-
2
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
-
Bryant HE, Schultz N, Thomas HD, et al. Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase. Nature. 2005;434:913-917.
-
(2005)
Nature
, vol.434
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
-
3
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
Farmer H, McCabe N, Lord CJ, et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature. 2005;434:917-921.
-
(2005)
Nature
, vol.434
, pp. 917-921
-
-
Farmer, H.1
McCabe, N.2
Lord, C.J.3
-
4
-
-
67650471685
-
Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
-
Fong PC, Boss DS, Yap TA, et al. Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med. 2009;361:123-134.
-
(2009)
N Engl J Med
, vol.361
, pp. 123-134
-
-
Fong, P.C.1
Boss, D.S.2
Yap, T.A.3
-
5
-
-
0037478605
-
Repeated observation of breast tumor subtypes in independent gene expression data sets
-
Sorlie T, Tibshirani R, Parker J, et al. Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci USA. 2003;100:8418-8423.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 8418-8423
-
-
Sorlie, T.1
Tibshirani, R.2
Parker, J.3
-
6
-
-
18244409687
-
Gene expression profiling predicts clinical outcome of breast cancer
-
van 't Veer LJ, Dai H, van de Vijver MJ, et al. Gene expression profiling predicts clinical outcome of breast cancer. Nature. 2002;415:530-536.
-
(2002)
Nature
, vol.415
, pp. 530-536
-
-
van 't Veer, L.J.1
Dai, H.2
van de Vijver, M.J.3
-
7
-
-
0035893363
-
Ku DNA end-binding protein modulates homologous repair of double-strand breaks in mammalian cells
-
Pierce AJ, Hu P, Han M, et al. Ku DNA end-binding protein modulates homologous repair of double-strand breaks in mammalian cells. Genes Dev. 2001;15:3237-3242.
-
(2001)
Genes Dev
, vol.15
, pp. 3237-3242
-
-
Pierce, A.J.1
Hu, P.2
Han, M.3
-
8
-
-
0034600975
-
Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells
-
Johnson RD, Jasin M. Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells. EMBO J. 2000;19: 3398-3407.
-
(2000)
EMBO J
, vol.19
, pp. 3398-3407
-
-
Johnson, R.D.1
Jasin, M.2
-
9
-
-
0032574750
-
Homology-directed repair is a major double-strand break repair pathway in mammalian cells
-
Liang F, Han M, Romanienko PJ, et al. Homology-directed repair is a major double-strand break repair pathway in mammalian cells. Proc Natl Acad Sci USA. 1998;95:5172-5177.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 5172-5177
-
-
Liang, F.1
Han, M.2
Romanienko, P.J.3
-
10
-
-
0031962185
-
Gene conversion tracts from double-strand break repair in mammalian cells
-
Elliott B, Richardson C, Winderbaum J, et al. Gene conversion tracts from double-strand break repair in mammalian cells. Mol Cell Biol. 1998;18:93-101.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 93-101
-
-
Elliott, B.1
Richardson, C.2
Winderbaum, J.3
-
11
-
-
0242384946
-
Rad51 recombinase and recombination mediators
-
Sung P, Krejci L, Van Komen S, et al. Rad51 recombinase and recombination mediators. J Biol Chem. 2003;278:42729-42732.
-
(2003)
J Biol Chem
, vol.278
, pp. 42729-42732
-
-
Sung, P.1
Krejci, L.2
Van Komen, S.3
-
12
-
-
0037773540
-
Loss of Bard1, the heterodimeric partner of the Brca1 tumor suppressor, results in early embryonic lethality and chromosomal instability
-
McCarthy EE, Celebi JT, Baer R, et al. Loss of Bard1, the heterodimeric partner of the Brca1 tumor suppressor, results in early embryonic lethality and chromosomal instability. Mol Cell Biol. 2003;23:5056-5063.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 5056-5063
-
-
McCarthy, E.E.1
Celebi, J.T.2
Baer, R.3
-
13
-
-
0142123148
-
BARD1 participates with BRCA1 in homology-directed repair of chromosome breaks
-
Westermark UK, Reyngold M, Olshen AB, et al. BARD1 participates with BRCA1 in homology-directed repair of chromosome breaks. Mol Cell Biol. 2003;23:7926-7936.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 7926-7936
-
-
Westermark, U.K.1
Reyngold, M.2
Olshen, A.B.3
-
14
-
-
0035083172
-
Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs
-
Takata M, Sasaki MS, Tachiiri S, et al. Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs. Mol Cell Biol. 2001;21:2858-2866.
-
(2001)
Mol Cell Biol
, vol.21
, pp. 2858-2866
-
-
Takata, M.1
Sasaki, M.S.2
Tachiiri, S.3
-
15
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The Breast Cancer Linkage Consortium
-
Easton DF, Bishop DT, Ford D, et al. Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium. Am J Hum Genet. 1993;52:678-701.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
-
16
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall JM, Lee MK, Newman B, et al. Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 1990;250:1684-1689.
-
(1990)
Science
, vol.250
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
-
17
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994;266: 66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
-
18
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science. 1994;265: 2088-2090.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
-
19
-
-
0032159062
-
Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells
-
Chen J, Silver DP, Walpita D, et al. Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells. Mol Cell. 1998;2:317-328.
-
(1998)
Mol Cell
, vol.2
, pp. 317-328
-
-
Chen, J.1
Silver, D.P.2
Walpita, D.3
-
20
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
Scully R, Chen J, Plug A, et al. Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell. 1997;88:265-275.
-
(1997)
Cell
, vol.88
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
-
21
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
-
Sharan SK, Morimatsu M, Albrecht U, et al. Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature. 1997;386:804-810.
-
(1997)
Nature
, vol.386
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
-
22
-
-
0033213392
-
Brca1 controls homologydirected DNA repair
-
Moynahan ME, Chiu JW, Koller BH, et al. Brca1 controls homologydirected DNA repair. Mol Cell. 1999;4:511-518.
-
(1999)
Mol Cell
, vol.4
, pp. 511-518
-
-
Moynahan, M.E.1
Chiu, J.W.2
Koller, B.H.3
-
23
-
-
0035874894
-
Homology-directed DNA repair, mitomycin-c resistance, and chromosome stability is restored with correction of a Brca1 mutation
-
Moynahan ME, Cui TY, Jasin M. Homology-directed DNA repair, mitomycin-c resistance, and chromosome stability is restored with correction of a Brca1 mutation. Cancer Res. 2001;61:4842-4850.
-
(2001)
Cancer Res
, vol.61
, pp. 4842-4850
-
-
Moynahan, M.E.1
Cui, T.Y.2
Jasin, M.3
-
24
-
-
0035099044
-
BRCA2 is required for homologydirected repair of chromosomal breaks
-
Moynahan ME, Pierce AJ, Jasin M. BRCA2 is required for homologydirected repair of chromosomal breaks. Mol Cell. 2001;7:263-272.
-
(2001)
Mol Cell
, vol.7
, pp. 263-272
-
-
Moynahan, M.E.1
Pierce, A.J.2
Jasin, M.3
-
25
-
-
0035801472
-
Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences
-
Tutt A, Bertwistle D, Valentine J, et al. Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences. EMBO J. 2001;20:4704-4716.
-
(2001)
EMBO J
, vol.20
, pp. 4704-4716
-
-
Tutt, A.1
Bertwistle, D.2
Valentine, J.3
-
26
-
-
0037115914
-
Homologous repair of DNA damage and tumorigenesis: The BRCA connection
-
Jasin M. Homologous repair of DNA damage and tumorigenesis: the BRCA connection. Oncogene. 2002;21:8981-8993.
-
(2002)
Oncogene
, vol.21
, pp. 8981-8993
-
-
Jasin, M.1
-
27
-
-
36949026476
-
BRCA2: A universal recombinase regulator
-
Thorslund T, West SC. BRCA2: a universal recombinase regulator. Oncogene. 2007;26:7720-7730.
-
(2007)
Oncogene
, vol.26
, pp. 7720-7730
-
-
Thorslund, T.1
West, S.C.2
-
28
-
-
0030894785
-
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations
-
Tirkkonen M, Johannsson O, Agnarsson BA, et al. Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res. 1997;57:1222-1227.
-
(1997)
Cancer Res
, vol.57
, pp. 1222-1227
-
-
Tirkkonen, M.1
Johannsson, O.2
Agnarsson, B.A.3
-
29
-
-
0036675318
-
Mammary tumors in mice conditionally mutant for Brca1 exhibit gross genomic instability and centrosome ampli-fication yet display a recurring distribution of genomic imbalances that is similar to human breast cancer
-
Weaver Z, Montagna C, Xu X, et al. Mammary tumors in mice conditionally mutant for Brca1 exhibit gross genomic instability and centrosome ampli-fication yet display a recurring distribution of genomic imbalances that is similar to human breast cancer. Oncogene. 2002;21:5097-5107.
-
(2002)
Oncogene
, vol.21
, pp. 5097-5107
-
-
Weaver, Z.1
Montagna, C.2
Xu, X.3
-
30
-
-
38049133119
-
BRCA2: Safeguarding the genome through homologous recombination
-
Rothstein R, ed, Berlin: Springer;
-
Christ N, Moynahan ME, Jasin M. BRCA2: safeguarding the genome through homologous recombination. In: Rothstein R, ed. Molecular Genetics of Recombination. Berlin: Springer; 2007:363-380.
-
(2007)
Molecular Genetics of Recombination
, pp. 363-380
-
-
Christ, N.1
Moynahan, M.E.2
Jasin, M.3
-
31
-
-
0037115915
-
The cancer connection: BRCA1 and BRCA2 tumor suppression in mice and humans
-
Moynahan ME. The cancer connection: BRCA1 and BRCA2 tumor suppression in mice and humans. Oncogene. 2002;21:8994-9007.
-
(2002)
Oncogene
, vol.21
, pp. 8994-9007
-
-
Moynahan, M.E.1
-
32
-
-
34249878748
-
Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2
-
Esashi F, Galkin VE, Yu X, et al. Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2. Nat Struct Mol Biol. 2007; 14:468-474.
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 468-474
-
-
Esashi, F.1
Galkin, V.E.2
Yu, X.3
-
33
-
-
0037375905
-
Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice
-
Donoho G, Brenneman MA, Cui TX, et al. Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice. Genes Chromosomes Cancer. 2003;36:317-331.
-
(2003)
Genes Chromosomes Cancer
, vol.36
, pp. 317-331
-
-
Donoho, G.1
Brenneman, M.A.2
Cui, T.X.3
-
34
-
-
0036174445
-
Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene
-
McAllister KA, Bennett LM, Houle CD, et al. Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene. Cancer Res. 2002;62:990-994.
-
(2002)
Cancer Res
, vol.62
, pp. 990-994
-
-
McAllister, K.A.1
Bennett, L.M.2
Houle, C.D.3
-
35
-
-
15844373362
-
CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair
-
Esashi F, Christ N, Gannon J, et al. CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair. Nature. 2005;434:598-604.
-
(2005)
Nature
, vol.434
, pp. 598-604
-
-
Esashi, F.1
Christ, N.2
Gannon, J.3
-
36
-
-
18544372595
-
BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure
-
Yang H, Jeffrey PD, Miller J, et al. BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. Science. 2002;297: 1837-1848.
-
(2002)
Science
, vol.297
, pp. 1837-1848
-
-
Yang, H.1
Jeffrey, P.D.2
Miller, J.3
-
37
-
-
33745018564
-
Suppression of the DNA repair defects of BRCA2-deficient cells with heterologous protein fusions
-
Saeki H, Siaud N, Christ N, et al. Suppression of the DNA repair defects of BRCA2-deficient cells with heterologous protein fusions. Proc Natl Acad Sci USA. 2006;103:8768-8773.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 8768-8773
-
-
Saeki, H.1
Siaud, N.2
Christ, N.3
-
38
-
-
0031031787
-
From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair
-
Callebaut I, Mornon JP. From BRCA1 to RAP1: a widespread BRCT module closely associated with DNA repair. FEBS Lett. 1997;400:25-30.
-
(1997)
FEBS Lett
, vol.400
, pp. 25-30
-
-
Callebaut, I.1
Mornon, J.P.2
-
39
-
-
0030187780
-
BRCA1 protein products. Functional motifs
-
Koonin EV, Altschul SF, Bork P. BRCA1 protein products. Functional motifs. Nat Genet. 1996;13:266-268.
-
(1996)
Nat Genet
, vol.13
, pp. 266-268
-
-
Koonin, E.V.1
Altschul, S.F.2
Bork, P.3
-
40
-
-
6344287454
-
Interactions between BRCT repeats and phosphoproteins: Tangled up in two
-
Glover JN, Williams RS, Lee MS. Interactions between BRCT repeats and phosphoproteins: tangled up in two. Trends Biochem Sci. 2004;29:579-585.
-
(2004)
Trends Biochem Sci
, vol.29
, pp. 579-585
-
-
Glover, J.N.1
Williams, R.S.2
Lee, M.S.3
-
41
-
-
0034809456
-
Crystal structure of the BRCT repeat region from the breast cancer-associated protein BRCA1
-
Williams RS, Green R, Glover JN. Crystal structure of the BRCT repeat region from the breast cancer-associated protein BRCA1. Nat Struct Biol. 2001;8:838-842.
-
(2001)
Nat Struct Biol
, vol.8
, pp. 838-842
-
-
Williams, R.S.1
Green, R.2
Glover, J.N.3
-
42
-
-
0142147272
-
The BRCT domain is a phospho-protein binding domain
-
Yu X, Chini CC, He M, et al. The BRCT domain is a phospho-protein binding domain. Science. 2003;302:639-642.
-
(2003)
Science
, vol.302
, pp. 639-642
-
-
Yu, X.1
Chini, C.C.2
He, M.3
-
43
-
-
34249946686
-
Abraxas and RAP80 form a BRCA1 protein complex required for the DNA damage response
-
Wang B, Matsuoka S, Ballif BA, et al. Abraxas and RAP80 form a BRCA1 protein complex required for the DNA damage response. Science. 2007;316: 1194-1198.
-
(2007)
Science
, vol.316
, pp. 1194-1198
-
-
Wang, B.1
Matsuoka, S.2
Ballif, B.A.3
-
44
-
-
36749025467
-
Ubc13/Rnf8 ubiquitin ligases control foci formation of the Rap80/Abraxas/Brca1/Brcc36 complex in response to DNA damage
-
Wang B, Elledge SJ. Ubc13/Rnf8 ubiquitin ligases control foci formation of the Rap80/Abraxas/Brca1/Brcc36 complex in response to DNA damage. Proc Natl Acad Sci USA. 2007;104:20759-20763.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 20759-20763
-
-
Wang, B.1
Elledge, S.J.2
-
45
-
-
34748890424
-
Activation of BRCA1/BRCA2-associated helicase BACH1 is required for timely progression through S phase
-
Kumaraswamy E, Shiekhattar R. Activation of BRCA1/BRCA2-associated helicase BACH1 is required for timely progression through S phase. Mol Cell Biol. 2007;27:6733-6741.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 6733-6741
-
-
Kumaraswamy, E.1
Shiekhattar, R.2
-
46
-
-
33745614048
-
BRCA1 ubiquitinates its phosphorylationdependent binding partner CtIP
-
Yu X, Fu S, Lai M, et al. BRCA1 ubiquitinates its phosphorylationdependent binding partner CtIP. Genes Dev. 2006;20:1721-1726.
-
(2006)
Genes Dev
, vol.20
, pp. 1721-1726
-
-
Yu, X.1
Fu, S.2
Lai, M.3
-
47
-
-
36549060102
-
Human CtIP promotes DNA end resection
-
Sartori AA, Lukas C, Coates J, et al. Human CtIP promotes DNA end resection. Nature. 2007;450:509-514.
-
(2007)
Nature
, vol.450
, pp. 509-514
-
-
Sartori, A.A.1
Lukas, C.2
Coates, J.3
-
48
-
-
44949114282
-
FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability
-
Wu Y, Shin-ya K, Brosh RM Jr. FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability. Mol Cell Biol. 2008;28:4116-4128.
-
(2008)
Mol Cell Biol
, vol.28
, pp. 4116-4128
-
-
Wu, Y.1
Shin-ya, K.2
Brosh Jr., R.M.3
-
49
-
-
0033400828
-
Genetic analysis of BRCA1 function in a defined tumor cell line
-
Scully R, Ganesan S, Vlasakova K, et al. Genetic analysis of BRCA1 function in a defined tumor cell line. Mol Cell. 1999;4:1093-1099.
-
(1999)
Mol Cell
, vol.4
, pp. 1093-1099
-
-
Scully, R.1
Ganesan, S.2
Vlasakova, K.3
-
50
-
-
66349096607
-
PALB2 is an integral component of the BRCA complex required for homologous recombination repair
-
Sy SM, Huen MS, Chen J. PALB2 is an integral component of the BRCA complex required for homologous recombination repair. Proc Natl Acad Sci USA. 2009;106:7155-7160.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 7155-7160
-
-
Sy, S.M.1
Huen, M.S.2
Chen, J.3
-
51
-
-
3142608985
-
Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains
-
Botuyan MV, Nomine Y, Yu X, et al. Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains. Structure. 2004;12:1137-1146.
-
(2004)
Structure
, vol.12
, pp. 1137-1146
-
-
Botuyan, M.V.1
Nomine, Y.2
Yu, X.3
-
52
-
-
2542489188
-
Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer
-
Clapperton JA, Manke IA, Lowery DM, et al. Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer. Nat Struct Mol Biol. 2004;11:512-518.
-
(2004)
Nat Struct Mol Biol
, vol.11
, pp. 512-518
-
-
Clapperton, J.A.1
Manke, I.A.2
Lowery, D.M.3
-
53
-
-
45749087347
-
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: A multi-modal approach
-
Tischkowitz M, Hamel N, Carvalho MA, et al. Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach. Eur J Hum Genet. 2008;16:820-832.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 820-832
-
-
Tischkowitz, M.1
Hamel, N.2
Carvalho, M.A.3
-
54
-
-
20644461718
-
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
-
Cantor SB, Bell DW, Ganesan S, et al. BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell. 2001;105:149-160.
-
(2001)
Cell
, vol.105
, pp. 149-160
-
-
Cantor, S.B.1
Bell, D.W.2
Ganesan, S.3
-
55
-
-
24944575242
-
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ
-
Litman R, Peng M, Jin Z, et al. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell. 2005;8:255-265.
-
(2005)
Cancer Cell
, vol.8
, pp. 255-265
-
-
Litman, R.1
Peng, M.2
Jin, Z.3
-
56
-
-
33745407668
-
Homologous recombination is required for genome stability in the absence of DOG-1 in Caenorhabditis elegans
-
Youds JL, O'Neil NJ, Rose AM. Homologous recombination is required for genome stability in the absence of DOG-1 in Caenorhabditis elegans. Genetics. 2006;173:697-708.
-
(2006)
Genetics
, vol.173
, pp. 697-708
-
-
Youds, J.L.1
O'Neil, N.J.2
Rose, A.M.3
-
57
-
-
33748519569
-
Gene function correlates with potential for G4 DNA formation in the human genome
-
Eddy J, Maizels N. Gene function correlates with potential for G4 DNA formation in the human genome. Nucleic Acids Res. 2006;34:3887-3896.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 3887-3896
-
-
Eddy, J.1
Maizels, N.2
-
58
-
-
53149127633
-
Spectrum of mutational events in the absence of DOG-1/FANCJ in Caenorhabditis elegans
-
Zhao Y, Tarailo-Graovac M, O'Neil NJ, et al. Spectrum of mutational events in the absence of DOG-1/FANCJ in Caenorhabditis elegans. DNA Repair (Amst). 2008;7:1846-1854.
-
(2008)
DNA Repair (Amst)
, vol.7
, pp. 1846-1854
-
-
Zhao, Y.1
Tarailo-Graovac, M.2
O'Neil, N.J.3
-
59
-
-
1442281478
-
The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations
-
Cantor S, Drapkin R, Zhang F, et al. The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations. Proc Natl Acad Sci USA. 2004;101:2357-2362.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 2357-2362
-
-
Cantor, S.1
Drapkin, R.2
Zhang, F.3
-
60
-
-
65549113446
-
FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchange
-
Sommers JA, Rawtani N, Gupta R, et al. FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchange. J Biol Chem. 2009;284:7505-7517.
-
(2009)
J Biol Chem
, vol.284
, pp. 7505-7517
-
-
Sommers, J.A.1
Rawtani, N.2
Gupta, R.3
-
61
-
-
47049108873
-
Expression of the BRCA1-interacting protein Brip1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy
-
Eelen G, Vanden Bempt I, Verlinden L, et al. Expression of the BRCA1-interacting protein Brip1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy. Oncogene. 2008;27:4233-4241.
-
(2008)
Oncogene
, vol.27
, pp. 4233-4241
-
-
Eelen, G.1
Vanden Bempt, I.2
Verlinden, L.3
-
62
-
-
43149118369
-
Cell cycle-dependent complex formation of BRCA1.CtIP.MRN is important for DNA double-strand break repair
-
Chen L, Nievera CJ, Lee AY, et al. Cell cycle-dependent complex formation of BRCA1.CtIP.MRN is important for DNA double-strand break repair. J Biol Chem. 2008;283:7713-7720.
-
(2008)
J Biol Chem
, vol.283
, pp. 7713-7720
-
-
Chen, L.1
Nievera, C.J.2
Lee, A.Y.3
-
63
-
-
67349246802
-
CtIP-BRCA1 modulates the choice of DNA doublestrand-break repair pathway throughout the cell cycle
-
Yun MH, Hiom K. CtIP-BRCA1 modulates the choice of DNA doublestrand-break repair pathway throughout the cell cycle. Nature. 2009;459: 460-463.
-
(2009)
Nature
, vol.459
, pp. 460-463
-
-
Yun, M.H.1
Hiom, K.2
-
64
-
-
17644375501
-
Inactivation of CtIP leads to early embryonic lethality mediated by G1 restraint and to tumorigenesis by haploid insuffi-ciency
-
Chen PL, Liu F, Cai S, et al. Inactivation of CtIP leads to early embryonic lethality mediated by G1 restraint and to tumorigenesis by haploid insuffi-ciency. Mol Cell Biol. 2005;25:3535-3542.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 3535-3542
-
-
Chen, P.L.1
Liu, F.2
Cai, S.3
-
65
-
-
33745200945
-
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2
-
Xia B, Sheng Q, Nakanishi K, et al. Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. Mol Cell. 2006;22:719-729.
-
(2006)
Mol Cell
, vol.22
, pp. 719-729
-
-
Xia, B.1
Sheng, Q.2
Nakanishi, K.3
-
66
-
-
49149115625
-
Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2
-
Kuznetsov SG, Liu P, Sharan SK. Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2. Nat Med. 2008;14:875-881.
-
(2008)
Nat Med
, vol.14
, pp. 875-881
-
-
Kuznetsov, S.G.1
Liu, P.2
Sharan, S.K.3
-
67
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
Reid S, Schindler D, Hanenberg H, et al. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet. 2007;39:162-164.
-
(2007)
Nat Genet
, vol.39
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
-
68
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
Xia B, Dorsman JC, Ameziane N, et al. Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet. 2007;39:159-161.
-
(2007)
Nat Genet
, vol.39
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
-
69
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
Rahman N, Seal S, Thompson D, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet. 2007; 39:165-167.
-
(2007)
Nat Genet
, vol.39
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
-
70
-
-
69949169651
-
Structural basis for recruitment of BRCA2 by PALB2
-
2009;10:990-996
-
Oliver AW, Swift S, Lord CJ, et al. Structural basis for recruitment of BRCA2 by PALB2. EMBO Rep. 2009;10:990-996.
-
EMBO Rep
-
-
Oliver, A.W.1
Swift, S.2
Lord, C.J.3
-
71
-
-
67651166786
-
PALB2 functionally connects the breast cancer susceptibility proteins BRCA1 and BRCA2
-
Zhang F, Fan Q, Ren K, et al. PALB2 functionally connects the breast cancer susceptibility proteins BRCA1 and BRCA2. Mol Cancer Res. 2009; 7:1110-1118.
-
(2009)
Mol Cancer Res
, vol.7
, pp. 1110-1118
-
-
Zhang, F.1
Fan, Q.2
Ren, K.3
-
72
-
-
62549115236
-
PALB2 links BRCA1 and BRCA2 in the DNA-damage response
-
Zhang F, Ma J, Wu J, et al. PALB2 links BRCA1 and BRCA2 in the DNA-damage response. Curr Biol. 2009;19:524-529.
-
(2009)
Curr Biol
, vol.19
, pp. 524-529
-
-
Zhang, F.1
Ma, J.2
Wu, J.3
-
73
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
Howlett NG, Taniguchi T, Olson S, et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science. 2002;297:606-609.
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
-
74
-
-
33846415079
-
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2
-
Alter BP, Rosenberg PS, Brody LC. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. J Med Genet. 2007;44:1-9.
-
(2007)
J Med Genet
, vol.44
, pp. 1-9
-
-
Alter, B.P.1
Rosenberg, P.S.2
Brody, L.C.3
-
75
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
Levran O, Attwooll C, Henry RT, et al. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat Genet. 2005;37:931-933.
-
(2005)
Nat Genet
, vol.37
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
-
76
-
-
34548759123
-
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
-
Wang W. Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins. Nat Rev Genet. 2007;8:735-748.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 735-748
-
-
Wang, W.1
-
77
-
-
69749106825
-
Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication
-
Shen X, Do H, Li Y, et al. Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication. Mol Cell. 2009;35:716-723.
-
(2009)
Mol Cell
, vol.35
, pp. 716-723
-
-
Shen, X.1
Do, H.2
Li, Y.3
-
78
-
-
0038744296
-
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: A combined analysis of 22 studies
-
Antoniou A, Pharoah PD, Narod S, et al. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet. 2003;72:1117-1130.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.D.2
Narod, S.3
-
79
-
-
33750465216
-
-
Seal S, Thompson D, Renwick A, et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006;38:1239-1241.
-
Seal S, Thompson D, Renwick A, et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006;38:1239-1241.
-
-
-
-
80
-
-
51649092869
-
Penetrance analysis of the PALB2 c. 1592delT founder mutation
-
Erkko H, Dowty JG, Nikkila J, et al. Penetrance analysis of the PALB2 c. 1592delT founder mutation. Clin Cancer Res. 2008;14:4667-4671.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 4667-4671
-
-
Erkko, H.1
Dowty, J.G.2
Nikkila, J.3
-
81
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
Erkko H, Xia B, Nikkila J, et al. A recurrent mutation in PALB2 in Finnish cancer families. Nature. 2007;446:316-319.
-
(2007)
Nature
, vol.446
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
-
82
-
-
52049086689
-
Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer
-
Atchley DP, Albarracin CT, Lopez A, et al. Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer. J Clin Oncol. 2008;26:4282-4288.
-
(2008)
J Clin Oncol
, vol.26
, pp. 4282-4288
-
-
Atchley, D.P.1
Albarracin, C.T.2
Lopez, A.3
-
83
-
-
0141429017
-
Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer
-
Foulkes WD, Stefansson IM, Chappuis PO, et al. Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. J Natl Cancer Inst. 2003;95:1482-1485.
-
(2003)
J Natl Cancer Inst
, vol.95
, pp. 1482-1485
-
-
Foulkes, W.D.1
Stefansson, I.M.2
Chappuis, P.O.3
-
84
-
-
2442614103
-
Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer
-
author reply 714
-
Palacios J, Honrado E, Osorio A, et al. Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. J Natl Cancer Inst. 2004;96: 712-714; author reply 714.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 712-714
-
-
Palacios, J.1
Honrado, E.2
Osorio, A.3
-
85
-
-
0032486752
-
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations
-
Lakhani SR, Jacquemier J, Sloane JP, et al. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J Natl Cancer Inst. 1998;90:1138-1145.
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 1138-1145
-
-
Lakhani, S.R.1
Jacquemier, J.2
Sloane, J.P.3
-
86
-
-
30944450821
-
Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma
-
Livasy CA, Karaca G, Nanda R, et al. Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma. Mod Pathol. 2006;19:264-271.
-
(2006)
Mod Pathol
, vol.19
, pp. 264-271
-
-
Livasy, C.A.1
Karaca, G.2
Nanda, R.3
-
87
-
-
33845953365
-
BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays
-
Bane AL, Beck JC, Bleiweiss I, et al. BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays. Am J Surg Pathol. 2007;31:121-128.
-
(2007)
Am J Surg Pathol
, vol.31
, pp. 121-128
-
-
Bane, A.L.1
Beck, J.C.2
Bleiweiss, I.3
-
88
-
-
34249857115
-
Analysis of PALB2/FANCNassociated breast cancer families
-
Tischkowitz M, Xia B, Sabbaghian N, et al. Analysis of PALB2/FANCNassociated breast cancer families. Proc Natl Acad Sci USA. 2007;104:6788-6793.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 6788-6793
-
-
Tischkowitz, M.1
Xia, B.2
Sabbaghian, N.3
-
89
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
Heikkinen T, Karkkainen H, Aaltonen K, et al. The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res. 2009;15:3214-3222.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 3214-3222
-
-
Heikkinen, T.1
Karkkainen, H.2
Aaltonen, K.3
-
90
-
-
58549086980
-
Analysis of FANCB and FANCN/ PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families
-
Garcia MJ, Fernandez V, Osorio A, et al. Analysis of FANCB and FANCN/ PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families. Breast Cancer Res Treat. 2009;113:545-551.
-
(2009)
Breast Cancer Res Treat
, vol.113
, pp. 545-551
-
-
Garcia, M.J.1
Fernandez, V.2
Osorio, A.3
-
91
-
-
61449204036
-
The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives
-
Cao AY, Huang J, Hu Z, et al. The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives. Breast Cancer Res Treat. 2009;114:457-462.
-
(2009)
Breast Cancer Res Treat
, vol.114
, pp. 457-462
-
-
Cao, A.Y.1
Huang, J.2
Hu, Z.3
-
92
-
-
40349111045
-
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women
-
Foulkes WD, Ghadirian P, Akbari MR, et al. Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women. Breast Cancer Res. 2007;9:R83.
-
(2007)
Breast Cancer Res
, vol.9
-
-
Foulkes, W.D.1
Ghadirian, P.2
Akbari, M.R.3
-
93
-
-
70449523582
-
PALB2 sequence variants in young South African breast cancer patients
-
Sluiter M, Mew S, van Rensburg EJ. PALB2 sequence variants in young South African breast cancer patients. Fam Cancer. 2009;8:347-353.
-
(2009)
Fam Cancer
, vol.8
, pp. 347-353
-
-
Sluiter, M.1
Mew, S.2
van Rensburg, E.J.3
-
94
-
-
51649108664
-
A novel breast cancerassociated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function
-
De Nicolo A, Tancredi M, Lombardi G, et al. A novel breast cancerassociated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function. Clin Cancer Res. 2008;14:4672-4680.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 4672-4680
-
-
De Nicolo, A.1
Tancredi, M.2
Lombardi, G.3
-
95
-
-
34447619477
-
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
-
Lewis AG, Flanagan J, Marsh A, et al. Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer. Breast Cancer Res. 2005;7:R1005-R1016.
-
(2005)
Breast Cancer Res
, vol.7
-
-
Lewis, A.G.1
Flanagan, J.2
Marsh, A.3
-
96
-
-
77951296890
-
Evaluation of variants in the CHEK2, BRIP1 and PALB2 genes in an Irish breast cancer cohort
-
September 18, doi:10.1007/s10549-009-0540-9. Available at
-
McInerney NM, Miller N, Rowan A, et al. Evaluation of variants in the CHEK2, BRIP1 and PALB2 genes in an Irish breast cancer cohort. Breast Cancer Res Treat. September 18, 2009. doi:10.1007/s10549-009-0540-9. Available at: http://www.springerlink.com/content/j606225875814430/.
-
(2009)
Breast Cancer Res Treat
-
-
McInerney, N.M.1
Miller, N.2
Rowan, A.3
-
97
-
-
36448996703
-
Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations
-
Fackenthal JD, Olopade OI. Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations. Nat Rev Cancer. 2007;7:937-948.
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 937-948
-
-
Fackenthal, J.D.1
Olopade, O.I.2
-
98
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium
-
Ford D, Easton DF, Stratton M, et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Am J Hum Genet. 1998;62:676-689.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
99
-
-
37549056200
-
The emerging landscape of breast cancer susceptibility
-
Stratton MR, Rahman N. The emerging landscape of breast cancer susceptibility. Nat Genet. 2008;40:17-22.
-
(2008)
Nat Genet
, vol.40
, pp. 17-22
-
-
Stratton, M.R.1
Rahman, N.2
-
100
-
-
4544374528
-
BRCA1 and BRCA2:1994 and beyond
-
Narod SA, Foulkes WD. BRCA1 and BRCA2:1994 and beyond. Nat Rev Cancer. 2004;4:665-676.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 665-676
-
-
Narod, S.A.1
Foulkes, W.D.2
-
101
-
-
21144436491
-
Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families
-
Hendrickson BC, Judkins T, Ward BD, et al. Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families. Genes Chromosomes Cancer. 2005;43:309-313.
-
(2005)
Genes Chromosomes Cancer
, vol.43
, pp. 309-313
-
-
Hendrickson, B.C.1
Judkins, T.2
Ward, B.D.3
-
103
-
-
33645084562
-
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
-
Walsh T, Casadei S, Coats KH, et al. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. JAMA. 2006;295:1379-1388.
-
(2006)
JAMA
, vol.295
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.H.3
-
104
-
-
42049084015
-
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH)
-
Staaf J, Torngren T, Rambech E, et al. Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH). Hum Mutat. 2008;29:555-564.
-
(2008)
Hum Mutat
, vol.29
, pp. 555-564
-
-
Staaf, J.1
Torngren, T.2
Rambech, E.3
-
105
-
-
77149166044
-
-
on-line breast cancer mutation data base. Available at
-
National Human Genome Research Institute. An open access on-line breast cancer mutation data base. Available at: http://research.nhgri.nih.gov/bic/.
-
An open access
-
-
-
106
-
-
70349696230
-
Expression of human BRCA1 variants in mouse ES cells allows functional analysis of BRCA1 mutations
-
Chang S, Biswas K, Martin BK, et al. Expression of human BRCA1 variants in mouse ES cells allows functional analysis of BRCA1 mutations. J Clin Invest. 2009;119:3160-3171.
-
(2009)
J Clin Invest
, vol.119
, pp. 3160-3171
-
-
Chang, S.1
Biswas, K.2
Martin, B.K.3
-
107
-
-
0028073794
-
BRCA1 mutations in primary breast and ovarian carcinomas
-
Futreal PA, Liu Q, Shattuck-Eidens D, et al. BRCA1 mutations in primary breast and ovarian carcinomas. Science. 1994;266:120-122.
-
(1994)
Science
, vol.266
, pp. 120-122
-
-
Futreal, P.A.1
Liu, Q.2
Shattuck-Eidens, D.3
-
108
-
-
0034607234
-
Promoter hypermethylation and BRCA1 inactivation in sporadic breast and ovarian tumors
-
Esteller M, Silva JM, Dominguez G, et al. Promoter hypermethylation and BRCA1 inactivation in sporadic breast and ovarian tumors. J Natl Cancer Inst. 2000;92:564-569.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 564-569
-
-
Esteller, M.1
Silva, J.M.2
Dominguez, G.3
-
109
-
-
18844410329
-
BRCA1 promoter methylation in sporadic breast tumors: Relationship to gene expression profiles
-
Matros E, Wang ZC, Lodeiro G, et al. BRCA1 promoter methylation in sporadic breast tumors: relationship to gene expression profiles. Breast Cancer Res Treat. 2005;91:179-186.
-
(2005)
Breast Cancer Res Treat
, vol.91
, pp. 179-186
-
-
Matros, E.1
Wang, Z.C.2
Lodeiro, G.3
-
110
-
-
33847022042
-
BRCA1 dysfunction in sporadic basal-like breast cancer
-
Turner NC, Reis-Filho JS, Russell AM, et al. BRCA1 dysfunction in sporadic basal-like breast cancer. Oncogene. 2007;26:2126-2132.
-
(2007)
Oncogene
, vol.26
, pp. 2126-2132
-
-
Turner, N.C.1
Reis-Filho, J.S.2
Russell, A.M.3
-
111
-
-
18744372123
-
BRCA1 supports XIST RNA concentration on the inactive X chromosome
-
Ganesan S, Silver DP, Greenberg RA, et al. BRCA1 supports XIST RNA concentration on the inactive X chromosome. Cell. 2002;111:393-405.
-
(2002)
Cell
, vol.111
, pp. 393-405
-
-
Ganesan, S.1
Silver, D.P.2
Greenberg, R.A.3
-
112
-
-
32044453343
-
X chromosomal abnormalities in basal-like human breast cancer
-
Richardson AL, Wang ZC, De Nicolo A, et al. X chromosomal abnormalities in basal-like human breast cancer. Cancer Cell. 2006;9:121-132.
-
(2006)
Cancer Cell
, vol.9
, pp. 121-132
-
-
Richardson, A.L.1
Wang, Z.C.2
De Nicolo, A.3
-
113
-
-
0035793052
-
Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approach
-
Beger C, Pierce LN, Kruger M, et al. Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approach. Proc Natl Acad Sci USA. 2001;98:130-135.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 130-135
-
-
Beger, C.1
Pierce, L.N.2
Kruger, M.3
-
114
-
-
39449107433
-
Promoter hypermethylation of the PALB2 susceptibility gene in inherited and sporadic breast and ovarian cancer
-
Potapova A, Hoffman AM, Godwin AK, et al. Promoter hypermethylation of the PALB2 susceptibility gene in inherited and sporadic breast and ovarian cancer. Cancer Res. 2008;68:998-1002.
-
(2008)
Cancer Res
, vol.68
, pp. 998-1002
-
-
Potapova, A.1
Hoffman, A.M.2
Godwin, A.K.3
-
115
-
-
24744468647
-
Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization
-
Jonsson G, Naylor TL, Vallon-Christersson J, et al. Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization. Cancer Res. 2005;65:7612-7621.
-
(2005)
Cancer Res
, vol.65
, pp. 7612-7621
-
-
Jonsson, G.1
Naylor, T.L.2
Vallon-Christersson, J.3
-
116
-
-
13444292834
-
Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations
-
van Beers EH, van Welsem T, Wessels LF, et al. Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations. Cancer Res. 2005;65:822-827.
-
(2005)
Cancer Res
, vol.65
, pp. 822-827
-
-
van Beers, E.H.1
van Welsem, T.2
Wessels, L.F.3
-
117
-
-
77149179427
-
Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes
-
Stefansson OA, Jonasson JG, Johannsson OT, et al. Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes. Breast Cancer Res. 2009;11:R47.
-
(2009)
Breast Cancer Res
, vol.11
-
-
Stefansson, O.A.1
Jonasson, J.G.2
Johannsson, O.T.3
-
118
-
-
6344234817
-
Genetic steps of mammalian homologous repair with distinct mutagenic consequences
-
Stark JM, Pierce AJ, Oh J, et al. Genetic steps of mammalian homologous repair with distinct mutagenic consequences. Mol Cell Biol. 2004;24:9305-9316.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 9305-9316
-
-
Stark, J.M.1
Pierce, A.J.2
Oh, J.3
-
119
-
-
10744233204
-
EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer
-
Hughes-Davies L, Huntsman D, Ruas M, et al. EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer. Cell. 2003;115:523-535.
-
(2003)
Cell
, vol.115
, pp. 523-535
-
-
Hughes-Davies, L.1
Huntsman, D.2
Ruas, M.3
-
120
-
-
24744443338
-
Genomic instability of human mammary epithelial cells overexpressing a truncated form of EMSY
-
Raouf A, Brown L, Vrcelj N, et al. Genomic instability of human mammary epithelial cells overexpressing a truncated form of EMSY. J Natl Cancer Inst. 2005;97:1302-1306.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 1302-1306
-
-
Raouf, A.1
Brown, L.2
Vrcelj, N.3
|