-
1
-
-
33747137903
-
Cancer in children and adolescents in Europe: developments over 20 years and future challenges
-
10.1016/j.ejca.2006.06.006, 16919780
-
Pritchard-Jones K, Kaatsch P, Steliarova-Foucher E, Stiller CA, Coebergh JW. Cancer in children and adolescents in Europe: developments over 20 years and future challenges. Eur J Cancer 2006, 42(13):2183-2190. 10.1016/j.ejca.2006.06.006, 16919780.
-
(2006)
Eur J Cancer
, vol.42
, Issue.13
, pp. 2183-2190
-
-
Pritchard-Jones, K.1
Kaatsch, P.2
Steliarova-Foucher, E.3
Stiller, C.A.4
Coebergh, J.W.5
-
2
-
-
6944226229
-
MRE11/RAD50/NBS1: complex activities
-
Assenmacher N, Hopfner KP. MRE11/RAD50/NBS1: complex activities. Chromosoma 2004, 113(4):157-166.
-
(2004)
Chromosoma
, vol.113
, Issue.4
, pp. 157-166
-
-
Assenmacher, N.1
Hopfner, K.P.2
-
3
-
-
0033544724
-
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
-
10.1016/S0092-8674(00)81547-0, 10612394
-
Stewart GS, Maser RS, Stankovic T, Bressan DA, Kaplan MI, Jaspers NG, Raams A, Byrd PJ, Petrini JH, Taylor AM. The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder. Cell 1999, 99(6):577-587. 10.1016/S0092-8674(00)81547-0, 10612394.
-
(1999)
Cell
, vol.99
, Issue.6
, pp. 577-587
-
-
Stewart, G.S.1
Maser, R.S.2
Stankovic, T.3
Bressan, D.A.4
Kaplan, M.I.5
Jaspers, N.G.6
Raams, A.7
Byrd, P.J.8
Petrini, J.H.9
Taylor, A.M.10
-
4
-
-
65149095154
-
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder
-
10.1016/j.ajhg.2009.04.010, 2681000, 19409520
-
Waltes R, Kalb R, Gatei M, Kijas AW, Stumm M, Sobeck A, Wieland B, Varon R, Lerenthal Y, Lavin MF, et al. Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am J Hum Genet 2009, 84(5):605-616. 10.1016/j.ajhg.2009.04.010, 2681000, 19409520.
-
(2009)
Am J Hum Genet
, vol.84
, Issue.5
, pp. 605-616
-
-
Waltes, R.1
Kalb, R.2
Gatei, M.3
Kijas, A.W.4
Stumm, M.5
Sobeck, A.6
Wieland, B.7
Varon, R.8
Lerenthal, Y.9
Lavin, M.F.10
-
5
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
10.1016/S0092-8674(00)81174-5, 9590180
-
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanova E, Cooper PR, Nowak NJ, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 1998, 93(3):467-476. 10.1016/S0092-8674(00)81174-5, 9590180.
-
(1998)
Cell
, vol.93
, Issue.3
, pp. 467-476
-
-
Varon, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanova, E.8
Cooper, P.R.9
Nowak, N.J.10
-
6
-
-
33746130359
-
Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia
-
10.1038/sj.leu.2404285, 16810201
-
Mosor M, Ziolkowska I, Pernak-Schwarz M, Januszkiewicz-Lewandowska D, Nowak J. Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia. Leukemia 2006, 20(8):1454-1456. 10.1038/sj.leu.2404285, 16810201.
-
(2006)
Leukemia
, vol.20
, Issue.8
, pp. 1454-1456
-
-
Mosor, M.1
Ziolkowska, I.2
Pernak-Schwarz, M.3
Januszkiewicz-Lewandowska, D.4
Nowak, J.5
-
7
-
-
44849105787
-
I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer
-
10.1007/s10549-007-9734-1, 17899368
-
Roznowski K, Januszkiewicz-Lewandowska D, Mosor M, Pernak M, Litwiniuk M, Nowak J. I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer. Breast Cancer Res Treat 2008, 110(2):343-348. 10.1007/s10549-007-9734-1, 17899368.
-
(2008)
Breast Cancer Res Treat
, vol.110
, Issue.2
, pp. 343-348
-
-
Roznowski, K.1
Januszkiewicz-Lewandowska, D.2
Mosor, M.3
Pernak, M.4
Litwiniuk, M.5
Nowak, J.6
-
8
-
-
34748906012
-
Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene
-
10.1111/j.1349-7006.2007.00594.x, 17894553
-
Ziolkowska I, Mosor M, Wierzbicka M, Rydzanicz M, Pernak-Schwarz M, Nowak J. Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene. Cancer Sci 2007, 98(11):1701-1705. 10.1111/j.1349-7006.2007.00594.x, 17894553.
-
(2007)
Cancer Sci
, vol.98
, Issue.11
, pp. 1701-1705
-
-
Ziolkowska, I.1
Mosor, M.2
Wierzbicka, M.3
Rydzanicz, M.4
Pernak-Schwarz, M.5
Nowak, J.6
-
9
-
-
40449131773
-
Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours
-
10.1016/j.ejca.2008.01.006, 18280732
-
Nowak J, Mosor M, Ziolkowska I, Wierzbicka M, Pernak-Schwarz M, Przyborska M, Roznowski K, Plawski A, Slomski R, Januszkiewicz D. Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours. Eur J Cancer 2008, 44(4):627-630. 10.1016/j.ejca.2008.01.006, 18280732.
-
(2008)
Eur J Cancer
, vol.44
, Issue.4
, pp. 627-630
-
-
Nowak, J.1
Mosor, M.2
Ziolkowska, I.3
Wierzbicka, M.4
Pernak-Schwarz, M.5
Przyborska, M.6
Roznowski, K.7
Plawski, A.8
Slomski, R.9
Januszkiewicz, D.10
-
10
-
-
3042818662
-
Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland
-
10.1002/ijc.20239, 15185344
-
Steffen J, Varon R, Mosor M, Maneva G, Maurer M, Stumm M, Nowakowska D, Rubach M, Kosakowska E, Ruka W, et al. Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. International journal of cancer Journal international du cancer 2004, 111(1):67-71. 10.1002/ijc.20239, 15185344.
-
(2004)
International journal of cancer Journal international du cancer
, vol.111
, Issue.1
, pp. 67-71
-
-
Steffen, J.1
Varon, R.2
Mosor, M.3
Maneva, G.4
Maurer, M.5
Stumm, M.6
Nowakowska, D.7
Rubach, M.8
Kosakowska, E.9
Ruka, W.10
-
11
-
-
10744233070
-
NBS1 is a prostate cancer susceptibility gene
-
10.1158/0008-5472.CAN-03-2502, 14973119
-
Cybulski C, Gorski B, Debniak T, Gliniewicz B, Mierzejewski M, Masojc B, Jakubowska A, Matyjasik J, Zlowocka E, Sikorski A, et al. NBS1 is a prostate cancer susceptibility gene. Cancer Res 2004, 64(4):1215-1219. 10.1158/0008-5472.CAN-03-2502, 14973119.
-
(2004)
Cancer Res
, vol.64
, Issue.4
, pp. 1215-1219
-
-
Cybulski, C.1
Gorski, B.2
Debniak, T.3
Gliniewicz, B.4
Mierzejewski, M.5
Masojc, B.6
Jakubowska, A.7
Matyjasik, J.8
Zlowocka, E.9
Sikorski, A.10
-
12
-
-
65649138379
-
Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis
-
10.1186/1471-2407-9-124, 2680905, 19393077
-
Lu M, Lu J, Yang X, Yang M, Tan H, Yun B, Shi L. Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis. BMC cancer 2009, 9:124. 10.1186/1471-2407-9-124, 2680905, 19393077.
-
(2009)
BMC cancer
, vol.9
, pp. 124
-
-
Lu, M.1
Lu, J.2
Yang, X.3
Yang, M.4
Tan, H.5
Yun, B.6
Shi, L.7
-
13
-
-
53049107194
-
Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia
-
10.1016/j.ejca.2008.06.026, 18691878
-
Mosor M, Ziolkowska I, Januszkiewicz-Lewandowska D, Nowak J. Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia. Eur J Cancer 2008, 44(15):2226-2232. 10.1016/j.ejca.2008.06.026, 18691878.
-
(2008)
Eur J Cancer
, vol.44
, Issue.15
, pp. 2226-2232
-
-
Mosor, M.1
Ziolkowska, I.2
Januszkiewicz-Lewandowska, D.3
Nowak, J.4
-
14
-
-
33747884830
-
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
-
3006189, 16474176
-
Heikkinen K, Rapakko K, Karppinen SM, Erkko H, Knuutila S, Lundan T, Mannermaa A, Borresen-Dale AL, Borg A, Barkardottir RB, et al. RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. Carcinogenesis 2006, 27(8):1593-1599. 3006189, 16474176.
-
(2006)
Carcinogenesis
, vol.27
, Issue.8
, pp. 1593-1599
-
-
Heikkinen, K.1
Rapakko, K.2
Karppinen, S.M.3
Erkko, H.4
Knuutila, S.5
Lundan, T.6
Mannermaa, A.7
Borresen-Dale, A.L.8
Borg, A.9
Barkardottir, R.B.10
-
15
-
-
33646372196
-
Evaluation of RAD50 in familial breast cancer predisposition
-
10.1002/ijc.21738, 16385572
-
Tommiska J, Seal S, Renwick A, Barfoot R, Baskcomb L, Jayatilake H, Bartkova J, Tallila J, Kaare M, Tamminen A, et al. Evaluation of RAD50 in familial breast cancer predisposition. International journal of cancer Journal international du cancer 2006, 118(11):2911-2916. 10.1002/ijc.21738, 16385572.
-
(2006)
International journal of cancer Journal international du cancer
, vol.118
, Issue.11
, pp. 2911-2916
-
-
Tommiska, J.1
Seal, S.2
Renwick, A.3
Barfoot, R.4
Baskcomb, L.5
Jayatilake, H.6
Bartkova, J.7
Tallila, J.8
Kaare, M.9
Tamminen, A.10
-
16
-
-
77956188699
-
RAD50 gene mutations are not likely a risk factor for breast cancer in Poland
-
10.1007/s10549-010-0992-y, 20571869
-
Mosor M, Ziolkowska-Suchanek I, Roznowski K, Baranowska M, Januszkiewicz-Lewandowska D, Nowak J. RAD50 gene mutations are not likely a risk factor for breast cancer in Poland. Breast Cancer Res Treat 2010, 123(2):607-609. 10.1007/s10549-010-0992-y, 20571869.
-
(2010)
Breast Cancer Res Treat
, vol.123
, Issue.2
, pp. 607-609
-
-
Mosor, M.1
Ziolkowska-Suchanek, I.2
Roznowski, K.3
Baranowska, M.4
Januszkiewicz-Lewandowska, D.5
Nowak, J.6
-
17
-
-
0035131930
-
Alterations of the double-strand break repair gene MRE11 in cancer
-
Fukuda T, Sumiyoshi T, Takahashi M, Kataoka T, Asahara T, Inui H, Watatani M, Yasutomi M, Kamada N, Miyagawa K. Alterations of the double-strand break repair gene MRE11 in cancer. Cancer Res 2001, 61(1):23-26.
-
(2001)
Cancer Res
, vol.61
, Issue.1
, pp. 23-26
-
-
Fukuda, T.1
Sumiyoshi, T.2
Takahashi, M.3
Kataoka, T.4
Asahara, T.5
Inui, H.6
Watatani, M.7
Yasutomi, M.8
Kamada, N.9
Miyagawa, K.10
-
18
-
-
1542542679
-
Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility
-
10.1136/jmg.40.12.e131, 1735331, 14684699
-
Heikkinen K, Karppinen SM, Soini Y, Makinen M, Winqvist R. Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility. J Med Genet 2003, 40(12):e131. 10.1136/jmg.40.12.e131, 1735331, 14684699.
-
(2003)
J Med Genet
, vol.40
, Issue.12
-
-
Heikkinen, K.1
Karppinen, S.M.2
Soini, Y.3
Makinen, M.4
Winqvist, R.5
-
19
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
10.1126/science.1133427, 16959974
-
Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Silliman N, et al. The consensus coding sequences of human breast and colorectal cancers. Science 2006, 314(5797):268-274. 10.1126/science.1133427, 16959974.
-
(2006)
Science
, vol.314
, Issue.5797
, pp. 268-274
-
-
Sjoblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
Barber, T.D.6
Mandelker, D.7
Leary, R.J.8
Ptak, J.9
Silliman, N.10
-
20
-
-
74049116628
-
Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15
-
10.1002/humu.21145, 2922057, 19847790
-
Sun C, Southard C, Witonsky DB, Olopade OI, Di Rienzo A. Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15. Hum Mutat 2010, 31(1):99-107. 10.1002/humu.21145, 2922057, 19847790.
-
(2010)
Hum Mutat
, vol.31
, Issue.1
, pp. 99-107
-
-
Sun, C.1
Southard, C.2
Witonsky, D.B.3
Olopade, O.I.4
Di Rienzo, A.5
-
21
-
-
33748420560
-
Investigating cis-acting regulatory variation using assays of relative allelic expression
-
10.1097/01.ypg.0000218612.35139.84, 16829785
-
Bray NJ, O'Donovan MC. Investigating cis-acting regulatory variation using assays of relative allelic expression. Psychiatr Genet 2006, 16(4):173-177. 10.1097/01.ypg.0000218612.35139.84, 16829785.
-
(2006)
Psychiatr Genet
, vol.16
, Issue.4
, pp. 173-177
-
-
Bray, N.J.1
O'Donovan, M.C.2
-
22
-
-
80053173229
-
An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predisposition
-
10.1186/1471-2350-12-121, 3198910, 21939546
-
Muller D, Rouleau E, Schultz I, Caputo S, Lefol C, Bieche I, Caron O, Nogues C, Limacher JM, Demange L, et al. An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predisposition. BMC Med Genet 2011, 12:121. 10.1186/1471-2350-12-121, 3198910, 21939546.
-
(2011)
BMC Med Genet
, vol.12
, pp. 121
-
-
Muller, D.1
Rouleau, E.2
Schultz, I.3
Caputo, S.4
Lefol, C.5
Bieche, I.6
Caron, O.7
Nogues, C.8
Limacher, J.M.9
Demange, L.10
-
23
-
-
77955405475
-
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
-
10.1093/bioinformatics/btq330, 2916720, 20562413
-
McLaren W, Pritchard B, Rios D, Chen Y, Flicek P, Cunningham F. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 2010, 26(16):2069-2070. 10.1093/bioinformatics/btq330, 2916720, 20562413.
-
(2010)
Bioinformatics
, vol.26
, Issue.16
, pp. 2069-2070
-
-
McLaren, W.1
Pritchard, B.2
Rios, D.3
Chen, Y.4
Flicek, P.5
Cunningham, F.6
-
24
-
-
84861859517
-
ENCODE whole-genome data in the UCSC Genome Browser: update 2012
-
(Database issue), 3245183, 22075998
-
Rosenbloom KR, Dreszer TR, Long JC, Malladi VS, Sloan CA, Raney BJ, Cline MS, Karolchik D, Barber GP, Clawson H, et al. ENCODE whole-genome data in the UCSC Genome Browser: update 2012. Nucleic Acids Res 2012, 40(Database issue):D912-D917. 3245183, 22075998.
-
(2012)
Nucleic Acids Res
, vol.40
-
-
Rosenbloom, K.R.1
Dreszer, T.R.2
Long, J.C.3
Malladi, V.S.4
Sloan, C.A.5
Raney, B.J.6
Cline, M.S.7
Karolchik, D.8
Barber, G.P.9
Clawson, H.10
-
25
-
-
84875945705
-
ENCODE data in the UCSC Genome Browser: year 5 update
-
(Database issue), 3531152, 23193274
-
Rosenbloom KR, Sloan CA, Malladi VS, Dreszer TR, Learned K, Kirkup VM, Wong MC, Maddren M, Fang R, Heitner SG, et al. ENCODE data in the UCSC Genome Browser: year 5 update. Nucleic Acids Res 2013, 41(Database issue):D56-D63. 3531152, 23193274.
-
(2013)
Nucleic Acids Res
, vol.41
-
-
Rosenbloom, K.R.1
Sloan, C.A.2
Malladi, V.S.3
Dreszer, T.R.4
Learned, K.5
Kirkup, V.M.6
Wong, M.C.7
Maddren, M.8
Fang, R.9
Heitner, S.G.10
-
26
-
-
56649086648
-
Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene
-
10.1016/j.molonc.2008.09.007, 19383352
-
Bartkova J, Tommiska J, Oplustilova L, Aaltonen K, Tamminen A, Heikkinen T, Mistrik M, Aittomaki K, Blomqvist C, Heikkila P. Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene. Mol Oncol 2008, 2(4):296-316. 10.1016/j.molonc.2008.09.007, 19383352.
-
(2008)
Mol Oncol
, vol.2
, Issue.4
, pp. 296-316
-
-
Bartkova, J.1
Tommiska, J.2
Oplustilova, L.3
Aaltonen, K.4
Tamminen, A.5
Heikkinen, T.6
Mistrik, M.7
Aittomaki, K.8
Blomqvist, C.9
Heikkila, P.10
-
27
-
-
12744273401
-
Identification and functional consequences of a novel MRE11 mutation affecting 10 Saudi Arabian patients with the ataxia telangiectasia-like disorder
-
Fernet M, Gribaa M, Salih MA, Seidahmed MZ, Hall J, Koenig M. Identification and functional consequences of a novel MRE11 mutation affecting 10 Saudi Arabian patients with the ataxia telangiectasia-like disorder. Hum Mol Genet 2005, 14(2):307-318.
-
(2005)
Hum Mol Genet
, vol.14
, Issue.2
, pp. 307-318
-
-
Fernet, M.1
Gribaa, M.2
Salih, M.A.3
Seidahmed, M.Z.4
Hall, J.5
Koenig, M.6
-
28
-
-
18344395671
-
Human MRE11 is inactivated in mismatch repair-deficient cancers
-
10.1093/embo-reports/kvf044, 1084012, 11850399
-
Giannini G, Ristori E, Cerignoli F, Rinaldi C, Zani M, Viel A, Ottini L, Crescenzi M, Martinotti S, Bignami M, et al. Human MRE11 is inactivated in mismatch repair-deficient cancers. EMBO Rep 2002, 3(3):248-254. 10.1093/embo-reports/kvf044, 1084012, 11850399.
-
(2002)
EMBO Rep
, vol.3
, Issue.3
, pp. 248-254
-
-
Giannini, G.1
Ristori, E.2
Cerignoli, F.3
Rinaldi, C.4
Zani, M.5
Viel, A.6
Ottini, L.7
Crescenzi, M.8
Martinotti, S.9
Bignami, M.10
-
29
-
-
80855133532
-
Crystal structure of human Mre11: understanding tumorigenic mutations
-
10.1016/j.str.2011.09.010, 22078559
-
Park YB, Chae J, Kim YC, Cho Y. Crystal structure of human Mre11: understanding tumorigenic mutations. Structure 2011, 19(11):1591-1602. 10.1016/j.str.2011.09.010, 22078559.
-
(2011)
Structure
, vol.19
, Issue.11
, pp. 1591-1602
-
-
Park, Y.B.1
Chae, J.2
Kim, Y.C.3
Cho, Y.4
-
30
-
-
33746375981
-
Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31
-
10.1038/sj.gene.6364307, 16724073
-
Onnie C, Fisher SA, King K, Mirza M, Roberts R, Forbes A, Sanderson J, Lewis CM, Mathew CG. Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31. Genes Immun 2006, 7(5):359-365. 10.1038/sj.gene.6364307, 16724073.
-
(2006)
Genes Immun
, vol.7
, Issue.5
, pp. 359-365
-
-
Onnie, C.1
Fisher, S.A.2
King, K.3
Mirza, M.4
Roberts, R.5
Forbes, A.6
Sanderson, J.7
Lewis, C.M.8
Mathew, C.G.9
-
31
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
10.1073/pnas.0903091106, 2716381, 19651600
-
Walter MJ, Payton JE, Ries RE, Shannon WD, Deshmukh H, Zhao Y, Baty J, Heath S, Westervelt P, Watson MA, et al. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci USA 2009, 106(31):12950-12955. 10.1073/pnas.0903091106, 2716381, 19651600.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.31
, pp. 12950-12955
-
-
Walter, M.J.1
Payton, J.E.2
Ries, R.E.3
Shannon, W.D.4
Deshmukh, H.5
Zhao, Y.6
Baty, J.7
Heath, S.8
Westervelt, P.9
Watson, M.A.10
-
32
-
-
60549106496
-
Rad50 c.687delT does not contribute significantly to familial breast cancer in a French population
-
10.1158/1055-9965.EPI-08-0971, 19190165
-
Uhrhammer N, Delort L, Bignon YJ. Rad50 c.687delT does not contribute significantly to familial breast cancer in a French population. Cancer Epidemiol Biomarkers Prev 2009, 18(2):684-685. 10.1158/1055-9965.EPI-08-0971, 19190165.
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, Issue.2
, pp. 684-685
-
-
Uhrhammer, N.1
Delort, L.2
Bignon, Y.J.3
-
33
-
-
77951297126
-
Some common mutations of RAD50 and NBS1 in western populations do not contribute significantly to Chinese non-BRCA1/2 hereditary breast cancer
-
10.1007/s10549-009-0629-1, 19904603
-
Cao AY, Hu Z, Yin WJ, Jin W, Shao ZM. Some common mutations of RAD50 and NBS1 in western populations do not contribute significantly to Chinese non-BRCA1/2 hereditary breast cancer. Breast Cancer Res Treat 2010, 121(1):247-249. 10.1007/s10549-009-0629-1, 19904603.
-
(2010)
Breast Cancer Res Treat
, vol.121
, Issue.1
, pp. 247-249
-
-
Cao, A.Y.1
Hu, Z.2
Yin, W.J.3
Jin, W.4
Shao, Z.M.5
-
34
-
-
77953020607
-
Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients
-
10.1007/s00401-009-0608-y, 19908051
-
Ciara E, Piekutowska-Abramczuk D, Popowska E, Grajkowska W, Barszcz S, Perek D, Dembowska-Baginska B, Perek-Polnik M, Kowalewska E, Czajnska A, et al. Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta Neuropathol 2010, 119(3):325-334. 10.1007/s00401-009-0608-y, 19908051.
-
(2010)
Acta Neuropathol
, vol.119
, Issue.3
, pp. 325-334
-
-
Ciara, E.1
Piekutowska-Abramczuk, D.2
Popowska, E.3
Grajkowska, W.4
Barszcz, S.5
Perek, D.6
Dembowska-Baginska, B.7
Perek-Polnik, M.8
Kowalewska, E.9
Czajnska, A.10
-
35
-
-
80051787595
-
Is the NBN gene mutation I171V a potential risk factor for malignant solid tumors in children?
-
10.1097/MPH.0b013e3181faf886, 21436738
-
Nowak J, Mosor M, Nowicka K, Rembowska J, Januszkiewicz D. Is the NBN gene mutation I171V a potential risk factor for malignant solid tumors in children?. J Pediatr Hematol Oncol 2011, 33(6):e248-e249. 10.1097/MPH.0b013e3181faf886, 21436738.
-
(2011)
J Pediatr Hematol Oncol
, vol.33
, Issue.6
-
-
Nowak, J.1
Mosor, M.2
Nowicka, K.3
Rembowska, J.4
Januszkiewicz, D.5
-
36
-
-
84860204988
-
Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions
-
10.1093/mutage/ger084, 22131123
-
Dzikiewicz-Krawczyk A, Mosor M, Januszkiewicz D, Nowak J. Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions. Mutagenesis 2012, 27(3):337-343. 10.1093/mutage/ger084, 22131123.
-
(2012)
Mutagenesis
, vol.27
, Issue.3
, pp. 337-343
-
-
Dzikiewicz-Krawczyk, A.1
Mosor, M.2
Januszkiewicz, D.3
Nowak, J.4
-
37
-
-
79951670633
-
Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population
-
10.1111/j.1600-0609.2010.01562.x, 21166880
-
Jiang L, Liang J, Jiang M, Yu X, Zheng J, Liu H, Wu D, Zhou Y. Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population. Eur J Haematol 2011, 86(3):199-205. 10.1111/j.1600-0609.2010.01562.x, 21166880.
-
(2011)
Eur J Haematol
, vol.86
, Issue.3
, pp. 199-205
-
-
Jiang, L.1
Liang, J.2
Jiang, M.3
Yu, X.4
Zheng, J.5
Liu, H.6
Wu, D.7
Zhou, Y.8
-
38
-
-
84877108475
-
Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: a meta-analysis
-
10.1007/s13277-013-0668-4, 23381647
-
Yao F, Fang Y, Chen B, Jin F, Wang S. Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: a meta-analysis. Tumour Biol 2013, 34(2):1255-1262. 10.1007/s13277-013-0668-4, 23381647.
-
(2013)
Tumour Biol
, vol.34
, Issue.2
, pp. 1255-1262
-
-
Yao, F.1
Fang, Y.2
Chen, B.3
Jin, F.4
Wang, S.5
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