-
1
-
-
78049485263
-
Estimates of worldwide burden of cancer in 2008
-
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCANN Int J Cancer. 2010;127(12):2893- 917.
-
(2010)
GLOBOCANN Int J Cancer
, vol.127
, Issue.12
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
Forman, D.4
Mathers, C.5
Parkin, D.M.6
-
2
-
-
33747126447
-
Estimating the burden of disease and the benefits of prevention
-
Hartge P. Estimating the burden of disease and the benefits of prevention. Epidemiology. 2006;17(5):498-9.
-
(2006)
Epidemiology
, vol.17
, Issue.5
, pp. 498-499
-
-
Hartge, P.1
-
3
-
-
33645180367
-
Overview of the etiology and epidemiology of lymphoma
-
In: Mauch PM, Armitage JO, Coiffier B, Dalla- Favera R, Harris NL, editors. Philadelphia: Lippincott Williams& Wilkins
-
Hartge P, Wang SS. Overview of the etiology and epidemiology of lymphoma. In: Mauch PM, Armitage JO, Coiffier B, Dalla- Favera R, Harris NL, editors. Non-Hodgkin's Lymphomas. Philadelphia: Lippincott Williams& Wilkins; 2004. p. 711-27.
-
(2004)
Non-Hodgkin's Lymphomas.
, pp. 711-727
-
-
Hartge, P.1
Wang, S.S.2
-
4
-
-
15944379516
-
Incidence and spectrum of non-Hodgkin lymphoma in Chinese migrants to British Columbia
-
Au WY, Gascoyne RD, Klasa RD, et al. Incidence and spectrum of non-Hodgkin lymphoma in Chinese migrants to British Columbia. Br J Haematol. 2005;128:792-6.
-
(2005)
Br J Haematol
, vol.128
, pp. 792-796
-
-
Au, W.Y.1
Gascoyne, R.D.2
Klasa, R.D.3
-
5
-
-
0030887767
-
Risk of cancer in migrants and their descendants in Israel: I Leukaemias and Lymphomas
-
Iscovich J, Parkin DM. Risk of cancer in migrants and their descendants in Israel: I. Leukaemias and lymphomas. Int J Cancer. 1997;70:649-53.
-
(1997)
Int J Cancer.
, vol.70
, pp. 649-653
-
-
Iscovich, J.1
Parkin, D.M.2
-
6
-
-
29744459902
-
Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: A report from the InterLymph Consortium
-
Rothman N, Skibola CF, Wang SS, et al. Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium. Lancet Oncol. 2006;7:27-38.
-
(2006)
Lancet Oncol
, vol.7
, pp. 27-38
-
-
Rothman, N.1
Skibola, C.F.2
Wang, S.S.3
-
7
-
-
34147154891
-
Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): A pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph)
-
Wang SS, Slager SL, Brennan P, et al. Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): a pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph). Blood. 2007;109:3479-88.
-
(2007)
Blood
, vol.109
, pp. 3479-3488
-
-
Wang, S.S.1
Slager, S.L.2
Brennan, P.3
-
8
-
-
0035839959
-
Mechanisms of chromosomal translocations in B cell lymphomas
-
Kuppers R, Dalla-Favera R. Mechanisms of chromosomal translocations in B cell lymphomas. Oncogene. 2001;20:5580-94.
-
(2001)
Oncogene
, vol.20
, pp. 5580-5594
-
-
Kuppers, R.1
Dalla-Favera, R.2
-
9
-
-
0141457927
-
The pathogenetic role of oncogenes deregulated by chromosomal translocation in B-cell malignancies
-
Dyer MJS. The pathogenetic role of oncogenes deregulated by chromosomal translocation in B-cell malignancies. Int J Hematol. 2003;77:315-20.
-
(2003)
Int J Hematol
, vol.77
, pp. 315-320
-
-
Dyer, M.J.S.1
-
10
-
-
16844381831
-
Mechanisms of B-cell lymphoma pathogenesis
-
Kuppers R. Mechanisms of B-cell lymphoma pathogenesis. Nat Rev Cancer. 2005;5:251-62.
-
(2005)
Nat Rev Cancer
, vol.5
, pp. 251-262
-
-
Kuppers, R.1
-
12
-
-
33751193888
-
Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes
-
Hill DA, Wang SS, Cerhan JR, et al. Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. Blood. 2006;108:3161-7.
-
(2006)
Blood
, vol.108
, pp. 3161-3167
-
-
Hill, D.A.1
Wang, S.S.2
Cerhan, J.R.3
-
13
-
-
0034626802
-
Cell-cycle-regulated DNA doublestranded breaks in somatic hypermutation of immunoglobulin genes
-
Papavasiliou FN, Schatz DG. Cell-cycle-regulated DNA doublestranded breaks in somatic hypermutation of immunoglobulin genes. Nature. 2000;408:216-21.
-
(2000)
Nature
, vol.408
, pp. 216-221
-
-
Papavasiliou, F.N.1
Schatz, D.G.2
-
14
-
-
33744464558
-
Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut
-
Shen M, Zheng T, Lan Q, Zhang Y, Zahm SH, Wang SS, et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut. Hum Genet. 2006;119: 659-68.
-
(2006)
Hum Genet
, vol.119
, pp. 659-668
-
-
Shen, M.1
Zheng, T.2
Lan, Q.3
Zhang, Y.4
Zahm, S.H.5
Wang, S.S.6
-
15
-
-
33644758044
-
Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma
-
Smedby KE, Lindgren CM, Hjalgrim H, Humphreys K, Schollkopf C, Chang ET, et al. Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma. Cancer Epidemiol Biomarkers Prev. 2006;15:258-65.
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 258-265
-
-
Smedby, K.E.1
Lindgren, C.M.2
Hjalgrim, H.3
Humphreys, K.4
Schollkopf, C.5
Chang, E.T.6
-
16
-
-
33344464252
-
Bladder cancer predisposition: A multigenic approach to DNA-repair and cellcycle-control genes
-
Wu X, Gu J, Grossman HB, et al. Bladder cancer predisposition: a multigenic approach to DNA-repair and cellcycle-control genes. Am J Hum Genet. 2006;78(3):464-79.
-
(2006)
Am J Hum Genet
, vol.78
, Issue.3
, pp. 464-479
-
-
Wu, X.1
Gu, J.2
Grossman, H.B.3
-
17
-
-
0036909535
-
Genetic variants of NHEJ DNA ligase IV can affect the risk of developing multiple myeloma, a tumour characterised by aberrant class switch recombination
-
Roddam PL, Rollinson S, O'Driscoll M, et al. Genetic variants of NHEJ DNA ligase IV can affect the risk of developing multiple myeloma, a tumour characterised by aberrant class switch recombination. J Med Genet. 2002;39(12):900-5.
-
(2002)
J Med Genet
, vol.39
, Issue.12
, pp. 900-905
-
-
Roddam, P.L.1
Rollinson, S.2
O'Driscoll, M.3
-
18
-
-
71749090715
-
Variants in DNA double-strand break repair genes and breast cancer susceptibility
-
Kuschel B, Auranen A, McBride S, et al. Variants in DNA double-strand break repair genes and breast cancer susceptibility. Hum Mol Genet. 2002;11(12):1399-407.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.12
, pp. 1399-1407
-
-
Kuschel, B.1
Auranen, A.2
McBride, S.3
-
19
-
-
34548056355
-
Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk
-
Figueroa JD, Malats N, Rothman N, et al. Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. Carcinogenesis. 2007;28(8):1788-93.
-
(2007)
Carcinogenesis
, vol.28
, Issue.8
, pp. 1788-1793
-
-
Figueroa, J.D.1
Malats, N.2
Rothman, N.3
-
20
-
-
36048929748
-
Association between the BRCA2 N372H variant and male breast cancer risk: A populationbased case-control study in Tuscany, Central Italy
-
Palli D, Falchetti M, Masala G, et al. Association between the BRCA2 N372H variant and male breast cancer risk: a populationbased case-control study in Tuscany, Central Italy. BMC Cancer. 2007;7:170.
-
(2007)
BMC Cancer
, vol.7
, pp. 170
-
-
Palli, D.1
Falchetti, M.2
Masala, G.3
-
21
-
-
0032555758
-
DNAtransposition by the RAG1 and RAG2 proteins: A possible source of oncogenic translocations
-
Hiom K, Melek M, Gellert M. DNAtransposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations. Cell. 1998;94:463-70.
-
(1998)
Cell
, vol.94
, pp. 463-470
-
-
Hiom, K.1
Melek, M.2
Gellert, M.3
-
22
-
-
0035353213
-
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome
-
Corneo B, Moshous D, Gungor T, et al. Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome. Blood. 2001;97:2772-6.
-
(2001)
Blood
, vol.97
, pp. 2772-2776
-
-
Corneo, B.1
Moshous, D.2
Gungor, T.3
-
23
-
-
0035161258
-
V(D)J recombination defects in lymphocytes due to RAG mutations: Severe immunodeficiency with a spectrum of clinical presentations
-
Villa A, Sobacchi C, Notarangelo LD, et al. V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. Blood. 2001; 97:81-8.
-
(2001)
Blood
, vol.97
, pp. 81-88
-
-
Villa, A.1
Sobacchi, C.2
Notarangelo, L.D.3
-
24
-
-
0034690249
-
Interplay of p53 and DNArepair protein XRCC4 in tumorigenesis, genomic stability and development
-
Gao Y, Ferguson DO, Xie W, et al. Interplay of p53 and DNArepair protein XRCC4 in tumorigenesis, genomic stability and development. Nature. 2000;404:897-900.
-
(2000)
Nature
, vol.404
, pp. 897-900
-
-
Gao, Y.1
Ferguson, D.O.2
Xie, W.3
-
25
-
-
0033768238
-
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability
-
Healey CS, Dunning AM, Teare MD, et al. A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability. Nat Genet. 2000;26:362-4.
-
(2000)
Nat Genet
, vol.26
, pp. 362-364
-
-
Healey, C.S.1
Dunning, A.M.2
Teare, M.D.3
-
26
-
-
0036120189
-
The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years
-
Spurdle AB, Hopper JL, Chen X, 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. 2002;11:413-6.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 413-416
-
-
Spurdle, A.B.1
Hopper, J.L.2
Chen, X.3
-
27
-
-
0037454803
-
BRCA2 Arg372His polymorphism and epithelial ovarian cancer risk
-
Auranen A, Spurdle AB, Chen X, et al. BRCA2 Arg372His polymorphism and epithelial ovarian cancer risk. Int J Cancer. 2003;103:427-30.
-
(2003)
Int J Cancer
, vol.103
, pp. 427-430
-
-
Auranen, A.1
Spurdle, A.B.2
Chen, X.3
-
28
-
-
0141925969
-
Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer
-
Wenham RM, Schildkraut JM, McLean K, et al. Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer. Clin Cancer Res. 2003;9:4396-403.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 4396-4403
-
-
Wenham, R.M.1
Schildkraut, J.M.2
McLean, K.3
-
30
-
-
0033523268
-
Cancer Risks in BRCA2 mutation carriers
-
The Breast Cancer Linkage Consortium
-
The Breast Cancer Linkage Consortium. Cancer Risks in BRCA2 mutation carriers. J Natl Cancer Inst. 1999;91:1310-6.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1310-1316
-
-
-
31
-
-
85117739599
-
RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphoma
-
Scott K, Adamson PJ, Barrans SL, Worrillow LJ, et al. RAG1 and BRCA2 polymorphisms in non-Hodgkin lymphoma. Blood. 2007;109(12):552-3.
-
(2007)
Blood
, vol.109
, Issue.12
, pp. 552-553
-
-
Scott, K.1
Adamson, P.J.2
Barrans, S.L.3
Worrillow, L.J.4
-
32
-
-
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. 1998;17: 2531-4.
-
(1998)
Oncogene
, vol.17
, pp. 2531-2534
-
-
Fuks, F.1
Milner, J.2
Kouzarides, T.3
-
34
-
-
29644437235
-
The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia
-
Zhoucun A, Zhang S, Yang Y, et al. The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia. Eur J Obstet Gynecol Reprod Biol. 2006;124:61-4.
-
(2006)
Eur J Obstet Gynecol Reprod Biol
, vol.124
, pp. 61-64
-
-
Zhoucun, A.1
Zhang, S.2
Yang, Y.3
-
35
-
-
24044521924
-
Current advances in unraveling the function of the Werner syndrome protein
-
Ozgenc A, Loeb LA. Current advances in unraveling the function of the Werner syndrome protein. Mutat Res. 2005;577(1-2): 237-51.
-
(2005)
Mutat Res
, vol.577
, Issue.1-2
, pp. 237-251
-
-
Ozgenc, A.1
Loeb, L.A.2
|