-
1
-
-
0342940785
-
Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2mutations and sporadic cases
-
Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2mutations and sporadic cases. Breast Cancer Linkage Consortium. Lancet 349, 1505-1510 (1997)
-
(1997)
Breast Cancer Linkage Consortium. Lancet
, vol.349
, pp. 1505-1510
-
-
-
2
-
-
0033740880
-
Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases
-
Anglian Breast Cancer Study Group
-
Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group. Br. J. Cancer 83, 1301-1308 (2000)
-
(2000)
Br. J. Cancer
, vol.83
, pp. 1301-1308
-
-
-
3
-
-
3342996598
-
ERBB2, TBX2, RPS6KB1, and MYC alterations in breast tissues of BRCA1 and BRCA2 mutation carriers
-
DOI 10.1002/gcc.20057
-
C. Adem, C.L. Soderberg, K. Hafner, C. Reynolds, J.M. Slezak, C.S. Sinclair, T.A. Sellers, D.J. Schaid, F. Couch, L.C. Hartmann, R.B. Jenkins, ERBB2, TBX2, RPS6KB1, and MYC alterations in breast tissues of BRCA1 and BRCA2 mutation carriers. Genes Chromosom. Cancer 41, 1-11 (2004) (Pubitemid 38988733)
-
(2004)
Genes Chromosomes and Cancer
, vol.41
, Issue.1
, pp. 1-11
-
-
Adem, C.1
Soderberg, C.L.2
Hafner, K.3
Reynolds, C.4
Slezak, J.M.5
Sinclair, C.S.6
Sellers, T.A.7
Schaid, D.J.8
Couch, F.9
Hartmann, L.C.10
Jenkins, R.B.11
-
4
-
-
0031983839
-
Inherited BRCA2 mutation associated with high grade breast cancer
-
DOI 10.1023/A:1005853022804
-
B.A. Agnarsson, J.G. Jonasson, I.B. Bjornsdottir, R.B. Barkardottir, V. Egilsson, H. Sigurdsson, Inherited BRCA2 mutation associated with high grade breast cancer. Breast Cancer Res. Treat. 47, 121- 127 (1998) (Pubitemid 28046083)
-
(1998)
Breast Cancer Research and Treatment
, vol.47
, Issue.2
, pp. 121-127
-
-
Agnarsson, B.A.1
Jonasson, J.G.2
Bjornsdottir, I.B.3
Barkardottir, R.B.4
Egilsson, V.5
Sigurdsson, H.6
-
5
-
-
0034940858
-
Mutation analysis of the CHK2 gene in families with hereditary breast cancer
-
DOI 10.1054/bjoc.2001.1858
-
M. Allinen, P. Huusko, S. Mantyniemi, V. Launonen, R. Winqvist, Mutation analysis of the CHK2 gene in families with hereditary breast cancer. Br. J. Cancer 85, 209-212 (2001) (Pubitemid 32695741)
-
(2001)
British Journal of Cancer
, vol.85
, Issue.2
, pp. 209-212
-
-
Allinen, M.1
Huusko, P.2
Mantyniemi, S.3
Launonen, V.4
Winqvist, R.5
-
6
-
-
0033766175
-
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
-
J. Alsner, M. Yilmaz, P. Guldberg, L.L. Hansen, J. Overgaard, Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients. Clin. Cancer Res. 6, 3923-3931 (2000)
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 3923-3931
-
-
Alsner, J.1
Yilmaz, M.2
Guldberg, P.3
Hansen, L.L.4
Overgaard, J.5
-
7
-
-
0029812426
-
A common BRCA1 mutation in Norwegian breast and ovarian cancer families? [7]
-
T.I. Andersen, A.L. Borresen, P. Moller, A common BRCA1 mutation in Norwegian breast and ovarian cancer families? Am. J. Hum. Genet. 59, 486-487 (1996) (Pubitemid 26266372)
-
(1996)
American Journal of Human Genetics
, vol.59
, Issue.2
, pp. 486-487
-
-
Andersen, T.I.1
Borresen, A.-L.2
Moller, P.3
-
8
-
-
33749002551
-
Models of genetic susceptibility to breast cancer
-
DOI 10.1038/sj.onc.1209879, PII 1209879
-
A.C. Antoniou, D.F. Easton, Models of genetic susceptibility to breast cancer. Oncogene 25, 5898-5905 (2006) (Pubitemid 44453445)
-
(2006)
Oncogene
, vol.25
, Issue.43
, pp. 5898-5905
-
-
Antoniou, A.C.1
Easton, D.F.2
-
9
-
-
22244467729
-
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: A combined analysis of 22 population based studies
-
DOI 10.1136/jmg.2004.024133
-
A.C. Antoniou, P.D. Pharoah, S. Narod, H.A. Risch, J.E. Eyfjord, J.L. Hopper, H. Olsson, O. Johannsson, A. Borg, B. Pasini, P. Radice, S. Manoukian, D.M. Eccles, N. Tang, E. Olah, H. Anton-Culver, E. Warner, J. Lubinski, J. Gronwald, B. Gorski, H. Tulinius, S. Thorlacius, H. Eerola, H. Nevanlinna, K. Syrjakoski, O.P. Kallioniemi, D. Thompson, C. Evans, J. Peto, F. Lalloo, D.G. Evans, D.F. Easton, Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: A combined analysis of 22 population based studies. J. Med. Genet. 42, 602-603 (2005) (Pubitemid 40993838)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.7
, pp. 602-603
-
-
Antoniou, A.C.1
Pharoah, P.D.P.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
Hopper, J.L.6
Olsson, H.7
Johannsson, O.8
Borg, A.9
Pasini, B.10
Radice, P.11
Manoukian, S.12
Eccles, D.M.13
Tang, N.14
Olah, E.15
Anton-Culver, H.16
Warner, E.17
Lubinski, J.18
Gronwald, J.19
Gorski, B.20
Tulinius, H.21
Thorlacius, S.22
Eerola, H.23
Nevanlinna, H.24
Syrjakoski, K.25
Kallioniemi, O.-P.26
Thompson, D.27
Evans, C.28
Peto, J.29
Lalloo, F.30
Evans, D.G.31
Easton, D.F.32
more..
-
10
-
-
0032400785
-
The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations: A population-based study
-
DOI 10.1002/(SICI)1097-0142(19981201)83:11<2335::AID-CNCR13>3.0. CO;2-N
-
J.E. Armes, A.J. Egan, M.C. Southey, G.S. Dite, M.R. McCredie, G.G. Giles, J.L. Hopper, D.J. Venter, The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations: A population-based study. Cancer 83, 2335-2345 (1998) (Pubitemid 28533503)
-
(1998)
Cancer
, vol.83
, Issue.11
, pp. 2335-2345
-
-
Armes, J.E.1
Egan, A.J.M.2
Southey, M.C.3
Dite, G.S.4
McCredie, M.R.E.5
Giles, G.G.6
Hopper, J.L.7
Venter, D.J.8
-
11
-
-
0033561620
-
Distinct molecular pathogeneses of early-onset breast cancers in BRCA1 and BRCA2 mutation carriers: A population-based study
-
J.E. Armes, L. Trute, D. White, M.C. Southey, F. Hammet, A. Tesoriero, A.M. Hutchins, G.S. Dite, M.R.McCredie, G.G. Giles, J. L. Hopper, D.J. Venter, Distinct molecular pathogeneses of earlyonset breast cancers in BRCA1 and BRCA2 mutation carriers: A population-based study. Cancer Res. 59, 2011-2017 (1999) (Pubitemid 29186179)
-
(1999)
Cancer Research
, vol.59
, Issue.8
, pp. 2011-2017
-
-
Armes, J.E.1
Trute, L.2
White, D.3
Southey, M.C.4
Hammel, F.5
Tesoriero, A.6
Hutchins, A.-M.7
Dite, G.S.8
McCredie, M.R.E.9
Giles, G.G.10
Hopper, J.L.11
Venter, D.J.12
-
12
-
-
20344377896
-
Placental cadherin and the basal epithelial phenotype of BRCA1-related breast cancer
-
DOI 10.1158/1078-0432.CCR-04-2064
-
J.B. Arnes, J.S. Brunet, I. Stefansson, L.R. Begin, N. Wong, P.O. Chappuis, L.A. Akslen, W.D. Foulkes, Placental cadherin and the basal epithelial phenotype of BRCA1-related breast cancer. Clin. Cancer Res. 11, 4003-4011 (2005) (Pubitemid 40791563)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.11
, pp. 4003-4011
-
-
Arnes, J.B.1
Brunet, J.-S.2
Stefansson, I.3
Begin, L.R.4
Wong, N.5
Chappuis, P.O.6
Akslen, L.A.7
Foulkes, W.D.8
-
13
-
-
63249089822
-
High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers
-
B. Arun, K.J. Vogel, A. Lopez, M. Hernandez, D. Atchley, K.R. Broglio, C.I. Amos, F. Meric-Bernstam, H. Kuerer, G.N. Hortobagyi, C.T. Albarracin, High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers. Cancer Prev. Res. (Phila. Pa.) 2, 122-127 (2009)
-
(2009)
Cancer Prev. Res. (Phila. Pa.)
, vol.2
, pp. 122-127
-
-
Arun, B.1
Vogel, K.J.2
Lopez, A.3
Hernandez, M.4
Atchley, D.5
Broglio, K.R.6
Amos, C.I.7
Kuerer, H.8
Hortobagyi, G.N.9
Albarracin, C.T.10
-
14
-
-
33845953365
-
BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays
-
DOI 10.1097/01.pas.0000213351.49767.0f, PII 0000047820070100000015
-
A.L. Bane, J.C. Beck, I. Bleiweiss, S.S. Buys, E. Catalano, M.B. Daly, G. Giles, A.K. Godwin, H. Hibshoosh, J.L. Hopper, E.M. John, L. Layfield, T. Longacre, A. Miron, R. Senie, M.C. Southey, D.W. West, A.S. Whittemore, H. Wu, I.L. Andrulis, F.P. O'Malley, BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays. Am. J. Surg. Pathol. 31, 121- 128 (2007) (Pubitemid 46036911)
-
(2007)
American Journal of Surgical Pathology
, vol.31
, Issue.1
, pp. 121-128
-
-
Bane, A.L.1
Beck, J.C.2
Bleiweiss, I.3
Buys, S.S.4
Catalano, E.5
Daly, M.B.6
Giles, G.7
Godwin, A.K.8
Hibshoosh, H.9
Hopper, J.L.10
John, E.M.11
Layfield, L.12
Longacre, T.13
Miron, A.14
Senie, R.15
Southey, M.C.16
West, D.W.17
Whittemore, A.S.18
Wu, H.19
Andrulis, I.L.20
O'Malley, F.P.21
more..
-
15
-
-
69049084367
-
Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors
-
A.L. Bane, D. Pinnaduwage, S. Colby, S.B. Bull, F.P. O'Malley, I.L. Andrulis, Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors. Breast Cancer Res. Treat. (2008)
-
(2008)
Breast Cancer Res. Treat.
-
-
Bane, A.L.1
Pinnaduwage, D.2
Colby, S.3
Bull, S.B.4
O'Malley, F.P.5
Andrulis, I.L.6
-
16
-
-
7144251883
-
The 185delAG BRCA1 mutation originated before the dispersion of Jews in the Diaspora and is not limited to Ashkenazim
-
DOI 10.1093/hmg/7.5.801
-
R.B. Bar-Sade, A. Kruglikova, B. Modan, E. Gak, G. Hirsh-Yechezkel, L. Theodor, I. Novikov, R. Gershoni-Baruch, S. Risel, M.Z. Papa, G. Ben-Baruch, E. Friedman, The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim. Hum. Mol. Genet. 7, 801-805 (1998) (Pubitemid 28221242)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.5
, pp. 801-805
-
-
Bruchim Bar-Sade, R.1
Kruglikova, A.2
Modan, B.3
Gak, E.4
Hirsh-Yechezkel, G.5
Theodor, L.6
Novikov, I.7
Gershoni-Baruch, R.8
Risel, S.9
Papa, M.Z.10
Ben-Baruch, G.11
Friedman, E.12
-
17
-
-
0027977943
-
E-cadherin gene mutations provide clues to diffuse type gastric carcinomas
-
K.F. Becker, M.J. Atkinson, U. Reich, I. Becker, H. Nekarda, J.R. Siewert, H. Hofler, E-cadherin gene mutations provide clues to diffuse type gastric carcinomas. Cancer Res. 54, 3845-3852 (1994) (Pubitemid 24241205)
-
(1994)
Cancer Research
, vol.54
, Issue.14
, pp. 3845-3852
-
-
Becker, K.-F.1
Atkinson, M.J.2
Reich, U.3
Becker, I.4
Nekarda, H.5
Siewert, J.R.6
Hofler, H.7
-
18
-
-
0033601346
-
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome
-
D.W. Bell, J.M. Varley, T.E. Szydlo, D.H. Kang, D.C. Wahrer, K. E. Shannon, M. Lubratovich, S.J. Verselis, K.J. Isselbacher, J.F. Fraumeni, J.M. Birch, F.P. Li, J.E. Garber, D.A. Haber, Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome. Science 286, 2528-2531 (1999)
-
(1999)
Science
, vol.286
, pp. 2528-2531
-
-
Bell, D.W.1
Varley, J.M.2
Szydlo, T.E.3
Kang, D.H.4
Wahrer, D.C.5
Shannon, K.E.6
Lubratovich, M.7
Verselis, S.J.8
Isselbacher, K.J.9
Fraumeni, J.F.10
Birch, J.M.11
Li, F.P.12
Garber, J.E.13
Haber, D.A.14
-
19
-
-
33745956231
-
Epigenetic silencing and deletion of the BRCA1 gene in sporadic breast cancer
-
V. Birgisdottir, O.A. Stefansson, S.K. Bodvarsdottir, H. Hilmarsdottir, J.G. Jonasson, J.E. Eyfjord, Epigenetic silencing and deletion of the BRCA1 gene in sporadic breast cancer. Breast Cancer Res. 8, R38 (2006)
-
(2006)
Breast Cancer Res.
, vol.8
-
-
Birgisdottir, V.1
Stefansson, O.A.2
Bodvarsdottir, S.K.3
Hilmarsdottir, H.4
Jonasson, J.G.5
Eyfjord, J.E.6
-
20
-
-
52949091170
-
NBS1 variant I171V and breast cancer risk
-
N. Bogdanova, P. Schurmann, R. Waltes, S. Feshchenko, I.V. Zalutsky, M. Bremer, T. Dork, NBS1 variant I171V and breast cancer risk. Breast Cancer Res. Treat. 112, 75-79 (2008)
-
(2008)
Breast Cancer Res. Treat.
, vol.112
, pp. 75-79
-
-
Bogdanova, N.1
Schurmann, P.2
Waltes, R.3
Feshchenko, S.4
Zalutsky, I.V.5
Bremer, M.6
Dork, T.7
-
21
-
-
0037443587
-
Levels of hypoxia-inducible factor-1α independently predict prognosis in patients with lymph node negative breast carcinoma
-
DOI 10.1002/cncr.11246
-
R. Bos, P. van der Groep, A.E. Greijer, A. Shvarts, S. Meijer, H. M. Pinedo, G.L. Semenza, P.J. van Diest, E. van der Wall, Levels of hypoxia-inducible factor-1alpha independently predict prognosis in patients with lymph node negative breast carcinoma. Cancer 97, 1573-1581 (2003) (Pubitemid 36297788)
-
(2003)
Cancer
, vol.97
, Issue.6
, pp. 1573-1581
-
-
Bos, R.1
Van Der Groep, P.2
Greijer, A.E.3
Shvarts, A.4
Meijer, S.5
Pinedo, H.M.6
Semenza, G.L.7
Van Diest, P.J.8
Van Der Wall, E.9
-
22
-
-
0035925072
-
Levels of hypoxia-inducible factor-1α during breast carcinogenesis
-
R. Bos, H. Zhong, C.F. Hanrahan, E.C. Mommers, G.L. Semenza, H.M. Pinedo, M.D. Abeloff, J.W. Simons, P.J. van Diest, E. van der Wall, Levels of hypoxia-inducible factor-1 alpha during breast carcinogenesis. J. Natl. Cancer Inst. 93, 309-314 (2001) (Pubitemid 32219818)
-
(2001)
Journal of the National Cancer Institute
, vol.93
, Issue.4
, pp. 309-314
-
-
Bos, R.1
Zhong, H.2
Hanrahan, C.F.3
Mommers, E.C.M.4
Semenza, G.L.5
Pinedo, H.M.6
Abeloff, M.D.7
Simons, J.W.8
Van Diest, P.J.9
Van Der Wall, E.10
-
23
-
-
33644700937
-
Survival and prognostic factors in BRCA1-associated breast cancer
-
DOI 10.1093/annonc/mdj095
-
C.T. Brekelmans, C. Seynaeve, M. Menke-Pluymers, H.T. Bruggenwirth, M.M. Tilanus-Linthorst, C.C. Bartels, M. Kriege, A.N. van Geel, C.M. Crepin, J.C. Blom, H. Meijers-Heijboer, J. G. Klijn, Survival and prognostic factors in BRCA1-associated breast cancer. Ann. Oncol. 17, 391-400 (2006) (Pubitemid 43329574)
-
(2006)
Annals of Oncology
, vol.17
, Issue.3
, pp. 391-400
-
-
Brekelmans, C.T.M.1
Seynaeve, C.2
Menke-Pluymers, M.3
Bruggenwirth, H.T.4
Tilanus-Linthorst, M.M.A.5
Bartels, C.C.M.6
Kriege, M.7
Van Geel, A.N.8
Crepin, C.M.G.9
Blom, J.C.10
Meijers-Heijboer, H.11
Klijn, J.G.M.12
-
25
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
-
DOI 10.1038/nature03443
-
H.E. Bryant, N. Schultz, H.D. Thomas, K.M. Parker, D. Flower, E. Lopez, S. Kyle, M. Meuth, N.J. Curtin, T. Helleday, Specific killing of BRCA2-deficient tumours with inhibitors of poly (ADP-ribose) polymerase. Nature 434, 913-917 (2005) (Pubitemid 40559005)
-
(2005)
Nature
, vol.434
, Issue.7035
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
Parker, K.M.4
Flower, D.5
Lopez, E.6
Kyle, S.7
Meuth, M.8
Curtin, N.J.9
Helleday, T.10
-
26
-
-
67349195962
-
Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients
-
T. Byrski, T. Huzarski, R. Dent, J. Gronwald, D. Zuziak, C. Cybulski, J. Kladny, B. Gorski, J. Lubinski, S.A. Narod, Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients. Breast Cancer Res. Treat. (2008)
-
(2008)
Breast Cancer Res. Treat.
-
-
Byrski, T.1
Huzarski, T.2
Dent, R.3
Gronwald, J.4
Zuziak, D.5
Cybulski, C.6
Kladny, J.7
Gorski, B.8
Lubinski, J.9
Narod, S.A.10
-
27
-
-
0031031787
-
From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair
-
DOI 10.1016/S0014-5793(96)01312-9, PII S0014579396013129
-
I. Callebaut, J.P. Mornon, From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair. FEBS Lett. 400, 25-30 (1997) (Pubitemid 27046815)
-
(1997)
FEBS Letters
, vol.400
, Issue.1
, pp. 25-30
-
-
Callebaut, I.1
Mornon, J.-P.2
-
28
-
-
0037403380
-
Improved survival in women with BRCA-associated ovarian carcinoma
-
DOI 10.1002/cncr.11310
-
I. Cass, R.L. Baldwin, T. Varkey, R. Moslehi, S.A. Narod, B.Y. Karlan, Improved survival in women with BRCA-associated ovarian carcinoma. Cancer 97, 2187-2195 (2003) (Pubitemid 36444059)
-
(2003)
Cancer
, vol.97
, Issue.9
, pp. 2187-2195
-
-
Cass, I.1
Baldwin, R.L.2
Varkey, T.3
Moslehi, R.4
Narod, S.A.5
Karlan, B.Y.6
-
29
-
-
0034028739
-
Clinico-pathological characteristics of BRCA1- and BRCA2-related breast cancer
-
P.O. Chappuis, V. Nethercot, W.D. Foulkes, Clinico-pathological characteristics of BRCA1-and BRCA2-related breast cancer. Semin. Surg. Oncol. 18, 287-295 (2000) (Pubitemid 30253021)
-
(2000)
Seminars in Surgical Oncology
, vol.18
, Issue.4
, pp. 287-295
-
-
Chappuis, P.O.1
Nethercot, V.2
Foulkes, W.D.3
-
30
-
-
33644549954
-
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance
-
G. Chenevix-Trench, S. Healey, S. Lakhani, P. Waring, M. Cummings, R. Brinkworth, A.M. Deffenbaugh, L.A. Burbidge, D. Pruss, T. Judkins, T. Scholl, A. Bekessy, A. Marsh, P. Lovelock, M. Wong, A. Tesoriero, H. Renard, M. Southey, J.L. Hopper, K. Yannoukakos, M. Brown, D. Easton, S.V. Tavtigian, D. Goldgar, A.B. Spurdle, Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance. Cancer Res. 66, 2019-2027 (2006)
-
(2006)
Cancer Res.
, vol.66
, pp. 2019-2027
-
-
Chenevix-Trench, G.1
Healey, S.2
Lakhani, S.3
Waring, P.4
Cummings, M.5
Brinkworth, R.6
Deffenbaugh, A.M.7
Burbidge, L.A.8
Pruss, D.9
Judkins, T.10
Scholl, T.11
Bekessy, A.12
Marsh, A.13
Lovelock, P.14
Wong, M.15
Tesoriero, A.16
Renard, H.17
Southey, M.18
Hopper, J.L.19
Yannoukakos, K.20
Brown, M.21
Easton, D.22
Tavtigian, S.V.23
Goldgar, D.24
Spurdle, A.B.25
more..
-
31
-
-
0032477349
-
Effect of BRCA1 and BRCA2 on the association between breast cancer risk and family history
-
E.B. Claus, J. Schildkraut, E.S. Iversen Jr., D. Berry, G. Parmigiani, Effect of BRCA1 and BRCA2 on the association between breast cancer risk and family history. J. Natl. Cancer Inst. 90, 1824-1829 (1998) (Pubitemid 28559895)
-
(1998)
Journal of the National Cancer Institute
, vol.90
, Issue.23
, pp. 1824-1829
-
-
Claus, E.B.1
Schildkraut, J.2
Iversen Jr., E.S.3
Berry, D.4
Parmigiani, G.5
-
32
-
-
0029007696
-
Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13
-
N. Collins, R. McManus, R. Wooster, J. Mangion, S. Seal, S.R. Lakhani, W. Ormiston, P.A. Daly, D. Ford, D.F. Easton et al., Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13. Oncogene 10, 1673-1675 (1995)
-
(1995)
Oncogene
, vol.10
, pp. 1673-1675
-
-
Collins, N.1
McManus, R.2
Wooster, R.3
Mangion, J.4
Seal, S.5
Lakhani, S.R.6
Ormiston, W.7
Daly, P.A.8
Ford, D.9
Easton, D.F.10
-
33
-
-
0029027365
-
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium
-
R.S. Cornelis, S.L. Neuhausen, O. Johansson, A. Arason, D. Kelsell, B.A. Ponder, P. Tonin, U. Hamann, A. Lindblom, P. Lalle et al., High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium. Genes Chromosom. Cancer 13, 203-210 (1995)
-
(1995)
Genes Chromosom. Cancer
, vol.13
, pp. 203-210
-
-
Cornelis, R.S.1
Neuhausen, S.L.2
Johansson, O.3
Arason, A.4
Kelsell, D.5
Ponder, B.A.6
Tonin, P.7
Hamann, U.8
Lindblom, A.9
Lalle, P.10
-
34
-
-
7844247959
-
P53 mutation with frequent novel codons but not a mutator phenotype in BRCA1- and BRCA2-associated breast tumours
-
T. Crook, L.A. Brooks, S. Crossland, P. Osin, K.T. Barker, J.Waller, E. Philp, P.D. Smith, I. Yulug, J. Peto, G. Parker, M.J. Allday, M.R. Crompton, B.A. Gusterson, p53 mutation with frequent novel condons but not a mutator phenotype in BRCA1-and BRCA2-associated breast tumours. Oncogene 17, 1681-1689 (1998) (Pubitemid 28482645)
-
(1998)
Oncogene
, vol.17
, Issue.13
, pp. 1681-1689
-
-
Crook, T.1
Brooks, L.A.2
Crossland, S.3
Osin, P.4
Barker, K.T.5
Waller, J.6
Philp, E.7
Smith, P.D.8
Yulug, I.9
Peto, J.10
Parker, G.11
Allday, M.J.12
Crompton, M.R.13
Gusterson, B.A.14
-
35
-
-
0037268338
-
The fanconi anaemia/BRCA pathway
-
DOI 10.1038/nrc970
-
A.D. D'Andrea, M. Grompe, The Fanconi anaemia/BRCA pathway. Nat. Rev. Cancer 3, 23-34 (2003) (Pubitemid 37328884)
-
(2003)
Nature Reviews Cancer
, vol.3
, Issue.1
, pp. 23-34
-
-
D'Andrea, A.D.1
Grompe, M.2
-
36
-
-
34249887673
-
Interaction with the BRCA2 C terminus protects RAD51-DNA filaments from disassembly by BRC repeats
-
DOI 10.1038/nsmb1251, PII NSMB1251
-
O.R. Davies, L. Pellegrini, Interaction with the BRCA2 C terminus protects RAD51-DNA filaments from disassembly by BRC repeats. Nat. Struct. Mol. Biol. 14, 475-483 (2007) (Pubitemid 46871813)
-
(2007)
Nature Structural and Molecular Biology
, vol.14
, Issue.6
, pp. 475-483
-
-
Davies, O.R.1
Pellegrini, L.2
-
37
-
-
70449534798
-
Methylation not a frequent "second hit" in tumors with germline BRCA mutations
-
A.M. Dworkin, A.D. Spearman, S.Y. Tseng, K. Sweet, A.E. Toland, Methylation not a frequent "second hit" in tumors with germline BRCA mutations. Fam. Cancer 8, 339-346 (2009)
-
(2009)
Fam. Cancer
, vol.8
, pp. 339-346
-
-
Dworkin, A.M.1
Spearman, A.D.2
Tseng, S.Y.3
Sweet, K.4
Toland, A.E.5
-
38
-
-
33644801945
-
Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer families
-
H. Eerola, P. Heikkila, A. Tamminen, K. Aittomaki, C. Blomqvist, H. Nevanlinna, Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer families. Breast Cancer Res. 7, R465-R469 (2005)
-
(2005)
Breast Cancer Res.
, vol.7
-
-
Eerola, H.1
Heikkila, P.2
Tamminen, A.3
Aittomaki, K.4
Blomqvist, C.5
Nevanlinna, H.6
-
39
-
-
53249097506
-
Hormone therapy and the risk of breast cancer in BRCA1 mutation carriers
-
A. Eisen, J. Lubinski, J. Gronwald, P. Moller, H.T. Lynch, J. Klijn, C. Kim-Sing, S.L. Neuhausen, L. Gilbert, P. Ghadirian, S. Manoukian, G. Rennert, E. Friedman, C. Isaacs, E. Rosen, B. Rosen, M. Daly, P. Sun, S.A. Narod, Hormone therapy and the risk of breast cancer in BRCA1 mutation carriers. J. Natl. Cancer Inst. 100, 1361-1367 (2008)
-
(2008)
J. Natl. Cancer Inst.
, vol.100
, pp. 1361-1367
-
-
Eisen, A.1
Lubinski, J.2
Gronwald, J.3
Moller, P.4
Lynch, H.T.5
Klijn, J.6
Kim-Sing, C.7
Neuhausen, S.L.8
Gilbert, L.9
Ghadirian, P.10
Manoukian, S.11
Rennert, G.12
Friedman, E.13
Isaacs, C.14
Rosen, E.15
Rosen, B.16
Daly, M.17
Sun, P.18
Narod, S.A.19
-
40
-
-
34249878748
-
Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2
-
DOI 10.1038/nsmb1245, PII NSMB1245
-
F. Esashi, V.E. Galkin, X. Yu, E.H. Egelman, S.C. West, Stabilization of RAD51 nucleoprotein filaments by the Cterminal region of BRCA2. Nat. Struct. Mol. Biol. 14, 468- 474 (2007) (Pubitemid 46871809)
-
(2007)
Nature Structural and Molecular Biology
, vol.14
, Issue.6
, pp. 468-474
-
-
Esashi, F.1
Galkin, V.E.2
Yu, X.3
Egelman, E.H.4
West, S.C.5
-
41
-
-
18244388241
-
DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis
-
M. Esteller, M.F. Fraga, M. Guo, J. Garcia-Foncillas, I. Hedenfalk, A.K. Godwin, J. Trojan, C. Vaurs-Barriere, Y.J. Bignon, S. Ramus, J. Benitez, T. Caldes, Y. Akiyama, Y. Yuasa, V. Launonen, M.J. Canal, R. Rodriguez, G. Capella, M.A. Peinado, A. Borg, L.A. Aaltonen, B.A. Ponder, S.B. Baylin, J.G. Herman, DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis. Hum. Mol. Genet. 10, 3001- 3007 (2001) (Pubitemid 34083486)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.26
, pp. 3001-3007
-
-
Esteller, M.1
Fraga, M.F.2
Guo, M.3
Garcia-Foncillas, J.4
Hedenfalk, I.5
Godwin, A.K.6
Trojan, J.7
Vaurs-Barriere, C.8
Bignon, Y.-J.9
Ramus, S.10
Benitez, J.11
Caldes, T.12
Akiyama, Y.13
Yuasa, Y.14
Launonen, V.15
Canal, M.J.16
Rodriguez, R.17
Capella, G.18
Peinado, M.A.19
Borg, A.20
Aaltonen, L.A.21
Ponder, B.A.22
Baylin, S.B.23
Herman, J.G.24
more..
-
42
-
-
0034607234
-
Promoter hypermethylation and BRCA1 inactivation in sporadic breast and ovarian tumors
-
M. Esteller, J.M. Silva, G. Dominguez, F. Bonilla, X. Matias-Guiu, E. Lerma, E. Bussaglia, J. Prat, I.C. Harkes, E.A. Repasky, E. Gabrielson, M. Schutte, S.B. Baylin, J.G. Herman, Promoter hypermethylation and BRCA1 inactivation in sporadic breast and ovarian tumors. J. Natl. Cancer Inst. 92, 564-569 (2000) (Pubitemid 30212318)
-
(2000)
Journal of the National Cancer Institute
, vol.92
, Issue.7
, pp. 564-569
-
-
Esteller, M.1
Silva, J.M.2
Dominguez, G.3
Bonilla, F.4
Matias-Guiu, X.5
Lerma, E.6
Bussaglia, E.7
Prat, J.8
Harkes, I.C.9
Repasky, E.A.10
Gabrielson, E.11
Schutte, M.12
Baylin, S.B.13
Herman, J.G.14
-
43
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
DOI 10.1038/nature03445
-
H. Farmer, N. McCabe, C.J. Lord, A.N. Tutt, D.A. Johnson, T.B. Richardson, M. Santarosa, K.J. Dillon, I. Hickson, C. Knights, N.M. Martin, S.P. Jackson, G.C. Smith, A. Ashworth, Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature 434, 917-921 (2005) (Pubitemid 40559006)
-
(2005)
Nature
, vol.434
, Issue.7035
, pp. 917-921
-
-
Farmer, H.1
McCabe, H.2
Lord, C.J.3
Tutt, A.H.J.4
Johnson, D.A.5
Richardson, T.B.6
Santarosa, M.7
Dillon, K.J.8
Hickson, I.9
Knights, C.10
Martin, N.M.B.11
Jackson, S.P.12
Smith, G.C.M.13
Ashworth, A.14
-
44
-
-
10744223743
-
+) Phenotype of BRCA1-Related Breast Cancer
-
DOI 10.1158/0008-5472.CAN-03-2970
-
W.D. Foulkes, J.S. Brunet, I.M. Stefansson, O. Straume, P.O. Chappuis, L.R. Begin, N. Hamel, J.R. Goffin, N. Wong, M. Trudel, L. Kapusta, P. Porter, L.A. Akslen, The prognostic implication of the basal-like (cyclin E high/p27 low/p53+/glomeruloid-microvascular-proliferation+) phenotype of BRCA1-related breast cancer. Cancer Res. 64, 830-835 (2004) (Pubitemid 38176880)
-
(2004)
Cancer Research
, vol.64
, Issue.3
, pp. 830-835
-
-
Foulkes, W.D.1
Brunet, J.-S.2
Stefansson, I.M.3
Straume, O.4
Chappuis, P.O.5
Begin, L.R.6
Hamel, N.7
Goffin, J.R.8
Wong, N.9
Trudel, M.10
Kapusta, L.11
Porter, P.12
Akslen, L.A.13
-
45
-
-
0141429017
-
Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer
-
W.D. Foulkes, I.M. Stefansson, P.O. Chappuis, L.R. Begin, J.R. Goffin, N. Wong, M. Trudel, L.A. Akslen, Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. J. Natl. Cancer Inst. 95, 1482-1485 (2003) (Pubitemid 37279334)
-
(2003)
Journal of the National Cancer Institute
, vol.95
, Issue.19
, pp. 1482-1485
-
-
Foulkes, W.D.1
Stefansson, I.M.2
Chappuis, P.O.3
Begin, L.R.4
Goffin, J.R.5
Wong, N.6
Trudel, M.7
Akslen, L.A.8
-
46
-
-
0033749946
-
Low expression of bcl-2 in Brca1-associated breast cancers
-
P. Freneaux, D. Stoppa-Lyonnet, E. Mouret, M. Kambouchner, A. Nicolas, B. Zafrani, A. Vincent-Salomon, A. Fourquet, H. Magdelenat, X. Sastre-Garau, Low expression of bcl-2 in Brca1-associated breast cancers. Br. J. Cancer 83, 1318-1322 (2000)
-
(2000)
Br. J. Cancer
, vol.83
, pp. 1318-1322
-
-
Freneaux, P.1
Stoppa-Lyonnet, D.2
Mouret, E.3
Kambouchner, M.4
Nicolas, A.5
Zafrani, B.6
Vincent-Salomon, A.7
Fourquet, A.8
Magdelenat, H.9
-
47
-
-
72449175818
-
Mammalian SUMO E3-ligases PIAS1 and PIAS4 promote responses to DNA double-strand breaks
-
Y. Galanty, R. Belotserkovskaya, J. Coates, S. Polo, K.M. Miller, S.P. Jackson, Mammalian SUMO E3-ligases PIAS1 and PIAS4 promote responses to DNA double-strand breaks. Nature 462, 935-939 (2009)
-
(2009)
Nature
, vol.462
, pp. 935-939
-
-
Galanty, Y.1
Belotserkovskaya, R.2
Coates, J.3
Polo, S.4
Miller, K.M.5
Jackson, S.P.6
-
48
-
-
0030940518
-
Recurrent germ-line BRCA1 mutations in extended african american families with early-onset breast cancer [1]
-
Q. Gao, S. Neuhausen, S. Cummings, M. Luce, O.I. Olopade, Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer. Am. J. Hum. Genet. 60, 1233-1236 (1997) (Pubitemid 27194108)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.5
, pp. 1233-1236
-
-
Gao, Q.1
Neuhausen, S.2
Cummings, S.3
Luce, M.4
Olopade, O.I.5
-
49
-
-
0037222380
-
TP53 mutations in familial breast cancer: Functional aspects
-
DOI 10.1002/humu.10173
-
M. Gasco, I.G. Yulug, T. Crook, TP53 mutations in familial breast cancer: Functional aspects. Hum. Mutat. 21, 301-306 (2003) (Pubitemid 36292972)
-
(2003)
Human Mutation
, vol.21
, Issue.3
, pp. 301-306
-
-
Gasco, M.1
Yulug, I.G.2
Crook, T.3
-
50
-
-
0031000719
-
Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia [3]
-
S.A. Gayther, P. Harrington, P. Russell, G. Kharkevich, R.F. Garkavtseva, B.A. Ponder, Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia. Am. J. Hum. Genet. 60, 1239-1242 (1997) (Pubitemid 27194110)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.5
, pp. 1239-1242
-
-
Gayther, S.A.1
Harrington, P.2
Russell, P.3
Kharkevich, G.4
Garkavtseva, R.F.5
Ponder, B.A.J.6
-
51
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
F.M. Giardiello, J.D. Brensinger, A.C. Tersmette, S.N. Goodman, G.M. Petersen, S.V. Booker, M. Cruz-Correa, J.A. Offerhaus, Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119, 1447-1453 (2000) (Pubitemid 32198669)
-
(2000)
Gastroenterology
, vol.119
, Issue.6
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
Goodman, S.N.4
Petersen, G.M.5
Booker, S.V.6
Cruz-Correa, M.7
Offerhaus, J.A.8
-
52
-
-
0035872462
-
TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: Distinctive spectrum and structural distribution
-
M.S. Greenblatt, P.O. Chappuis, J.P. Bond, N. Hamel, W.D. Foulkes, TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: Distinctive spectrum and structural distribution. Cancer Res. 61, 4092-4097 (2001) (Pubitemid 32720976)
-
(2001)
Cancer Research
, vol.61
, Issue.10
, pp. 4092-4097
-
-
Greenblatt, M.S.1
Chappuis, P.O.2
Bond, J.P.3
Hamel, N.4
Foulkes, W.D.5
-
53
-
-
0036494110
-
Molecular-cytogenetic analysis of HER-2/neu gene in BRCA1-associated breast cancers
-
T.A. Grushko, M.A. Blackwood, P.L. Schumm, F.G. Hagos, M. O. Adeyanju, M.D. Feldman, M.O. Sanders, B.L. Weber, O.I. Olopade, Molecular-cytogenetic analysis of HER-2/neu gene in BRCA1-associated breast cancers. Cancer Res. 62, 1481-1488 (2002) (Pubitemid 34407811)
-
(2002)
Cancer Research
, vol.62
, Issue.5
, pp. 1481-1488
-
-
Grushko, T.A.1
Blackwood, M.A.2
Schumm, P.L.3
Hagos, F.G.4
Adeyanju, M.O.5
Feldman, M.D.6
Sanders, M.O.7
Weber, B.L.8
Olopade, O.I.9
-
54
-
-
0029149274
-
Loss of heterozygosity at chromosome 11 in breast cancer: Association of prognostic factors with genetic alterations
-
J. Gudmundsson, R.B. Barkardottir, G. Eiriksdottir, T. Baldursson, A. Arason, V. Egilsson, S. Ingvarsson, Loss of heterozygosity at chromosome 11 in breast cancer: Association of prognostic factors with genetic alterations. Br. J. Cancer 72, 696-701 (1995)
-
(1995)
Br. J. Cancer
, vol.72
, pp. 696-701
-
-
Gudmundsson, J.1
Barkardottir, R.B.2
Eiriksdottir, G.3
Baldursson, T.4
Arason, A.5
Egilsson, V.6
Ingvarsson, S.7
-
55
-
-
0029917946
-
Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype
-
J. Gudmundsson, G. Johannesdottir, A. Arason, J.T. Bergthorsson, S. Ingvarsson, V. Egilsson, R.B. Barkardottir, Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype. Am. J. Hum. Genet. 58, 749-756 (1996) (Pubitemid 26086665)
-
(1996)
American Journal of Human Genetics
, vol.58
, Issue.4
, pp. 749-756
-
-
Gudmundsson, J.1
Johannesdottir, G.2
Arason, A.3
Bergthorsson, J.T.4
Ingvarsson, S.5
Egilsson, V.6
Barkardottir, R.B.7
-
56
-
-
0037420026
-
BRCA2 germline mutations in familial pancreatic carcinoma
-
S.A. Hahn, B. Greenhalf, I. Ellis, M. Sina-Frey, H. Rieder, B. Korte, B. Gerdes, R. Kress, A. Ziegler, J.A. Raeburn, D. Campra, R. Grutzmann, H. Rehder,M. Rothmund,W. Schmiegel, J.P. Neoptolemos, D.K. Bartsch, BRCA2 germline mutations in familial pancreatic carcinoma. J. Natl. Cancer Inst. 95, 214-221 (2003) (Pubitemid 36240634)
-
(2003)
Journal of the National Cancer Institute
, vol.95
, Issue.3
, pp. 214-221
-
-
Hahn, S.A.1
Greenhalf, B.2
Ellis, I.3
Sina-Frey, M.4
Rieder, H.5
Korte, B.6
Gerdes, B.7
Kress, R.8
Ziegler, A.9
Raeburn, J.A.10
Campra, D.11
Grutzmann, R.12
Rehder, H.13
Rothmund, M.14
Schmiegel, W.15
Neoptolemos, J.P.16
Bartsch, D.K.17
-
57
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
J.M. Hall, M.K. Lee, B. Newman, J.E. Morrow, L.A. Anderson, B. Huey, M.C. King, Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250, 1684-1689 (1990) (Pubitemid 120031871)
-
(1990)
Science
, vol.250
, Issue.4988
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
Morrow, J.E.4
Anderson, L.A.5
Huey, B.6
King, M.-C.7
-
58
-
-
0033804445
-
Hereditary breast cancer: High risk genes, genetic testing and clinical implications
-
U. Hamann, Hereditary breast cancer: High risk genes, genetic testing and clinical implications. Clin. Lab. 46, 447-461 (2000)
-
(2000)
Clin. Lab.
, vol.46
, pp. 447-461
-
-
Hamann, U.1
-
59
-
-
0036724986
-
BRCA1 induces DNA damage recognition factors and enhances nucleotide excision repair
-
DOI 10.1038/ng953
-
A.R. Hartman, J.M. Ford, BRCA1 induces DNA damage recognition factors and enhances nucleotide excision repair. Nat. Genet. 32, 180-184 (2002) (Pubitemid 34977215)
-
(2002)
Nature Genetics
, vol.32
, Issue.1
, pp. 180-184
-
-
Hartman, A.-R.1
Ford, J.M.2
-
60
-
-
33744782567
-
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
-
DOI 10.1158/1078-0432.CCR-06-0083
-
N. Hearle, V. Schumacher, F.H. Menko, S. Olschwang, L.A. Boardman, J.J. Gille, J.J. Keller, A.M. Westerman, R.J. Scott, W. Lim, J.D. Trimbath, F.M. Giardiello, S.B. Gruber, G.J. Offerhaus, F. W. de Rooij, J.H. Wilson, A. Hansmann, G. Moslein, B. Royer-Pokora, T. Vogel, R.K. Phillips, A.D. Spigelman, R.S. Houlston, Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin. Cancer Res. 12, 3209-3215 (2006) (Pubitemid 43837371)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.10
, pp. 3209-3215
-
-
Hearle, N.1
Schumacher, V.2
Menko, F.H.3
Olschwang, S.4
Boardman, L.A.5
Gille, J.J.P.6
Keller, J.J.7
Westerman, A.M.8
Scott, R.J.9
Lim, W.10
Trimbath, J.D.11
Giardiello, F.M.12
Gruber, S.B.13
Offerhaus, G.J.A.14
De Rooij, F.W.M.15
Wilson, J.H.P.16
Hansmann, A.17
Moslein, G.18
Royer-Pokora, B.19
Vogel, T.20
Phillips, R.K.S.21
Spigelman, A.D.22
Houlston, R.S.23
more..
-
61
-
-
0035931947
-
Gene-expression profiles in hereditary breast cancer
-
DOI 10.1056/NEJM200102223440801
-
I. Hedenfalk, D. Duggan, Y. Chen, M. Radmacher, M. Bittner, R. Simon, P. Meltzer, B. Gusterson, M. Esteller, O.P. Kallioniemi, B.Wilfond, A. Borg, J. Trent, M. Raffeld, Z. Yakhini, A. Ben-Dor, E. Dougherty, J. Kononen, L. Bubendorf, W. Fehrle, S. Pittaluga, S. Gruvberger, N. Loman, O. Johannsson, H. Olsson, G. Sauter, Gene-expression profiles in hereditary breast cancer. N. Engl. J. Med. 344, 539-548 (2001) (Pubitemid 32167867)
-
(2001)
New England Journal of Medicine
, vol.344
, Issue.8
, pp. 539-548
-
-
Hedenfalk, I.1
Duggan, D.2
Chen, Y.3
Radmacher, M.4
Bittner, M.5
Simon, R.6
Meltzer, P.7
Gusterson, B.8
Esteller, M.9
Raffeld, M.10
Yakhini, Z.11
Ben-Dor, A.12
Dougherty, E.13
Kononen, J.14
Bubendorf, L.15
Fehrle, W.16
Pittaluga, S.17
Gruvberger, S.18
Loman, N.19
Johannsson, O.20
Olsson, H.21
Wilfond, B.22
Sauter, G.23
Kallioniemi, O.-P.24
Borg, A.25
Trent, J.26
more..
-
62
-
-
0037418232
-
Molecular classification of familial non-BRCA1/BRCA2 breast cancer
-
DOI 10.1073/pnas.0533805100
-
I. Hedenfalk, M. Ringner, A. Ben-Dor, Z. Yakhini, Y. Chen, G. Chebil, R. Ach, N. Loman, H. Olsson, P.Meltzer, A. Borg, J. Trent, Molecular classification of familial non-BRCA1/BRCA2 breast cancer. Proc. Natl. Acad. Sci. USA 100, 2532-2537 (2003) (Pubitemid 36297533)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.5
, pp. 2532-2537
-
-
Hedenfalk, I.1
Ringner, M.2
Ben-Dor, A.3
Yakhini, Z.4
Chen, Y.5
Chebil, G.6
Ach, R.7
Loman, N.8
Olsson, H.9
Meltzer, P.10
Borg, A.11
Trent, J.12
-
63
-
-
36348972261
-
Prophylactic mastectomy in BRCA1/2 mutation carriers and women at risk of hereditary breast cancer: Long-term experiences at the Rotterdam family cancer clinic
-
DOI 10.1245/s10434-007-9449-x
-
B.A. Heemskerk-Gerritsen, C.T. Brekelmans, M.B. Menke-Pluymers, A.N. van Geel, M.M. Tilanus-Linthorst, C.C. Bartels, M. Tan, H.E. Meijers-Heijboer, J.G. Klijn, C. Seynaeve, Prophylactic mastectomy in BRCA1/2 mutation carriers and women at risk of hereditary breast cancer: Long-term experiences at the Rotterdam Family Cancer Clinic. Ann. Surg. Oncol. 14, 3335-3344 (2007) (Pubitemid 350160099)
-
(2007)
Annals of Surgical Oncology
, vol.14
, Issue.12
, pp. 3335-3344
-
-
Heemskerk-Gerritsen, B.A.M.1
Brekelmans, C.T.M.2
Menke-Pluymers, M.B.E.3
Van Geel, A.N.4
Tilanus-Linthorst, M.M.A.5
Bartels, C.C.M.6
Tan, M.7
Meijers-Heijboer, H.E.J.8
Klijn, J.G.M.9
Seynaeve, C.10
-
64
-
-
84871137081
-
-
In preparation
-
M.R. Heerma van Voss, P. van der Groep, J. Bart, E. van derWall, P. J. van Diest, Expression of the stem cell marker ALDH1 in BRCA1 related breast cancer, In preparation
-
Expression of the Stem Cell Marker ALDH1 in BRCA1 Related Breast Cancer
-
-
Heerma Van Voss, M.R.1
Van Der Groep, P.2
Bart, J.3
Van Der Wall, E.4
Van Diest, P.J.5
-
65
-
-
84871121150
-
Expression of the stem cell marker ALDH1 in the normal breast of BRCA1 mutation carriers
-
M.R. Heerma van Voss, P. van der Groep, J. Bart, E. van derWall, P. J. van Diest, Expression of the stem cell marker ALDH1 in the normal breast of BRCA1 mutation carriers. Breast Cancer Res. Treat.
-
Breast Cancer Res. Treat
-
-
Heerma Van Voss, M.R.1
Van Der Groep, P.2
Bart, J.3
Van Der Wall, E.4
Van Diest, P.J.5
-
66
-
-
85027916783
-
Lympho-vascular invasion in BRCA related breast cancer compared to sporadic controls
-
M.R. Heerma van Voss, P. van der Groep, J. Bart, E. van derWall, P.J. van Diest, Lympho-vascular invasion in BRCA related breast cancer compared to sporadic controls. BMC Cancer 10, 145
-
BMC Cancer
, vol.10
, pp. 145
-
-
Heerma Van Voss, M.R.1
Van Der Groep, P.2
Bart, J.3
Van Der Wall, E.4
Van Diest, P.J.5
-
67
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
T. Heikkinen, H. Karkkainen, K. Aaltonen, R.L. Milne, P. Heikkila, K. Aittomaki, C. Blomqvist, H. Nevanlinna, The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin. Cancer Res. 15, 3214-3222 (2009)
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 3214-3222
-
-
Heikkinen, T.1
Karkkainen, H.2
Aaltonen, K.3
Milne, R.L.4
Heikkila, P.5
Aittomaki, K.6
Blomqvist, C.7
Nevanlinna, H.8
-
68
-
-
25444471892
-
Poly(ADP-ribose) polymerase (PARP-1) in homologous recombination and as a target for cancer therapy
-
T. Helleday, H.E. Bryant, N. Schultz, Poly(ADP-ribose) polymerase (PARP-1) in homologous recombination and as a target for cancer therapy. Cell Cycle 4, 1176-1178 (2005) (Pubitemid 41365386)
-
(2005)
Cell Cycle
, vol.4
, Issue.9
, pp. 1176-1178
-
-
Helleday, T.1
Bryant, H.E.2
Schultz, N.3
-
69
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
DOI 10.1038/34432
-
A. Hemminki, D. Markie, I. Tomlinson, E. Avizienyte, S. Roth, A. Loukola, G. Bignell, W. Warren, M. Aminoff, P. Hoglund, H. Jarvinen, P. Kristo, K. Pelin, M. Ridanpaa, R. Salovaara, T. Toro, W. Bodmer, S. Olschwang, A.S. Olsen, M.R. Stratton, A. de la Chapelle, L.A. Aaltonen, A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391, 184-187 (1998) (Pubitemid 28092478)
-
(1998)
Nature
, vol.391
, Issue.6663
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
Bignell, G.7
Warren, W.8
Aminoff, M.9
Hoglund, P.10
Jarvinen, H.11
Kristo, P.12
Pelin, K.13
Ridanpaa, M.14
Salovaara, R.15
Toro, T.16
Bodmer, W.17
Olschwang, S.18
Olsen, A.S.19
Stratton, M.R.20
De La Chapelle, A.21
Aaltonen, L.A.22
more..
-
70
-
-
3242670404
-
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance
-
DOI 10.1053/j.gastro.2004.03.068, PII S0016508504005785
-
Y.M. Hendriks, A. Wagner, H. Morreau, F. Menko, A. Stormorken, F. Quehenberger, L. Sandkuijl, P. Moller, M. Genuardi, H. Van Houwelingen, C. Tops, M. Van Puijenbroek, P. Verkuijlen, G. Kenter, A. Van Mil, H. Meijers-Heijboer, G.B. Tan, M.H. Breuning, R. Fodde, J.T. Wijnen, A.H. Brocker-Vriends, H. Vasen, Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance. Gastroenterology 127, 17-25 (2004) (Pubitemid 38962270)
-
(2004)
Gastroenterology
, vol.127
, Issue.1
, pp. 17-25
-
-
Hendriks, Y.M.C.1
Wagner, A.2
Morreau, H.3
Menko, F.4
Stormorken, A.5
Quehenberger, F.6
Sandkuijl, L.7
Moller, P.8
Genuardi, M.9
Van Houwelingen, H.10
Tops, C.11
Van Puijenbroek, M.12
Verkuijlen, P.13
Kenter, G.14
Van Mil, A.15
Meijers-Heijboer, H.16
Tan, G.B.17
Breuning, M.H.18
Fodde, R.19
Wijnen, J.T.H.20
Brocker-Vriends, A.H.J.T.21
Vasen, H.22
more..
-
71
-
-
33747478190
-
Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and fallopian tube in women at hereditary high risk of breast and ovarian cancer
-
DOI 10.1002/ijc.21988
-
B.B. Hermsen, P.J. van Diest, J. Berkhof, F.H. Menko, J.J. Gille, J.M. Piek, S. Meijer, H.A. Winters, P. Kenemans, S. Mensdorff-Pouilly, R.H. Verheijen, Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancer. Int. J. Cancer 119, 1412-1418 (2006) (Pubitemid 44258819)
-
(2006)
International Journal of Cancer
, vol.119
, Issue.6
, pp. 1412-1418
-
-
Hermsen, B.B.J.1
Van Diest, P.J.2
Berkhof, J.3
Menko, F.H.4
Gille, J.J.P.5
Piek, J.M.J.6
Meijer, S.7
Winters, H.A.H.8
Kenemans, P.9
Von Mensdorff-Pouilly, S.10
Verheijen, R.H.M.11
-
72
-
-
19944361851
-
Lobulitis is a frequent finding in prophylactically removed breast tissue from women at hereditary high risk of breast cancer
-
DOI 10.1002/path.1774
-
B.B. Hermsen, S. von Mensdorff-Pouilly, H.F. Fabry, H.A. Winters, P. Kenemans, R.H. Verheijen, P.J. van Diest, Lobulitis is a frequent finding in prophylactically removed breast tissue from women at hereditary high risk of breast cancer. J. Pathol. 206, 220-223 (2005) (Pubitemid 40754026)
-
(2005)
Journal of Pathology
, vol.206
, Issue.2
, pp. 220-223
-
-
Hemsen, B.B.J.1
Von Mensdorff-Pouilly, S.2
Fabry, H.F.J.3
Winters, H.A.H.4
Kenemans, P.5
Verheijen, R.H.M.6
Van Diest, P.J.7
-
73
-
-
0037380994
-
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
-
F.B. Hogervorst, P.M. Nederlof, J.J. Gille, C.J. McElgunn, M. Grippeling, R. Pruntel, R. Regnerus, T. van Welsem, R. van Spaendonk, F.H. Menko, I. Kluijt, C. Dommering, S. Verhoef, J. P. Schouten, L.J. van't Veer, G. Pals, Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method. Cancer Res. 63, 1449-1453 (2003) (Pubitemid 36373627)
-
(2003)
Cancer Research
, vol.63
, Issue.7
, pp. 1449-1453
-
-
Hogervorst, F.B.L.1
Nederlof, P.M.2
Gille, J.J.P.3
McElgunn, C.J.4
Grippeling, M.5
Pruntel, R.6
Regnerus, R.7
Van Welsem, T.8
Van Spaendonk, R.9
Menko, F.H.10
Kluijt, I.11
Dommering, C.12
Verhoef, S.13
Schouten, J.P.14
Van'T Veer, L.J.15
Pals, G.16
-
74
-
-
65949105079
-
High incidence of protein-truncating TP53 mutations in BRCA1-related breast cancer
-
H. Holstege, S.A. Joosse, C.T. van Oostrom, P.M. Nederlof, A. de Vries, J. Jonkers, High incidence of protein-truncating TP53 mutations in BRCA1-related breast cancer. Cancer Res. 69, 3625-3633 (2009)
-
(2009)
Cancer Res.
, vol.69
, pp. 3625-3633
-
-
Holstege, H.1
Joosse, S.A.2
Van Oostrom, C.T.3
Nederlof, P.M.4
De Vries, A.5
Jonkers, J.6
-
75
-
-
25144506227
-
The molecular pathology of hereditary breast cancer: Genetic testing and therapeutic implications
-
DOI 10.1038/modpathol.3800453, PII 3800453
-
E. Honrado, J. Benitez, J. Palacios, The molecular pathology of hereditary breast cancer: Genetic testing and therapeutic implications. Mod. Pathol. 18, 1305-1320 (2005) (Pubitemid 41348649)
-
(2005)
Modern Pathology
, vol.18
, Issue.10
, pp. 1305-1320
-
-
Honrado, E.1
Benitez, J.2
Palacios, J.3
-
76
-
-
36248970130
-
Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families
-
DOI 10.1038/modpathol.3800969, PII 3800969
-
E. Honrado, A. Osorio, R.L. Milne, M.F. Paz, L. Melchor, A. Cascon, M. Urioste, A. Cazorla, O. Diez, E. Lerma, M. Esteller, J. Palacios, J. Benitez, Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families. Mod. Pathol. 20, 1298-1306 (2007) (Pubitemid 350126855)
-
(2007)
Modern Pathology
, vol.20
, Issue.12
, pp. 1298-1306
-
-
Honrado, E.1
Osorio, A.2
Milne, R.L.3
Paz, M.F.4
Melchor, L.5
Cascon, A.6
Urioste, M.7
Cazorla, A.8
Diez, O.9
Lerma, E.10
Esteller, M.11
Palacios, J.12
Benitez, J.13
-
77
-
-
33749025026
-
Pathology and gene expression of hereditary breast tumors associated with BRCA1, BRCA2 and CHEK2 gene mutations
-
DOI 10.1038/sj.onc.1209875, PII 1209875
-
E. Honrado, A. Osorio, J. Palacios, J. Benitez, Pathology and gene expression of hereditary breast tumors associated with BRCA1, BRCA2 and CHEK2 gene mutations. Oncogene 25, 5837-5845 (2006) (Pubitemid 44453439)
-
(2006)
Oncogene
, vol.25
, Issue.43
, pp. 5837-5845
-
-
Honrado, E.1
Osorio, A.2
Palacios, J.3
Benitez, J.4
-
78
-
-
33748984965
-
Numerous high-risk epithelial lesions in familial breast cancer
-
DOI 10.1016/j.ejca.2006.05.027, PII S0959804906005296
-
N. Hoogerbrugge, P. Bult, J.J. Bonenkamp, M.J. Ligtenberg, L. A. Kiemeney, J.A. de Hullu, C. Boetes, M.F. Niermeijer, H.G. Brunner, Numerous high-risk epithelial lesions in familial breast cancer. Eur. J. Cancer 42, 2492-2498 (2006) (Pubitemid 44442941)
-
(2006)
European Journal of Cancer
, vol.42
, Issue.15
, pp. 2492-2498
-
-
Hoogerbrugge, N.1
Bult, P.2
Bonenkamp, J.J.3
Ligtenberg, M.J.L.4
Kiemeney, L.A.5
De Hullu, J.A.6
Boetes, C.7
Niermeijer, M.F.8
Brunner, H.G.9
-
79
-
-
18744377172
-
High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer
-
N. Hoogerbrugge, P. Bult, L.M. de Widt-Levert, L.V. Beex, L.A. Kiemeney, M.J. Ligtenberg, L.F. Massuger, C. Boetes, P. Manders, H.G. Brunner, High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer. J. Clin. Oncol. 21, 41-45 (2003)
-
(2003)
J. Clin. Oncol.
, vol.21
, pp. 41-45
-
-
Hoogerbrugge, N.1
Bult, P.2
De Widt-Levert, L.M.3
Beex, L.V.4
Kiemeney, L.A.5
Ligtenberg, M.J.6
Massuger, L.F.7
Boetes, C.8
Manders, P.9
Brunner, H.G.10
-
80
-
-
17444447998
-
Evidence of founder mutations in finnish BRCA1 and BRCA2 families [4]
-
DOI 10.1086/301880
-
P. Huusko, K. Paakkonen, V. Launonen, M. Poyhonen, G. Blanco, A. Kauppila, U. Puistola, H. Kiviniemi, M. Kujala, J. Leisti, R. Winqvist, Evidence of founder mutations in Finnish BRCA1 and BRCA2 families. Am. J. Hum. Genet. 62, 1544- 1548 (1998) (Pubitemid 28307128)
-
(1998)
American Journal of Human Genetics
, vol.62
, Issue.6
, pp. 1544-1548
-
-
Huusko, P.1
Paakkonen, K.2
Launonen, V.3
Poyhonen, M.4
Blanco, G.5
Kauppila, A.6
Puistola, U.7
Kiviniemi, H.8
Kujala, M.9
Leisti, J.10
Winqvist, R.11
-
81
-
-
17644368911
-
Pathology of breast cancer in women with constitutional CHEK2 mutations
-
DOI 10.1007/s10549-004-3778-2
-
T. Huzarski, C. Cybulski, W. Domagala, J. Gronwald, T. Byrski, M. Szwiec, S. Woyke, S.A. Narod, J. Lubinski, Pathology of breast cancer in women with constitutional CHEK2 mutations. Breast Cancer Res. Treat. 90, 187-189 (2005) (Pubitemid 40568901)
-
(2005)
Breast Cancer Research and Treatment
, vol.90
, Issue.2
, pp. 187-189
-
-
Huzarski, T.1
Cybulski, C.2
Domagala, W.3
Gronwald, J.4
Byrski, T.5
Szwiec, M.6
Woyke, S.7
Narod, S.A.8
Lubinski, J.9
-
82
-
-
0029156036
-
Germline mutation of BRCA1 in Japanese breast cancer families
-
R. Inoue, T. Fukutomi, T. Ushijima, Y. Matsumoto, T. Sugimura, M. Nagao, Germline mutation of BRCA1 in Japanese breast cancer families. Cancer Res. 55, 3521-3524 (1995)
-
(1995)
Cancer Res.
, vol.55
, pp. 3521-3524
-
-
Inoue, R.1
Fukutomi, T.2
Ushijima, T.3
Matsumoto, Y.4
Sugimura, T.5
Nagao, M.6
-
83
-
-
0036497966
-
Prevalence of the BRCA2 6174 del T mutation in Israeli uveal melanoma patients
-
DOI 10.1002/ijc.10155
-
J. Iscovich, M. Abdulrazik, C. Cour, A. Fischbein, J. Pe'er, D.E. Goldgar, Prevalence of the BRCA2 6174 del T mutation in Israeli uveal melanoma patients. Int. J. Cancer 98, 42-44 (2002) (Pubitemid 34113416)
-
(2002)
International Journal of Cancer
, vol.98
, Issue.1
, pp. 42-44
-
-
Iscovich, J.1
Abdulrazik, M.2
Cour, C.3
Fischbein, A.4
Pe'Er, J.5
Goldgar, D.E.6
-
84
-
-
50849134167
-
Histopathological findings and follow-up after prophylactic mastectomy and immediate breast reconstruction in 100 women from families with hereditary breast cancer
-
A.E. Isern, N. Loman, J. Malina, H. Olsson, A. Ringberg, Histopathological findings and follow-up after prophylactic mastectomy and immediate breast reconstruction in 100 women from families with hereditary breast cancer. Eur. J. Surg. Oncol. 34, 1148-1154 (2008)
-
(2008)
Eur. J. Surg. Oncol.
, vol.34
, pp. 1148-1154
-
-
Isern, A.E.1
Loman, N.2
Malina, J.3
Olsson, H.4
Ringberg, A.5
-
85
-
-
0035047680
-
Connecting Fanconi anemia to BRCA1
-
DOI 10.1038/86458
-
H. Joenje, F. Arwert, Connecting Fanconi anemia to BRCA1. Nat. Med. 7, 406-407 (2001) (Pubitemid 32298534)
-
(2001)
Nature Medicine
, vol.7
, Issue.4
, pp. 406-407
-
-
Joenje, H.1
Arwert, F.2
-
86
-
-
19144364122
-
Founding BRCA1 mutations in hereditary breast and ovarian cancer in Southern Sweden
-
O. Johannsson, E.A. Ostermeyer, S. Hakansson, L.S. Friedman, U. Johansson, G. Sellberg, K. Brondum-Nielsen, V. Sele, H. Olsson, M.C. King, A. Borg, Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden. Am. J. Hum. Genet. 58, 441-450 (1996) (Pubitemid 26062474)
-
(1996)
American Journal of Human Genetics
, vol.58
, Issue.3
, pp. 441-450
-
-
Johannsson, O.1
Ostermeyer, E.A.2
Hakansson, S.3
Friedman, L.S.4
Johansson, U.5
Sellberg, G.6
Brondum-Nielsen, K.7
Sele, V.8
Olsson, H.9
King, M.-C.10
Borg, A.11
-
87
-
-
0031105976
-
Tumour biological features of BRCA1-induced breast and ovarian cancer
-
O.T. Johannsson, I. Idvall, C. Anderson, A. Borg, R.B. Barkardottir, V. Egilsson, H. Olsson, Tumour biological features of BRCA1-induced breast and ovarian cancer. Eur. J. Cancer 33, 362-371 (1997)
-
(1997)
Eur. J. Cancer
, vol.33
, pp. 362-371
-
-
Johannsson, O.T.1
Idvall, I.2
Anderson, C.3
Borg, A.4
Barkardottir, R.B.5
Egilsson, V.6
Olsson, H.7
-
88
-
-
0030792818
-
Influence of BRCA1 mutations on nuclear grade and estrogen receptor status of breast carcinoma in Ashkenazi Jewish women
-
DOI 10.1002/(SICI)1097-0142(19970801)80:3<435::AID-CNCR11>3.0.CO;2- Y
-
S.E. Karp, P.N. Tonin, L.R. Begin, J.J. Martinez, J.C. Zhang, M. N. Pollak, W.D. Foulkes, Influence of BRCA1 mutations on nuclear grade and estrogen receptor status of breast carcinoma in Ashkenazi Jewish women. Cancer 80, 435-441 (1997) (Pubitemid 27323413)
-
(1997)
Cancer
, vol.80
, Issue.3
, pp. 435-441
-
-
Karp, S.E.1
Tonin, P.N.2
Begin, L.R.3
Martinez, J.J.4
Zhang, J.C.5
Pollak, M.N.6
Foulkes, W.D.7
-
89
-
-
34447500612
-
Risk-reducing salpingo-oophorectomy in patients with germline mutations in BRCA1 or BRCA2
-
DOI 10.1200/JCO.2007.11.3449
-
N.D. Kauff, R.R. Barakat, Risk-reducing salpingo-oophorectomy in patients with germline mutations in BRCA1 or BRCA2. J. Clin. Oncol. 25, 2921-2927 (2007) (Pubitemid 47123156)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.20
, pp. 2921-2927
-
-
Kauff, N.D.1
Barakat, R.R.2
-
90
-
-
0037378455
-
Epithelial lesions in prophylactic mastectomy specimens from women with BRCA mutations
-
DOI 10.1002/cncr.11225
-
N.D. Kauff, E. Brogi, L. Scheuer, D.R. Pathak, P.I. Borgen, C.A. Hudis, K. Offit, M.E. Robson, Epithelial lesions in prophylactic mastectomy specimens from women with BRCA mutations. Cancer 97, 1601-1608 (2003) (Pubitemid 36350702)
-
(2003)
Cancer
, vol.97
, Issue.7
, pp. 1601-1608
-
-
Kauff, N.D.1
Brogi, E.2
Scheuer, L.3
Pathak, D.R.4
Borgen, P.I.5
Hudis, C.A.6
Offit, K.7
Robson, M.E.8
-
91
-
-
0032806475
-
Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation
-
G. Keller, H. Vogelsang, I. Becker, J. Hutter, K. Ott, S. Candidus, T. Grundei, K.F. Becker, J. Mueller, J.R. Siewert, H. Hofler, Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation. Am. J. Pathol. 155, 337-342 (1999) (Pubitemid 29370383)
-
(1999)
American Journal of Pathology
, vol.155
, Issue.2
, pp. 337-342
-
-
Keller, G.1
Vogelsang, H.2
Becker, I.3
Hutter, J.4
Ott, K.5
Candidus, S.6
Grundei, T.7
Becker, K.-F.8
Mueller, J.9
Siewert, J.R.10
Hofler, H.11
-
92
-
-
34548564536
-
Heterogenic loss of the wild-type BRCA allele in human breast tumorigenesis
-
DOI 10.1245/s10434-007-9372-1
-
T.A. King, W. Li, E. Brogi, C.J. Yee, M.L. Gemignani, N. Olvera, D.A. Levine, L. Norton, M.E. Robson, K. Offit, P.I. Borgen, J. Boyd, Heterogenic loss of the wild-type BRCA allele in human breast tumorigenesis. Ann. Surg. Oncol. 14, 2510- 2518 (2007) (Pubitemid 47389559)
-
(2007)
Annals of Surgical Oncology
, vol.14
, Issue.9
, pp. 2510-2518
-
-
King, T.A.1
Li, W.2
Brogi, E.3
Yee, C.J.4
Gemignani, M.L.5
Olvera, N.6
Levine, D.A.7
Norton, L.8
Robson, M.E.9
Offit, K.10
Borgen, P.I.11
Boyd, J.12
-
93
-
-
2442440933
-
BRCA Mutations and Risk of Prostate Cancer in Ashkenazi Jews
-
DOI 10.1158/1078-0432.CCR-03-0604
-
T. Kirchhoff, N.D. Kauff, N. Mitra, K. Nafa, H. Huang, C. Palmer, T. Gulati, E. Wadsworth, S. Donat, M.E. Robson, N.A. Ellis, K. Offit, BRCA mutations and risk of prostate cancer in Ashkenazi Jews. Clin. Cancer Res. 10, 2918-2921 (2004) (Pubitemid 38619665)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.9
, pp. 2918-2921
-
-
Kirchhoff, T.1
Kauff, N.D.2
Mitra, N.3
Nafa, K.4
Huang, H.5
Palmer, C.6
Gulati, T.7
Wadsworth, E.8
Donat, S.9
Robson, M.E.10
Ellis, N.A.11
Offit, K.12
-
94
-
-
0029972806
-
P53: Puzzle and paradigm
-
L.J. Ko, C. Prives, p53: Puzzle and paradigm. Genes Dev. 10, 1054-1072 (1996) (Pubitemid 26152848)
-
(1996)
Genes and Development
, vol.10
, Issue.9
, pp. 1054-1072
-
-
Ko, L.J.1
Prives, C.2
-
95
-
-
0030187780
-
BRCA1 protein products. Functional motifs
-
E.V. Koonin, S.F. Altschul, P. Bork, BRCA1 protein products. Functional motifs. Nat. Genet. 13, 266-268 (1996)
-
(1996)
Nat. Genet.
, vol.13
, pp. 266-268
-
-
Koonin, E.V.1
Altschul, S.F.2
Bork, P.3
-
96
-
-
48149106931
-
Distant disease-free interval, site of first relapse and postrelapse survival in BRCA1-and BRCA2-associated compared to sporadic breast cancer patients
-
M. Kriege, C. Seynaeve, H. Meijers-Heijboer, J.M. Collee, M. B. Menke-Pluymers, C.C. Bartels, M.M. Tilanus-Linthorst, A. van den Ouweland, B. van Geel, C.T. Brekelmans, J.G. Klijn, Distant disease-free interval, site of first relapse and postrelapse survival in BRCA1-and BRCA2-associated compared to sporadic breast cancer patients. Breast Cancer Res. Treat. 111, 303-311 (2008)
-
(2008)
Breast Cancer Res. Treat.
, vol.111
, pp. 303-311
-
-
Kriege, M.1
Seynaeve, C.2
Meijers-Heijboer, H.3
Collee, J.M.4
Menke-Pluymers, M.B.5
Bartels, C.C.6
Tilanus-Linthorst, M.M.7
Van Den Ouweland, A.8
Van Geel, B.9
Brekelmans, C.T.10
Klijn, J.G.11
-
97
-
-
0036775583
-
Multiple fibroadenomas harbouring carcinoma in situ in a woman with a family history of breast/ovarian cancer
-
DOI 10.1136/jcp.55.10.795
-
A. Kuijper, S.S. Preisler-Adams, F.D. Rahusen, J.J. Gille, E. van der Wall, P.J. van Diest, Multiple fibroadenomas harbouring carcinoma in situ in a woman with a family history of breast/ ovarian cancer. J. Clin. Pathol. 55, 795-797 (2002) (Pubitemid 35231919)
-
(2002)
Journal of Clinical Pathology
, vol.55
, Issue.10
, pp. 795-797
-
-
Kuijper, A.1
Preisler-Adams, S.S.2
Rahusen, F.D.3
Gille, J.J.P.4
Van Der Wall, E.5
Van Diest, P.J.6
-
98
-
-
12944286550
-
The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
-
S.R. Lakhani, B.A. Gusterson, J. Jacquemier, J.P. Sloane, T.J. Anderson, M.J. van de Vijver, D. Venter, A. Freeman, A. Antoniou, L. McGuffog, E. Smyth, C.M. Steel, N. Haites, R.J. Scott, D. Goldgar, S. Neuhausen, P.A. Daly, W. Ormiston, R. McManus, S. Scherneck, B.A. Ponder, P.A. Futreal, J. Peto, D. Stoppa-Lyonnet, Y.J. Bignon, M.R. Stratton, The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2. Clin. Cancer Res. 6, 782-789 (2000) (Pubitemid 30159330)
-
(2000)
Clinical Cancer Research
, vol.6
, Issue.3
, pp. 782-789
-
-
Lakhani, S.R.1
Gusterson, B.A.2
Jacquemier, J.3
Sloane, J.P.4
Anderson, T.J.5
Van De Vijver, M.J.6
Venter, D.7
Freeman, A.8
Antoniou, A.9
McGuffog, L.10
Smyth, E.11
Steel, C.M.12
Haites, N.13
Scott, R.J.14
Goldgar, D.15
Neuhausen, S.16
Daly, P.A.17
Ormiston, W.18
McManus, R.19
Scherneck, S.20
Ponder, B.A.J.21
Futreal, P.A.22
Peto, J.23
Stoppa-Lyonnet, D.24
Bignon, Y.-J.25
Struewing, J.P.26
Bishop, D.T.27
Klijn, J.G.M.28
Devilee, P.29
Cornelisse, C.J.30
Lasset, C.31
Lenoir, G.32
Barkardottir, R.B.33
Egilsson, V.34
Hamann, U.35
Chang-Claude, J.36
Sobol, H.37
Weber, B.38
Easton, D.F.39
Stratton, M.R.40
more..
-
99
-
-
0032486752
-
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations
-
S.R. Lakhani, J. Jacquemier, J.P. Sloane, B.A. Gusterson, T.J. Anderson, M.J. van de Vijver, L.M. Farid, D. Venter, A. Antoniou, A. Storfer-Isser, E. Smyth, C.M. Steel, N. Haites, R. J. Scott, D. Goldgar, S. Neuhausen, P.A. Daly, W. Ormiston, R. McManus, S. Scherneck, B.A. Ponder, D. Ford, J. Peto, D. Stoppa-Lyonnet, Y.J. Bignon, J.P. Struewing, N.K. Spurr, D.T. Bishop, J.G. Klijn, P. Devilee, C.J. Cornelisse, C. Lasset, G. Lenoir, R.B. Barkardottir, V. Egilsson, U. Hamann, J. Chang-Claude, H. Sobol, B. Weber, M.R. Stratton, D.F. Easton, Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J. Natl. Cancer Inst. 90, 1138-1145 (1998) (Pubitemid 28380718)
-
(1998)
Journal of the National Cancer Institute
, vol.90
, Issue.15
, pp. 1138-1145
-
-
Lakhani, S.R.1
Jacquemier, J.2
Sloane, J.P.3
Gusterson, B.A.4
Anderson, T.J.5
Van De Vijver, M.J.6
Farid, L.M.7
Venter, D.8
Antoniou, A.9
Storfer-Isser, A.10
Smyth, E.11
Steel, C.M.12
Haites, N.13
Scott, R.J.14
Goldgar, D.15
Neuhausen, S.16
Daly, P.A.17
Ormiston, W.18
McManus, R.19
Scherneck, S.20
Ponder, B.A.J.21
Ford, D.22
Peto, J.23
Stoppa-Lyonnet, D.24
Bignon, Y.-J.25
Struewing, J.P.26
Spurr, N.K.27
Bishop, D.T.28
Klijn, J.G.M.29
Devilee, P.30
Cornelisse, C.J.31
Lasset, C.32
Lenoir, G.33
Barkardottir, R.B.34
Egilsson, V.35
Hamann, U.36
Chang-Claude, J.37
Sobol, H.38
Weber, B.39
Stratton, M.R.40
Easton, D.F.41
more..
-
100
-
-
22344443194
-
Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype
-
DOI 10.1158/1078-0432.CCR-04-2424
-
S.R. Lakhani, J.S. Reis-Filho, L. Fulford, F. Penault-Llorca, M. van der Vijver, S. Parry, T. Bishop, J. Benitez, C. Rivas, Y.J. Bignon, J. Chang-Claude, U. Hamann, C.J. Cornelisse, P. Devilee, M.W. Beckmann, C. Nestle-Kramling, P.A. Daly, N. Haites, J. Varley, F. Lalloo, G. Evans, C. Maugard, H. Meijers-Heijboer, J.G. Klijn, E. Olah, B.A. Gusterson, S. Pilotti, P. Radice, S. Scherneck, H. Sobol, J. Jacquemier, T. Wagner, J. Peto, M.R. Stratton, L. McGuffog, D.F. Easton, Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype. Clin. Cancer Res. 11, 5175-5180 (2005) (Pubitemid 41003703)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.14
, pp. 5175-5180
-
-
Lakhani, S.R.1
Reis-Filho, J.S.2
Fulford, L.3
Renault-Llorca, F.4
Van Vijver, M.D.5
Parry, S.6
Bishop, T.7
Benitez, J.8
Rivas, C.9
Bignon, Y.-J.10
Chang-Claude, J.11
Hamann, U.12
Cornelisse, C.J.13
Devilee, P.14
Beckmann, M.W.15
Nestle-Kramling, C.16
Daly, P.A.17
Haites, N.18
Varley, J.19
Lalloo, F.20
Evans, G.21
Maugard, C.22
Meijers-Heijboer, H.23
Klijn, J.G.M.24
Olah, E.25
Gusterson, B.A.26
Pilotti, S.27
Radice, P.28
Scherneck, S.29
Sobol, H.30
Jacquemier, J.31
Wagner, T.32
Peto, J.33
Stratton, M.R.34
McGuffog, L.35
Easton, D.F.36
more..
-
101
-
-
0036569877
-
The pathology of familial breast cancer: Predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2
-
DOI 10.1200/JCO.2002.09.023
-
S.R. Lakhani, M.J. Van De Vijver, J. Jacquemier, T.J. Anderson, P.P. Osin, L. McGuffog, D.F. Easton, The pathology of familial breast cancer: Predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2. J. Clin. Oncol. 20, 2310-2318 (2002) (Pubitemid 34441658)
-
(2002)
Journal of Clinical Oncology
, vol.20
, Issue.9
, pp. 2310-2318
-
-
Lakhani, S.R.1
Van De Vijver, M.J.2
Jacquemier, J.3
Anderson, T.J.4
Osin, P.P.5
McGuffog, L.6
Easton, D.F.7
-
102
-
-
36949013395
-
ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks
-
DOI 10.1038/sj.onc.1210880, PII 1210880
-
M.F. Lavin, ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks. Oncogene 26, 7749-7758 (2007) (Pubitemid 350242462)
-
(2007)
Oncogene
, vol.26
, Issue.56
, pp. 7749-7758
-
-
Lavin, M.F.1
-
103
-
-
0034307185
-
BRCA1 and BRCA2 are necessary for the transcription-coupled repair of the oxidative 8-oxoguanine lesion in human cells
-
F. Le Page,V. Randrianarison,D.Marot, J. Cabannes,M. Perricaudet, J. Feunteun, A. Sarasin, BRCA1 and BRCA2 are necessary for the transcription- coupled repair of the oxidative 8-oxoguanine lesion in human cells. Cancer Res. 60, 5548-5552 (2000)
-
(2000)
Cancer Res.
, vol.60
, pp. 5548-5552
-
-
Le Page, F.1
Randrianarison, V.2
Marot, D.3
Cabannes, J.4
Perricaudet, M.5
Feunteun, J.6
Sarasin, A.7
-
104
-
-
44849135866
-
Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: Results from a population-based study of young breast cancer patients
-
E. Lee, R. McKean-Cowdin, H. Ma, Z. Chen, D. Van Den Berg, B.E. Henderson, L. Bernstein, G. Ursin, Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: Results from a population-based study of young breast cancer patients. Breast Cancer Res. 10, R19 (2008)
-
(2008)
Breast Cancer Res
, vol.10
-
-
Lee, E.1
McKean-Cowdin, R.2
Ma, H.3
Chen, Z.4
Van Den Berg, D.5
Henderson, B.E.6
Bernstein, L.7
Ursin, G.8
-
105
-
-
0036928961
-
Pathologic findings in prophylactic oophorectomy specimens in high-risk women
-
DOI 10.1006/gyno.2002.6779
-
K. Leeper, R. Garcia, E. Swisher, B. Goff, B. Greer, P. Paley, Pathologic findings in prophylactic oophorectomy specimens in high-risk women. Gynecol. Oncol. 87, 52-56 (2002) (Pubitemid 36027101)
-
(2002)
Gynecologic Oncology
, vol.87
, Issue.1
, pp. 52-56
-
-
Leeper, K.1
Garcia, R.2
Swisher, E.3
Goff, B.4
Greer, B.5
Paley, P.6
-
106
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
DOI 10.1126/science.275.5308.1943
-
J. Li, C. Yen, D. Liaw, K. Podsypanina, S. Bose, S.I. Wang, J. Puc, C. Miliaresis, L. Rodgers, R. McCombie, S.H. Bigner, B.C. Giovanella, M. Ittmann, B. Tycko, H. Hibshoosh, M.H. Wigler, R. Parsons, PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 275, 1943-1947 (1997) (Pubitemid 27148818)
-
(1997)
Science
, vol.275
, Issue.5308
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.H.16
Parsons, R.17
-
107
-
-
33846306403
-
Management of BRCA1/2 associated breast cancer: A systematic qualitative review of the state of knowledge in 2006
-
DOI 10.1016/j.ejca.2006.07.019, PII S0959804906008082
-
F.P. Liebens, B. Carly, A. Pastijn, S. Rozenberg, Management of BRCA1/2 associated breast cancer: A systematic qualitative review of the state of knowledge in 2006. Eur. J. Cancer 43, 238-257 (2007) (Pubitemid 46123983)
-
(2007)
European Journal of Cancer
, vol.43
, Issue.2
, pp. 238-257
-
-
Liebens, F.P.1
Carly, B.2
Pastijn, A.3
Rozenberg, S.4
-
108
-
-
2942527434
-
Relative frequency and morphology of cancers in STK11 mutation carriers
-
DOI 10.1053/j.gastro.2004.03.014
-
W. Lim, S. Olschwang, J.J. Keller, A.M. Westerman, F.H. Menko, L.A. Boardman, R.J. Scott, J. Trimbath, F.M. Giardiello, S.B. Gruber, J.J. Gille, G.J. Offerhaus, F.W. de Rooij, J.H. Wilson, A.D. Spigelman, R.K. Phillips, R.S. Houlston, Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology 126, 1788-1794 (2004) (Pubitemid 38736344)
-
(2004)
Gastroenterology
, vol.126
, Issue.7
, pp. 1788-1794
-
-
Lim, W.1
Olschwang, S.2
Keller, J.J.3
Westerman, A.M.4
Menko, F.H.5
Boardman, L.A.6
Scott, R.J.7
Trimbath, J.8
Giardiello, F.M.9
Gruber, S.B.10
Gille, J.J.P.11
Offerhaus, G.J.A.12
De Rooij, F.W.M.13
Wilson, J.H.P.14
Spigelman, A.D.15
Phillips, R.K.S.16
Houlston, R.S.17
-
109
-
-
44349189973
-
Expression of estrogen receptor beta in the breast carcinoma of BRCA1 mutation carriers
-
M.M. Litwiniuk, K. Roznowski, V. Filas, D.D. Godlewski, M. Stawicka, R. Kaleta, J. Breborowicz, Expression of estrogen receptor beta in the breast carcinoma of BRCA1 mutation carriers. BMC Cancer 8, 100 (2008)
-
(2008)
BMC Cancer
, vol.8
, pp. 100
-
-
Litwiniuk, M.M.1
Roznowski, K.2
Filas, V.3
Godlewski, D.D.4
Stawicka, M.5
Kaleta, R.6
Breborowicz, J.7
-
110
-
-
0033613222
-
RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination
-
DOI 10.1073/pnas.96.20.11364
-
K.L. Lorick, J.P. Jensen, S. Fang, A.M. Ong, S. Hatakeyama, A. M. Weissman, RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination. Proc. Natl. Acad. Sci. USA 96, 11364-11369 (1999) (Pubitemid 29487386)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.20
, pp. 11364-11369
-
-
Lorick, K.L.1
Jensen, J.P.2
Fang, S.3
Ong, A.M.4
Hatakeyama, S.5
Weissman, A.M.6
-
111
-
-
0031690463
-
Pathobiologic characteristics of hereditary breast cancer
-
DOI 10.1016/S0046-8177(98)90427-0
-
B.J. Lynch, J.A. Holden, S.S. Buys, S.L. Neuhausen, D.K. Gaffney, Pathobiologic characteristics of hereditary breast cancer. Hum. Pathol. 29, 1140-1144 (1998) (Pubitemid 28467537)
-
(1998)
Human Pathology
, vol.29
, Issue.10
, pp. 1140-1144
-
-
Lynch, B.J.1
Holden, J.A.2
Buys, S.S.3
Neuhausen, S.L.4
Gaffney, D.K.5
-
112
-
-
13344262707
-
Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage
-
DOI 10.1002/(SICI)1097-0142(19960215)77:4<697::AID-CNCR16>3.0.CO;2- W
-
J.N. Marcus, P. Watson, D.L. Page, S.A. Narod, G.M. Lenoir, P. Tonin, L. Linder-Stephenson, G. Salerno, T.A. Conway, H.T. Lynch, Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage. Cancer 77, 697-709 (1996) (Pubitemid 26055395)
-
(1996)
Cancer
, vol.77
, Issue.4
, pp. 697-709
-
-
Marcus, J.N.1
Watson, P.2
Page, D.L.3
Narod, S.A.4
Lenoir, G.M.5
Tonin, P.6
Linder-Stephenson, L.7
Salerno, G.8
Conway, T.A.9
Lynch, H.T.10
-
113
-
-
0030789568
-
BRCA2 hereditary breast cancer pathophenotype
-
DOI 10.1023/A:1005830230664
-
J.N. Marcus, P. Watson, D.L. Page, S.A. Narod, P. Tonin, G.M. Lenoir, O. Serova, H.T. Lynch, BRCA2 hereditary breast cancer pathophenotype. Breast Cancer Res. Treat. 44, 275-277 (1997) (Pubitemid 27296388)
-
(1997)
Breast Cancer Research and Treatment
, vol.44
, Issue.3
, pp. 275-277
-
-
Marcus, J.N.1
Watson, P.2
Page, D.L.3
Narod, S.A.4
Tonin, P.5
Lenoir, G.M.6
Serova, O.7
Lynch, H.T.8
-
114
-
-
0032853452
-
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
-
DOI 10.1093/hmg/8.8.1461
-
D.J. Marsh, J.B. Kum, K.L. Lunetta, M.J. Bennett, R.J. Gorlin, S.F. Ahmed, J. Bodurtha, C. Crowe, M.A. Curtis, M. Dasouki, T. Dunn, H. Feit, M.T. Geraghty, J.M. Graham Jr., S.V. Hodgson, A. Hunter, B.R. Korf, D. Manchester, S. Miesfeldt, V.A. Murday, K.L. Nathanson, M. Parisi, B. Pober, C. Romano, C. Eng et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum. Mol. Genet. 8, 1461-1472 (1999) (Pubitemid 29374079)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.8
, pp. 1461-1472
-
-
Marsh, D.J.1
Kum, J.B.2
Lunetta, K.L.3
Bennett, M.J.4
Gorlin, R.J.5
Ahmed, S.F.6
Bodurtha, J.7
Crowe, C.8
Curtis, M.A.9
Dasouki, M.10
Dunn, T.11
Feit, H.12
Geraghty, M.T.13
Graham Jr., J.M.14
Hodgson, S.V.15
Hunter, A.16
Korf, B.R.17
Manchester, D.18
Miesfeldt, S.19
Murday, V.A.20
Nathanson, K.L.21
Parisi, M.22
Pober, B.23
Romano, C.24
Tolmie, J.L.25
Trembath, R.26
Winter, R.M.27
Zackai, E.H.28
Zori, R.T.29
Weng, L.-P.30
Dahia, P.L.M.31
Eng, C.32
more..
-
115
-
-
0032484084
-
Linkage of ATM to cell cycle regulation by the Chk2 protein kinase
-
S. Matsuoka, M. Huang, S.J. Elledge, Linkage of ATM to cell cycle regulation by the Chk2 protein kinase. Science 282, 1893- 1897 (1998) (Pubitemid 28555269)
-
(1998)
Science
, vol.282
, Issue.5395
, pp. 1893-1897
-
-
Matsuoka, S.1
Huang, M.2
Elledge, S.J.3
-
116
-
-
33750331063
-
Body Image After Bilateral Prophylactic Mastectomy: An Integrative Literature Review
-
DOI 10.1016/j.jmwh.2006.07.002, PII S1526952306003321
-
A. McGaughey, Body image after bilateral prophylactic mastectomy: An integrative literature review. J. Midwifery Womens Health 51, e45-e49 (2006) (Pubitemid 44615967)
-
(2006)
Journal of Midwifery and Women's Health
, vol.51
, Issue.6
-
-
McGaughey, A.1
-
117
-
-
18544389716
-
Lowpenetrance susceptibility to breast cancer due to CHEK2 delC in noncarriers of BRCA1 or BRCA2 mutations
-
H. Meijers-Heijboer, A. van den Ouweland, J. Klijn, M. Wasielewski, A. de Snoo, R. Oldenburg, A. Hollestelle, M. Houben, E. Crepin, M. van
-
(2002)
Nat. Genet.
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
Van Den Ouweland, A.2
Klijn, J.3
Wasielewski, M.4
De Snoo, A.5
Oldenburg, R.6
Hollestelle, A.7
Houben, M.8
Crepin, E.9
Van Veghel-Plandsoen, M.10
Elstrodt, F.11
Van Duijn, C.12
Bartels, C.13
Meijers, C.14
Schutte, M.15
McGuffog, L.16
Thompson, D.17
Easton, D.18
Sodha, N.19
Seal, S.20
Barfoot, R.21
Mangion, J.22
Eccles, D.23
Eeles, R.24
Evans, D.G.25
Houlston, R.26
Murday, V.27
Narod, S.28
Peretz, T.29
Peto, J.30
Phelan, C.31
Zhang, H.X.32
Szabo, C.33
Devilee, P.34
Goldgar, D.35
Futreal, P.A.36
Nathanson, K.L.37
Weber, B.38
Rahman, N.39
Stratton, M.R.40
more..
-
118
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Y. Miki, J. Swensen, D. Shattuck-Eidens, P.A. Futreal, K. Harshman, S. Tavtigian, Q. Liu, C. Cochran, L.M. Bennett, W. Ding et al., A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266, 66-71 (1994) (Pubitemid 24345325)
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
119
-
-
0030966227
-
RAB22 and RAB163/mouse BRCA2: Proteins that specifically interact with the RAD51 protein
-
DOI 10.1073/pnas.94.13.6927
-
R. Mizuta, J.M. LaSalle, H.L. Cheng, A. Shinohara, H. Ogawa, N. Copeland, N.A. Jenkins, M. Lalande, F.W. Alt, RAB22 and RAB163/mouse BRCA2: Proteins that specifically interact with the RAD51 protein. Proc. Natl. Acad. Sci. USA 94, 6927-6932 (1997) (Pubitemid 27281967)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.13
, pp. 6927-6932
-
-
Mizuta, R.1
LaSalle, J.M.2
Cheng, H.-L.3
Shinohara, A.4
Ogawa, H.5
Copeland, N.6
Jenkins, N.A.7
Lalande, M.8
Alt, F.W.9
-
120
-
-
0038364017
-
Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families
-
DOI 10.1093/hmg/ddg120
-
M. Montagna, M. Dalla Palma, C. Menin, S. Agata, A. De Nicolo, L. Chieco-Bianchi, E. D'Andrea, 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) (Pubitemid 36553525)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.9
, pp. 1055-1061
-
-
Montagna, M.1
Palma, M.D.2
Menin, C.3
Agata, S.4
De Nicolo, A.5
Chieco-Bianchi, L.6
D'Andrea, E.D.7
-
121
-
-
72449163470
-
The SUMO modification pathway is involved in the BRCA1 response to genotoxic stress
-
J.R. Morris, C. Boutell, M. Keppler, R. Densham, D. Weekes, A. Alamshah, L. Butler, Y. Galanty, L. Pangon, T. Kiuchi, T. Ng, E. Solomon, The SUMO modification pathway is involved in the BRCA1 response to genotoxic stress. Nature 462, 886-890 (2009)
-
(2009)
Nature
, vol.462
, pp. 886-890
-
-
Morris, J.R.1
Boutell, C.2
Keppler, M.3
Densham, R.4
Weekes, D.5
Alamshah, A.6
Butler, L.7
Galanty, Y.8
Pangon, L.9
Kiuchi, T.10
Ng, T.11
Solomon, E.12
-
122
-
-
0035874894
-
Homology-directed DNA repair, mitomycin-C resistance, and chromosome stability is restored with correction of a Brca1 mutation
-
M.E. Moynahan, T.Y. Cui, M. Jasin, Homology-directed dna repair, mitomycin-c resistance, and chromosome stability is restored with correction of a Brca1 mutation. Cancer Res. 61, 4842-4850 (2001) (Pubitemid 32691900)
-
(2001)
Cancer Research
, vol.61
, Issue.12
, pp. 4842-4850
-
-
Moynahan, M.E.1
Cui, T.Y.2
Jasin, M.3
-
123
-
-
42449107062
-
Familial breast-ovarian cancer locus on chromosome 17q12-q23
-
S.A. Narod, J. Feunteun, H.T. Lynch, P. Watson, T. Conway, J. Lynch, G.M. Lenoir, Familial breast-ovarian cancer locus on chromosome 17q12-q23. Lancet 338, 82-83 (1991)
-
(1991)
Lancet
, vol.338
, pp. 82-83
-
-
Narod, S.A.1
Feunteun, J.2
Lynch, H.T.3
Watson, P.4
Conway, T.5
Lynch, J.6
Lenoir, G.M.7
-
124
-
-
4544374528
-
BRCA1 and BRCA2: 1994 and beyond
-
DOI 10.1038/nrc1431
-
S.A. Narod, W.D. Foulkes, BRCA1 and BRCA2: 1994 and beyond. Nat. Rev. Cancer 4, 665-676 (2004) (Pubitemid 39215065)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.9
, pp. 665-676
-
-
Narod, S.A.1
Foulkes, W.D.2
-
125
-
-
0030140025
-
Localization of the gene for Cowden disease to chromosome 10q22-23
-
M.R. Nelen, G.W. Padberg, E.A. Peeters, A.Y. Lin, B. van den Helm, R.R. Frants, V. Coulon, A.M. Goldstein, M.M. van Reen, D.F. Easton, R.A. Eeles, S. Hodgsen, J.J. Mulvihill, V.A. Murday, M.A. Tucker, E.C. Mariman, T.M. Starink, B.A. Ponder, H.H. Ropers, H. Kremer, M. Longy, C. Eng, Localization of the gene for Cowden disease to chromosome 10q22-23. Nat. Genet. 13, 114-116 (1996) (Pubitemid 126528240)
-
(1996)
Nature Genetics
, vol.13
, Issue.1
, pp. 114-116
-
-
Nelen, M.R.1
Padberg, G.W.2
Peeters, E.A.J.3
Lin, A.Y.4
Van Den Helm, B.5
Frants, R.R.6
Coulon, V.7
Goldstein, A.M.8
Van Reen, M.M.M.9
Easton, D.F.10
Eeles, R.A.11
Hodgson, S.12
Mulvihill, J.J.13
Murday, V.A.14
Tucker, M.A.15
Mariman, E.C.M.16
Starink, T.M.17
Ponder, B.A.J.18
Ropers, H.H.19
Kremer, H.20
Longy, M.21
Eng, C.22
more..
-
126
-
-
0030138354
-
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
-
S. Neuhausen, T. Gilewski, L. Norton, T. Tran, P. McGuire, J. Swensen, H. Hampel, P. Borgen, K. Brown, M. Skolnick, D. Shattuck-Eidens, S. Jhanwar, D. Goldgar, K. Offit, Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer. Nat. Genet. 13, 126-128 (1996)
-
(1996)
Nat. Genet.
, vol.13
, pp. 126-128
-
-
Neuhausen, S.1
Gilewski, T.2
Norton, L.3
Tran, T.4
McGuire, P.5
Swensen, J.6
Hampel, H.7
Borgen, P.8
Brown, K.9
Skolnick, M.10
Shattuck-Eidens, D.11
Jhanwar, S.12
Goldgar, D.13
Offit, K.14
-
127
-
-
0027960790
-
Loss of heterozygosity in familial tumors from three BRCA1-linked kindreds
-
S.L. Neuhausen, C.J. Marshall, Loss of heterozygosity in familial tumors from three BRCA1-linked kindreds. Cancer Res. 54, 6069-6072 (1994) (Pubitemid 24378631)
-
(1994)
Cancer Research
, vol.54
, Issue.23
, pp. 6069-6072
-
-
Neuhausen, S.L.1
Marshall, C.J.2
-
128
-
-
0842302522
-
BRCA1 and BRCA2 founder mutations and the risk of colorectal cancer
-
B.L. Niell, G. Rennert, J.D. Bonner, R. Almog, L.P. Tomsho, S. B. Gruber, BRCA1 and BRCA2 founder mutations and the risk of colorectal cancer. J. Natl. Cancer Inst. 96, 15-21 (2004) (Pubitemid 38180955)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.1
, pp. 15-21
-
-
Niell, B.L.1
Rennert, G.2
Bonner, J.D.3
Almog, R.4
Tomsho, L.P.5
Gruber, S.B.6
-
129
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
DOI 10.1038/ng1096-188
-
C. Oddoux, J.P. Struewing, C.M. Clayton, S. Neuhausen, L.C. Brody, M. Kaback, B. Haas, L. Norton, P. Borgen, S. Jhanwar, D. Goldgar, H. Ostrer, K. Offit, The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat. Genet. 14, 188-190 (1996) (Pubitemid 26338802)
-
(1996)
Nature Genetics
, vol.14
, Issue.2
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
Neuhausen, S.4
Brody, L.C.5
Kaback, M.6
Haas, B.7
Norton, L.8
Borgen, P.9
Jhanwar, S.10
Goldgar, D.11
Ostrer, H.12
Offit, K.13
-
130
-
-
15844375655
-
Germline BRCA1 185delAG mutations in Jewish women with breast cancer
-
DOI 10.1016/S0140-6736(96)91484-1
-
K. Offit, T. Gilewski, P. McGuire, A. Schluger, H. Hampel, K. Brown, J. Swensen, S. Neuhausen, M. Skolnick, L. Norton, D. Goldgar, Germline BRCA1 185delAG mutations in Jewish women with breast cancer. Lancet 347, 1643-1645 (1996) (Pubitemid 26177382)
-
(1996)
Lancet
, vol.347
, Issue.9016
, pp. 1643-1645
-
-
Offit, K.1
Gilewski, T.2
McGuire, P.3
Schluger, A.4
Hampel, H.5
Brown, K.6
Swensen, J.7
Neuhausen, S.8
Skolnick, M.9
Norton, L.10
Goldgar, D.11
-
131
-
-
0031137173
-
Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients
-
H. Ozcelik, B. Schmocker, N. Di Nicola, X.H. Shi, B. Langer, M. Moore, B.R. Taylor, S.A. Narod, G. Darlington, I.L. Andrulis, S. Gallinger, M. Redston, Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients. Nat. Genet. 16, 17-18 (1997)
-
(1997)
Nat. Genet.
, vol.16
, pp. 17-18
-
-
Ozcelik, H.1
Schmocker, B.2
Di Nicola, N.3
Shi, X.H.4
Langer, B.5
Moore, M.6
Taylor, B.R.7
Narod, S.A.8
Darlington, G.9
Andrulis, I.L.10
Gallinger, S.11
Redston, M.12
-
132
-
-
11844253144
-
ERBB2 And MYC alterations In BRCA1-and BRCA2-associated cancers
-
author reply 206
-
J. Palacios, E. Honrado, J.C. Cigudosa, J. Benitez, ERBB2 and MYC alterations in BRCA1-and BRCA2-associated cancers. Genes Chromosom. Cancer 42, 204-205 (2005). author reply 206
-
(2005)
Genes Chromosom. Cancer
, vol.42
, pp. 204-205
-
-
Palacios, J.1
Honrado, E.2
Cigudosa, J.C.3
Benitez, J.4
-
133
-
-
20144387584
-
Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers
-
DOI 10.1007/s10549-004-1536-0
-
J. Palacios, E. Honrado, A. Osorio, A. Cazorla, D. Sarrio, A. Barroso, S. Rodriguez, J.C. Cigudosa, O. Diez, C. Alonso, E. Lerma, J. Dopazo, C. Rivas, J. Benitez, Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers. Breast Cancer Res. Treat. 90, 5-14 (2005) (Pubitemid 40486996)
-
(2005)
Breast Cancer Research and Treatment
, vol.90
, Issue.1
, pp. 5-14
-
-
Palacios, J.1
Honrado, E.2
Osorio, A.3
Cazorla, A.4
Sarrio, D.5
Barroso, A.6
Rodriguez, S.7
Cigudosa, J.C.8
Diez, O.9
Alonso, C.10
Lerma, E.11
Dopazo, J.12
Rivas, C.13
Benitez, J.14
-
134
-
-
12444324167
-
Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: Differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers
-
J. Palacios, E. Honrado, A. Osorio, A. Cazorla, D. Sarrio, A. Barroso, S. Rodriguez, J.C. Cigudosa, O. Diez, C. Alonso, E. Lerma, L. Sanchez, C. Rivas, J. Benitez, Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: Differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers. Clin. Cancer Res. 9, 3606-3614 (2003) (Pubitemid 37169224)
-
(2003)
Clinical Cancer Research
, vol.9
, Issue.10
, pp. 3606-3614
-
-
Palacios, J.1
Honrado, E.2
Osorio, A.3
Cazorla, A.4
Sarrio, D.5
Barroso, A.6
Rodriguez, S.7
Cigudosa, J.C.8
Diez, O.9
Alonso, C.10
Lerma, E.11
Sanchez, L.12
Rivas, C.13
Benitez, J.14
-
135
-
-
0031990269
-
Involvement of Brca2 in DNA repair
-
K.J. Patel, V.P. Yu, H. Lee, A. Corcoran, F.C. Thistlethwaite, M. J. Evans, W.H. Colledge, L.S. Friedman, B.A. Ponder, A.R. Venkitaraman, Involvement of Brca2 in DNA repair. Mol. Cell 1, 347-357 (1998) (Pubitemid 128378883)
-
(1998)
Molecular Cell
, vol.1
, Issue.3
, pp. 347-357
-
-
Patel, K.J.1
Yu, V.P.C.C.2
Lee, H.3
Corcoran, A.4
Thistlethwaite, F.C.5
Evans, M.J.6
Colledge, W.H.7
Friedman, L.S.8
Ponder, B.A.J.9
Venkitaraman, A.R.10
-
136
-
-
16944365091
-
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families
-
T. Peelen, M. van Vliet, A. Petrij-Bosch, R. Mieremet, C. Szabo, A.M. van den Ouweland, F. Hogervorst, R. Brohet, M.J. Ligtenberg, E. Teugels, R. van der Luijt, A.H. van der Hout, J. J. Gille, G. Pals, I. Jedema, R. Olmer, I. van Leeuwen, B. Newman, M. Plandsoen, M. van der Est, G. Brink, S. Hageman, P.J. Arts, M.M. Bakker, P. Devilee et al., A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families. Am. J. Hum. Genet. 60, 1041-1049 (1997) (Pubitemid 27194088)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.5
, pp. 1041-1049
-
-
Peelen, T.1
Van Vliet, M.2
Petrij-Bosch, A.3
Mieremet, R.4
Szabo, C.5
Van Den Ouweland, A.M.W.6
Hogervorst, F.7
Brohet, R.8
Ligtenberg, M.J.L.9
Teugels, E.10
Van Der Luijt, R.11
Van Der Hout, A.H.12
Gille, J.J.P.13
Pals, G.14
Jedema, I.15
Olmer, R.16
Van Leeuwen, I.17
Newman, B.18
Plandsoen, M.19
Van Der Est, M.20
Brink, G.21
Hageman, S.22
Arts, P.J.W.23
Bakker, M.M.24
Willems, H.W.25
Van Der Looij, E.26
Neyns, B.27
Bonduelle, M.28
Jansen, R.29
Oosterwijk, J.C.30
Sijmons, R.31
Smeets, H.J.M.32
Van Asperen, C.J.33
Meijers-Heijboer, H.34
Klijn, J.G.M.35
De Greve, J.36
King, M.-C.37
Menko, F.H.38
Brunner, H.G.39
Halley, D.40
Van Ommen, G.-J.B.41
Vasen, H.F.A.42
Cornelisse, C.J.43
Van 't Veer, L.J.44
De Knijff, P.45
Bakker, E.46
Devilee, P.47
more..
-
137
-
-
0034680102
-
Molecular portraits of human breast tumours
-
C.M. Perou, T. Sorlie, M.B. Eisen, M. van de Rijn, S.S. Jeffrey, C. A. Rees, J.R. Pollack, D.T. Ross, H. Johnsen, L.A. Akslen, O. Fluge, A. Pergamenschikov, C.Williams, S.X. Zhu, P.E. Lonning, A.L. Borresen-Dale, P.O. Brown, D. Botstein, Molecular portraits of human breast tumours. Nature 406, 747-752 (2000)
-
(2000)
Nature
, vol.406
, pp. 747-752
-
-
Perou, C.M.1
Sorlie, T.2
Eisen, M.B.3
Van De Rijn, M.4
Jeffrey, S.S.5
Rees, C.A.6
Pollack, J.R.7
Ross, D.T.8
Johnsen, H.9
Akslen, L.A.10
Fluge, O.11
Pergamenschikov, A.12
Williams, C.13
Zhu, S.X.14
Lonning, P.E.15
Borresen-Dale, A.L.16
Brown, P.O.17
Botstein, D.18
-
138
-
-
0033516265
-
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early- onset breast cancer
-
J. Peto, N. Collins, R. Barfoot, S. Seal, W. Warren, N. Rahman, D.F. Easton, C. Evans, J. Deacon, M.R. Stratton, Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J. Natl. Cancer Inst. 91, 943-949 (1999) (Pubitemid 29272520)
-
(1999)
Journal of the National Cancer Institute
, vol.91
, Issue.11
, pp. 943-949
-
-
Peto, J.1
Collins, N.2
Barfoot, R.3
Seal, S.4
Warren, W.5
Rahman, N.6
Easton, D.F.7
Evans, C.8
Deacon, J.9
Stratton, M.R.10
-
139
-
-
16944363592
-
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
-
DOI 10.1038/ng1197-341
-
A. Petrij-Bosch, T. Peelen, M. van Vliet, R. van Eijk, R. Olmer, M. Drusedau, F.B. Hogervorst, S. Hageman, P.J. Arts, M.J. Ligtenberg, H. Meijers-Heijboer, J.G. Klijn, H.F. Vasen, C.J. Cornelisse, L.J. van't Veer, E. Bakker, G.J. van Ommen, P. Devilee, BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nat. Genet. 17, 341-345 (1997) (Pubitemid 27476002)
-
(1997)
Nature Genetics
, vol.17
, Issue.3
, pp. 341-345
-
-
Petrij-Bosch, A.1
Peelen, T.2
Van Vliet, M.3
Van Eijk, R.4
Olmer, R.5
Drusedau, M.6
Hogervorst, F.B.L.7
Hageman, S.8
Arts, P.J.W.9
Ligtenberg, M.J.L.10
Meijers-Heijboer, H.11
Klijn, J.G.M.12
Vasen, H.F.A.13
Cornelisse, C.J.14
Van't Veer, L.J.15
Bakker, E.16
Van Ommen, G.-J.B.17
Devilee, P.18
-
140
-
-
45949085378
-
Polygenes, risk prediction, and targeted prevention of breast cancer
-
DOI 10.1056/NEJMsa0708739
-
P.D. Pharoah, A.C. Antoniou, D.F. Easton, B.A. Ponder, Polygenes, risk prediction, and targeted prevention of breast cancer. N. Engl. J. Med. 358, 2796-2803 (2008) (Pubitemid 351930854)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.26
, pp. 2796-2803
-
-
Pharoah, P.D.P.1
Antoniou, A.C.2
Easton, D.F.3
Ponder, B.A.J.4
-
141
-
-
0033518891
-
Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutations
-
K.A. Phillips, K. Nichol, H. Ozcelik, J. Knight, S.J. Done, P.J. Goodwin, I.L. Andrulis, Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutations. J. Natl. Cancer Inst. 91, 469-473 (1999) (Pubitemid 29128285)
-
(1999)
Journal of the National Cancer Institute
, vol.91
, Issue.5
, pp. 469-473
-
-
Phillips, K.-A.1
Nichol, K.2
Ozcelik, H.3
Knight, J.4
Done, S.J.5
Goodwin, P.J.6
Andrulis, I.L.7
-
142
-
-
0035828559
-
Tubal ligation and risk of ovarian cancer
-
J.M. Piek, P.J. van Diest, R.P. Zweemer, P. Kenemans, R.H. Verheijen, Tubal ligation and risk of ovarian cancer. Lancet 358, 844 (2001)
-
(2001)
Lancet
, vol.358
, pp. 844
-
-
Piek, J.M.1
Van Diest, P.J.2
Zweemer, R.P.3
Kenemans, P.4
Verheijen, R.H.5
-
143
-
-
33746708760
-
Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer
-
DOI 10.1007/s10549-006-9184-1
-
S.M. Pinilla, E. Honrado, D. Hardisson, J. Benitez, J. Palacios, Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer. Breast Cancer Res. Treat. 99, 85-90 (2006) (Pubitemid 44168607)
-
(2006)
Breast Cancer Research and Treatment
, vol.99
, Issue.1
, pp. 85-90
-
-
Rodriguez Pinilla, S.M.1
Honrado, E.2
Hardisson, D.3
Benitez, J.4
Palacios, J.5
-
144
-
-
33646808638
-
A conserved pathway to activate BRCA1-dependent ubiquitylation at DNA damage sites
-
J. Polanowska, J.S. Martin, T. Garcia-Muse, M.I. Petalcorin, S.J. Boulton, A conserved pathway to activate BRCA1-dependent ubiquitylation at DNA damage sites. EMBO J. 25, 2178-2188 (2006)
-
(2006)
EMBO J.
, vol.25
, pp. 2178-2188
-
-
Polanowska, J.1
Martin, J.S.2
Garcia-Muse, T.3
Petalcorin, M.I.4
Boulton, S.J.5
-
145
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
DOI 10.1038/ng1959, PII NG1959
-
N. Rahman, S. Seal, D. Thompson, P. Kelly, A. Renwick, A. Elliott, S. Reid, K. Spanova, R. Barfoot, T. Chagtai, H. Jayatilake, L. McGuffog, S. Hanks, D.G. Evans, D. Eccles, D. F. Easton, M.R. Stratton, PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat. Genet. 39, 165-167 (2007) (Pubitemid 46184346)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
146
-
-
0036754170
-
Prophylactic oophorectomy in BRCA1 and BRCA2 mutation carriers
-
DOI 10.1016/S0959-8049(02)80012-0, PII S0959804902002691
-
T.R. Rebbeck, Prophylactic oophorectomy in BRCA1 and BRCA2 mutation carriers. Eur. J. Cancer 38(Suppl 6), S15- S17 (2002) (Pubitemid 35284376)
-
(2002)
European Journal of Cancer
, vol.38
, Issue.SUPPL. 6
-
-
Rebbeck, T.R.1
-
147
-
-
34447303102
-
Clinical outcomes of breast cancer in carriers of BRCA1 and BRCA2 mutations
-
DOI 10.1056/NEJMoa070608
-
G. Rennert, S. Bisland-Naggan, O. Barnett-Griness, N. Bar-Joseph, S. Zhang, H.S. Rennert, S.A. Narod, Clinical outcomes of breast cancer in carriers of BRCA1 and BRCA2 mutations. N. Engl. J. Med. 357, 115-123 (2007) (Pubitemid 47057729)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.2
, pp. 115-123
-
-
Rennert, G.1
Bisland-Naggan, S.2
Barnett-Griness, O.3
Bar-Joseph, N.4
Zhang, S.5
Rennert, H.S.6
Narod, S.A.7
-
148
-
-
33746491583
-
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
-
DOI 10.1038/ng1837, PII NG1837
-
A. Renwick, D. Thompson, S. Seal, P. Kelly, T. Chagtai, M. Ahmed, B. North, H. Jayatilake, R. Barfoot, K. Spanova, L. McGuffog, D.G. Evans, D. Eccles, D.F. Easton, M.R. Stratton, N. Rahman, ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat. Genet. 38, 873-875 (2006) (Pubitemid 44141653)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
Kelly, P.4
Chagtai, T.5
Ahmed, M.6
North, B.7
Jayatilake, H.8
Barfoot, R.9
Spanova, K.10
McGuffog, L.11
Evans, D.G.12
Eccles, D.13
Easton, D.F.14
Stratton, M.R.15
Rahman, N.16
-
151
-
-
34548853409
-
Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas
-
DOI 10.1136/jcp.2006.042143
-
S.M. Rodriguez-Pinilla, D. Sarrio, E. Honrado, G. Moreno-Bueno, D. Hardisson, F. Calero, J. Benitez, J. Palacios, Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas. J. Clin. Pathol. 60, 1006-1012 (2007) (Pubitemid 47441933)
-
(2007)
Journal of Clinical Pathology
, vol.60
, Issue.9
, pp. 1006-1012
-
-
Rodriguez-Pinilla, S.M.1
Sarrio, D.2
Honrado, E.3
Moreno-Bueno, G.4
Hardisson, D.5
Calero, F.6
Benitez, J.7
Palacios, J.8
-
152
-
-
0035942190
-
Cancer-predisposing mutations within the RING domain of BRCA1: Loss of ubiquitin protein ligase activity and protection from radiation hypersensitivity
-
DOI 10.1073/pnas.081068398
-
H. Ruffner, C.A. Joazeiro, D. Hemmati, T. Hunter, I.M. Verma, Cancer-predisposing mutations within the RING domain of BRCA1: Loss of ubiquitin protein ligase activity and protection from radiation hypersensitivity. Proc. Natl. Acad. Sci. USA 98, 5134-5139 (2001) (Pubitemid 32397095)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.9
, pp. 5134-5139
-
-
Ruffner, H.1
Joazeiro, C.A.P.2
Hemmati, D.3
Hunter, T.4
Verma, I.M.5
-
153
-
-
0029057336
-
A single ataxia telangiectasia gene with a product similar to PI-3 kinase
-
K. Savitsky, A. Bar-Shira, S. Gilad, G. Rotman, Y. Ziv, L. Vanagaite, D.A. Tagle, S. Smith, T. Uziel, S. Sfez, M. Ashkenazi, I. Pecker, M. Frydman, R. Harnik, S.R. Patanjali, A. Simmons, G.A. Clines, A. Sartiel, R.A. Gatti, L. Chessa, O. Sanal, M.F. Lavin, N.G. Jaspers, A.M. Taylor, C.F. Arlett, T. Miki, S.M. Weissman, M. Lovett, F.S. Collins, Y. Shiloh, A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268, 1749-1753 (1995)
-
(1995)
Science
, vol.268
, pp. 1749-1753
-
-
Savitsky, K.1
Bar-Shira, A.2
Gilad, S.3
Rotman, G.4
Ziv, Y.5
Vanagaite, L.6
Tagle, D.A.7
Smith, S.8
Uziel, T.9
Sfez, S.10
Ashkenazi, M.11
Pecker, I.12
Frydman, M.13
Harnik, R.14
Patanjali, S.R.15
Simmons, A.16
Clines, G.A.17
Sartiel, A.18
Gatti, R.A.19
Chessa, L.20
Sanal, O.21
Lavin, M.F.22
Jaspers, N.G.23
Taylor, A.M.24
Arlett, C.F.25
Miki, T.26
Weissman, S.M.27
Lovett, M.28
Collins, F.S.29
Shiloh, Y.30
more..
-
154
-
-
46449107403
-
Hereditary diffuse gastric cancer: Association with lobular breast cancer
-
K.A. Schrader, S. Masciari, N. Boyd, S. Wiyrick, P. Kaurah, J. Senz, W. Burke, H.T. Lynch, J.E. Garber, D.G. Huntsman, Hereditary diffuse gastric cancer: Association with lobular breast cancer. Fam Cancer 7, 73-82 (2008)
-
(2008)
Fam Cancer
, vol.7
, pp. 73-82
-
-
Schrader, K.A.1
Masciari, S.2
Boyd, N.3
Wiyrick, S.4
Kaurah, P.5
Senz, J.6
Burke, W.7
Lynch, H.T.8
Garber, J.E.9
Huntsman, D.G.10
-
155
-
-
0345669750
-
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility
-
DOI 10.1086/373965
-
M. Schutte, S. Seal, R. Barfoot, H. Meijers-Heijboer, M. Wasielewski, D.G. Evans, D. Eccles, C. Meijers, F. Lohman, J. Klijn, A. van den Ouweland, P.A. Futreal, K.L. Nathanson, B.L. Weber, D.F. Easton, M.R. Stratton, N. Rahman, Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility. Am. J. Hum. Genet. 72, 1023- 1028 (2003) (Pubitemid 36403321)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.4
, pp. 1023-1028
-
-
Schutte, M.1
Seal, S.2
Barfoot, R.3
Meijers-Heijboer, H.4
Wasielewski, M.5
Evans, D.G.6
Eccles, D.7
Meijers, C.8
Lohman, F.9
Klijn, J.10
Van Den Ouweland, A.11
Futreal, P.A.12
Nathanson, K.L.13
Weber, B.L.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
Brady, A.18
Cole, T.19
Collins, A.20
Cox, H.21
Donaldson, A.22
Eeles, R.23
Evans, D.24
Gregory, H.25
Gray, J.26
Houlston, R.27
Lalloo, F.28
Lucassen, A.29
Mackay, J.30
Mitchell, G.31
Morrison, P.32
Murday, V.33
Narod, S.34
Patterson, J.35
Peretz, T.36
Phelan, C.M.37
Rogers, M.38
Schofield, A.39
Tonin, P.40
Weber, W.41
more..
-
156
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
DOI 10.1016/S0092-8674(00)81847-4
-
R. Scully, J. Chen, A. Plug, Y. Xiao, D. Weaver, J. Feunteun, T. Ashley, D.M. Livingston, Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell 88, 265-275 (1997) (Pubitemid 28015875)
-
(1997)
Cell
, vol.88
, Issue.2
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
Xiao, Y.4
Weaver, D.5
Feunteun, J.6
Ashley, T.7
Livingston, D.M.8
-
157
-
-
0034707053
-
In search of the tumoursuppressor functions of BRCA1 and BRCA2
-
R. Scully, D.M. Livingston, In search of the tumoursuppressor functions of BRCA1 and BRCA2. Nature 408, 429-432 (2000)
-
(2000)
Nature
, vol.408
, pp. 429-432
-
-
Scully, R.1
Livingston, D.M.2
-
158
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
DOI 10.1038/ng1902, PII NG1902
-
S. Seal, D. Thompson, A. Renwick, A. Elliott, P. Kelly, R. Barfoot, T. Chagtai, H. Jayatilake, M. Ahmed, K. Spanova, B. North, L. McGuffog, D.G. Evans, D. Eccles, D.F. Easton, M.R. Stratton, N. Rahman, Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat. Genet. 38, 1239-1241 (2006) (Pubitemid 44646283)
-
(2006)
Nature Genetics
, vol.38
, Issue.11
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
159
-
-
68449101315
-
Breast cancer immunohistochemistry can be useful in triage of some HNPCC families
-
S. Shanley, C. Fung, J. Milliken, J. Leary, R. Barnetson, M. Schnitzler, J. Kirk, Breast cancer immunohistochemistry can be useful in triage of some HNPCC families. Fam. Cancer (2009)
-
(2009)
Fam. Cancer
-
-
Shanley, S.1
Fung, C.2
Milliken, J.3
Leary, J.4
Barnetson, R.5
Schnitzler, M.6
Kirk, J.7
-
160
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
-
S.K. Sharan, M. Morimatsu, U. Albrecht, D.S. Lim, E. Regel, C. Dinh, A. Sands, G. Eichele, P. Hasty, A. Bradley, Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature 386, 804-810 (1997) (Pubitemid 27181248)
-
(1997)
Nature
, vol.386
, Issue.6627
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
Lim, D.-S.4
Regel, E.5
Dinh, C.6
Sands, A.7
Eichele, G.8
Hasty, P.9
Bradley, A.10
-
161
-
-
0034671945
-
Oncogenic mutations of the p53 tumor suppressor: The demons of the guardian of the genome
-
A. Sigal, V. Rotter, Oncogenic mutations of the p53 tumor suppressor: The demons of the guardian of the genome. Cancer Res. 60, 6788-6793 (2000) (Pubitemid 32059139)
-
(2000)
Cancer Research
, vol.60
, Issue.24
, pp. 6788-6793
-
-
Sigal, A.1
Rotter, V.2
-
162
-
-
0027939506
-
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families
-
DOI 10.1038/ng1294-392
-
J. Simard, P. Tonin, F. Durocher, K. Morgan, J. Rommens, S. Gingras, C. Samson, J.F. Leblanc, C. Belanger, F. Dion et al., Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families. Nat. Genet. 8, 392-398 (1994) (Pubitemid 24375607)
-
(1994)
Nature Genetics
, vol.8
, Issue.4
, pp. 392-398
-
-
Simard, J.1
Tonin, P.2
Durocher, F.3
Morgan, K.4
Rommens, J.5
Gingras, S.6
Samson, C.7
Leblanc, J.-F.8
Belanger, C.9
Dion, F.10
Liu, Q.11
Skolnick, M.12
Goldgar, D.13
Shattuck-Eidens, D.14
Labrie, F.15
Narod, S.A.16
-
163
-
-
0029804093
-
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1
-
T.M. Smith, M.K. Lee, C.I. Szabo, N. Jerome, M. McEuen, M. Taylor, L. Hood, M.C. King, Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. Genome Res. 6, 1029-1049 (1996) (Pubitemid 26413615)
-
(1996)
Genome Research
, vol.6
, Issue.11
, pp. 1029-1049
-
-
Smith, T.M.1
Lee, M.K.2
Szabo, C.I.3
Jerome, N.4
McEuen, M.5
Taylor, M.6
Hood, L.7
King, M.-C.8
-
164
-
-
0037478605
-
Repeated observation of breast tumor subtypes in independent gene expression data sets
-
DOI 10.1073/pnas.0932692100
-
T. Sorlie, R. Tibshirani, J. Parker, T. Hastie, J.S. Marron, A. Nobel, S. Deng, H. Johnsen, R. Pesich, S. Geisler, J. Demeter, C. M. Perou, P.E. Lonning, P.O. Brown, A.L. Borresen-Dale, D. Botstein, Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc. Natl. Acad. Sci. USA 100, 8418-8423 (2003) (Pubitemid 36842560)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.14
, pp. 8418-8423
-
-
Sorlie, T.1
Tibshirani, R.2
Parker, J.3
Hastie, T.4
Marron, J.S.5
Nobel, A.6
Deng, S.7
Johnsen, H.8
Pesich, R.9
Geisler, S.10
Demeter, J.11
Perou, C.M.12
Lonning, P.E.13
Brown, P.O.14
Borresen-Dale, A.-L.15
Botstein, D.16
-
165
-
-
56749160290
-
Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance
-
A.D. Spearman, K. Sweet, X.P. Zhou, J. McLennan, F.J. Couch, A.E. Toland, Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance. J. Clin. Oncol. 26, 5393-5400 (2008)
-
(2008)
J. Clin. Oncol.
, vol.26
, pp. 5393-5400
-
-
Spearman, A.D.1
Sweet, K.2
Zhou, X.P.3
McLennan, J.4
Couch, F.J.5
Toland, A.E.6
-
166
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
DOI 10.1038/ng0497-356
-
P.A. Steck, M.A. Pershouse, S.A. Jasser, W.K. Yung, H. Lin, A. H. Ligon, L.A. Langford, M.L. Baumgard, T. Hattier, T. Davis, C. Frye, R. Hu, B. Swedlund, D.H. Teng, S.V. Tavtigian, Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat. Genet. 15, 356-362 (1997) (Pubitemid 27147102)
-
(1997)
Nature Genetics
, vol.15
, Issue.4
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
Yung, W.K.A.4
Lin, H.5
Ligon, A.H.6
Langford, L.A.7
Baumgard, M.L.8
Hattier, T.9
Davis, T.10
Frye, C.11
Hu, R.12
Swedlund, B.13
Teng, D.H.F.14
Tavtigian, S.V.15
-
167
-
-
0028141722
-
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q
-
DOI 10.1038/ng0594-103
-
M.R. Stratton, D. Ford, S. Neuhasen, S. Seal, R. Wooster, L.S. Friedman, M.C. King, V. Egilsson, P. Devilee, R. McManus et al., Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q. Nat. Genet. 7, 103-107 (1994) (Pubitemid 24232389)
-
(1994)
Nature Genetics
, vol.7
, Issue.1
, pp. 103-107
-
-
Stratton, M.R.1
Ford, D.2
Neuhasen, S.3
Seal, S.4
Wooster, R.5
Friedman, L.S.6
King, M.-C.7
Egilsson, V.8
Devilee, P.9
McManus, R.10
Daly, P.A.11
Smyth, E.12
Ponder, B.A.J.13
Peto, J.14
Cannon-Albright, L.15
Easton, D.F.16
Goldgar, D.E.17
-
168
-
-
0029083814
-
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
-
J.P. Struewing, D. Abeliovich, T. Peretz, N. Avishai, M.M. Kaback, F.S. Collins, L.C. Brody, The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nat. Genet. 11, 198-200 (1995)
-
(1995)
Nat. Genet.
, vol.11
, pp. 198-200
-
-
Struewing, J.P.1
Abeliovich, D.2
Peretz, T.3
Avishai, N.4
Kaback, M.M.5
Collins, F.S.6
Brody, L.C.7
-
169
-
-
54949134514
-
Methylation is less abundant in BRCA1-associated compared with sporadic breast cancer
-
K.P. Suijkerbuijk, M.J. Fackler, S. Sukumar, C.H. van Gils, T. van Laar, E. van der Wall, M. Vooijs, P.J. van Diest, Methylation is less abundant in BRCA1-associated compared with sporadic breast cancer. Ann. Oncol. 19, 1870-1874 (2008)
-
(2008)
Ann. Oncol.
, vol.19
, pp. 1870-1874
-
-
Suijkerbuijk, K.P.1
Fackler, M.J.2
Sukumar, S.3
Van Gils, C.H.4
Van Laar, T.5
Van Der Wall, E.6
Vooijs, M.7
Van Diest, P.J.8
-
170
-
-
53649089909
-
Hereditary breast cancer: From molecular pathology to tailored therapies
-
D.S. Tan, C. Marchio, J.S. Reis-Filho, Hereditary breast cancer: From molecular pathology to tailored therapies. J. Clin. Pathol. 61, 1073-1082 (2008)
-
(2008)
J. Clin. Pathol.
, vol.61
, pp. 1073-1082
-
-
Tan, D.S.1
Marchio, C.2
Reis-Filho, J.S.3
-
171
-
-
49249136904
-
Promoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors
-
T. Tapia, S.V. Smalley, P. Kohen, A. Munoz, L.M. Solis, A. Corvalan, P. Faundez, L. Devoto, M. Camus, M. Alvarez, P. Carvallo, Promoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors. Epigenetics 3, 157-163 (2008)
-
(2008)
Epigenetics
, vol.3
, pp. 157-163
-
-
Tapia, T.1
Smalley, S.V.2
Kohen, P.3
Munoz, A.4
Solis, L.M.5
Corvalan, A.6
Faundez, P.7
Devoto, L.8
Camus, M.9
Alvarez, M.10
Carvallo, P.11
-
172
-
-
0038147067
-
BRCA1 expression modulates chemosensitivity of BRCA1-defective HCC1937 human breast cancer cells
-
DOI 10.1038/sj.bjc.6600859
-
P. Tassone, P. Tagliaferri, A. Perricelli, S. Blotta, B. Quaresima, M.L. Martelli, A. Goel, V. Barbieri, F. Costanzo, C.R. Boland, S. Venuta, BRCA1 expression modulates chemosensitivity of BRCA1-defective HCC1937 human breast cancer cells. Br. J. Cancer 88, 1285-1291 (2003) (Pubitemid 36606348)
-
(2003)
British Journal of Cancer
, vol.88
, Issue.8
, pp. 1285-1291
-
-
Tassone, P.1
Tagliaferri, P.2
Perricelli, A.3
Blotta, S.4
Quaresima, B.5
Martelli, M.L.6
Goel, A.7
Barbieri, V.8
Costanzo, F.9
Boland, C.R.10
Venuta, S.11
-
173
-
-
20544474516
-
Cancer risks and mortality in heterozygous ATM mutation carriers
-
DOI 10.1093/jnci/dji141
-
D. Thompson, S. Duedal, J. Kirner, L. McGuffog, J. Last, A. Reiman, P. Byrd, M. Taylor, D.F. Easton, Cancer risks and mortality in heterozygous ATM mutation carriers. J. Natl. Cancer Inst. 97, 813-822 (2005) (Pubitemid 40909124)
-
(2005)
Journal of the National Cancer Institute
, vol.97
, Issue.11
, pp. 813-822
-
-
Thompson, D.1
Duedal, S.2
Kirner, J.3
McGuffog, L.4
Last, J.5
Reiman, A.6
Byrd, P.7
Taylor, M.8
Easton, D.F.9
-
174
-
-
9144251028
-
The genetic epidemiology of breast cancer genes
-
DOI 10.1023/B:JOMG.0000048770.90334.3b, Chromosomal Instability and Breast Cancer Pathogenesis
-
D. Thompson, D. Easton, The genetic epidemiology of breast cancer genes. J. Mammary Gland Biol. Neoplasia 9, 221-236 (2004) (Pubitemid 39545740)
-
(2004)
Journal of Mammary Gland Biology and Neoplasia
, vol.9
, Issue.3
, pp. 221-236
-
-
Thompson, D.1
Easton, D.2
-
175
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
S. Thorlacius, G. Olafsdottir, L. Tryggvadottir, S. Neuhausen, J. G. Jonasson, S.V. Tavtigian, H. Tulinius, H.M. Ogmundsdottir, J. E. Eyfjord, A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat. Genet. 13, 117-119 (1996) (Pubitemid 126528241)
-
(1996)
Nature Genetics
, vol.13
, Issue.1
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Tryggvadottir, L.3
Neuhausen, S.4
Jonasson, J.G.5
Tavtigian, S.V.6
Tulinius, H.7
Ogmundsdottir, H.M.8
Eyfjord, J.E.9
-
176
-
-
36949026476
-
BRCA2: A universal recombinase regulator
-
DOI 10.1038/sj.onc.1210870, PII 1210870
-
T. Thorslund, S.C. West, BRCA2: A universal recombinase regulator. Oncogene 26, 7720-7730 (2007) (Pubitemid 350242452)
-
(2007)
Oncogene
, vol.26
, Issue.56
, pp. 7720-7730
-
-
Thorslund, T.1
West, S.C.2
-
177
-
-
0030894785
-
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations
-
M. Tirkkonen, O. Johannsson, B.A. Agnarsson, H. Olsson, S. Ingvarsson, R. Karhu, M. Tanner, J. Isola, R.B. Barkardottir, A. Borg, O.P. Kallioniemi, Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res. 57, 1222-1227 (1997) (Pubitemid 27152540)
-
(1997)
Cancer Research
, vol.57
, Issue.7
, pp. 1222-1227
-
-
Tirkkonen, M.1
Johannsson, O.2
Agnarsson, B.A.3
Olsson, H.4
Ingvarsson, S.5
Karhu, R.6
Tanner, M.7
Isola, J.8
Barkardottir, R.B.9
Borg, A.10
Kallioniemi, O.-P.11
-
178
-
-
0036076032
-
Loss of heterozygosity analysis: Practically and conceptually flawed?
-
DOI 10.1002/gcc.10085
-
I.P. Tomlinson, M.B. Lambros, R.R. Roylance, Loss of heterozygosity analysis: Practically and conceptually flawed? Genes Chromosom. Cancer 34, 349-353 (2002) (Pubitemid 34787455)
-
(2002)
Genes Chromosomes and Cancer
, vol.34
, Issue.4
, pp. 349-353
-
-
Tomlinson, I.P.M.1
Lambros, M.B.K.2
Roylance, R.R.3
Cleton-Jansen, A.-M.4
-
179
-
-
16044366171
-
Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families
-
DOI 10.1038/nm1196-1179
-
P. Tonin, B. Weber, K. Offit, F. Couch, T.R. Rebbeck, S. Neuhausen, A.K. Godwin, M. Daly, J. Wagner-Costalos, D. Berman, G. Grana, E. Fox, M.F. Kane, R.D. Kolodner, M. Krainer, D.A. Haber, J.P. Struewing, E. Warner, B. Rosen, C. Lerman, B. Peshkin, L. Norton, O. Serova, W.D. Foulkes, J.E. Garber et al., Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families. Nat. Med. 2, 1179-1183 (1996) (Pubitemid 26375392)
-
(1996)
Nature Medicine
, vol.2
, Issue.11
, pp. 1179-1183
-
-
Tonin, P.1
Weber, B.2
Offit, K.3
Couch, F.4
Rebbeck, T.R.5
Neuhausen, S.6
Godwin, A.K.7
Daly, M.8
Wagner-Costalos, J.9
Berman, D.10
Grana, G.11
Fox, E.12
Kane, M.F.13
Kolodner, R.D.14
Krainer, M.15
Haber, D.A.16
Struewing, J.P.17
Warner, E.18
Rosen, B.19
-
180
-
-
35549006364
-
Combining carefully selected drug, patient genetics may lead to total tumor death
-
1509
-
R.S. Tuma, Combining carefully selected drug, patient genetics may lead to total tumor death. J. Natl. Cancer Inst. 99, 1505-1506, 1509 (2007)
-
(2007)
J. Natl. Cancer Inst.
, vol.99
, pp. 1505-1506
-
-
Tuma, R.S.1
-
181
-
-
21644482340
-
Targeting the DNA repair defect of BRCA tumours
-
DOI 10.1016/j.coph.2005.03.006, PII S1471489205000767
-
N. Turner, A. Tutt, A. Ashworth, Targeting the DNA repair defect of BRCA tumours. Curr. Opin. Pharmacol. 5, 388-393 (2005) (Pubitemid 40932041)
-
(2005)
Current Opinion in Pharmacology
, vol.5
, Issue.4 SPEC. ISS.
, pp. 388-393
-
-
Turner, N.1
Tutt, A.2
Ashworth, A.3
-
182
-
-
18444379055
-
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
-
DOI 10.1086/341943
-
P. Vahteristo, J. Bartkova, H. Eerola, K. Syrjakoski, S. Ojala, O. Kilpivaara, A. Tamminen, J. Kononen, K. Aittomaki, P. Heikkila, K. Holli, C. Blomqvist, J. Bartek, O.P. Kallioniemi, H. Nevanlinna, A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am. J. Hum. Genet. 71, 432-438 (2002) (Pubitemid 34800260)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.2
, pp. 432-438
-
-
Vahteristo, P.1
Bartkova, J.2
Eerola, H.3
Syrjakoski, K.4
Ojala, S.5
Kilpivaara, O.6
Tamminen, A.7
Kononen, J.8
Aittomaki, K.9
Heikkila, P.10
Holli, K.11
Blomqvist, C.12
Bartek, J.13
Kallioniemi, O.-P.14
Nevanlinna, H.15
-
183
-
-
0035421321
-
P53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: Further evidence of CHK2 in inherited cancer predisposition
-
P. Vahteristo, A. Tamminen, P. Karvinen, H. Eerola, C. Eklund, L.A. Aaltonen, C. Blomqvist, K. Aittomaki, H. Nevanlinna, p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: Further evidence of CHK2 in inherited cancer predisposition. Cancer Res. 61, 5718-5722 (2001) (Pubitemid 32769084)
-
(2001)
Cancer Research
, vol.61
, Issue.15
, pp. 5718-5722
-
-
Vahteristo, P.1
Tamminen, A.2
Karvinen, P.3
Eerola, H.4
Eklund, C.5
Aaltonen, L.A.6
Blomqvist, C.7
Aittomaki, K.8
Nevanlinna, H.9
-
184
-
-
18244409687
-
Gene expression profiling predicts clinical outcome of breast cancer
-
DOI 10.1038/415530a
-
L.J. van't Veer, H. Dai, M.J. van de Vijver, Y.D. He, A.A. Hart, M. Mao, H.L. Peterse, K. van der Kooy, M.J. Marton, A.T. Witteveen, G.J. Schreiber, R.M. Kerkhoven, C. Roberts, P.S. Linsley, R. Bernards, S.H. Friend, Gene expression profiling predicts clinical outcome of breast cancer. Nature 415, 530-536 (2002) (Pubitemid 34130608)
-
(2002)
Nature
, vol.415
, Issue.6871
, pp. 530-536
-
-
Van't Veer, L.J.1
Dai, H.2
Van De Vijver, M.J.3
He, Y.D.4
Hart, A.A.M.5
Mao, M.6
Peterse, H.L.7
Van Der Kooy, K.8
Marton, M.J.9
Witteveen, A.T.10
Schreiber, G.J.11
Kerkhoven, R.M.12
Roberts, C.13
Linsley, P.S.14
Bernards, R.15
Friend, S.H.16
-
185
-
-
13444292834
-
Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations
-
E.H. van Beers, T. van Welsem, L.F. Wessels, Y. Li, R.A. Oldenburg, P. Devilee, C.J. Cornelisse, S. Verhoef, F.B. Hogervorst, L.J. van't Veer, P.M. Nederlof, Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations. Cancer Res. 65, 822-827 (2005) (Pubitemid 40216440)
-
(2005)
Cancer Research
, vol.65
, Issue.3
, pp. 822-827
-
-
Van Beers, E.H.1
Van Welsem, T.2
Wessels, L.F.A.3
Li, Y.4
Oldenburg, R.A.5
Devilee, P.6
Cornelisse, C.J.7
Verhoef, S.8
Hogervorst, F.B.L.9
Van't Veer, L.J.10
Nederlof, P.M.11
-
186
-
-
51649118874
-
High frequency of HIF-1alpha overexpression in BRCA1 related breast cancer
-
P. van der Groep, A. Bouter, F.H. Menko, E. van der Wall, P.J. van Diest, High frequency of HIF-1alpha overexpression in BRCA1 related breast cancer. Breast Cancer Res. Treat. 111, 475-480 (2008)
-
(2008)
Breast Cancer Res. Treat.
, vol.111
, pp. 475-480
-
-
Van Der Groep, P.1
Bouter, A.2
Menko, F.H.3
Van Der Wall, E.4
Van Diest, P.J.5
-
187
-
-
2442614103
-
Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer
-
author reply 714
-
P. van der Groep, A. Bouter, R. van der Zanden, F.H. Menko, H. Buerger, R.H.Verheijen, E. van derWall, P.J. van Diest, Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. J Natl Cancer Inst 96, 712-713 (2004). author reply 714
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 712-713
-
-
Van Der Groep, P.1
Bouter, A.2
Van Der Zanden, R.3
Menko, F.H.4
Buerger, H.5
Verheijen, R.H.6
Van Der Wall, E.7
Van Diest, P.J.8
-
188
-
-
33745057445
-
Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data
-
DOI 10.1136/jcp.2005.032151
-
P. van der Groep, A. Bouter, R. van der Zanden, I. Siccama, F.H. Menko, J.J. Gille, C. van Kalken, E. van der Wall, R.H. Verheijen, P.J. van Diest, Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data. J. Clin. Pathol. 59, 611-617 (2006) (Pubitemid 43886045)
-
(2006)
Journal of Clinical Pathology
, vol.59
, Issue.6
, pp. 611-617
-
-
Van Der Groep, P.1
Bouter, A.2
Van Der Zanden, R.3
Siccama, I.4
Menko, F.H.5
Gille, J.J.P.6
Van Kalken, C.7
Van Der Wall, E.8
Verheijen, R.H.M.9
Van Diest, P.J.10
-
189
-
-
36549083551
-
Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer
-
DOI 10.1007/s10549-007-9534-7
-
P. van der Groep, M. Hoelzel, H. Buerger, H. Joenje, J.P. de Winter, P.J. van Diest, Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer. Breast Cancer Res. Treat. 107, 41-47 (2008) (Pubitemid 350179594)
-
(2008)
Breast Cancer Research and Treatment
, vol.107
, Issue.1
, pp. 41-47
-
-
Van Der Groep, P.1
Hoelzel, M.2
Buerger, H.3
Joenje, H.4
De Winter, J.P.5
Van Diest, P.J.6
-
190
-
-
70349696551
-
Molecular profile of ductal carcinoma in situ of the breast in BRCA1 and BRCA2 germline mutation carriers
-
P. van der Groep, P.J. van Diest, F.H. Menko, J. Bart, E.G. de Vries, E. van der Wall, Molecular profile of ductal carcinoma in situ of the breast in BRCA1 and BRCA2 germline mutation carriers. J. Clin. Pathol. 62, 926-930 (2009)
-
(2009)
J. Clin. Pathol.
, vol.62
, pp. 926-930
-
-
Van Der Groep, P.1
Van Diest, P.J.2
Menko, F.H.3
Bart, J.4
De Vries, E.G.5
Van Der Wall, E.6
-
191
-
-
31544467620
-
EGFR expression predicts BRCA1 status in patients with breast cancer [3]
-
DOI 10.1158/1078-0432.CCR-05-2098
-
P.J. van Diest, P. van der Groep, E. van der Wall, EGFR expression predicts BRCA1 status in patients with breast cancer. Clin Cancer Res 12, 670 (2006). author reply 671 (Pubitemid 43166165)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.2
, pp. 670
-
-
Van Diest, P.J.1
Van Der Groep, P.2
Van Der Wall, E.3
-
192
-
-
0034772774
-
Breast tumor immunophenotype of BRCA1-mutation carriers is influenced by age at diagnosis
-
S.A. Vaziri, L.M. Krumroy, P. Elson, G.T. Budd, G. Darlington, J. Myles, R.R. Tubbs, G. Casey, Breast tumor immunophenotype of BRCA1-mutation carriers is influenced by age at diagnosis. Clin. Cancer Res. 7, 1937-1945 (2001) (Pubitemid 32994828)
-
(2001)
Clinical Cancer Research
, vol.7
, Issue.7
, pp. 1937-1945
-
-
Vaziri, S.A.J.1
Krumroy, L.M.2
Elson, P.3
Budd, G.T.4
Darlington, G.5
Myles, J.6
Tubbs, R.R.7
Casey, G.8
-
193
-
-
1942502234
-
Tracing the network connecting BRCA and Fanconi anaemia proteins
-
A.R. Venkitaraman, Tracing the network connecting BRCA and Fanconi anaemia proteins. Nat. Rev. Cancer 4, 266-276 (2004) (Pubitemid 38525282)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.4
, pp. 266-276
-
-
Venkitaraman, A.R.1
-
194
-
-
17344392776
-
Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1
-
DOI 10.1016/S0140-6736(97)07065-7
-
L.C. Verhoog, C.T. Brekelmans, C. Seynaeve, L.M. van den Bosch, G. Dahmen, A.N. van Geel, M.M. Tilanus-Linthorst, C. C. Bartels, A. Wagner, A. van den Ouweland, P. Devilee, E.J. Meijers-Heijboer, J.G. Klijn, Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1. Lancet 351, 316-321 (1998) (Pubitemid 28052696)
-
(1998)
Lancet
, vol.351
, Issue.9099
, pp. 316-321
-
-
Verhoog, L.C.1
Brekelmans, C.T.M.2
Seynaeve, C.3
Van Den Bosch, L.M.C.4
Dahmen, G.5
Van Geel, A.N.6
Tilanus-Linthorst, M.M.A.7
Bartels, C.C.M.8
Wagner, A.9
Van Den Ouweland, A.10
Devilee, P.11
Meijers-Heijboer, E.J.12
Klijn, J.G.M.13
-
195
-
-
19944434232
-
Differential prognostic impact of hypoxia induced and diffuse HIF-1α expression in invasive breast cancer
-
DOI 10.1136/jcp.2004.019885
-
M.M. Vleugel, A.E. Greijer, A. Shvarts, P. van der Groep, M. van Berkel, Y. Aarbodem, H. van Tinteren, A.L. Harris, P.J. van Diest, E. van der Wall, Differential prognostic impact of hypoxia induced and diffuse HIF-1alpha expression in invasive breast cancer. J. Clin. Pathol. 58, 172-177 (2005) (Pubitemid 40193803)
-
(2005)
Journal of Clinical Pathology
, vol.58
, Issue.2
, pp. 172-177
-
-
Vleugel, M.M.1
Greijer, A.E.2
Shvarts, A.3
Van Der Groep, P.4
Van Berkel, M.5
Aarbodem, Y.6
Van Tinteren, H.7
Harris, A.L.8
Van Diest, P.J.9
Van Der Wall, E.10
-
197
-
-
0034655991
-
BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures
-
Y. Wang, D. Cortez, P. Yazdi, N. Neff, S.J. Elledge, J. Qin, BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes Dev. 14, 927-939 (2000) (Pubitemid 30253002)
-
(2000)
Genes and Development
, vol.14
, Issue.8
, pp. 927-939
-
-
Wang, Y.1
Cortez, D.2
Yazdi, P.3
Neff, N.4
Elledge, S.J.5
Qin, J.6
-
198
-
-
0035057806
-
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer
-
P.L. Welcsh, M.C. King, BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. Hum. Mol. Genet. 10, 705-713 (2001) (Pubitemid 32331579)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.7
, pp. 705-713
-
-
Welcsh, P.L.1
King, M.-C.2
-
199
-
-
0036895886
-
Molecular classification of breast carcinomas by comparative genomic hybridization: A specific somatic genetic profile for BRCA1 tumors
-
L.F. Wessels, T. van Welsem, A.A. Hart, L.J. van't Veer, M.J. Reinders, P.M. Nederlof, Molecular classification of breast carcinomas by comparative genomic hybridization: A specific somatic genetic profile for BRCA1 tumors. Cancer Res. 62, 7110-7117 (2002) (Pubitemid 35424107)
-
(2002)
Cancer Research
, vol.62
, Issue.23
, pp. 7110-7117
-
-
Wessels, L.F.A.1
Van Welsem, T.2
Hart, A.A.M.3
Van'T Veer, L.J.4
Reinders, M.J.T.5
Nederlof, P.M.6
-
200
-
-
0031466027
-
RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2
-
DOI 10.1074/jbc.272.51.31941
-
A.K. Wong, R. Pero, P.A. Ormonde, S.V. Tavtigian, P.L. Bartel, RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2. J. Biol. Chem. 272, 31941-31944 (1997) (Pubitemid 28011857)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.51
, pp. 31941-31944
-
-
Wong, A.K.C.1
Pero, R.2
Ormonde, P.A.3
Tavtigian, S.V.4
Bartel, P.L.5
-
201
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
DOI 10.1038/378789a0
-
R. Wooster, G. Bignell, J. Lancaster, S. Swift, S. Seal, J. Mangion, N. Collins, S. Gregory, C. Gumbs, G. Micklem, Identification of the breast cancer susceptibility gene BRCA2. Nature 378, 789-792 (1995) (Pubitemid 26004412)
-
(1995)
Nature
, vol.378
, Issue.6559
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
Barfoot, R.11
Hamoudl, R.12
Patel, S.13
Rice, C.14
Biggs, P.15
Hashim, Y.16
Smith, A.17
Connor, F.18
Arason, A.19
Gudmundsson, J.20
Ficenec, D.21
Kelsell, D.22
Ford, D.23
Tonin, P.24
Bishop, D.T.25
Spurr, N.K.26
Ponder, B.A.J.27
Eeles, R.28
Peto, J.29
Devilee, P.30
Cornelisse, C.31
Lynch, H.32
Narod, S.33
Lenoir, G.34
Egilsson, V.35
Barkadottir, R.B.36
Easton, D.F.37
Bentley, D.R.38
Futreal, P.A.39
Ashworth, A.40
Stratton, M.R.41
more..
-
202
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
R. Wooster, S.L. Neuhausen, J. Mangion, Y. Quirk, D. Ford, N. Collins, K. Nguyen, S. Seal, T. Tran, D. Averill et al., Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 265, 2088-2090 (1994) (Pubitemid 24325690)
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
203
-
-
0035951809
-
Characterization of tumorassociated Chk2 mutations
-
X. Wu, S.R. Webster, J. Chen, Characterization of tumorassociated Chk2 mutations. J. Biol. Chem. 276, 2971-2974 (2001)
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 2971-2974
-
-
Wu, X.1
Webster, S.R.2
Chen, J.3
-
204
-
-
0033179235
-
BRCA2 is required for ionizing radiation-induced assembly of Rad51 complex in vivo
-
S.S. Yuan, S.Y. Lee, G. Chen, M. Song, G.E. Tomlinson, E.Y. Lee, BRCA2 is required for ionizing radiation-induced assembly of Rad51 complex in vivo. Cancer Res. 59, 3547-3551 (1999) (Pubitemid 29381849)
-
(1999)
Cancer Research
, vol.59
, Issue.15
, pp. 3547-3551
-
-
Yuan, S.-S.F.1
Lee, S.-Y.2
Chen, G.3
Song, M.4
Tomlinson, G.E.5
Lee, E.Y.-H.P.6
-
205
-
-
0033618621
-
Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response
-
Q. Zhong, C.F. Chen, S. Li, Y. Chen, C.C. Wang, J. Xiao, P.L. Chen, Z.D. Sharp, W.H. Lee, Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response. Science 285, 747-750 (1999)
-
(1999)
Science
, vol.285
, pp. 747-750
-
-
Zhong, Q.1
Chen, C.F.2
Li, S.3
Chen, Y.4
Wang, C.C.5
Xiao, J.6
Chen, P.L.7
Sharp, Z.D.8
Lee, W.H.9
-
206
-
-
0033976892
-
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations
-
DOI 10.1006/gyno.1999.5623
-
R.P. Zweemer, P.J. van Diest, R.H. Verheijen, A. Ryan, J.J. Gille, R.H. Sijmons, I.J. Jacobs, F.H. Menko, P. Kenemans, Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations. Gynecol. Oncol. 76, 45-50 (2000) (Pubitemid 30048318)
-
(2000)
Gynecologic Oncology
, vol.76
, Issue.1
, pp. 45-50
-
-
Zweemer, R.P.1
Van Diest, P.J.2
Verheijen, R.H.M.3
Ryan, A.4
Gille, J.J.P.5
Sijmons, R.H.6
Jacobs, I.J.7
Menko, F.H.8
Kenemans, P.9
|