-
1
-
-
0035895504
-
Human DNA repair genes
-
Wood, R. D., Mitchell, M., Sgouros, J. & Lindahl, T. Human DNA repair genes. Science 291, 1284-9 (2001).
-
(2001)
Science
, vol.291
, pp. 1284-1289
-
-
Wood, R.D.1
Mitchell, M.2
Sgouros, J.3
Lindahl, T.4
-
2
-
-
0242331221
-
Mechanisms of human DNA repair: An update
-
Christmann, M., Tomicic, M. T., Roos, W. P. & Kaina, B. Mechanisms of human DNA repair: an update. Toxicology 193, 3-34 (2003).
-
(2003)
Toxicology
, vol.193
, pp. 3-34
-
-
Christmann, M.1
Tomicic, M.T.2
Roos, W.P.3
Kaina, B.4
-
3
-
-
0036261707
-
Sensing and repairing DNA double-strand breaks
-
Jackson, S. P. Sensing and repairing DNA double-strand breaks. Carcinogenesis 23, 687-96 (2002).
-
(2002)
Carcinogenesis
, vol.23
, pp. 687-696
-
-
Jackson, S.P.1
-
4
-
-
0035500805
-
Double-strand breaks and tumorigenesis
-
Pierce, A. J. et al. Double-strand breaks and tumorigenesis. Trends Cell Biol 11, S52-9 (2001).
-
(2001)
Trends Cell Biol
, vol.11
, pp. S52-S59
-
-
Pierce, A.J.1
-
5
-
-
34249911218
-
RAD51, BRCA2 and DNA repair: A partial resolution
-
Lord, C. J. & Ashworth, A. RAD51, BRCA2 and DNA repair: a partial resolution. Nat Struct Mol Biol 14, 461-2 (2007).
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 461-462
-
-
Lord, C.J.1
Ashworth, A.2
-
6
-
-
34249887673
-
Interaction with the BRCA2 C terminus protects RAD51-DNA filaments from disassembly by BRC repeats
-
Davies, O. R. & Pellegrini, L. Interaction with the BRCA2 C terminus protects RAD51-DNA filaments from disassembly by BRC repeats. Nat Struct Mol Biol 14, 475-83 (2007).
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 475-483
-
-
Davies, O.R.1
Pellegrini, L.2
-
7
-
-
34249878748
-
Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2
-
Esashi, F., Galkin, V. E., Yu, X., Egelman, E. H. & West, S. C. Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2. Nat Struct Mol Biol 14, 468-74 (2007).
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 468-474
-
-
Esashi, F.1
Galkin, V.E.2
Yu, X.3
Egelman, E.H.4
West, S.C.5
-
8
-
-
2242443513
-
Insights into DNA recombination from the structure of a RAD51-BRCA2 complex
-
Pellegrini, L. et al. Insights into DNA recombination from the structure of a RAD51-BRCA2 complex. Nature 420, 287-93 (2002).
-
(2002)
Nature
, vol.420
, pp. 287-293
-
-
Pellegrini, L.1
-
9
-
-
0037169354
-
Cancer susceptibility and the functions of BRCA1 and BRCA2
-
Venkitaraman, A. R. Cancer susceptibility and the functions of BRCA1 and BRCA2. Cell 108, 171-82 (2002).
-
(2002)
Cell
, vol.108
, pp. 171-182
-
-
Venkitaraman, A.R.1
-
10
-
-
0036578764
-
Polygenic susceptibility to breast cancer and implications for prevention
-
Pharoah, P. D. et al. Polygenic susceptibility to breast cancer and implications for prevention. Nat Genet 31, 33-6 (2002).
-
(2002)
Nat Genet
, vol.31
, pp. 33-36
-
-
Pharoah, P.D.1
-
11
-
-
0032512067
-
BRCA2 associates with acetyltransferase activity when bound to P/CAF
-
Fuks, F., Milner, J. & Kouzarides, T. BRCA2 associates with acetyltransferase activity when bound to P/CAF. Oncogene 17, 2531-4 (1998).
-
(1998)
Oncogene
, vol.17
, pp. 2531-2534
-
-
Fuks, F.1
Milner, J.2
Kouzarides, T.3
-
12
-
-
0033768238
-
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability
-
Healey, C. S. et al. A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability. Nat Genet 26, 362-4 (2000).
-
(2000)
Nat Genet
, vol.26
, pp. 362-364
-
-
Healey, C.S.1
-
13
-
-
26444479826
-
Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk
-
Millikan, R. C., Player, J. S., Decotret, A. R., Tse, C. K. & Keku, T. Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk. Cancer Epidemiol Biomarkers Prev 14, 2326-34 (2005).
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 2326-2334
-
-
Millikan, R.C.1
Player, J.S.2
Decotret, A.R.3
Tse, C.K.4
Keku, T.5
-
14
-
-
0036120189
-
The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years
-
Spurdle, A. B. et al. The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years. Cancer Epidemiol Biomarkers Prev 11, 413-6 (2002).
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 413-416
-
-
Spurdle, A.B.1
-
15
-
-
33749571327
-
Commonly studied single-nucleotide polymorphisms and breast cancer: Results from the breast cancer association consortium
-
Breast Cancer Association Consortium. Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium. J Natl Cancer Inst 98, 1382-96 (2006).
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1382-1396
-
-
-
16
-
-
77956185031
-
BRCA2 N372H polymorphism and breast cancer susceptibility: A meta-analysis involving 44,903 subjects
-
Qiu, L. X. et al. BRCA2 N372H polymorphism and breast cancer susceptibility: a meta-analysis involving 44,903 subjects. Breast Cancer Res Treat 123, 487-90 (2010).
-
(2010)
Breast Cancer Res Treat
, vol.123
, pp. 487-490
-
-
Qiu, L.X.1
-
17
-
-
18544375922
-
No association between BRCA2 N372H and breast cancer risk
-
Cox, D. G., Hankinson, S. E. & Hunter, D. J. No association between BRCA2 N372H and breast cancer risk. Cancer Epidemiol Biomarkers Prev 14, 1353-4 (2005).
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 1353-1354
-
-
Cox, D.G.1
Hankinson, S.E.2
Hunter, D.J.3
-
18
-
-
68949084967
-
Missense polymorphisms in BRCA1 and BRCA2 and risk of breast and ovarian cancer
-
Dombernowsky, S. L. et al. Missense polymorphisms in BRCA1 and BRCA2 and risk of breast and ovarian cancer. Cancer Epidemiol Biomarkers Prev 18, 2339-42 (2009).
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 2339-2342
-
-
Dombernowsky, S.L.1
-
19
-
-
19544364468
-
Common variation in BRCA2 and breast cancer risk: A haplotype-based analysis in the multiethnic cohort
-
Freedman, M. L. et al. Common variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort. Hum Mol Genet 13, 2431-41 (2004).
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2431-2441
-
-
Freedman, M.L.1
-
20
-
-
33645744903
-
Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: Two population-based studies in USA and Poland, and meta-analyses
-
Garcia-Closas, M. et al. Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses. Hum Genet 119, 376-88 (2006).
-
(2006)
Hum Genet
, vol.119
, pp. 376-388
-
-
Garcia-Closas, M.1
-
21
-
-
57049115891
-
Association of polymorphisms of N372H in BRCA2 gene and 135G/C in RAD51 gene and breast cancers
-
Hu, R. et al. [Association of polymorphisms of N372H in BRCA2 gene and 135G/C in RAD51 gene and breast cancers]. Sichuan Da Xue Xue Bao Yi Xue Ban 39, 973-5 (2008).
-
(2008)
Sichuan da Xue Xue Bao Yi Xue Ban
, vol.39
, pp. 973-975
-
-
Hu, R.1
-
22
-
-
0037390199
-
Association of BRCA2 polymorphism at codon 784 (Met/Val) with breast cancer risk and prognosis
-
Ishitobi, M. et al. Association of BRCA2 polymorphism at codon 784 (Met/Val) with breast cancer risk and prognosis. Clin Cancer Res 9, 1376-80 (2003).
-
(2003)
Clin Cancer Res
, vol.9
, pp. 1376-1380
-
-
Ishitobi, M.1
-
23
-
-
34447295643
-
Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility
-
Johnson, N. et al. Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility. Hum Mol Genet 16, 1051-7 (2007).
-
(2007)
Hum Mol Genet
, vol.16
, pp. 1051-1057
-
-
Johnson, N.1
-
24
-
-
80051993060
-
Association study between signal nucleotide plymorphism of BRCA2 and susceptibility to sporadic breast cancer in han Chinese women from jiangxi province
-
Li, X. et al. Association study between signal nucleotide plymorphism of BRCA2 and susceptibility to sporadic breast cancer in Han Chinese women from Jiangxi province. Chin J Cancer Prev Treat 18, 489-493 (2011).
-
(2011)
Chin J Cancer Prev Treat
, vol.18
, pp. 489-493
-
-
Li, X.1
-
25
-
-
2942628016
-
Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations
-
Menzel, H. J. et al. Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations. Br J Cancer 90, 1989-94 (2004).
-
(2004)
Br J Cancer
, vol.90
, pp. 1989-1994
-
-
Menzel, H.J.1
-
26
-
-
80052743253
-
Novel sequence variants and common recurrent polymorphisms of BRCA2 in Sri Lankan breast cancer patients and a family with BRCA1 mutations
-
S, D. E. S. et al.
-
S, D. E. S. et al. Novel sequence variants and common recurrent polymorphisms of BRCA2 in Sri Lankan breast cancer patients and a family with BRCA1 mutations. Exp Ther Med 2, 1163-1170 (2011).
-
(2011)
Exp Ther Med
, vol.2
, pp. 1163-1170
-
-
-
27
-
-
40249088775
-
Disease family history and modification of breast cancer risk in common BRCA2 variants
-
Seymour, I. J. C. S. & Zampiga, V. Disease family history and modification of breast cancer risk in common BRCA2 variants. Oncol Rep 19, 783-786 (2008).
-
(2008)
Oncol Rep
, vol.19
, pp. 783-786
-
-
Seymour, I.J.C.S.1
Zampiga, V.2
-
29
-
-
0037454803
-
BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk
-
Auranen, A. et al. BRCA2 Arg372Hispolymorphism and epithelial ovarian cancer risk. Int J Cancer 103, 427-30 (2003).
-
(2003)
Int J Cancer
, vol.103
, pp. 427-430
-
-
Auranen, A.1
-
30
-
-
38849190562
-
Association between single-nucleotide polymorphisms in hormonemetabolism and DNA repair genes and epithelial ovarian cancer: Results from two Australian studies and an additional validation set
-
Beesley, J. et al. Association between single-nucleotide polymorphisms in hormonemetabolism and DNA repair genes and epithelial ovarian cancer: results from two Australian studies and an additional validation set. Cancer Epidemiol Biomarkers Prev 16, 2557-65 (2007).
-
(2007)
Cancer Epidemiol Biomarkers Prev
, vol.16
, pp. 2557-2565
-
-
Beesley, J.1
-
31
-
-
0141925969
-
Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer
-
Wenham, R.M. et al. Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer. Clin Cancer Res 9, 4396-403 (2003).
-
(2003)
Clin Cancer Res
, vol.9
, pp. 4396-4403
-
-
Wenham, R.M.1
-
32
-
-
33751193888
-
Risk of non-hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes
-
Hill, D. A. et al. Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. Blood 108, 3161-7 (2006).
-
(2006)
Blood
, vol.108
, pp. 3161-3167
-
-
Hill, D.A.1
-
33
-
-
84866272444
-
Association of follicular lymphoma risk with BRCA2 N372H polymorphism in slovak population
-
Salagovic, J., Klimcakova, L., Ilencikova, D. & Kafkova, A. Association of follicular lymphoma risk with BRCA2 N372H polymorphism in Slovak population. Med Oncol 29, 1173-8 (2012).
-
(2012)
Med Oncol
, vol.29
, pp. 1173-1178
-
-
Salagovic, J.1
Klimcakova, L.2
Ilencikova, D.3
Kafkova, A.4
-
34
-
-
34250015545
-
RAG1 and BRCA2 polymorphisms in non-hodgkin lymphoma
-
Scott, K. et al. RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphoma. Blood 109, 5522-3 (2007).
-
(2007)
Blood
, vol.109
, pp. 5522-5523
-
-
Scott, K.1
-
35
-
-
36248960241
-
Polymorphisms in DNA repair genes and risk of non-hodgkin's lymphoma in New South Wales, Australia
-
Shen, M. et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin's lymphoma in New South Wales, Australia. Haematologica 92, 1180-5 (2007).
-
(2007)
Haematologica
, vol.92
, pp. 1180-1185
-
-
Shen, M.1
-
36
-
-
33744464558
-
Polymorphisms in DNA repair genes and risk of non-hodgkin lymphoma among women in Connecticut
-
Shen, M. et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut. Hum Genet 119, 659-68 (2006).
-
(2006)
Hum Genet
, vol.119
, pp. 659-668
-
-
Shen, M.1
-
37
-
-
33745952966
-
Variants in the ATM-BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia
-
Rudd, M. F., Sellick, G. S., Webb, E. L., Catovsky, D. & Houlston, R. S. Variants in the ATM-BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia. Blood 108, 638-44 (2006).
-
(2006)
Blood
, vol.108
, pp. 638-644
-
-
Rudd, M.F.1
Sellick, G.S.2
Webb, E.L.3
Catovsky, D.4
Houlston, R.S.5
-
38
-
-
77950689168
-
Genetic variation in DNA repair genes and prostate cancer risk: Results from a population-based study
-
Agalliu, I. et al. Genetic variation in DNA repair genes and prostate cancer risk: results from a population-based study. Cancer Causes Control 21, 289-300 (2010).
-
(2010)
Cancer Causes Control
, vol.21
, pp. 289-300
-
-
Agalliu, I.1
-
39
-
-
0037254305
-
Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China
-
Hu, N. et al. Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China. Cancer Detect Prev 27, 132-8 (2003).
-
(2003)
Cancer Detect Prev
, vol.27
, pp. 132-138
-
-
Hu, N.1
-
40
-
-
33344464252
-
Bladder cancer predisposition: Amultigenic approach to DNA-repair and cell-cycle-control genes
-
Wu, X. et al. Bladder cancer predisposition: amultigenic approach to DNA-repair and cell-cycle-control genes. Am J Hum Genet 78, 464-79 (2006).
-
(2006)
Am J Hum Genet
, vol.78
, pp. 464-479
-
-
Wu, X.1
-
41
-
-
37149000722
-
Common variants of DNA repair genes and malignant melanoma
-
Debniak, T. et al. Common variants of DNA repair genes and malignant melanoma. Eur J Cancer 44, 110-4 (2008).
-
(2008)
Eur J Cancer
, vol.44
, pp. 110-114
-
-
Debniak, T.1
-
42
-
-
84855654225
-
Multiple pathway-based genetic variations associated with tobacco related multiple primary neoplasms
-
Kotnis, A. et al. Multiple pathway-based genetic variations associated with tobacco related multiple primary neoplasms. PLoS One 7, e30013 (2012).
-
(2012)
PLoS One
, vol.7
, pp. e30013
-
-
Kotnis, A.1
-
43
-
-
0036907407
-
Polymorphisms in DNArepair genes and associations with cancer risk
-
Goode, E. L., Ulrich, C. M. & Potter, J. D. Polymorphisms in DNArepair genes and associations with cancer risk. Cancer Epidemiol Biomarkers Prev 11, 1513-30 (2002).
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 1513-1530
-
-
Goode, E.L.1
Ulrich, C.M.2
Potter, J.D.3
-
44
-
-
36248960241
-
Polymorphisms in DNA repair genes and risk of non-hodgkin's lymphoma in New South Wales, Australia
-
Shen, M. et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin's lymphoma in New South Wales, Australia. Haematologica 92, 1180-1185 (2007).
-
(2007)
Haematologica
, vol.92
, pp. 1180-1185
-
-
Shen, M.1
-
45
-
-
68549101842
-
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: Explanation and elaboration
-
Liberati, A. et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ 339, b2700 (2009).
-
(2009)
BMJ
, vol.339
, pp. b2700
-
-
Liberati, A.1
-
46
-
-
84906706005
-
Association of MTHFR C677T and A1298C polymorphisms with non-hodgkin lymphoma susceptibility: Evidence from ameta-analysis
-
He, J. et al. Association of MTHFR C677T and A1298C polymorphisms with non-Hodgkin lymphoma susceptibility: Evidence from ameta-analysis. Sci Rep 4, 6159 (2014).
-
(2014)
Sci Rep
, vol.4
, pp. 6159
-
-
He, J.1
|