-
1
-
-
0015043748
-
Mutation and Cancer: Statistical Study of Retinoblastoma
-
5279523 10.1073/pnas.68.4.820
-
Knudson AG (1971) Mutation and Cancer: Statistical Study of Retinoblastoma. Proc Natl Acad Sci USA 68:820-823
-
(1971)
Proc Natl Acad Sci USA
, vol.68
, pp. 820-823
-
-
Knudson, A.G.1
-
2
-
-
0033677022
-
Frequent association of β-catenin and WT1 mutations in Wilms tumors
-
11103785 1:CAS:528:DC%2BD3cXos1Sksbc%3D
-
Maiti S, Alam R, Amos CI, Huff V (2000) Frequent association of β-catenin and WT1 mutations in Wilms tumors. Cancer Res 60:6288-6292
-
(2000)
Cancer Res
, vol.60
, pp. 6288-6292
-
-
Maiti, S.1
Alam, R.2
Amos, C.I.3
Huff, V.4
-
3
-
-
52049100974
-
Clinical Relevance of Mutations in the Wilms Tumor Suppressor 1 Gene WT1 and the Cadherin-associated Protein β1 Gene CTNNB1 for Patients with Wilms Tumors
-
18618575 10.1002/cncr.23672
-
Royer-Pokora B, Weirich A, Schumacher V, Uschkereit C, Beier M, Leuschner I, Graf N, Autschbach F, Schneider D, von Harrach M (2008) Clinical Relevance of Mutations in the Wilms Tumor Suppressor 1 Gene WT1 and the Cadherin-associated Protein β1 Gene CTNNB1 for Patients with Wilms Tumors. Cancer 113:1080-1089
-
(2008)
Cancer
, vol.113
, pp. 1080-1089
-
-
Royer-Pokora, B.1
Weirich, A.2
Schumacher, V.3
Uschkereit, C.4
Beier, M.5
Leuschner, I.6
Graf, N.7
Autschbach, F.8
Schneider, D.9
Von Harrach, M.10
-
4
-
-
33746644763
-
Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor
-
10.1002/pbc.20891
-
Breslow NE, Beckwith JB, Perlman EJ, Reeve AE (2006) Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor. Pediatr Bood Cancer 47:260-267
-
(2006)
Pediatr Bood Cancer
, vol.47
, pp. 260-267
-
-
Breslow, N.E.1
Beckwith, J.B.2
Perlman, E.J.3
Reeve, A.E.4
-
5
-
-
0030889197
-
Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology
-
9108089 10.1073/pnas.94.8.3972 1:CAS:528:DyaK2sXis1ehsLg%3D
-
Schumacher V, Schneider S, Figge A, Wildhardt G, Harms D, Schmidt D, Weirich A, Ludwig R, Royer-Pokora B (1997) Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. Proc Natl Acad Sci USA 94:3972-3977
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3972-3977
-
-
Schumacher, V.1
Schneider, S.2
Figge, A.3
Wildhardt, G.4
Harms, D.5
Schmidt, D.6
Weirich, A.7
Ludwig, R.8
Royer-Pokora, B.9
-
6
-
-
17544395621
-
Correlation between a specific Wilms tumours suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
-
12471221 10.1136/jmg.39.12.e83 1:STN:280:DC%2BD38jgvFemtA%3D%3D
-
Shibata R, Hashigushi A, Sakamoto J, Yamada T, Umezawa A, Hata J (2002) Correlation between a specific Wilms tumours suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT). J Med Genet 39:e83
-
(2002)
J Med Genet
, vol.39
, pp. 83
-
-
Shibata, R.1
Hashigushi, A.2
Sakamoto, J.3
Yamada, T.4
Umezawa, A.5
Hata, J.6
-
7
-
-
2542462400
-
Twenty-four new cases of WT1 germ line mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development
-
15150775 10.1002/ajmg.a.30015
-
Royer-Pokora B, Beier M, Henzler M, Alam R, Schumacher V, Weirich A, Huff V (2004) Twenty-four new cases of WT1 germ line mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development. Am J Med Genet Part A 127A:249-257
-
(2004)
Am J Med Genet Part A
, vol.127
, pp. 249-257
-
-
Royer-Pokora, B.1
Beier, M.2
Henzler, M.3
Alam, R.4
Schumacher, V.5
Weirich, A.6
Huff, V.7
-
8
-
-
7044262957
-
Frequency and heritability of WT1 mutations in nonsyndromic Wilms tumor patients: A UK Children's Cancer Study Group Study
-
15483024 10.1200/JCO.2004.02.136 1:CAS:528:DC%2BD2cXpslOrs7Y%3D
-
Little SE, Hanks SP, King-Underwood L, Jones C, Rapley EA, Rahman N, Pritchard-Jones K (2004) Frequency and heritability of WT1 mutations in nonsyndromic Wilms tumor patients: a UK Children's Cancer Study Group Study. J Clin Oncol 22:4140-4146
-
(2004)
J Clin Oncol
, vol.22
, pp. 4140-4146
-
-
Little, S.E.1
Hanks, S.P.2
King-Underwood, L.3
Jones, C.4
Rapley, E.A.5
Rahman, N.6
Pritchard-Jones, K.7
-
9
-
-
34250738407
-
Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation
-
17551084 10.1136/jmg.2006.047530 1:CAS:528:DC%2BD2sXnvFOisbc%3D
-
Uschkereit C, Perez N, de Torres C, Küff M, Mora J, Royer-Pokora B (2007) Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation. J Med Genet 44:393-396
-
(2007)
J Med Genet
, vol.44
, pp. 393-396
-
-
Uschkereit, C.1
Perez, N.2
De Torres, C.3
Küff, M.4
Mora, J.5
Royer-Pokora, B.6
-
11
-
-
80053633503
-
A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript
-
21940503 10.1073/pnas.1110904108 1:CAS:528:DC%2BC3MXhtlWksrfO
-
Onyango P, Feinberg AP (2011) A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript. Proc Natl Acad Sci USA 108:16759-16764
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 16759-16764
-
-
Onyango, P.1
Feinberg, A.P.2
-
12
-
-
78650943634
-
Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation
-
21123950 10.1172/JCI43772 1:CAS:528:DC%2BC3MXis1ynuw%3D%3D
-
Hu Q, Gao F, Tian W, Ruteshouser EC, Wang Y, Lazar A, Stewart J, Strong LC, Behringer RR, Huff V (2011) Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation. J Clin Invest 121:174-183
-
(2011)
J Clin Invest
, vol.121
, pp. 174-183
-
-
Hu, Q.1
Gao, F.2
Tian, W.3
Ruteshouser, E.C.4
Wang, Y.5
Lazar, A.6
Stewart, J.7
Strong, L.C.8
Behringer, R.R.9
Huff, V.10
-
13
-
-
0025271523
-
Nephrogenic rests, nephroblasto-matosis, and the pathogenesis of Wilms tumor
-
2156243 10.3109/15513819009067094 1:STN:280:DyaK3c7pt1CqsQ%3D%3D
-
Beckwith JB, Kiviat NB, Bonadio JF (1990) Nephrogenic rests, nephroblasto-matosis, and the pathogenesis of Wilms tumor. Pediatr Pathol 10:1-36
-
(1990)
Pediatr Pathol
, vol.10
, pp. 1-36
-
-
Beckwith, J.B.1
Kiviat, N.B.2
Bonadio, J.F.3
-
14
-
-
34548458923
-
Molecular pathology and epidemiology of nephrogenic rests and Wilms tumors
-
10.1097/01.mph.0000212981.67114.ec 1:CAS:528:DC%2BD2sXhtFClu7%2FM
-
Fukuzawa R, Reeve AE (2007) Molecular pathology and epidemiology of nephrogenic rests and Wilms tumors. Pediatr Hematol Oncol 29:589-594
-
(2007)
Pediatr Hematol Oncol
, vol.29
, pp. 589-594
-
-
Fukuzawa, R.1
Reeve, A.E.2
-
15
-
-
33846846526
-
An X chromosome gene, WTX, is commonly inactivated in Wilms tumor
-
17204608 10.1126/science.1137509 1:CAS:528:DC%2BD2sXhtVyis7c%3D
-
Rivera MN, Kim WJ, Wells J, Driscoll DR, Brannigan BW, Kim JC, Feinberg AP, Gerald WL, Vargas SO, Chin L, Iafrate AJ, Bell DW, Haber DA (2007) An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science 315:642-645
-
(2007)
Science
, vol.315
, pp. 642-645
-
-
Rivera, M.N.1
Kim, W.J.2
Wells, J.3
Driscoll, D.R.4
Brannigan, B.W.5
Kim, J.C.6
Feinberg, A.P.7
Gerald, W.L.8
Vargas, S.O.9
Chin, L.10
Iafrate, A.J.11
Bell, D.W.12
Haber, D.A.13
-
16
-
-
43049157909
-
Wilms Tumor Genetics: Mutations in WT1, WTX, and CTNNB1 Account for only about One-Third of Tumors
-
18311776 10.1002/gcc.20553 1:CAS:528:DC%2BD1cXlslCksLs%3D
-
Ruteshouser EC, Robinson SM, Huff V (2008) Wilms Tumor Genetics: Mutations in WT1, WTX, and CTNNB1 Account for Only About One-Third of Tumors. Genes Chromosomes Cancer 47:461-470
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 461-470
-
-
Ruteshouser, E.C.1
Robinson, S.M.2
Huff, V.3
-
17
-
-
79955530313
-
Analysis of Wilms Tumors Using SNP Mapping Array-Based Comparative Genomic Hybridization
-
21544195 10.1371/journal.pone.0018941 1:CAS:528:DC%2BC3MXlsVansb4%3D
-
Hawthorn L, Cowell KJ (2011) Analysis of Wilms Tumors Using SNP Mapping Array-Based Comparative Genomic Hybridization. PLoS One 6:e18941
-
(2011)
PLoS One
, vol.6
, pp. 18941
-
-
Hawthorn, L.1
Cowell, K.J.2
-
18
-
-
33749031535
-
The many facets of the Wilms' tumour gene, WT1
-
16987884 10.1093/hmg/ddl196 1:CAS:528:DC%2BD28XpvFGlsL8%3D
-
Hohenstein P, Hastie ND (2006) The many facets of the Wilms' tumour gene, WT1. Hum Mol Genet 15:R196-R201
-
(2006)
Hum Mol Genet
, vol.15
-
-
Hohenstein, P.1
Hastie, N.D.2
-
19
-
-
0027182741
-
WT-1 is required for early kidney development
-
8395349 10.1016/0092-8674(93)90515-R 1:CAS:528:DyaK3sXlsFKrurg%3D
-
Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R (1993) WT-1 is required for early kidney development. Cell 74:679-691
-
(1993)
Cell
, vol.74
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
20
-
-
1642514813
-
Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation
-
14645201 10.1093/hmg/ddh015 1:CAS:528:DC%2BD2cXmsVGl
-
Davies JA, Ladomery M, Hohenstein P, Michael L, Shafe A, Spraggon L, Hastie N (2004) Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation. Hum Mol Genet 13:235-246
-
(2004)
Hum Mol Genet
, vol.13
, pp. 235-246
-
-
Davies, J.A.1
Ladomery, M.2
Hohenstein, P.3
Michael, L.4
Shafe, A.5
Spraggon, L.6
Hastie, N.7
-
21
-
-
77952538909
-
Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm
-
20106868 10.1093/hmg/ddq042 1:CAS:528:DC%2BC3cXksFKnsL8%3D
-
Royer-Pokora B, Busch M, Beier M, Duhme C, de Torres C, Mora J, Brandt A, Royer HD (2010) Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm. Hum Mol Genet 19:1651-1668
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1651-1668
-
-
Royer-Pokora, B.1
Busch, M.2
Beier, M.3
Duhme, C.4
De Torres, C.5
Mora, J.6
Brandt, A.7
Royer, H.D.8
-
22
-
-
33845269523
-
Surveillance for Wilms tumour in at-risk children: Pragmatic recommendations for best practice
-
16857697 10.1136/adc.2006.101295 1:STN:280:DC%2BD28nnvV2rsg%3D%3D
-
Scott RH, Walker L, Olsen OE, Levitt G, Kenney I, Maher E, Owens CM, Pritchard-Jones K, Craft A, Rahman N (2006) Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice. Arch Dis Child 91:995-999
-
(2006)
Arch Dis Child
, vol.91
, pp. 995-999
-
-
Scott, R.H.1
Walker, L.2
Olsen, O.E.3
Levitt, G.4
Kenney, I.5
Maher, E.6
Owens, C.M.7
Pritchard-Jones, K.8
Craft, A.9
Rahman, N.10
-
23
-
-
33749266701
-
Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
-
16690728 10.1136/jmg.2006.041723 1:CAS:528:DC%2BD28XhtFGrt7fK
-
Scott RH, Stiller CA, Walker L, Rahman N (2006) Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet 43:705-714
-
(2006)
J Med Genet
, vol.43
, pp. 705-714
-
-
Scott, R.H.1
Stiller, C.A.2
Walker, L.3
Rahman, N.4
-
24
-
-
33644665922
-
WAGR syndrome: A clinical review of 54 cases
-
16199712 10.1542/peds.2004-0467
-
Fischbach BV, Trout KL, Lewis J, Luis CA, Sika M (2005) WAGR syndrome: a clinical review of 54 cases. Pediatrics 116:984-988
-
(2005)
Pediatrics
, vol.116
, pp. 984-988
-
-
Fischbach, B.V.1
Trout, K.L.2
Lewis, J.3
Luis, C.A.4
Sika, M.5
-
25
-
-
1542648311
-
Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: A report from the National Wilms Tumor Study Group
-
14673045 10.1200/JCO.2003.06.096
-
Breslow E, Norris R, Norkool PA, Kang T, Beckwith JB, Perlman EJ, Ritchey ML, Green DM, Nichols KE (2003) Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group. J Clin Oncol 21:4579-4585
-
(2003)
J Clin Oncol
, vol.21
, pp. 4579-4585
-
-
Breslow, E.1
Norris, R.2
Norkool, P.A.3
Kang, T.4
Beckwith, J.B.5
Perlman, E.J.6
Ritchey, M.L.7
Green, D.M.8
Nichols, K.E.9
-
26
-
-
2642664516
-
Software and database for the analysis of mutations in the human WT1 gene
-
9399851 10.1093/nar/26.1.271 1:CAS:528:DyaK1cXovVeiuw%3D%3D
-
Jeanpierre C, Béroud C, Niaudet P, Junien C (1998) Software and database for the analysis of mutations in the human WT1 gene. Nucl Acids Res 26:271-274
-
(1998)
Nucl Acids Res
, vol.26
, pp. 271-274
-
-
Jeanpierre, C.1
Béroud, C.2
Niaudet, P.3
Junien, C.4
-
27
-
-
0030017174
-
Evidence for a familial Wilms tumour gene (FWT1) on chromosome 17q12-q21
-
10.1038/ng0896-461
-
Rahman N, Arbour L, Tonin P, Renshaw J, Pelletier J, Baruchel S, Pritchard-Jones K, Stratton MR, Narod SA (1996) Evidence for a familial Wilms tumour gene (FWT1) on chromosome 17q12-q21. Nat Genet 4:461-463
-
(1996)
Nat Genet
, vol.4
, pp. 461-463
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Renshaw, J.4
Pelletier, J.5
Baruchel, S.6
Pritchard-Jones, K.7
Stratton, M.R.8
Narod, S.A.9
-
28
-
-
0034685457
-
Penetrance of mutations in the familial Wilms tumor gene FWT1
-
10772684 10.1093/jnci/92.8.650 1:CAS:528:DC%2BD3cXjt1Slt7w%3D
-
Rahman N, Arbour L, Houlston R, Bonaïti-Pellié C, Abidi F, Tranchemontagne J, Ford D, Narod S, Pritchard-Jones K, Foulkes WD, Schwartz C, Stratton MR (2000) Penetrance of mutations in the familial Wilms tumor gene FWT1. J Natl Cancer Inst 92:650-652
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 650-652
-
-
Rahman, N.1
Arbour, L.2
Houlston, R.3
Bonaïti-Pellié, C.4
Abidi, F.5
Tranchemontagne, J.6
Ford, D.7
Narod, S.8
Pritchard-Jones, K.9
Foulkes, W.D.10
Schwartz, C.11
Stratton, M.R.12
-
29
-
-
0030803486
-
The familial Wilms tumour susceptibility gene, FWT1, may not be a tumour suppressor gene
-
9223674 10.1038/sj.onc.1201107 1:CAS:528:DyaK2sXksF2itrY%3D
-
Rahman N, Arbour L, Tonin P, Baruchel S, Pritchard-Jones K, Narod SA, Stratton MR (1997) The familial Wilms tumour susceptibility gene, FWT1, may not be a tumour suppressor gene. Oncogene 14:3099-3102
-
(1997)
Oncogene
, vol.14
, pp. 3099-3102
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Baruchel, S.4
Pritchard-Jones, K.5
Narod, S.A.6
Stratton, M.R.7
-
30
-
-
0032053822
-
Linkage of familial Wilms tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors
-
9537236 1:CAS:528:DyaK1cXit1eksrw%3D
-
McDonald JM, Douglass EC, Fisher R, Geiser CF, Krill CE, Strong LC, Virshup D, Huff V (1998) Linkage of familial Wilms tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. Cancer Res 58:1387-1390
-
(1998)
Cancer Res
, vol.58
, pp. 1387-1390
-
-
McDonald, J.M.1
Douglass, E.C.2
Fisher, R.3
Geiser, C.F.4
Krill, C.E.5
Strong, L.C.6
Virshup, D.7
Huff, V.8
-
31
-
-
0030940740
-
Evidence for genetic heterogeneity in familial Wilms tumor
-
9157975 1:CAS:528:DyaK2sXjtlGlt7g%3D
-
Huff V, Amos CI, Douglass EC, Fisher R, Geiser CF, Krill CE, Li FP, Strong LC, McDonald JM (1997) Evidence for genetic heterogeneity in familial Wilms tumor. Cancer Res 57:1859-1862
-
(1997)
Cancer Res
, vol.57
, pp. 1859-1862
-
-
Huff, V.1
Amos, C.I.2
Douglass, E.C.3
Fisher, R.4
Geiser, C.F.5
Krill, C.E.6
Li, F.P.7
Strong, L.C.8
McDonald, J.M.9
-
32
-
-
21644461973
-
Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis
-
10.1002/ajmg.a.30729
-
Rump P, Zeegers MP, van Essen AJ (2005) Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis. Am J Med Genet 136A:95-104
-
(2005)
Am J Med Genet
, vol.136
, pp. 95-104
-
-
Rump, P.1
Zeegers, M.P.2
Van Essen, A.J.3
-
33
-
-
84856866623
-
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome
-
22015620 10.1007/s00467-011-2009-4
-
Mussa A, Peruzzi L, Chiesa N, De Crescenzo A, Russo S, Melis D, Tarani L, Baldassarre G, Larizza L, Riccio A, Silengo M, Ferrero GB (2011) Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome. Pediatr Nephrol 27:397-406
-
(2011)
Pediatr Nephrol
, vol.27
, pp. 397-406
-
-
Mussa, A.1
Peruzzi, L.2
Chiesa, N.3
De Crescenzo, A.4
Russo, S.5
Melis, D.6
Tarani, L.7
Baldassarre, G.8
Larizza, L.9
Riccio, A.10
Silengo, M.11
Ferrero, G.B.12
-
34
-
-
79956209250
-
Clinical and Molecular Description of a Wilms Tumor in a Patient with Tuberous Sclerosis Complex
-
10.1002/ajmg.a.34001 1:CAS:528:DC%2BC3MXmsVCgu7g%3D
-
Spreafico F, Notarangelo LD, Schumacher RF, Savoldi G, Gamba B, Terenziani M, Collini P, Fasoli S, Giordano L, Luisa B, Porta F, Massimo M, Radice P, Perotti D (2011) Clinical and Molecular Description of a Wilms Tumor in a Patient With Tuberous Sclerosis Complex. Am J Med Genet Part A 155:1419-1424
-
(2011)
Am J Med Genet Part A
, vol.155
, pp. 1419-1424
-
-
Spreafico, F.1
Notarangelo, L.D.2
Schumacher, R.F.3
Savoldi, G.4
Gamba, B.5
Terenziani, M.6
Collini, P.7
Fasoli, S.8
Giordano, L.9
Luisa, B.10
Porta, F.11
Massimo, M.12
Radice, P.13
Perotti, D.14
-
35
-
-
13444274594
-
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour
-
for the Familial Wilms Tumour Collaboration
-
Reid S, Renwick A, Seal S, Baskcomb L, Barfoot R, Jayatilake H, The Breast Cancer Suspectibility Collaboration (UK), Pritchard-Jones K, Stratton MR, Ridolfi-Lüthy A, Rahman N, for the Familial Wilms Tumour Collaboration (2005) Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour. J Med Genet 42:147-151
-
(2005)
J Med Genet
, vol.42
, pp. 147-151
-
-
Reid S, R.1
-
36
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
17200672 10.1038/ng1942 1:CAS:528:DC%2BD2sXpvFekug%3D%3D
-
Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP (2007) Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet 39:159-161
-
(2007)
Nat Genet
, vol.39
, 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
-
37
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
10.1038/ng1947
-
Reis S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N (2007) Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet 39:162-164
-
(2007)
Nat Genet
, vol.39
, pp. 162-164
-
-
Reis, 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..
-
38
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR
-
Rahman N, Seal S, Thompson D, Kelly P, Renwick A, Elliott A, Reid S, Spanova K, Barfoot R, Chagtai T, Jayatilake H, McGuffog L, Hanks S, Evans DG, Eccles D; Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR (2007) PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet 39:165-167
-
(2007)
Nat Genet
, vol.39
, 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
-
39
-
-
28144453343
-
Clear Cell sarcoma of the Kidney: Up-regulation of neuronal Markers with Activation of the Sonic Hedgehog and Akt Pathways
-
Cutcliffe C, Kersey D, Huang C-C, Zeng Y, Walterhouse D, Perlman EJ for the Renal Tumor Committee of the Children's Oncology Group 10.1158/1078-0432. CCR-05-1354
-
Cutcliffe C, Kersey D, Huang C-C, Zeng Y, Walterhouse D, Perlman EJ for the Renal Tumor Committee of the Children's Oncology Group (2005) Clear Cell sarcoma of the Kidney: Up-regulation of neuronal Markers with Activation of the Sonic Hedgehog and Akt Pathways. Clin Cancer Res 11:7986-7994
-
(2005)
Clin Cancer Res
, vol.11
, pp. 7986-7994
-
-
-
40
-
-
33847635763
-
Recurring translocation (10;17) and deletion (14q) in clear cell sarcoma of the kidney
-
17516747
-
Brownlee NA, Perkins A, Stewart W, Jackle B, Pettenati MJ, Koty PP, Iskandar SS, Garvin AJ (2007) Recurring translocation (10;17) and deletion (14q) in clear cell sarcoma of the kidney. Arch Pathol Lab Med 131:446-451
-
(2007)
Arch Pathol Lab Med
, vol.131
, pp. 446-451
-
-
Brownlee, N.A.1
Perkins, A.2
Stewart, W.3
Jackle, B.4
Pettenati, M.J.5
Koty, P.P.6
Iskandar, S.S.7
Garvin, A.J.8
-
41
-
-
2642647094
-
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
-
9671307 10.1038/28212 1:CAS:528:DyaK1cXksFyltr0%3D
-
Versteege I, Sevenet N, Lange J, Rousseau-Merck M, Ambros P, Handgretinger R, Aurias A, Delattre O (1998) Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature 394:203-206
-
(1998)
Nature
, vol.394
, pp. 203-206
-
-
Versteege, I.1
Sevenet, N.2
Lange, J.3
Rousseau-Merck, M.4
Ambros, P.5
Handgretinger, R.6
Aurias, A.7
Delattre, O.8
-
42
-
-
78649675614
-
Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors
-
21108436 10.1002/pbc.22831
-
Eaton KW, Tooke LS, Wainwright LM, Judkins AR, Biegel JA (2011) Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors. Pediatr Blood Cancer 56:7-15
-
(2011)
Pediatr Blood Cancer
, vol.56
, pp. 7-15
-
-
Eaton, K.W.1
Tooke, L.S.2
Wainwright, L.M.3
Judkins, A.R.4
Biegel, J.A.5
-
43
-
-
17444422189
-
Snf5 tumor suppressor couples chromatin remodeling, checkpoint control, and chromosomal stability
-
15837618 10.1016/j.ccr.2005.04.001 1:CAS:528:DC%2BD2MXjvFSkurs%3D
-
Imbalzano AN, Jones SN (2005) Snf5 tumor suppressor couples chromatin remodeling, checkpoint control, and chromosomal stability. Cancer Cell 7:294-295
-
(2005)
Cancer Cell
, vol.7
, pp. 294-295
-
-
Imbalzano, A.N.1
Jones, S.N.2
-
44
-
-
0042452295
-
Highly penetrant, rapid tumorigenesis through conditional inversion of the tumor suppressor gene Snf5
-
12450796 10.1016/S1535-6108(02)00185-X 1:CAS:528:DC%2BD38Xptlalurg%3D
-
Roberts CA, Leroux MM, Fleming MD, Orkin SH (2002) Highly penetrant, rapid tumorigenesis through conditional inversion of the tumor suppressor gene Snf5. Cancer Cell 2:415-425
-
(2002)
Cancer Cell
, vol.2
, pp. 415-425
-
-
Roberts, C.A.1
Leroux, M.M.2
Fleming, M.D.3
Orkin, S.H.4
-
45
-
-
22844447414
-
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney
-
10.1002/humu.20195 1:CAS:528:DC%2BD2MXhtVGnsL3J
-
Wieser R, Fritz B, Ullmann R, Müller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H (2005) Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney. Hum Mutation 26:78-83
-
(2005)
Hum Mutation
, vol.26
, pp. 78-83
-
-
Wieser, R.1
Fritz, B.2
Ullmann, R.3
Müller, I.4
Galhuber, M.5
Storlazzi, C.T.6
Ramaswamy, A.7
Christiansen, H.8
Shimizu, N.9
Rehder, H.10
-
46
-
-
34547813165
-
High-density single nucleotide polymorphism array analysis in patients with germ line deletions of 22q11.2 and malignant rhabdoid tumor
-
17541642 10.1007/s00439-007-0386-3 1:CAS:528:DC%2BD2sXoslGhtrw%3D
-
Jackson EM, Shaikh TH, Gururangan S, Jones MC, Malkin D, Nikkel SM, Zuppan CW, Wainwright LM, Zhang F, Biegel JA (2007) High-density single nucleotide polymorphism array analysis in patients with germ line deletions of 22q11.2 and malignant rhabdoid tumor. Hum Genet 122:117-127
-
(2007)
Hum Genet
, vol.122
, pp. 117-127
-
-
Jackson, E.M.1
Shaikh, T.H.2
Gururangan, S.3
Jones, M.C.4
Malkin, D.5
Nikkel, S.M.6
Zuppan, C.W.7
Wainwright, L.M.8
Zhang, F.9
Biegel, J.A.10
-
47
-
-
79955014650
-
Wilms Tumor in a patient with 22q11.2 Microdeletion
-
10.1002/ajmg.a.33957 1:CAS:528:DC%2BC3MXkvVKrs7Y%3D
-
Finch PT, Pivnick EK, Furman W, Odom C (2011) Wilms Tumor in a patient With 22q11.2 Microdeletion. Am J Med Genet Part A 155:1162-1164
-
(2011)
Am J Med Genet Part A
, vol.155
, pp. 1162-1164
-
-
Finch, P.T.1
Pivnick, E.K.2
Furman, W.3
Odom, C.4
-
48
-
-
33845577118
-
Population-based study of renal cell carcinoma in children in Germany, 1980-2005: More frequently localized tumors and underlying disorders compared with adult counterparts
-
17109448 10.1002/cncr.22346
-
Selle B, Furtwängler R, Graf N, Kaatsch P, Bruder E, Leuschner I (2006) Population-based study of renal cell carcinoma in children in Germany, 1980-2005: more frequently localized tumors and underlying disorders compared with adult counterparts. Cancer 107:2906-2914
-
(2006)
Cancer
, vol.107
, pp. 2906-2914
-
-
Selle, B.1
Furtwängler, R.2
Graf, N.3
Kaatsch, P.4
Bruder, E.5
Leuschner, I.6
-
49
-
-
64549113699
-
Paediatric renal tumours: Recent developments, new entities and pathological features
-
10.1111/j.1365-2559.2008.03110.x
-
Sebire NJ, Vujanic GM (2009) Paediatric renal tumours: recent developments, new entities and pathological features. Histopathol 54:516-528
-
(2009)
Histopathol
, vol.54
, pp. 516-528
-
-
Sebire, N.J.1
Vujanic, G.M.2
-
50
-
-
1842647388
-
-
Lyon, France JARC Press
-
Eble JN, Sauter G, Epstein JL (eds) (2004) World Health Organization Classification of Tumours, in Tumors of the kidney: Tumours of the Urinary System and Male Genital Organs. Lyon, France JARC Press 37-38
-
(2004)
World Health Organization Classification of Tumours, in Tumors of the Kidney: Tumours of the Urinary System and Male Genital Organs
, pp. 37-38
-
-
Eble, J.N.1
Sauter, G.2
Epstein, J.L.3
-
51
-
-
0037609538
-
Cloning of an Alpha-TFEB fusion in renal tumors harbouring the t(6;11)(p21;q13) chromosome translocation
-
12719541 10.1073/pnas.0931430100 1:CAS:528:DC%2BD3sXjvFOltLo%3D
-
Davis JJ, His B-L, Arroya JD, Vergas SO, Yeh YA, Motyckova G, Valencia P, Perez-Atayde AR, Argani P, Ladanyi M, Fletcher JA, Fisher DE (2003) Cloning of an Alpha-TFEB fusion in renal tumors harbouring the t(6;11)(p21;q13) chromosome translocation. Proc Natl Acad Sci 100:6051-6056
-
(2003)
Proc Natl Acad Sci
, vol.100
, pp. 6051-6056
-
-
Davis, J.J.1
His, B.-L.2
Arroya, J.D.3
Vergas, S.O.4
Yeh, Y.A.5
Motyckova, G.6
Valencia, P.7
Perez-Atayde, A.R.8
Argani, P.9
Ladanyi, M.10
Fletcher, J.A.11
Fisher, D.E.12
-
52
-
-
34247570879
-
Mesenchymal stem cell features of Ewing tumors
-
17482132 10.1016/j.ccr.2007.02.027 1:CAS:528:DC%2BD2sXlsVahu7c%3D
-
Tirode F, Laud-Duval K, Prieur A, Delorme B, Charbord P, Delattre O (2007) Mesenchymal stem cell features of Ewing tumors. Cancer Cell 11:421-429
-
(2007)
Cancer Cell
, vol.11
, pp. 421-429
-
-
Tirode, F.1
Laud-Duval, K.2
Prieur, A.3
Delorme, B.4
Charbord, P.5
Delattre, O.6
-
53
-
-
17044427464
-
The EWS-WT1 gene fusion in desmoplastic small round cell tumor
-
15826834 10.1016/j.semcancer.2005.01.005 1:CAS:528:DC%2BD2MXjtF2itL4%3D
-
Gerald WL, Haber DA (2005) The EWS-WT1 gene fusion in desmoplastic small round cell tumor. Semin Cancer Biol 15:197-205
-
(2005)
Semin Cancer Biol
, vol.15
, pp. 197-205
-
-
Gerald, W.L.1
Haber, D.A.2
-
54
-
-
0033853824
-
Primary renal synovial sarcoma
-
10935649 10.1097/00000478-200008000-00006 1:STN:280: DC%2BD3czpvFOjsg%3D%3D
-
Argani P, Faria PA, Epstein JI, Reuter VE, Perlman EJ, Beckwith JB, Ladanyi M (2000) Primary renal synovial sarcoma. Am J Surg Pathol 24:1087-1096
-
(2000)
Am J Surg Pathol
, vol.24
, pp. 1087-1096
-
-
Argani, P.1
Faria, P.A.2
Epstein, J.I.3
Reuter, V.E.4
Perlman, E.J.5
Beckwith, J.B.6
Ladanyi, M.7
-
55
-
-
70949102042
-
Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1
-
19936258 10.1371/journal.pone.0007904
-
Cironi L, Provero P, Riggi N, Janiszewska M, Suva D, Suva M-L, Kindler V, Stamenkovic I (2009) Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1. PLoS One 4:e7904
-
(2009)
PLoS One
, vol.4
, pp. 7904
-
-
Cironi, L.1
Provero, P.2
Riggi, N.3
Janiszewska, M.4
Suva, D.5
Suva, M.-L.6
Kindler, V.7
Stamenkovic, I.8
|