
-
-
84861527388
-
The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
-
Curtis C, Shah SP, Chin SF, Turashvili G, Rueda OM, Dunning MJ, et al. The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups. Nature 2012;486:346-52.
-
(2012)
Nature
, vol.486
, pp. 346-352
-
-
Curtis, C.1
Shah, S.P.2
Chin, S.F.3
Turashvili, G.4
Rueda, O.M.5
Dunning, M.J.6
-
9
-
-
79960015997
-
Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies
-
Lehmann BD, Bauer JA, Chen X, Sanders ME, Chakravarthy AB, Shyr Y, et al. Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest 2011;121:2750-67.
-
(2011)
J Clin Invest
, vol.121
, pp. 2750-2767
-
-
Lehmann, B.D.1
Bauer, J.A.2
Chen, X.3
Sanders, M.E.4
Chakravarthy, A.B.5
Shyr, Y.6
-
10
-
-
84862907494
-
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
-
Mavaddat N, Barrowdale D, Andrulis IL, Domchek SM, Eccles D, Nevanlinna H, et al. Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). Cancer Epidemiol Biomarkers Prev 2012;21:134-47.
-
(2012)
Cancer Epidemiol Biomarkers Prev
, vol.21
, pp. 134-147
-
-
Mavaddat, N.1
Barrowdale, D.2
Andrulis, I.L.3
Domchek, S.M.4
Eccles, D.5
Nevanlinna, H.6
-
11
-
-
84858295021
-
BRCA1 testing should be offered to individuals with triplenegative breast cancer diagnosed below 50 years
-
Robertson L, Hanson H, Seal S, Warren-Perry M, Hughes D, Howell I, et al. BRCA1 testing should be offered to individuals with triplenegative breast cancer diagnosed below 50 years. Br J Cancer 2012;106:1234-8.
-
(2012)
Br J Cancer
, vol.106
, pp. 1234-1238
-
-
Robertson, L.1
Hanson, H.2
Seal, S.3
Warren-Perry, M.4
Hughes, D.5
Howell, I.6
-
12
-
-
52049086689
-
Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer
-
Atchley DP, Albarracin CT, Lopez A, Valero V, Amos CI, Gonzalez-Angulo AM, et al. Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer. J Clin Oncol 2008;26:4282-8.
-
(2008)
J Clin Oncol
, vol.26
, pp. 4282-4288
-
-
Atchley, D.P.1
Albarracin, C.T.2
Lopez, A.3
Valero, V.4
Amos, C.I.5
Gonzalez-Angulo, A.M.6
-
13
-
-
79960834725
-
Relative contributions of BRCA1 and BRCA2 mutations to "triple-negative" breast cancer in Ashkenazi Women
-
Comen E, Davids M, Kirchhoff T, Hudis C, Offit K, Robson M. Relative contributions of BRCA1 and BRCA2 mutations to "triple-negative" breast cancer in Ashkenazi Women. Breast Cancer Res Treat 2011; 129:185-90.
-
(2011)
Breast Cancer Res Treat
, vol.129
, pp. 185-190
-
-
Comen, E.1
Davids, M.2
Kirchhoff, T.3
Hudis, C.4
Offit, K.5
Robson, M.6
-
14
-
-
84877028141
-
Comprehensive molecular portraits of human breast tumors
-
The Cancer Genome Atlas Network
-
The Cancer Genome Atlas Network. Comprehensive molecular portraits of human breast tumors. Nature 2012;490:61-70.
-
(2012)
Nature
, vol.490
, pp. 61-70
-
-
-
15
-
-
77955439715
-
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing
-
Walsh T, Lee MK, Casadei S, Thornton AM, Stray SM, Pennil C, et al. Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Proc Natl Acad Sci U S A 2010;107:12629-33.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 12629-12633
-
-
Walsh, T.1
Lee, M.K.2
Casadei, S.3
Thornton, A.M.4
Stray, S.M.5
Pennil, C.6
-
16
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, Ballinger DG, et al. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 2007;447:1087-93.
-
(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
Ballinger, D.G.6
-
17
-
-
34250001297
-
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, Hankinson SE, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 2007;39:870-4.
-
(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
Hankinson, S.E.6
-
18
-
-
34250002140
-
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
-
Stacey SN, Manolescu A, Sulem P, Rafnar T, Gudmundsson J, Gudjonsson SA, et al. Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet 2007;39:865-9.
-
(2007)
Nat Genet
, vol.39
, pp. 865-869
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
Rafnar, T.4
Gudmundsson, J.5
Gudjonsson, S.A.6
-
19
-
-
44349087530
-
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer
-
Stacey SN, Manolescu A, Sulem P, Thorlacius S, Gudjonsson SA, Jonsson GF, et al. Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet 2008;40:703-6.
-
(2008)
Nat Genet
, vol.40
, pp. 703-706
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
Thorlacius, S.4
Gudjonsson, S.A.5
Jonsson, G.F.6
-
20
-
-
67349237973
-
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
-
Ahmed S, Thomas G, Ghoussaini M, Healey CS, Humphreys MK, Platte R, et al. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet 2009;41:585-90.
-
(2009)
Nat Genet
, vol.41
, pp. 585-590
-
-
Ahmed, S.1
Thomas, G.2
Ghoussaini, M.3
Healey, C.S.4
Humphreys, M.K.5
Platte, R.6
-
21
-
-
67349158067
-
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
-
Thomas G, Jacobs KB, Kraft P, Yeager M, Wacholder S, Cox DG, et al. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat Genet 2009;41:579-84.
-
(2009)
Nat Genet
, vol.41
, pp. 579-584
-
-
Thomas, G.1
Jacobs, K.B.2
Kraft, P.3
Yeager, M.4
Wacholder, S.5
Cox, D.G.6
-
22
-
-
61349163553
-
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
-
Zheng W, Long J, Gao YT, Li C, Zheng Y, Xiang YB, et al. Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat Genet 2009;41:324-8.
-
(2009)
Nat Genet
, vol.41
, pp. 324-328
-
-
Zheng, W.1
Long, J.2
Gao, Y.T.3
Li, C.4
Zheng, Y.5
Xiang, Y.B.6
-
23
-
-
77952887426
-
Genome-wide association study identifies five new breast cancer susceptibility loci
-
Turnbull C, Ahmed S, Morrison J, Pernet D, Renwick A, Maranian M, et al. Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet 2010;42:504-7.
-
(2010)
Nat Genet
, vol.42
, pp. 504-507
-
-
Turnbull, C.1
Ahmed, S.2
Morrison, J.3
Pernet, D.4
Renwick, A.5
Maranian, M.6
-
24
-
-
79952329937
-
Novel breast cancer susceptibility locus at 9q31.2: Results of a genome-wide association study
-
Fletcher O, Johnson N, Orr N, Hosking FJ, Gibson LJ, Walker K, et al. Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. J Natl Cancer Inst 2011;103: 425-35.
-
(2011)
J Natl Cancer Inst
, vol.103
, pp. 425-435
-
-
Fletcher, O.1
Johnson, N.2
Orr, N.3
Hosking, F.J.4
Gibson, L.J.5
Walker, K.6
-
25
-
-
84862776961
-
Genome-wide association analysis identifies three new breast cancer susceptibility loci
-
Ghoussaini M, Fletcher O, Michailidou K, Turnbull C, Schmidt MK, Dicks E, et al. Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat Genet 2012;44:312-8.
-
(2012)
Nat Genet
, vol.44
, pp. 312-318
-
-
Ghoussaini, M.1
Fletcher, O.2
Michailidou, K.3
Turnbull, C.4
Schmidt, M.K.5
Dicks, E.6
-
26
-
-
82255183150
-
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
-
Haiman CA, Chen GK, Vachon CM, Canzian F, Dunning A, Millikan RC, et al. A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat Genet 2011;43:1210-4.
-
(2011)
Nat Genet
, vol.43
, pp. 1210-1214
-
-
Haiman, C.A.1
Chen, G.K.2
Vachon, C.M.3
Canzian, F.4
Dunning, A.5
Millikan, R.C.6
-
27
-
-
77957568513
-
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptornegative breast cancer in the general population
-
Antoniou AC, Wang X, Fredericksen ZS, McGuffog L, Tarrell R, Sinilnikova OM, et al. A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptornegative breast cancer in the general population. Nat Genet 2010;42:885-92.
-
(2010)
Nat Genet
, vol.42
, pp. 885-892
-
-
Antoniou, A.C.1
Wang, X.2
Fredericksen, Z.S.3
McGuffog, L.4
Tarrell, R.5
Sinilnikova, O.M.6
-
28
-
-
84984992122
-
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
-
Siddiq A, Couch FJ, Chen GK, Lindstrom S, Eccles D, Millikan RC, et al. A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum Mol Genet 2012;21:5373-84.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 5373-5384
-
-
Siddiq, A.1
Couch, F.J.2
Chen, G.K.3
Lindstrom, S.4
Eccles, D.5
Millikan, R.C.6
-
29
-
-
33847337318
-
A common coding variant in CASP8 is associated with breast cancer risk
-
Cox A, Dunning AM, Garcia-Closas M, Balasubramanian S, Reed MW, Pooley KA, et al. A common coding variant in CASP8 is associated with breast cancer risk. Nat Genet 2007;39:352-8.
-
(2007)
Nat Genet
, vol.39
, pp. 352-358
-
-
Cox, A.1
Dunning, A.M.2
Garcia-Closas, M.3
Balasubramanian, S.4
Reed, M.W.5
Pooley, K.A.6
-
30
-
-
84875703379
-
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
-
In press
-
Michailidou K, Hall P, Gonzalez-Neira A, Ghoussaini M, Dennis J, Milne R, et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet. In press, 2013.
-
(2013)
Nat Genet.
-
-
Michailidou, K.1
Hall, P.2
Gonzalez-Neira, A.3
Ghoussaini, M.4
Dennis, J.5
Milne, R.6
-
31
-
-
84875701351
-
Genome-wide association studies identify four ERnegative specific breast cancer risk loci
-
In press
-
Garcia-Closas M, Couch F, Lindstrom S, Michailidou K, Schmidt MK, Brook M, et al. Genome-wide association studies identify four ERnegative specific breast cancer risk loci. Nat Genet. In press, 2013.
-
(2013)
Nat Genet.
-
-
Garcia-Closas, M.1
Couch, F.2
Lindstrom, S.3
Michailidou, K.4
Schmidt, M.K.5
Brook, M.6
-
32
-
-
81255209196
-
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: Findings from the Breast Cancer Association Consortium
-
Figueroa JD, Garcia-Closas M, Humphreys M, Platte R, Hopper JL, Southey MC, et al. Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. Hum Mol Genet 2011;20:4693-706.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 4693-4706
-
-
Figueroa, J.D.1
Garcia-Closas, M.2
Humphreys, M.3
Platte, R.4
Hopper, J.L.5
Southey, M.C.6
-
33
-
-
80053366674
-
Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: Findings from the Breast Cancer Association Consortium
-
Broeks A, Schmidt MK, Sherman ME, Couch FJ, Hopper JL, Dite GS, et al. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. Hum Mol Genet 2011;20:3289-303.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3289-3303
-
-
Broeks, A.1
Schmidt, M.K.2
Sherman, M.E.3
Couch, F.J.4
Hopper, J.L.5
Dite, G.S.6
-
34
-
-
77957343700
-
Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus
-
Stacey SN, Sulem P, Zanon C, Gudjonsson SA, Thorleifsson G, Helgason A, et al. Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus. PLoS Genet 2010;6:e1001029.
-
(2010)
PLoS Genet
, vol.6
-
-
Stacey, S.N.1
Sulem, P.2
Zanon, C.3
Gudjonsson, S.A.4
Thorleifsson, G.5
Helgason, A.6
-
35
-
-
84859375225
-
19p13.1 is a triple negative-specific breast cancer susceptibility locus
-
Stevens KN, Fredericksen Z, Vachon CM, Wang X, Margolin S, Lindblom A, et al. 19p13.1 is a triple negative-specific breast cancer susceptibility locus. Cancer Res 2012;72:1795-803.
-
(2012)
Cancer Res
, vol.72
, pp. 1795-1803
-
-
Stevens, K.N.1
Fredericksen, Z.2
Vachon, C.M.3
Wang, X.4
Margolin, S.5
Lindblom, A.6
-
36
-
-
84875717832
-
Multiple independent TERT variants associated with telomere length and risks of breast and ovarian cancer
-
In press
-
Bojesen S, Pooley K, Johnatty SE, Beesley J, Michailidou K, Tyrer J, et al. Multiple independent TERT variants associated with telomere length and risks of breast and ovarian cancer. Nat Genet. In press, 2013.
-
(2013)
Nat Genet.
-
-
Bojesen, S.1
Pooley, K.2
Johnatty, S.E.3
Beesley, J.4
Michailidou, K.5
Tyrer, J.6
-
37
-
-
80053375835
-
Common breast cancer susceptibility loci are associated with triplenegative breast cancer
-
Stevens KN, Vachon CM, Lee AM, Slager S, Lesnick T, Olswold C, et al. Common breast cancer susceptibility loci are associated with triplenegative breast cancer. Cancer Res 2011;71:6240-9.
-
(2011)
Cancer Res
, vol.71
, pp. 6240-6249
-
-
Stevens, K.N.1
Vachon, C.M.2
Lee, A.M.3
Slager, S.4
Lesnick, T.5
Olswold, C.6
-
38
-
-
67349158309
-
No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: A multi-center cohort study
-
Rebbeck TR, Antoniou AC, Llopis TC, Nevanlinna H, Aittomaki K, Simard J, et al. No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study. Breast Cancer Res Treat 2009;115:185-92.
-
(2009)
Breast Cancer Res Treat
, vol.115
, pp. 185-192
-
-
Rebbeck, T.R.1
Antoniou, A.C.2
Llopis, T.C.3
Nevanlinna, H.4
Aittomaki, K.5
Simard, J.6
-
39
-
-
78649980806
-
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction
-
Antoniou AC, Beesley J, McGuffog L, Sinilnikova OM, Healey S, Neuhausen SL, et al. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. Cancer Res 2010;70:9742-54.
-
(2010)
Cancer Res
, vol.70
, pp. 9742-9754
-
-
Antoniou, A.C.1
Beesley, J.2
McGuffog, L.3
Sinilnikova, O.M.4
Healey, S.5
Neuhausen, S.L.6
-
40
-
-
79960819760
-
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
-
Antoniou AC, Kartsonaki C, Sinilnikova OM, Soucy P, McGuffog L, Healey S, et al. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. Hum Mol Genet 2011;20:3304-21.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3304-3321
-
-
Antoniou, A.C.1
Kartsonaki, C.2
Sinilnikova, O.M.3
Soucy, P.4
McGuffog, L.5
Healey, S.6
-
41
-
-
84862821318
-
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
-
Antoniou AC, Kuchenbaecker KB, Soucy P, Beesley J, Chen X, McGuffog L, et al. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Res 2012;14:R33.
-
(2012)
Breast Cancer Res
, vol.14
-
-
Antoniou, A.C.1
Kuchenbaecker, K.B.2
Soucy, P.3
Beesley, J.4
Chen, X.5
McGuffog, L.6
-
42
-
-
79551621885
-
Genetic modifiers of cancer risk for BRCA1 and BRCA2 mutation carriers
-
Milne RL, Antoniou AC. Genetic modifiers of cancer risk for BRCA1 and BRCA2 mutation carriers. Ann Oncol 2011;22 Suppl 1:i11-7.
-
(2011)
Ann Oncol
, vol.22
, Issue.SUPPL. 1
-
-
Milne, R.L.1
Antoniou, A.C.2
-
43
-
-
84858750992
-
Regulation of the human catalytic subunit of telomerase (hTERT)
-
Daniel M, Peek GW, Tollefsbol TO. Regulation of the human catalytic subunit of telomerase (hTERT). Gene 2012;498:135-46.
-
(2012)
Gene
, vol.498
, pp. 135-146
-
-
Daniel, M.1
Peek, G.W.2
Tollefsbol, T.O.3
-
44
-
-
77953545169
-
Puzzling over MDM4-p53 network
-
Mancini F, Di Conza G, Monti O, Macchiarulo A, Pellicciari R, Pontecorvi A, et al. Puzzling over MDM4-p53 network. Int J Biochem Cell Biol 2010;42:1080-3.
-
(2010)
Int J Biochem Cell Biol
, vol.42
, pp. 1080-1083
-
-
Mancini, F.1
Di Conza, G.2
Monti, O.3
Macchiarulo, A.4
Pellicciari, R.5
Pontecorvi, A.6
-
45
-
-
63049083118
-
MERIT40 facilitates BRCA1 localization and DNA damage repair
-
Feng L, Huang J, Chen J. MERIT40 facilitates BRCA1 localization and DNA damage repair. Genes Dev 2009;23:719-28.
-
(2009)
Genes Dev
, vol.23
, pp. 719-728
-
-
Feng, L.1
Huang, J.2
Chen, J.3
-
46
-
-
84855485251
-
Telomere dysfunction and chromosome instability
-
Murnane JP. Telomere dysfunction and chromosome instability. Mutat Res 2012;730:28-36.
-
(2012)
Mutat Res
, vol.730
, pp. 28-36
-
-
Murnane, J.P.1
-
47
-
-
77956640538
-
To fuse or not to fuse: How do checkpoint and DNA repair proteins maintain telomeres?
-
Subramanian L, Nakamura TM. To fuse or not to fuse: how do checkpoint and DNA repair proteins maintain telomeres? Front Biosci 2010;15:1105-18.
-
(2010)
Front Biosci
, vol.15
, pp. 1105-1118
-
-
Subramanian, L.1
Nakamura, T.M.2
-
48
-
-
84863994288
-
Dissecting the heterogeneity of triple-negative breast cancer
-
Metzger-Filho O, Tutt A, de Azambuja E, Saini KS, Viale G, Loi S, et al. Dissecting the heterogeneity of triple-negative breast cancer. J Clin Oncol 2012;30:1879-87.
-
(2012)
J Clin Oncol
, vol.30
, pp. 1879-1887
-
-
Metzger-Filho, O.1
Tutt, A.2
De Azambuja, E.3
Saini, K.S.4
Viale, G.5
Loi, S.6
-
49
-
-
77949578084
-
Performance of common genetic variants in breastcancer risk models
-
Wacholder S, Hartge P, Prentice R, Garcia-Closas M, Feigelson HS, Diver WR, et al. Performance of common genetic variants in breastcancer risk models. N Engl J Med 2010;362:986-93.
-
(2010)
N Engl J Med
, vol.362
, pp. 986-993
-
-
Wacholder, S.1
Hartge, P.2
Prentice, R.3
Garcia-Closas, M.4
Feigelson, H.S.5
Diver, W.R.6
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