-
1
-
-
52949096470
-
Genetic predisposition to breast cancer: Past, present, and future
-
Turnbull, C. & Rahman, N. Genetic predisposition to breast cancer: past, present, and future. Annu. Rev. Genomics Hum. Genet. 9, 321-345 (2008).
-
(2008)
Annu. Rev. Genomics Hum. Genet
, vol.9
, pp. 321-345
-
-
Turnbull, C.1
Rahman, N.2
-
2
-
-
50649091874
-
Structural and functional relationships of the XPF/MUS81 family of proteins
-
Ciccia, A., McDonald, N. & West, S.C. Structural and functional relationships of the XPF/MUS81 family of proteins. Annu. Rev. Biochem. 77, 259-287 (2008).
-
(2008)
Annu. Rev. Biochem
, vol.77
, pp. 259-287
-
-
Ciccia, A.1
McDonald, N.2
West, S.C.3
-
3
-
-
34548759123
-
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
-
DOI 10.1038/nrg2159, PII NRG2159
-
Wang, W. Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins. Nat. Rev. Genet. 8, 735-748 (2007). (Pubitemid 47429206)
-
(2007)
Nature Reviews Genetics
, vol.8
, Issue.10
, pp. 735-748
-
-
Wang, W.1
-
4
-
-
67650403821
-
Genotype-phenotype correlations in Fanconi anemia
-
Neveling, K., Endt, D., Hoehn, H. & Schindler, D. Genotype-phenotype correlations in Fanconi anemia. Mutat. Res. 668, 73-91 (2009).
-
(2009)
Mutat. Res
, vol.668
, pp. 73-91
-
-
Neveling, K.1
Endt, D.2
Hoehn, H.3
Schindler, D.4
-
5
-
-
77951747926
-
Mutation of the RAD51C gene in Fanconi anemia
-
advance online publication doi:10.1038/ng.570 (18 April 2010)
-
Vaz, F. et al. Mutation of the RAD51C gene in Fanconi anemia. Nat. Genet. advance online publication, doi:10.1038/ng.570 (18 April 2010).
-
Nat. Genet
-
-
Vaz, F.1
-
6
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
Howlett, N.G. et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 297, 606-609 (2002).
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
-
7
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
DOI 10.1038/ng1947, PII NG1947
-
Reid, S. et al. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat. Genet. 39, 162-164 (2007). (Pubitemid 46184345)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
Neveling, K.7
Kelly, P.8
Seal, S.9
Freund, M.10
Wurm, M.11
Batish, S.D.12
Lach, F.P.13
Yetgin, S.14
Neitzel, H.15
Ariffin, H.16
Tischkowitz, M.17
Mathew, C.G.18
Auerbach, A.D.19
Rahman, N.20
more..
-
8
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
DOI 10.1038/ng1942, PII NG1942
-
Xia, B. et al. Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat. Genet. 39, 159-161 (2007). (Pubitemid 46184344)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
De Vries, Y.4
Rooimans, M.A.5
Sheng, Q.6
Pals, G.7
Errami, A.8
Gluckman, E.9
Llera, J.10
Wang, W.11
Livingston, D.M.12
Joenje, H.13
De Winter, J.P.14
-
9
-
-
13944268723
-
The RAD51 gene family, genetic instability and cancer
-
DOI 10.1016/j.canlet.2004.08.018
-
Thacker, J. The RAD51 gene family, genetic instability and cancer. Cancer Lett. 219, 125-135 (2005). (Pubitemid 40269475)
-
(2005)
Cancer Letters
, vol.219
, Issue.2
, pp. 125-135
-
-
Thacker, J.1
-
10
-
-
33745237158
-
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
-
Arking, D.E. et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006).
-
(2006)
Nat. Genet
, vol.38
, pp. 644-651
-
-
Arking, D.E.1
-
11
-
-
10744224600
-
A novel approach to describe a U1 snRNA binding site
-
DOI 10.1093/nar/gkg901
-
Freund, M. et al. A novel approach to describe a U1 snRNA binding site. Nucleic Acids Res. 31, 6963-6975 (2003). (Pubitemid 37508803)
-
(2003)
Nucleic Acids Research
, vol.31
, Issue.23
, pp. 6963-6975
-
-
Freund, M.1
Asang, C.2
Kammler, S.3
Konermann, C.4
Krummheuer, J.5
Hipp, M.6
Meyer, I.7
Gierling, W.8
Theiss, S.9
Preuss, T.10
Schindler, D.11
Kjems, J.12
Schaal, H.13
-
12
-
-
77951769519
-
Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2
-
(8 August 2009)
-
Betz, B. et al. Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2. J. Cancer Res. Clin. Oncol. published online (8 August 2009).
-
J. Cancer Res. Clin. Oncol. Published Online
-
-
Betz, B.1
-
13
-
-
16044366110
-
Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells
-
DOI 10.1038/nm0896-876
-
Hanenberg, H. et al. Colocalization of retrovirus and target cells on specifc fbronectin fragments increases genetic transduction of mammalian cells. Nat. Med. 2, 876-882 (1996). (Pubitemid 26296757)
-
(1996)
Nature Medicine
, vol.2
, Issue.8
, pp. 876-882
-
-
Hanenberg, H.1
Xiao, X.L.2
Dilloo, D.3
Hashino, K.4
Kato, I.5
Williams, D.A.6
-
14
-
-
0035083172
-
Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs
-
DOI 10.1128/MCB.21.8.2858-2866.2001
-
Takata, M. et al. Chromosome instability and defective recombinational repair in knockout mutants of the fve Rad51 paralogs. Mol. Cell. Biol. 21, 2858-2866 (2001). (Pubitemid 32244929)
-
(2001)
Molecular and Cellular Biology
, vol.21
, Issue.8
, pp. 2858-2866
-
-
Takata, M.1
Sasaki, M.S.2
Tachiiri, S.3
Fukushima, T.4
Sonoda, E.5
Schild, D.6
Thompson, L.H.7
Takeda, S.8
-
15
-
-
66149151303
-
RAD51C facilitates checkpoint signaling by promoting CHK2 phosphorylation
-
Badie, S. et al. RAD51C facilitates checkpoint signaling by promoting CHK2 phosphorylation. J. Cell Biol. 185, 587-600 (2009).
-
(2009)
J. Cell Biol
, vol.185
, pp. 587-600
-
-
Badie, S.1
-
16
-
-
0346340054
-
RAD51C is required for holliday junction processing in mammalian cells
-
DOI 10.1126/science.1093037
-
Liu, Y., Masson, J.Y., Shah, R., O′Regan, P. & West, S.C. RAD51C is required for Holliday junction processing in mammalian cells. Science 303, 243-246 (2004). (Pubitemid 38057577)
-
(2004)
Science
, vol.303
, Issue.5655
, pp. 243-246
-
-
Liu, Y.1
Masson, J.-Y.2
Shah, R.3
O'Regan, P.4
West, S.C.5
-
17
-
-
67651163668
-
The ATR-Chk1 pathway plays a role in the generation of centrosome aberrations induced by Rad51C dysfunction
-
Katsura, M. et al. The ATR-Chk1 pathway plays a role in the generation of centrosome aberrations induced by Rad51C dysfunction. Nucleic Acids Res. 37, 3959-3968 (2009).
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 3959-3968
-
-
Katsura, M.1
-
18
-
-
0142178215
-
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
DOI 10.1126/science.1088759
-
King, M.C., Marks, J.H. & Mandell, J.B. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 302, 643-646 (2003). (Pubitemid 37310920)
-
(2003)
Science
, vol.302
, Issue.5645
, pp. 643-646
-
-
King, M.-C.1
Marks, J.H.2
Mandell, J.B.3
-
19
-
-
0032486752
-
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations
-
Lakhani, S.R. et al. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J. Natl. Cancer Inst. 90, 1138-1145 (1998).
-
(1998)
J. Natl. Cancer Inst
, vol.90
, pp. 1138-1145
-
-
Lakhani, S.R.1
-
20
-
-
11144354423
-
Pathology of ovarian cancers in BRCA1 and BRCA2 carriers
-
DOI 10.1158/1078-0432.CCR-1029-3
-
Lakhani, S.R. et al. Pathology of ovarian cancers in BRCA1 and BRCA2 carriers. Clin. Cancer Res. 10, 2473-2481 (2004). (Pubitemid 38445709)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.7
, pp. 2473-2481
-
-
Lakhani, S.R.1
Manek, S.2
Penault-Llorca, F.3
Flanagan, A.4
Arnout, L.5
Merrett, S.6
McGuffog, L.7
Steele, D.8
Devilee, P.9
Klijn, J.G.M.10
Meijers-Heijboer, H.11
Radice, P.12
Pilotti, S.13
Nevanlinna, H.14
Butzow, R.15
Sobol, H.16
Jacquemier, J.17
Lyonet, D.S.18
Neuhausen, S.L.19
Weber, B.20
Wagner, T.21
Winqvist, R.22
Bignon, Y.-J.23
Monti, F.24
Schmitt, F.25
Lenoir, G.26
Seitz, S.27
Hamman, U.28
Pharoah, P.29
Lane, G.30
Ponder, B.31
Bishop, D.T.32
Easton, D.F.33
more..
-
21
-
-
22344443194
-
Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype
-
Lakhani, S.R. et al. Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype. Clin. Cancer Res. 11, 5175-5180 (2005).
-
(2005)
Clin. Cancer Res
, vol.11
, pp. 5175-5180
-
-
Lakhani, S.R.1
-
22
-
-
0032029599
-
Isolation and characterization of RAD51C, a new human member of the RAD51 family of related genes
-
DOI 10.1093/nar/26.5.1179
-
Dosanjh, M.K. et al. Isolation and characterization of RAD51C, a new human member of the RAD51 family of related genes. Nucleic Acids Res. 26, 1179-1184 (1998). (Pubitemid 28291687)
-
(1998)
Nucleic Acids Research
, vol.26
, Issue.5
, pp. 1179-1184
-
-
Dosanjh, M.K.1
Collins, D.W.2
Fan, W.3
Lennon, G.G.4
Albala, J.S.5
Shen, Z.6
Schild, D.7
-
23
-
-
59149088203
-
Loss of Rad51c leads to embryonic lethality and modulation of Trp53-dependent tumorigenesis in mice
-
Kuznetsov, S.G., Haines, D.C., Martin, B.K. & Sharan, S.K. Loss of Rad51c leads to embryonic lethality and modulation of Trp53-dependent tumorigenesis in mice. Cancer Res. 69, 863-872 (2009).
-
(2009)
Cancer Res
, vol.69
, pp. 863-872
-
-
Kuznetsov, S.G.1
Haines, D.C.2
Martin, B.K.3
Sharan, S.K.4
-
24
-
-
67349158067
-
A multistage genome-wide association study in breast cancer identifes two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
-
Thomas, G. et al. A multistage genome-wide association study in breast cancer identifes two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat. Genet. 41, 579-584 (2009).
-
(2009)
Nat. Genet
, vol.41
, pp. 579-584
-
-
Thomas, G.1
-
25
-
-
64849092309
-
Exomic sequencing identifes PALB2 as a pancreatic cancer susceptibility gene
-
Jones, S. et al. Exomic sequencing identifes PALB2 as a pancreatic cancer susceptibility gene. Science 324, 217 (2009).
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
-
26
-
-
33846850422
-
Ten genes for inherited breast cancer
-
DOI 10.1016/j.ccr.2007.01.010, PII S1535610807000256
-
Walsh, T. & King, M.C. Ten genes for inherited breast cancer. Cancer Cell 11, 103-105 (2007). (Pubitemid 46209856)
-
(2007)
Cancer Cell
, vol.11
, Issue.2
, pp. 103-105
-
-
Walsh, T.1
King, M.-C.2
-
27
-
-
0036466858
-
German Consortium for Hereditary Breast and Ovarian Cancer Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profles and frequencies for the German population
-
Meindl, A. & German Consortium for Hereditary Breast and Ovarian Cancer Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profles and frequencies for the German population. Int. J. Cancer 97, 472-480 (2002).
-
(2002)
Int. J. Cancer
, vol.97
, pp. 472-480
-
-
Meindl, A.1
-
28
-
-
46749157576
-
MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: Novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases
-
DOI 10.1002/humu.20723
-
Engert, S. et al. MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases. Hum. Mutat. 29, 948-958 (2008). (Pubitemid 351951289)
-
(2008)
Human Mutation
, vol.29
, Issue.7
, pp. 948-958
-
-
Engert, S.1
Wappenschmidt, B.2
Betz, B.3
Kast, K.4
Kutsche, M.5
Hellebrand, H.6
Goecke, T.O.7
Kiechle, M.8
Niederacher, D.9
Schmutzler, R.K.10
Meindl, A.11
-
29
-
-
23844467739
-
KORA - A research platform for population based health research
-
DOI 10.1055/s-2005-858235
-
Holle, R., Happich, M., Lowel, H. & Wichmann, H.E. KORA-a research platform for population based health research. Gesundheitswesen 67 (Suppl. 1), S19-S25 (2005). (Pubitemid 41153389)
-
(2005)
Gesundheitswesen
, vol.67
, Issue.SUPPL. 1
-
-
Holle, R.1
Happich, M.2
Lowel, H.3
Wichmann, H.E.4
-
30
-
-
23844472247
-
KORA-gen - Resource for population genetics, controls and a broad spectrum of disease phenotypes
-
DOI 10.1055/s-2005-858226
-
Wichmann, H.E., Gieger, C. & Illig, T. KORA-gen-resource for population genetics, controls and a broad spectrum of disease phenotypes. Gesundheitswesen 67 (Suppl. 1), S26-S30 (2005). (Pubitemid 41153390)
-
(2005)
Gesundheitswesen
, vol.67
, Issue.SUPPL. 1
-
-
Wichmann, H.-E.1
Gieger, C.2
Illig, T.3
-
31
-
-
0033621054
-
Chip-based genotyping by mass spectrometry
-
DOI 10.1073/pnas.96.18.10016
-
Tang, K. et al. Chip-based genotyping by mass spectrometry. Proc. Natl. Acad. Sci. USA 96, 10016-10020 (1999). (Pubitemid 29422504)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.18
, pp. 10016-10020
-
-
Tang, K.1
Fu, D.-J.2
Julien, D.3
Braun, A.4
Cantor, C.R.5
Kostek, H.6
-
32
-
-
25144471268
-
Extended base pair complementarity between U1 snRNA and the 5′ splice site does not inhibit splicing in higher eukaryotes, but rather increases 5′ splice site recognition
-
DOI 10.1093/nar/gki824
-
Freund, M. et al. Extended base pair complementarity between U1 snRNA and the 5′ splice site does not inhibit splicing in higher eukaryotes, but rather increases 5′ splice site recognition. Nucleic Acids Res. 33, 5112-5119 (2005). (Pubitemid 41487819)
-
(2005)
Nucleic Acids Research
, vol.33
, Issue.16
, pp. 5112-5119
-
-
Freund, M.1
Hicks, M.J.2
Konermann, C.3
Otte, M.4
Hertel, K.J.5
Schaal, H.6
-
33
-
-
0031564330
-
+ hematopoietic cells
-
Hanenberg, H. et al. Optimization of fbronectin-assisted retroviral gene transfer into human CD34+ hematopoietic cells. Hum. Gene Ther. 8, 2193-2206 (1997). (Pubitemid 28043557)
-
(1997)
Human Gene Therapy
, vol.8
, Issue.18
, pp. 2193-2206
-
-
Hanenberg, H.1
Hashino, K.2
Konishi, H.3
Hock, R.A.4
Kato, I.5
Williams, D.A.6
-
34
-
-
18444378426
-
Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool
-
DOI 10.1016/S0301-472X(02)00782-8, PII S0301472X02007828
-
Hanenberg, H. et al. Phenotypic correction of primary Fanconi anemia T cells from patients with retroviral vectors as a diagnostic tool. Exp. Hematol. 30, 410-420 (2002). (Pubitemid 34556732)
-
(2002)
Experimental Hematology
, vol.30
, Issue.5
, pp. 410-420
-
-
Hanenberg, H.1
Batish, S.D.2
Pollok, K.E.3
Vieten, L.4
Verlander, P.C.5
Leurs, C.6
Cooper, R.J.7
Gottsche, K.8
Haneline, L.9
Clapp, D.W.10
Lobitz, S.11
Williams, D.A.12
Auerbach, A.D.13
-
35
-
-
84870186364
-
Functional knock-down of human RAD51 for testing the Fanconi anemia-BRCA connection
-
(eds. Schindler, D. & Hoehn, H.) Karger, Basel, Switzerland
-
Rio, P. & Hanenberg, H. Functional knock-down of human RAD51 for testing the Fanconi anemia-BRCA connection. in Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging (eds. Schindler, D. & Hoehn, H.) 211-225 (Karger, Basel, Switzerland, 2007).
-
(2007)
Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging
, pp. 211-225
-
-
Rio, P.1
Hanenberg, H.2
|