-
2
-
-
0346644386
-
Focus on embryonal malignancies
-
J. M. Maris and C. T. Denny, Focus on embryonal malignancies, Cancer Cell 2 (2002), 447-450.
-
(2002)
Cancer Cell
, vol.2
, pp. 447-450
-
-
Maris, J.M.1
Denny, C.T.2
-
3
-
-
1842831283
-
Conserved mechanisms across development and tumorigenesis revealed by a mouse development perspective of human cancers
-
A. T. Kho, Q. Zhao, Z. Cai, A. J. Butte, J. Y. Kim, S. L. Pomeroy et al. , Conserved mechanisms across development and tumorigenesis revealed by a mouse development perspective of human cancers, Genes Dev 18 (2004), 629-640.
-
(2004)
Genes. Dev.
, vol.18
, pp. 629-640
-
-
Kho, A.T.1
Zhao, Q.2
Cai, Z.3
Butte, A.J.4
Kim, J.Y.5
Pomeroy, S.L.6
-
4
-
-
0346307645
-
Profiling gene expression in kidney development
-
B. Dekel, Profiling gene expression in kidney development, Nephron Exp Nephrol 95 (2003), e1-6.
-
(2003)
Nephron. Exp. Nephrol.
, vol.95
-
-
Dekel, B.1
-
5
-
-
49249104685
-
Pediatric malignant germ cell tumors show characteristic transcriptome profiles
-
R. D. Palmer, N. L. Barbosa-Morais, E. L. Gooding, B. Muralidhar, C. M. Thornton, M. R. Pett et al. , Pediatric malignant germ cell tumors show characteristic transcriptome profiles, Cancer Res 68 (2008), 4239-4247.
-
(2008)
Cancer Res.
, vol.68
, pp. 4239-4247
-
-
Palmer, R.D.1
Barbosa-Morais, N.L.2
Gooding, E.L.3
Muralidhar, B.4
Thornton, C.M.5
Pett, M.R.6
-
6
-
-
12144291333
-
Germline mutations of the paired-like homeobox 2b phox2b gene in neuroblastoma
-
D. Trochet, F. Bourdeaut, I. Janoueix-Lerosey, A. Deville, L. de Pontual, G. Schleiermacher et al. , Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma, Am J Hum Genet 74 (2004), 761-764.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 761-764
-
-
Trochet, D.1
Bourdeaut, F.2
Janoueix-Lerosey, I.3
Deville, A.4
De Pontual, L.5
Schleiermacher, G.6
-
8
-
-
0039712065
-
Mutation and childhood cancer: A probabilistic model for the incidence of retinoblastoma
-
U S A
-
A. G. Knudson, H. W. Jr. , Hethcote andB. W. Brown, Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma, Proc Natl Acad Sci U S A 72 (1975), 5116-5120.
-
(1975)
Proc. Natl. Acad. Sci.
, vol.72
, pp. 5116-5120
-
-
Knudson, A.G.1
Hethcote Jr., H.W.2
Brown, B.W.3
-
9
-
-
0001736811
-
Diagnostic pathology of pediatric malignancies
-
P. A. Pizzo and D. G. Poplack eds Philadelphia: Lippincott Williams and Wilkins
-
T. J. H. Triche and P. H. B. Sorensen, Diagnostic Pathology of Pediatric Malignancies, in: Principles and Practice of Pediatric Oncology, P. A. Pizzo and D. G. Poplack, eds, Philadelphia: Lippincott Williams and Wilkins, 2006, pp. 185-235.
-
(2006)
Principles and Practice of Pediatric Oncology
, pp. 185-235
-
-
Triche, T.J.H.1
Sorensen, P.H.B.2
-
10
-
-
0036183742
-
Recent advances inwilms tumor genetics
-
J. S. Dome andM. J. Coppes, Recent advances inWilms tumor genetics, Curr Opin Pediatr 14 (2002), 5-11.
-
(2002)
Curr. Opin. Pediatr.
, vol.14
, pp. 5-11
-
-
Dome, J.S.1
Coppes, M.J.2
-
11
-
-
0344198135
-
Biology of childhood osteogenic sarcoma and potential targets for therapeutic development: Meeting summary
-
R. Gorlick, P. Anderson, I. Andrulis, C. Arndt, G. P. Beardsley, M. Bernstein et al. , Biology of childhood osteogenic sarcoma and potential targets for therapeutic development: meeting summary, Clin Cancer Res 9 (2003), 5442-5453.
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 5442-5453
-
-
Gorlick, R.1
Anderson, P.2
Andrulis, I.3
Arndt, C.4
Beardsley, G.P.5
Bernstein, M.6
-
12
-
-
19644386697
-
EWS-FLI1 fusion protein upregulates critical genes in neural crest development and isresponsible for the observed phenotype of ewings family of tumors
-
S. Hu-Lieskovan, J. Zhang, L. Wu, H. Shimada, D. E. Schofield and T. J. Triche, EWS-FLI1 fusion protein upregulates critical genes in neural crest development and isresponsible for the observed phenotype of Ewing's family of tumors, Cancer Res 65 (2005), 4633-4644.
-
(2005)
Cancer Res.
, vol.65
, pp. 4633-4644
-
-
Hu-Lieskovan, S.1
Zhang, J.2
Wu, L.3
Shimada, H.4
Schofield, D.E.5
Triche, T.J.6
-
13
-
-
24944582403
-
Expression profiles of osteosarcoma that can predict response to chemotherapy
-
T. K. Man, M. Chintagumpala, J. Visvanathan, J. Shen, L. Perlaky, J. Hicks et al. , Expression profiles of osteosarcoma that can predict response to chemotherapy, Cancer Res 65 (2005), 8142-8150.
-
(2005)
Cancer Res.
, vol.65
, pp. 8142-8150
-
-
Man, T.K.1
Chintagumpala, M.2
Visvanathan, J.3
Shen, J.4
Perlaky, L.5
Hicks, J.6
-
14
-
-
51649092873
-
Molecular characterization of the pediatric preclinical testing panel
-
G. Neale, X. Su, C. L. Morton, D. Phelps, R. Gorlick, R. B. Lock et al. , Molecular characterization of the pediatric preclinical testing panel, Clin Cancer Res 14 (2008), 4572-4583.
-
(2008)
Clin. Cancer Res.
, vol.14
, pp. 4572-4583
-
-
Neale, G.1
Su, X.2
Morton, C.L.3
Phelps, D.4
Gorlick, R.5
Lock, R.B.6
-
15
-
-
0001803359
-
-
P. A. Pizzo D. G. Poplack eds Philadelphia: Lippincott Williams and Wilkins
-
G. M. Brodeur and J. M. Maris, Neuroblastoma, in: Principles and Practice of Pediatric Oncology, P. A. Pizzo, D. G. Poplack, eds, Philadelphia: Lippincott Williams and Wilkins, 2006, pp. 905-932.
-
(2006)
Neuroblastoma Principles and Practice of Pediatric Oncology
, pp. 905-932
-
-
Brodeur, G.M.1
Maris, J.M.2
-
16
-
-
0022388606
-
Association of multiple copies of the nmyc oncogene with rapid progression of neuroblastomas
-
R. C. Seeger, G. M. Brodeur, H. Sather, A. Dalton, S. E. Siegel, K. Y. Wong et al. , Association of multiple copies of the Nmyc oncogene with rapid progression of neuroblastomas, N Engl J Med 313 (1985), 1111-1116.
-
(1985)
N. Engl. J. Med.
, vol.313
, pp. 1111-1116
-
-
Seeger, R.C.1
Brodeur, G.M.2
Sather, H.3
Dalton, A.4
Siegel, S.E.5
Wong, K.Y.6
-
17
-
-
0033600283
-
Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma
-
N. Bown, S. Cotterill, M. Lastowska, S. O'Neill, A. D. Pearson, D. Plantaz et al. , Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma, N Engl J Med 340 (1999), 1954-1961.
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 1954-1961
-
-
Bown, N.1
Cotterill, S.2
Lastowska, M.3
O'neill, S.4
Pearson, A.D.5
Plantaz Et Al., D.6
-
18
-
-
0031425266
-
Analysis of 1;17 translocation breakpoints in neuroblastoma: Implications for mapping of neuroblastoma genes
-
N. Van Roy, G. Laureys, M. Van Gele, G. Opdenakker, R. Miura, P. van der Drift et al. , Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes, Eur J Cancer 33 (1997), 1974-1978.
-
(1997)
Eur. J. Cancer
, vol.33
, pp. 1974-1978
-
-
Van Roy, N.1
Laureys, G.2
Van Gele, M.3
Opdenakker, G.4
Miura, R.5
Drift Der P.Van6
-
19
-
-
0034598797
-
High expression of survivin mapped to 17q25 is significantly associated with poor prognostic factors and promotes cell survival in human neuroblastoma
-
A. Islam, H. Kageyama, N. Takada, T. Kawamoto, H. Takayasu, E. Isogai et al. , High expression of Survivin, mapped to 17q25, is significantly associated with poor prognostic factors and promotes cell survival in human neuroblastoma, Oncogene 19 (2000), 617-623.
-
(2000)
Oncogene
, vol.19
, pp. 617-623
-
-
Islam, A.1
Kageyama, H.2
Takada, N.3
Kawamoto, T.4
Takayasu, H.5
Isogai, E.6
-
20
-
-
85047695614
-
The N-myc and c-myc downstream pathways include the chromosome 17q genes nm23- h1 and nm23-h2
-
M. B. Godfried, M. Veenstra, P. v Sluis, K. Boon, R. v Asperen, M. C. Hermus et al. , The N-myc and c-myc downstream pathways include the chromosome 17q genes nm23- H1 and nm23-H2, Oncogene 21 (2002), 2097-2101.
-
(2002)
Oncogene
, vol.21
, pp. 2097-2101
-
-
Godfried, M.B.1
Veenstra, M.2
Sluis, P.V.3
Boon, K.4
Asperen, R.V.5
Hermus Et Al., M.C.6
-
21
-
-
0025979843
-
Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: A pediatric oncology group study
-
A. T. Look, F. A. Hayes, J. J. Shuster, E. C. Douglass, R. P. Castleberry, L. C. Bowman et al. , Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study, J Clin Oncol 9 (1991), 581-591.
-
(1991)
J. Clin. Oncol.
, vol.9
, pp. 581-591
-
-
Look, A.T.1
Hayes, F.A.2
Shuster, J.J.3
Douglass, E.C.4
Castleberry, R.P.5
Bowman, L.C.6
-
22
-
-
28144453057
-
Chromosome 1p and 11q deletions and outcome in neuroblastoma
-
E. F. Attiyeh, W. B. London, Y. P. Mosse, Q. Wang, C. Winter, D. Khazi et al. , Chromosome 1p and 11q deletions and outcome in neuroblastoma, N Engl J Med 353 (2005), 2243-2253.
-
(2005)
N. Engl. J. Med.
, vol.353
, pp. 2243-2253
-
-
Attiyeh, E.F.1
London, W.B.2
Mosse, Y.P.3
Wang, Q.4
Winter, C.5
Khazi, D.6
-
23
-
-
0033822026
-
Liver transplantation in eastern europe
-
J. Spicak, S. Vitko, M. Ryska, P. Trunecka, F. Belina, M. Krawczyk et al. , Liver transplantation in Eastern Europe, Liver Transpl 6 (2000), 665-669.
-
(2000)
Liver Transpl.
, vol.6
, pp. 665-669
-
-
Spicak, J.1
Vitko, S.2
Ryska, M.3
Trunecka, P.4
Belina, F.5
Krawczyk, M.6
-
24
-
-
20944437124
-
Definition and characterization of a region of 1p36. 3 consistently deleted in neuroblastoma
-
P. S. White, P. M. Thompson, T. Gotoh, E. R. Okawa, J. Igarashi, M. Kok et al. , Definition and characterization of a region of 1p36. 3 consistently deleted in neuroblastoma, Oncogene 24 (2005), 2684-2694.
-
(2005)
Oncogene
, vol.24
, pp. 2684-2694
-
-
White, P.S.1
Thompson, P.M.2
Gotoh, T.3
Okawa, E.R.4
Igarashi, J.5
Kok, M.6
-
25
-
-
0027531016
-
Association between high levels of expression of the trk gene and favorable outcome in human neuroblastoma
-
A. Nakagawara, M. Arima-Nakagawara, N. J. Scavarda, C. G. Azar, A. B. Cantor and G. M. Brodeur, Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma, N Engl JMed 328 (1993), 847-854.
-
(1993)
N. Engl. J. Med.
, vol.328
, pp. 847-854
-
-
Nakagawara, A.1
Arima-Nakagawara, M.2
Scavarda, N.J.3
Azar, C.G.4
Cantor, A.B.5
Brodeur, G.M.6
-
26
-
-
0028107269
-
Expression and function of TRK-B and BDNF in human neuroblastomas
-
A. Nakagawara, C. G. Azar, N. J. Scavarda and G. M. Brodeur, Expression and function of TRK-B and BDNF in human neuroblastomas, Mol Cell Biol 14 (1994), 759-767.
-
(1994)
Mol. Cell Biol.
, vol.14
, pp. 759-767
-
-
Nakagawara, A.1
Azar, C.G.2
Scavarda, N.J.3
Brodeur, G.M.4
-
27
-
-
54049094708
-
Identification of ALK as a major familial neuroblastoma predisposition gene
-
Y. P. Mosse,M. Laudenslager, L. Longo, K. A. Cole, A. Wood, E. F. Attiyeh et al. , Identification of ALK as a major familial neuroblastoma predisposition gene, Nature 455 (2008), 930-935.
-
(2008)
Nature
, vol.455
, pp. 930-935
-
-
Mossem. Laudenslager, Y.P.1
Longo, L.2
Cole, K.A.3
Wood, A.4
Attiyeh, E.F.5
-
28
-
-
54049149961
-
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
-
I. Janoueix-Lerosey, D. Lequin, L. Brugieres, A. Ribeiro, L. de Pontual, V. Combaret et al. , Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma, Nature 455 (2008), 967-970.
-
(2008)
Nature
, vol.455
, pp. 967-970
-
-
Janoueix-Lerosey, I.1
Lequin, D.2
Brugieres, L.3
Ribeiro, A.4
De Pontual, L.5
Combaret, V.6
-
29
-
-
54049118823
-
Oncogenic mutations of ALK kinase in neuroblastoma
-
Y. Chen, J. Takita, Y. L. Choi, M. Kato, M. Ohira, M. Sanada et al. , Oncogenic mutations of ALK kinase in neuroblastoma, Nature 455 (2008), 971-974.
-
(2008)
Nature
, vol.455
, pp. 971-974
-
-
Chen, Y.1
Takita, J.2
Choi, Y.L.3
Kato, M.4
Ohira, M.5
Sanada, M.6
-
30
-
-
54049120220
-
Activating mutations in ALK provide a therapeutic target in neuroblastoma
-
R. E. George, T. Sanda, M. Hanna, S. Frohling, W. ,2nd. Luther, J. Zhang et al. , Activating mutations in ALK provide a therapeutic target in neuroblastoma, Nature 455 (2008),975-978.
-
(2008)
Nature
, vol.455
, pp. 975-978
-
-
George, R.E.1
Sanda, T.2
Hanna, M.3
Frohling, S.4
Luther II, W.5
Zhang, J.6
-
31
-
-
0037112452
-
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13
-
J. M. Maris, M. J. Weiss, Y. Mosse, G. Hii, C. Guo, P. S. White et al. , Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13, Cancer Res 62 (2002), 6651-6658.
-
(2002)
Cancer Res.
, vol.62
, pp. 6651-6658
-
-
Maris, J.M.1
Weiss, M.J.2
Mosse, Y.3
Hii, G.4
Guo, C.5
White, P.S.6
-
32
-
-
33847281230
-
Undifferentiated sarcomas
-
D. G. Pizzo PaP ed. Philadelphia: Lippincott Williams and Wilkins
-
L. H. J. M. Wexler, W. H. Helman, L. J. Rhabdomyosarcomas and Undifferentiated Sarcomas, in: Principles and Practice of Pediatric Oncology, D. G. Pizzo PaP, ed. , Philadelphia: Lippincott Williams and Wilkins, 2006, pp. 185-235.
-
(2006)
Principles and Practice of Pediatric Oncology
, pp. 185-235
-
-
Wexler, L.H.J.M.1
Helman, W.H.2
Rhabdomyosarcomas, L.J.3
-
33
-
-
0033888976
-
Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass
-
P. Dias, B. Chen, B. Dilday, H. Palmer, H. Hosoi, S. Singh et al. , Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass, Am J Pathol 156 (2000), 399-408.
-
(2000)
Am. J. Pathol.
, vol.156
, pp. 399-408
-
-
Dias, P.1
Chen, B.2
Dilday, B.3
Palmer, H.4
Hosoi, H.5
Singh, S.6
-
34
-
-
0035031713
-
Pathologic classification of rhabdomyosarcomas and correlations with molecular studies
-
D. M. Parham, Pathologic classification of rhabdomyosarcomas and correlations with molecular studies, Mod Pathol 14 (2001), 506-514.
-
(2001)
Mod. Pathol.
, vol.14
, pp. 506-514
-
-
Parham, D.M.1
-
35
-
-
0032199723
-
Intergroup Rhabdomyosarcoma Study: Update for pathologists
-
S. J. Qualman, C. M. Coffin, W. A. Newton, H. Hojo, T. J. Triche, D. M. Parham et al. , Intergroup Rhabdomyosarcoma Study: update for pathologists, Pediatr Dev Pathol 1 (1998), 550-561.
-
(1998)
Pediatr. Dev. Pathol.
, vol.1
, pp. 550-561
-
-
Qualman, S.J.1
Coffin, C.M.2
Newton, W.A.3
Hojo, H.4
Triche, T.J.5
Parham, D.M.6
-
36
-
-
0036514765
-
Risk assignment in pediatric soft-tissue sarcomas: An evolving molecular classification
-
S. J. Qualman and R. A. Morotti, Risk assignment in pediatric soft-tissue sarcomas: an evolving molecular classification, Curr Oncol Rep 4 (2002), 123-130.
-
(2002)
Curr. Oncol. Rep.
, vol.4
, pp. 123-130
-
-
Qualman, S.J.1
Morotti, R.A.2
-
37
-
-
0023048925
-
Consistent chromosomal translocation in alveolar rhabdomyosarcoma
-
C. Turc-Carel, S. Lizard-Nacol, E. Justrabo, M. Favrot, T. Philip and E. Tabone, Consistent chromosomal translocation in alveolar rhabdomyosarcoma, Cancer Genet Cytogenet 19 (1986), 361-362.
-
(1986)
Cancer Genet. Cytogenet.
, vol.19
, pp. 361-362
-
-
Turc-Carel, C.1
Lizard-Nacol, S.2
Justrabo, E.3
Favrot, M.4
Philip, T.5
Tabone, E.6
-
38
-
-
85047698674
-
Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma
-
M. Valentine, E. C. Douglass and A. T. Look, Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma, Cytogenet Cell Genet 52 (1989), 128-132.
-
(1989)
Cytogenet Cell Genet
, vol.52
, pp. 128-132
-
-
Valentine, M.1
Douglass, E.C.2
Look, A.T.3
-
39
-
-
0027534945
-
Rearrangement of the pax3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
-
F. G. Barr, N. Galili, J. Holick, J. A. Biegel, G. Rovera and B. S. Emanuel, Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma, Nat Genet 3 (1993), 113-117.
-
(1993)
Nat. Genet.
, vol.3
, pp. 113-117
-
-
Barr, F.G.1
Galili, N.2
Holick, J.3
Biegel, J.A.4
Rovera, G.5
Emanuel, B.S.6
-
40
-
-
0027521658
-
Fusion of a fork head domain gene to pax3 in the solid tumour alveolar rhabdomyosarcoma
-
N. Galili, R. J. Davis, W. J. Fredericks, S. Mukhopadhyay, F. J. 3rd. Rauscher, B. S. Emanuel et al. , Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma, Nat Genet 5 (1993), 230-235.
-
(1993)
Nat. Genet.
, vol.5
, pp. 230-235
-
-
Galili, N.1
Davis, R.J.2
Fredericks, W.J.3
Mukhopadhyay, S.4
Rauscher Iii, F.J.5
Emanuel, B.S.6
-
41
-
-
0026340855
-
Chromosomal translocation t 1;13 p36;q14 in a case of rhabdomyosarcoma
-
J. A. Biegel, R. S. Meek, A. H. Parmiter, K. Conard and B. S. Emanuel, Chromosomal translocation t(1;13)(p36;q14) in a case of rhabdomyosarcoma, Genes Chromosomes Cancer 3 (1991), 483-484.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 483-484
-
-
Biegel, J.A.1
Meek, R.S.2
Parmiter, A.H.3
Conard, K.4
Emanuel, B.S.5
-
42
-
-
0028364374
-
Fusion of PAX7 to FKHR by the variant t 1;13 p36;q14 translocation in alveolar rhabdomyosarcoma
-
R. J. Davis, C. M. D'Cruz, M. A. Lovell, J. A. Biegel and F. G. Barr, Fusion of PAX7 to FKHR by the variant t(1;13) (p36;q14) translocation in alveolar rhabdomyosarcoma, Cancer Res 54 (1994), 2869-2872.
-
(1994)
Cancer Res.
, vol.54
, pp. 2869-2872
-
-
Davis, R.J.1
D'cruz, C.M.2
Lovell, M.A.3
Biegel, J.A.4
Barr, F.G.5
-
43
-
-
4143150844
-
Gene expression signatures identify rhabdomyosarcoma subtypes and detect a novel t2;2 q35;p23 translocation fusing pax3 to ncoa1
-
M. Wachtel, M. Dettling, E. Koscielniak, S. Stegmaier, J. Treuner, K. Simon-Klingenstein et al. , Gene expression signatures identify rhabdomyosarcoma subtypes and detect a novel t(2;2)(q35;p23) translocation fusing PAX3 to NCOA1, Cancer Res 64 (2004), 5539-5545.
-
(2004)
Cancer Res.
, vol.64
, pp. 5539-5545
-
-
Wachtel, M.1
Dettling, M.2
Koscielniak, E.3
Stegmaier, S.4
Treuner, J.5
Simon-Klingenstein, K.6
-
44
-
-
18244374534
-
Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcomawhereas amplification predominates in embryonal with anaplasia and alveolar subtypes
-
J. A. Bridge, J. Liu, S. J. Qualman, R. Suijkerbuijk, G. Wenger, J. Zhang et al. , Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma,whereas amplification predominates in embryonal with anaplasia and alveolar subtypes, Genes Chromosomes Cancer 33 (2002), 310-321.
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 310-321
-
-
Bridge, J.A.1
Liu, J.2
Qualman, S.J.3
Suijkerbuijk, R.4
Wenger, G.5
Zhang, J.6
-
45
-
-
0024958667
-
Molecular differential pathology of rhabdomyosarcoma
-
H. Scrable, D. Witte, H. Shimada, T. Seemayer, W. W. Sheng, S. Soukup et al. , Molecular differential pathology of rhabdomyosarcoma, Genes Chromosomes Cancer 1 (1989), 23-35.
-
(1989)
Genes. Chromosomes Cancer
, vol.1
, pp. 23-35
-
-
Scrable, H.1
Witte, D.2
Shimada, H.3
Seemayer, T.4
Sheng, W.W.5
Soukup, S.6
-
46
-
-
0034080846
-
Cytogenetic and molecular genetic techniques as adjunctive approaches in the diagnosis of bone and soft tissue tumors
-
J. A. Bridge and A. A. Sandberg, Cytogenetic and molecular genetic techniques as adjunctive approaches in the diagnosis of bone and soft tissue tumors, Skeletal Radiol 29 (2000), 249-258.
-
(2000)
Skeletal. Radiol.
, vol.29
, pp. 249-258
-
-
Bridge, J.A.1
Sandberg, A.A.2
-
47
-
-
14644435739
-
Upstream cpg island methylation of the pax3 gene in human rhabdomyosarcomas
-
R. T. Kurmasheva, C. A. Peterson, D. M. Parham, B. Chen, R. E. McDonald and C. A. Cooney, Upstream CpG island methylation of the PAX3 gene in human rhabdomyosarcomas, Pediatr Blood Cancer 44 (2005), 328-337.
-
(2005)
Pediatr. Blood Cancer
, vol.44
, pp. 328-337
-
-
Kurmasheva, R.T.1
Peterson, C.A.2
Parham, D.M.3
Chen, B.4
McDonald, R.E.5
Cooney, C.A.6
-
48
-
-
0033539498
-
Cdna microarrays detect activation of a myogenic transcription program by the pax3-fkhr fusion oncogene
-
USA
-
J. Khan,M. L. Bittner, L. H. Saal, U. Teichmann, D. O. Azorsa, G. C. Gooden et al. , cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene, Proc NatlAcad SciUSA 96 (1999), 13264-13269.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 13264-13269
-
-
Khan, J.1
Bittner, M.L.2
Saal, L.H.3
Teichmann, U.4
Azorsa, D.O.5
Gooden, G.C.6
-
49
-
-
0029980113
-
Mechanism for transcriptional gain of function resulting from chromosomal translocation in alveolar rhabdomyosarcoma
-
U S A
-
J. L. Bennicelli, R. H. Edwards and F. G. Barr, Mechanism for transcriptional gain of function resulting from chromosomal translocation in alveolar rhabdomyosarcoma, Proc Natl Acad Sci U S A 93 (1996), 5455-5459.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 5455-5459
-
-
Bennicelli, J.L.1
Edwards, R.H.2
Barr, F.G.3
-
50
-
-
34248176755
-
FOXO1a acts as a selective tumor suppressor in alveolar rhabdomyosarcoma
-
P. R. Bois, K. Izeradjene, P. J. Houghton, J. L. Cleveland, J. A. Houghton and G. C. Grosveldz, FOXO1a acts as a selective tumor suppressor in alveolar rhabdomyosarcoma, J Cell Biol 177 (2007), 563.
-
(2007)
J. Cell Biol.
, vol.177
, pp. 563
-
-
Bois, P.R.1
Izeradjene, K.2
Houghton, P.J.3
Cleveland, J.L.4
Houghton, J.A.5
Grosveldz, G.C.6
-
51
-
-
15744400937
-
Novel genes possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma detected by genomic expression profiling
-
S. Bortoluzzi, A. Bisognin, C. Romualdi and G. A. Danieli, Novel genes, possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma, detected by genomic expression profiling, Gene 348 (2005), 65-71.
-
(2005)
Gene.
, vol.348
, pp. 65-71
-
-
Bortoluzzi, S.1
Bisognin, A.2
Romualdi, C.3
Danieli, G.A.4
-
52
-
-
0025054481
-
Myod induces growth arrest independent of differentiation in normal and transformed cells
-
U S A
-
M. Crescenzi, T. P. Fleming, A. B. Lassar, H. Weintraub and S. A. Aaronson, MyoD induces growth arrest independent of differentiation in normal and transformed cells, Proc Natl Acad Sci U S A 87 (1990), 8442-8446.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 8442-8446
-
-
Crescenzi, M.1
Fleming, T.P.2
Lassar, A.B.3
Weintraub, H.4
Aaronson, S.A.5
-
53
-
-
0025277030
-
Cell proliferation inhibited by myod1 independently of myogenic differentiation
-
V. Sorrentino, R. Pepperkok, R. L. Davis, W. Ansorge and L. Philipson, Cell proliferation inhibited by MyoD1 independently of myogenic differentiation, Nature 345 (1990), 813-815.
-
(1990)
Nature
, vol.345
, pp. 813-815
-
-
Sorrentino, V.1
Pepperkok, R.2
Davis, R.L.3
Ansorge, W.4
Philipson, L.5
-
54
-
-
0025311120
-
Mechanisms of p53 loss in human sarcomas
-
U S A
-
L. M. Mulligan, G. J. Matlashewski, H. J. Scrable and W. K. Cavenee, Mechanisms of p53 loss in human sarcomas, Proc Natl Acad Sci U S A 87 (1990), 5863-5867.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 5863-5867
-
-
Mulligan, L.M.1
Matlashewski, G.J.2
Scrable, H.J.3
Cavenee, W.K.4
-
55
-
-
0032417124
-
N-myc gene amplification in rhabdomyosarcoma detected by fluorescence in situ hybridization: Its correlation with histologic features
-
Y. Hachitanda, S. Toyoshima, K. Akazawa and M. Tsuneyoshi, N-myc gene amplification in rhabdomyosarcoma detected by fluorescence in situ hybridization: its correlation with histologic features, Mod Pathol 11 (1998), 1222-1227.
-
(1998)
Mod. Pathol.
, vol.11
, pp. 1222-1227
-
-
Hachitanda, Y.1
Toyoshima, S.2
Akazawa, K.3
Tsuneyoshi, M.4
-
56
-
-
0028353848
-
MYCN gene amplification in rhabdomyosarcoma
-
D. Driman, P. S. Thorner, M. L. Greenberg, S. Chilton- MacNeill and J. Squire, MYCN gene amplification in rhabdomyosarcoma, Cancer 73 (1994), 2231-2237.
-
(1994)
Cancer
, vol.73
, pp. 2231-2237
-
-
Driman, D.1
Thorner, P.S.2
Greenberg, M.L.3
Chilton- MacNeill, S.4
Squire, J.5
-
57
-
-
0029929274
-
Analysis of cyclin-dependent kinase inhibitor genes cdkn2a cdkn2b andcdkn2c in childhood rhabdomyosarcoma
-
A. Iolascon, M. F. Faienza, B. Coppola, A. Rosolen, G. Basso, F. Della Ragione et al. , Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A,CDKN2B, andCDKN2C) in childhood rhabdomyosarcoma, Genes Chromosomes Cancer 15 (1996), 217-222.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 217-222
-
-
Iolascon, A.1
Faienza, M.F.2
Coppola, B.3
Rosolen, A.4
Basso, G.5
Della Ragione, F.6
-
58
-
-
20044391414
-
Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype
-
D. Williamson, Y. J. Lu, T. Gordon, R. Sciot, A. Kelsey, C. Fisher et al. , Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype, J Clin Oncol 23 (2005), 880-888.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 880-888
-
-
Williamson, D.1
Lu, Y.J.2
Gordon, T.3
Sciot, R.4
Kelsey, A.5
Fisher, C.6
-
59
-
-
10044288449
-
Rhabdomyosarcoma: Value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype: An analysis of 109 paraffin-embedded specimens
-
I. Hostein, M. Andraud-Fregeville, L. Guillou, M. J. Terrier- Lacombe, C. Deminiere, D. Ranchere et al. , Rhabdomyosarcoma: value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype: an analysis of 109 paraffin-embedded specimens, Cancer 101 (2004), 2817-2824.
-
(2004)
Cancer
, vol.101
, pp. 2817-2824
-
-
Hostein, I.1
Andraud-Fregeville, M.2
Guillou, L.3
Terrier- Lacombe, M.J.4
Deminiere, C.5
Ranchere, D.6
-
60
-
-
53449087711
-
Diffuse myogenin expression by immunohistochemistry is an independent marker of poor survival in pediatric rhabdomyosarcoma: A tissue microarray study of 71 primary tumors including correlation with molecular phenotype
-
A. Heerema-McKenney, L. C. Wijnaendts, J. F. Pulliam, D. Lopez-Terrada, J. K. McKenney, S. Zhu et al. , Diffuse myogenin expression by immunohistochemistry is an independent marker of poor survival in pediatric rhabdomyosarcoma: a tissue microarray study of 71 primary tumors including correlation with molecular phenotype, Am J Surg Pathol 32 (2008), 1513-1522.
-
(2008)
Am. J. Surg. Pathol.
, vol.32
, pp. 1513-1522
-
-
Heerema-Mckenney, A.1
Wijnaendts, L.C.2
Pulliam, J.F.3
Lopez-Terrada, D.4
McKenney, J.K.5
Zhu, S.6
-
61
-
-
0036605806
-
Pax3-fkhr and pax7- fkhr gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: A report from the children's oncology group
-
P. H. Sorensen, J. C. Lynch, S. J. Qualman, R. Tirabosco, J. F. Lim, H. M. Maurer et al. , PAX3-FKHR and PAX7- FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: a report from the children's oncology group, J Clin Oncol 20 (2002), 2672-2679.
-
(2002)
J. Clin. Oncol.
, vol.20
, pp. 2672-2679
-
-
Sorensen, P.H.1
Lynch, J.C.2
Qualman, S.J.3
Tirabosco, R.4
Lim, J.F.5
Maurer, H.M.6
-
62
-
-
0037102443
-
Genetic heterogeneity in the alveolar rhabdomyosarcoma subset without typical gene fusions
-
F. G. Barr, S. J. Qualman, M. H. Macris, N. Melnyk, E. R. Lawlor, D. M. Strzelecki et al. , Genetic heterogeneity in the alveolar rhabdomyosarcoma subset without typical gene fusions, Cancer Res 62 (2002), 4704-4710.
-
(2002)
Cancer Res.
, vol.62
, pp. 4704-4710
-
-
Barr, F.G.1
Qualman, S.J.2
MacRis, M.H.3
Melnyk, N.4
Lawlor, E.R.5
Strzelecki, D.M.6
-
63
-
-
0028888439
-
Molecular assays for chromosomal translocations in the diagnosis of pediatric soft tissue sarcomas
-
F. G. Barr, J. Chatten, C. M. D'Cruz, A. E. Wilson, L. E. Nauta, L. M. Nycum et al. , Molecular assays for chromosomal translocations in the diagnosis of pediatric soft tissue sarcomas, Jama 273 (1995), 553-557.
-
(1995)
Jama
, vol.273
, pp. 553-557
-
-
Barr, F.G.1
Chatten, J.2
D'cruz, C.M.3
Wilson, A.E.4
Nauta, L.E.5
Nycum, L.M.6
-
64
-
-
0028928079
-
Detection of the t 2;13 q35;q14 and pax3-fkhr fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization
-
J. A. Biegel, L. M. Nycum, V. Valentine, F. G. Barr and D. N. Shapiro, Detection of the t(2;13)(q35;q14) and PAX3-FKHR fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization, Genes Chromosomes Cancer 12 (1995), 186-192.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 186-192
-
-
Biegel, J.A.1
Nycum, L.M.2
Valentine, V.3
Barr, F.G.4
Shapiro, D.N.5
-
65
-
-
0035105525
-
Use of reverse transcriptase polymerase chain reaction for diagnosis and staging of alveolar rhabdomyosarcoma ewing sarcoma family of tumors and desmoplastic small round cell tumor
-
U. H. Athale, S. A. Shurtleff, J. J. Jenkins, C. A. Poquette, M. Tan, J. R. Downing et al. , Use of reverse transcriptase polymerase chain reaction for diagnosis and staging of alveolar rhabdomyosarcoma, Ewing sarcoma family of tumors, and desmoplastic small round cell tumor, J Pediatr Hematol Oncol 23 (2001), 99-104.
-
(2001)
J. Pediatr. Hematol. Oncol.
, vol.23
, pp. 99-104
-
-
Athale, U.H.1
Shurtleff, S.A.2
Jenkins, J.J.3
Poquette, C.A.4
Tan, M.5
Downing, J.R.6
-
66
-
-
39349089647
-
-
D. G. Pizzo PaP ed. Philadelphia: Lippincott Williams and Wilkins
-
M. P. G. Link, M. C. Meyers and P. A. Osteosarcoma, in: Principles and Practice of Pediatric Oncology, D. G. Pizzo PaP, ed. , Philadelphia: Lippincott Williams and Wilkins, 2006, pp. 1074-1115.
-
(2006)
Principles and Practice of Pediatric Oncology
, pp. 1074-1115
-
-
Link, M.P.G.1
Meyers, M.C.2
Osteosarcoma, P.A.3
-
68
-
-
0027219679
-
Cytogenetic findings in 33 osteosarcomas
-
F. Mertens, N. Mandahl, C. Orndal, B. Baldetorp, H. C. Bauer, A. Rydholm et al. , Cytogenetic findings in 33 osteosarcomas, Int J Cancer 55 (1993), 44-50.
-
(1993)
Int. J. Cancer
, vol.55
, pp. 44-50
-
-
Mertens, F.1
Mandahl, N.2
Orndal, C.3
Baldetorp, B.4
Bauer, H.C.5
Rydholm, A.6
-
69
-
-
0027939487
-
Cytogenetic aberrations in osteosarcomas nonrandom deletions rings and double-minute chromosomes
-
J. A. Fletcher, M. C. Gebhardt and H. P. Kozakewich, Cytogenetic aberrations in osteosarcomas. Nonrandom deletions, rings, and double-minute chromosomes, Cancer Genet Cytogenet 77 (1994), 81-88.
-
(1994)
Cancer Genet. Cytogenet.
, vol.77
, pp. 81-88
-
-
Fletcher, J.A.1
Gebhardt, M.C.2
Kozakewich, H.P.3
-
70
-
-
0030964763
-
Cytogenetic findings in 73 osteosarcoma specimens and a review of the literature
-
J. A. Bridge, M. Nelson, E. McComb, M. H. McGuire, H. Rosenthal, G. Vergara et al. , Cytogenetic findings in 73 osteosarcoma specimens and a review of the literature, Cancer Genet Cytogenet 95 (1997), 74-87.
-
(1997)
Cancer Genet. Cytogenet.
, vol.95
, pp. 74-87
-
-
Bridge, J.A.1
Nelson, M.2
McComb, E.3
McGuire, M.H.4
Rosenthal, H.5
Vergara, G.6
-
71
-
-
0042745572
-
Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: Osteosarcoma and related tumors
-
A. A. Sandberg and J. A. Bridge, Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors, Cancer Genet Cytogenet 145 (2003), 1-30.
-
(2003)
Cancer Genet Cytogenet
, vol.145
, pp. 1-30
-
-
Sandberg, A.A.1
Bridge, J.A.2
-
72
-
-
0344973662
-
Comparative genomic hybridization of low-grade central osteosarcoma
-
M. Tarkkanen, T. Bohling, G. Gamberi, P. Ragazzini, M. S. Benassi, A. Kivioja et al. , Comparative genomic hybridization of low-grade central osteosarcoma, Mod Pathol 11 (1998), 421-426.
-
(1998)
Mod. Pathol.
, vol.11
, pp. 421-426
-
-
Tarkkanen, M.1
Bohling, T.2
Gamberi, G.3
Ragazzini, P.4
Benassi, M.S.5
Kivioja, A.6
-
73
-
-
4344633830
-
High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalinfixed paraffin-embedded tissue
-
M. Zielenska, P. Marrano, P. Thorner, J. Pei, B. Beheshti, M. Ho et al. , High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalinfixed paraffin-embedded tissue, Cytogenet Genome Res 107 (2004), 77-82.
-
(2004)
Cytogenet. Genome. Res.
, vol.107
, pp. 77-82
-
-
Zielenska, M.1
Marrano, P.2
Thorner, P.3
Pei, J.4
Beheshti, B.5
Ho, M.6
-
74
-
-
0035918534
-
Presence of telomerase activity in different musculoskeletal tumor histotypes and correlation with aggressiveness
-
L. Sangiorgi, G. A. Gobbi, E. Lucarelli, S. M. Sartorio, M. Mordenti, I. Ghedini et al. , Presence of telomerase activity in different musculoskeletal tumor histotypes and correlation with aggressiveness, Int J Cancer 95 (2001), 156-161.
-
(2001)
Int. J. Cancer
, vol.95
, pp. 156-161
-
-
Sangiorgi, L.1
Gobbi, G.A.2
Lucarelli, E.3
Sartorio, S.M.4
Mordenti, M.5
Ghedini, I.6
-
75
-
-
0344837710
-
Absence of a telomere maintenance mechanism as a favorable prognostic factor in patients with osteosarcoma
-
G. A. Ulaner, H. Y. Huang, J. Otero, Z. Zhao, L. Ben-Porat, J. M. Satagopan et al. , Absence of a telomere maintenance mechanism as a favorable prognostic factor in patients with osteosarcoma, Cancer Res 63 (2003), 1759-1763.
-
(2003)
Cancer Res.
, vol.63
, pp. 1759-1763
-
-
Ulaner, G.A.1
Huang, H.Y.2
Otero, J.3
Zhao, Z.4
Ben-Porat, L.5
Satagopan, J.M.6
-
76
-
-
0027978368
-
Amplification of multiple genes from chromosomal region 12q13-14 in human malignant gliomas: Preliminary mapping of the amplicons shows preferential involvement of CDK4 SAS and MDM2
-
G. R. J. Reifenberger, K. Ichimura, P. S. Meltzer and V. P. Collins, Amplification of multiple genes from chromosomal region 12q13-14 in human malignant gliomas: preliminary mapping of the amplicons shows preferential involvement of CDK4, SAS, and MDM2, Cancer Res 54 (1994), 4299-4303.
-
(1994)
Cancer Res.
, vol.54
, pp. 4299-4303
-
-
Reifenberger, G.R.J.1
Ichimura, K.2
Meltzer, P.S.3
Collins, V.P.4
-
77
-
-
0033006029
-
DNAsequence copy number increase at 8q: A potential new prognostic marker in high-grade osteosarcoma
-
M. Tarkkanen, I. Elomaa, C. Blomqvist, A. H. Kivioja, P. Kellokumpu-Lehtinen, T. Bohling et al. , DNAsequence copy number increase at 8q: a potential new prognostic marker in high-grade osteosarcoma, Int J Cancer 84 (1999), 114-121.
-
(1999)
Int. J. Cancer
, vol.84
, pp. 114-121
-
-
Tarkkanen, M.1
Elomaa, I.2
Blomqvist, C.3
Kivioja, A.H.4
Kellokumpu-Lehtinen, P.5
Bohling, T.6
-
78
-
-
0022402666
-
Osteosarcoma and retinoblastoma: A shared chromosomal mechanism revealing recessive predisposition
-
U S A
-
M. F. Hansen, A. Koufos, B. L. Gallie, R. A. Phillips, O. Fodstad, A. Brogger et al. , Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition, Proc Natl Acad Sci U S A 82 (1985), 6216-6220.
-
(1985)
Proc. Natl. Acad. Sci.
, vol.82
, pp. 6216-6220
-
-
Hansen, M.F.1
Koufos, A.2
Gallie, B.L.3
Phillips, R.A.4
Fodstad, O.5
Brogger, A.6
-
79
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
-
S. H. Friend, R. Bernards, S. Rogelj, R. A. Weinberg, J. M. Rapaport, D. M. Albert et al. , A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma, Nature 323 (1986), 643-646.
-
(1986)
Nature
, vol.323
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
Weinberg, R.A.4
Rapaport, J.M.5
Albert, D.M.6
-
80
-
-
0023777950
-
Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma
-
J. Toguchida, K. Ishizaki, M. S. Sasaki, M. Ikenaga, M. Sugimoto, Y. Kotoura et al. , Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma, Cancer Res 48 (1988), 3939-3943.
-
(1988)
Cancer Res.
, vol.48
, pp. 3939-3943
-
-
Toguchida, J.1
Ishizaki, K.2
Sasaki, M.S.3
Ikenaga, M.4
Sugimoto, M.5
Kotoura, Y.6
-
81
-
-
0028955652
-
MDM2 and cdk4 gene amplification in ewings sarcoma
-
M. Ladanyi, R. Lewis, S. C. Jhanwar, W. Gerald, A. G. Huvos and J. H. Healey, MDM2 and CDK4 gene amplification in Ewing's sarcoma, J Pathol 175 (1995), 211-217.
-
(1995)
J. Pathol.
, vol.175
, pp. 211-217
-
-
Ladanyi, M.1
Lewis, R.2
Jhanwar, S.C.3
Gerald, W.4
Huvos, A.G.5
Healey, J.H.6
-
82
-
-
0032991072
-
Analysis of sas gene and cdk4 and mdm2 proteins in low-grade osteosarcoma
-
P. Ragazzini, G. Gamberi, M. S. Benassi, C. Orlando, R. Sestini, C. Ferrari et al. , Analysis of SAS gene and CDK4 and MDM2 proteins in low-grade osteosarcoma, Cancer Detect Prev 23 (1999), 129-136.
-
(1999)
Cancer Detect. Prev.
, vol.23
, pp. 129-136
-
-
Ragazzini, P.1
Gamberi, G.2
Benassi, M.S.3
Orlando, C.4
Sestini, R.5
Ferrari, C.6
-
83
-
-
0026464556
-
Mutation spectrum of the p53 gene in bone and soft tissue sarcomas
-
J. Toguchida, T. Yamaguchi, B. Ritchie, R. L. Beauchamp, S. H. Dayton, G. E. Herrera et al. , Mutation spectrum of the p53 gene in bone and soft tissue sarcomas, Cancer Res 52 (1992), 6194-6199.
-
(1992)
Cancer Res.
, vol.52
, pp. 6194-6199
-
-
Toguchida, J.1
Yamaguchi, T.2
Ritchie, B.3
Beauchamp, R.L.4
Dayton, S.H.5
Herrera, G.E.6
-
84
-
-
0023576046
-
Rearrangement of the p53 gene in human osteogenic sarcomas
-
U S A
-
H. Masuda, C. Miller, H. P. Koeffler, H. Battifora and M. J. Cline, Rearrangement of the p53 gene in human osteogenic sarcomas, Proc Natl Acad Sci U S A 84 (1987), 7716-7719.
-
(1987)
Proc. Natl. Acad. Sci.
, vol.84
, pp. 7716-7719
-
-
Masuda, H.1
Miller, C.2
Koeffler, H.P.3
Battifora, H.4
Cline, M.J.5
-
85
-
-
0026776432
-
Tumor suppressor gene Rb and p53 mutations in osteosarcoma
-
ix- x.
-
R. R. Schreck, Tumor suppressor gene (Rb and p53) mutations in osteosarcoma, Pediatr Hematol Oncol 9 (1992), ix- x.
-
(1992)
Pediatr. Hematol. Oncol.
, vol.9
-
-
Schreck, R.R.1
-
86
-
-
0141705379
-
The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability
-
U S A
-
M. Overholtzer, P. H. Rao, R. Favis, R. Lu, M. B. Elowitz, F. Barany et al. , The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability, Proc Natl Acad Sci U S A 100 (2003), 11547-11552.
-
(2003)
Proc. Natl. Acad. Sci.
, vol.100
, pp. 11547-11552
-
-
Overholtzer, M.1
Rao, P.H.2
Favis, R.3
Lu, R.4
Elowitz, M.B.5
Barany, F.6
-
87
-
-
20144381477
-
TP53 mutations and outcome in osteosarcoma: A prospective multicenter study
-
J. S. Wunder, N. Gokgoz, R. Parkes, S. B. Bull, S. Eskandarian, A. M. Davis et al. , TP53 mutations and outcome in osteosarcoma: a prospective, multicenter study, J Clin Oncol 23 (2005), 1483-1490.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 1483-1490
-
-
Wunder, J.S.1
Gokgoz, N.2
Parkes, R.3
Bull, S.B.4
Eskandarian, S.5
Davis, A.M.6
-
88
-
-
0029918497
-
Alterations of the p15 p16and p18 genes in osteosarcoma
-
C. W. Miller, A. Aslo, M. J. Campbell, N. Kawamata, B. C. Lampkin and H. P. Koeffler, Alterations of the p15, p16,and p18 genes in osteosarcoma, Cancer Genet Cytogenet 86 (1996), 136-142.
-
(1996)
Cancer Genet. Cytogenet.
, vol.86
, pp. 136-142
-
-
Miller, C.W.1
Aslo, A.2
Campbell, M.J.3
Kawamata, N.4
Lampkin, B.C.5
Koeffler, H.P.6
-
89
-
-
2442471534
-
Aberrations of p16INK4A p14ARF and p15INK4B genes in pediatric solid tumors
-
K. Obana, H. W. Yang, H. Y. Piao, T. Taki, K. Hashizume, R. Hanada et al. , Aberrations of p16INK4A, p14ARF and p15INK4B genes in pediatric solid tumors, Int J Oncol 23 (2003), 1151-1157.
-
(2003)
Int. J. Oncol.
, vol.23
, pp. 1151-1157
-
-
Obana, K.1
Yang, H.W.2
Piao, H.Y.3
Taki, T.4
Hashizume, K.5
Hanada, R.6
-
90
-
-
0038221272
-
Genetic and epigenetic alterations of the cell cycle regulators and tumor suppressor genes in pediatric osteosarcomas
-
A. Patino-Garcia, E. S. Pineiro, M. Z. Diez, L. G. Iturriagagoitia, F. A. Klussmann and L. S. Ariznabarreta, Genetic and epigenetic alterations of the cell cycle regulators and tumor suppressor genes in pediatric osteosarcomas, J Pediatr Hematol Oncol 25 (2003), 362-367.
-
(2003)
J. Pediatr. Hematol. Oncol.
, vol.25
, pp. 362-367
-
-
Patino-Garcia, A.1
Pineiro, E.S.2
Diez, M.Z.3
Iturriagagoitia, L.G.4
Klussmann, F.A.5
Ariznabarreta, L.S.6
-
91
-
-
0034661248
-
Analysis of the p16ink4 p14arf p15 tp53 and mdm2 genes and their prognostic implications in osteosarcoma and ewing sarcoma
-
T. Tsuchiya, K. Sekine, S. Hinohara, T. Namiki, T. Nobori and Y. Kaneko, Analysis of the p16INK4, p14ARF, p15, TP53, and MDM2 genes and their prognostic implications in osteosarcoma and Ewing sarcoma, Cancer Genet Cytogenet 120 (2000), 91-98.
-
(2000)
Cancer Genet. Cytogenet.
, vol.120
, pp. 91-98
-
-
Tsuchiya, T.1
Sekine, K.2
Hinohara, S.3
Namiki, T.4
Nobori, T.5
Kaneko, Y.6
-
92
-
-
0036211680
-
Alterations in the ink4a/arf locus and their effects on the growth of human osteosarcoma cell lines
-
Y. B. Park,M. J. Park, K. Kimura, K. Shimizu, S. H. Lee and J. Yokota, Alterations in the INK4a/ARF locus and their effects on the growth of human osteosarcoma cell lines, Cancer Genet Cytogenet 133 (2002), 105-111.
-
(2002)
Cancer Genet. Cytogenet.
, vol.133
, pp. 105-111
-
-
Park, Y.B.1
Park, M.J.2
Kimura, K.3
Shimizu, K.4
Lee, S.H.5
Yokota, J.6
-
93
-
-
0034841867
-
Aberrant expression of tumor suppressor proteins in the Ewing family of tumors
-
A. Maitra, H. Roberts, A. G. Weinberg and J. Geradts, Aberrant expression of tumor suppressor proteins in the Ewing family of tumors, Arch Pathol Lab Med 125 (2001), 1207-1212.
-
(2001)
Arch. Pathol. Lab. Med.
, vol.125
, pp. 1207-1212
-
-
Maitra, A.1
Roberts, H.2
Weinberg, A.G.3
Geradts, J.4
-
94
-
-
0031783711
-
C-myc and c-fos in human osteosarcoma: Prognostic value of mrna and protein expression
-
G. Gamberi, M. S. Benassi, T. Bohling, P. Ragazzini, L. Molendini, M. R. Sollazzo et al. , C-myc and c-fos in human osteosarcoma: prognostic value of mRNA and protein expression, Oncology 55 (1998), 556-563.
-
(1998)
Oncology
, vol.55
, pp. 556-563
-
-
Gamberi, G.1
Benassi, M.S.2
Bohling, T.3
Ragazzini, P.4
Molendini, L.5
Sollazzo, M.R.6
-
95
-
-
9344255443
-
Multidrug resistance and malignancy in human osteosarcoma
-
K. Scotlandi, M. Serra, G. Nicoletti, M. Vaccari, M. C. Manara, G. Nini et al. , Multidrug resistance and malignancy in human osteosarcoma, Cancer Res 56 (1996), 2434-2439.
-
(1996)
Cancer Res.
, vol.56
, pp. 2434-2439
-
-
Scotlandi, K.1
Serra, M.2
Nicoletti, G.3
Vaccari, M.4
Manara, M.C.5
Nini, G.6
-
96
-
-
0032856174
-
Expression of her2/erbb-2 correlates with survival in osteosarcoma
-
R. Gorlick, A. G. Huvos, G. Heller, A. Aledo, G. P. Beardsley, J. H. Healey et al. , Expression of HER2/erbB-2 correlates with survival in osteosarcoma, J Clin Oncol 17 (1999), 2781-2788.
-
(1999)
J. Clin. Oncol.
, vol.17
, pp. 2781-2788
-
-
Gorlick, R.1
Huvos, A.G.2
Heller, G.3
Aledo, A.4
Beardsley, G.P.5
Healey, J.H.6
-
97
-
-
0034546526
-
Novel findings in gene expression detected in human osteosarcoma by cdna microarray
-
M. Wolf, W. El-Rifai, M. Tarkkanen, J. Kononen, M. Serra, E. F. Eriksen et al. , Novel findings in gene expression detected in human osteosarcoma by cDNA microarray, Cancer Genet Cytogenet 123 (2000), 128-132.
-
(2000)
Cancer Genet. Cytogenet.
, vol.123
, pp. 128-132
-
-
Wolf, M.1
El-Rifai, W.2
Tarkkanen, M.3
Kononen, J.4
Serra, M.5
Eriksen, E.F.6
-
98
-
-
0141889935
-
High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use ofcghanalysis of cdna microarrays
-
J. A. Squire, J. Pei, P. Marrano, B. Beheshti, J. Bayani, G. Lim et al. , High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use ofCGHanalysis of cDNA microarrays, Genes Chromosomes Cancer 38 (2003), 215-225.
-
(2003)
Genes Chromosomes Cancer
, vol.38
, pp. 215-225
-
-
Squire, J.A.1
Pei, J.2
Marrano, P.3
Beheshti, B.4
Bayani, J.5
Lim, G.6
-
99
-
-
0345304776
-
Biological properties and gene expression associated with metastatic potential of human osteosarcoma
-
T. Nakano, M. Tani, Y. Ishibashi, K. Kimura, Y. B. Park, N. Imaizumi et al. , Biological properties and gene expression associated with metastatic potential of human osteosarcoma, Clin Exp Metastasis 20 (2003), 665-674.
-
(2003)
Clin. Exp. Metastasis
, vol.20
, pp. 665-674
-
-
Nakano, T.1
Tani, M.2
Ishibashi, Y.3
Kimura, K.4
Park, Y.B.5
Imaizumi, N.6
-
101
-
-
84880185406
-
-
Principles and Practice of Pediatric Oncology, D. G. Pizzo PaP, ed. , Philadelphia: Lippincott Williams and Wilkins
-
M. K. Bernstein, H. Paulussen, M. Randall, R. L. Schluck, A. Teot, L. A. Juergens, H. Ewing Sarcoma Family of Tumors, in: Principles and Practice of Pediatric Oncology, D. G. Pizzo PaP, ed. , Philadelphia: Lippincott Williams and Wilkins, 2006, pp. 1002-1032.
-
(2006)
Sarcoma Family of Tumors
, pp. 1002-1032
-
-
Bernstein, M.K.1
Paulussen, H.2
Randall, M.3
Schluck, R.L.4
Teot, A.5
Juergens, L.A.6
Ewing, H.7
-
102
-
-
38949211947
-
-
Washington: ARP Press
-
K. Unni, C. Inwards, J. Bridge, L. Kindblom and L. Wild, Tumors of the bones and joints, Washington: ARP Press; 2005.
-
(2005)
Tumors of the Bones and Joints
-
-
Unni, K.1
Inwards, C.2
Bridge, J.3
Kindblom, L.4
Wild, L.5
-
103
-
-
0021066625
-
Chromosomal translocation 11; 22 in cell lines of ewings sarcoma
-
C. Turc-Carel, I. Philip, M. P. Berger, T. Philip and G. Lenoir, [Chromosomal translocation (11; 22) in cell lines of Ewing's sarcoma], C R Seances Acad Sci III 296 (1983), 1101-1103.
-
(1983)
C R Seances Acad. Sci. III
, vol.296
, pp. 1101-1103
-
-
Turc-Carel, C.1
Philip, I.2
Berger, M.P.3
Philip, T.4
Lenoir, G.5
-
104
-
-
0021262110
-
Translocation involving chromosome 22 in ewings sarcoma a cytogenetic study of four fresh tumors
-
A. Aurias, C. Rimbaut, D. Buffe, J. M. Zucker and A. Mazabraud, Translocation involving chromosome 22 in Ewing's sarcoma. A cytogenetic study of four fresh tumors, Cancer Genet Cytogenet 12 (1984), 21-25.
-
(1984)
Cancer Genet. Cytogenet.
, vol.12
, pp. 21-25
-
-
Aurias, A.1
Rimbaut, C.2
Buffe, D.3
Zucker, J.M.4
Mazabraud, A.5
-
105
-
-
0021252642
-
Chromosome study of ewing's sarcoma es cell lines consistency of a reciprocal translocation t 11;22 q24;q12
-
C. Turc-Carel, I. Philip, M. P. Berger, T. Philip and G. M. Lenoir, Chromosome study of Ewing's sarcoma (ES) cell lines. Consistency of a reciprocal translocation t(11;22) (q24;q12), Cancer Genet Cytogenet 12 (1984), 1-19.
-
(1984)
Cancer Genet Cytogenet
, vol.12
, pp. 1-19
-
-
Turc-Carel, C.1
Philip, I.2
Berger, M.P.3
Philip, T.4
Lenoir, G.M.5
-
106
-
-
0021702084
-
Chromosome translocation in peripheral neuroepithelioma
-
J. Whang-Peng, T. J. Triche, T. Knutsen, J. Miser, E. C. Douglass and M. A. Israel, Chromosome translocation in peripheral neuroepithelioma, N Engl J Med 311 (1984), 584-585.
-
(1984)
N. Engl. J. Med.
, vol.311
, pp. 584-585
-
-
Whang-Peng, J.1
Triche, T.J.2
Knutsen, T.3
Miser, J.4
Douglass, E.C.5
Israel, M.A.6
-
107
-
-
0028307384
-
A second ewings sarcoma translocation t 21;22 fuses the ews gene to another etsfamily transcription factor erg
-
P. H. Sorensen, S. L. Lessnick, D. Lopez-Terrada, X. F. Liu, T. J. Triche and C. T. Denny, A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETSfamily transcription factor, ERG, Nat Genet 6 (1994), 146-151.
-
(1994)
Nat. Genet.
, vol.6
, pp. 146-151
-
-
Sorensen, P.H.1
Lessnick, S.L.2
Lopez-Terrada, D.3
Liu, X.F.4
Triche, T.J.5
Denny, C.T.6
-
108
-
-
0033668831
-
Updates on cytogenetics and molecular genetics of bone and soft tissue tumors: Ewing sarcoma and peripheral primitive neuroectodermal tumors
-
A. A. Sandberg and J. A. Bridge, Updates on cytogenetics and molecular genetics of bone and soft tissue tumors: Ewing sarcoma and peripheral primitive neuroectodermal tumors, Cancer Genet Cytogenet 123 (2000), 1-26.
-
(2000)
Cancer Genet. Cytogenet.
, vol.123
, pp. 1-26
-
-
Sandberg, A.A.1
Bridge, J.A.2
-
109
-
-
0022623831
-
Cytogenetic characterization of selected small round cell tumors of childhood
-
J. Whang-Peng, T. J. Triche, T. Knutsen, J. Miser, S. Kao- Shan, S. Tsai et al. , Cytogenetic characterization of selected small round cell tumors of childhood, Cancer Genet Cytogenet 21 (1986), 185-208.
-
(1986)
Cancer Genet Cytogenet
, vol.21
, pp. 185-208
-
-
Whang-Peng, J.1
Triche, T.J.2
Knutsen, T.3
Miser, J.4
Kao- Shan, S.5
Tsai, S.6
-
110
-
-
0026686674
-
Gene fusion with an ets dna-binding domain caused by chromosome translocation in human tumours
-
O. Delattre, J. Zucman, B. Plougastel, C. Desmaze, T. Melot, M. Peter et al. , Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours, Nature 359 (1992), 162-165.
-
(1992)
Nature
, vol.359
, pp. 162-165
-
-
Delattre, O.1
Zucman, J.2
Plougastel, B.3
Desmaze, C.4
Melot, T.5
Peter, M.6
-
111
-
-
0026746009
-
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t 11;22 translocation breakpoints
-
J. Zucman, O. Delattre, C. Desmaze, B. Plougastel, I. Joubert, T. Melot et al. , Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints, Genes Chromosomes Cancer 5 (1992), 71-277.
-
(1992)
Genes. Chromosomes Cancer
, vol.5
, pp. 71-277
-
-
Zucman, J.1
Delattre, O.2
Desmaze, C.3
Plougastel, B.4
Joubert, I.5
Melot, T.6
-
112
-
-
0027230568
-
Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the dna-binding domain encoded by fli1 for transformation
-
U S A
-
W. A. May, M. L. Gishizky, S. L. Lessnick, L. B. Lunsford, B. C. Lewis, O. Delattre et al. , Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation, Proc Natl Acad Sci U S A 90 (1993), 5752-5756.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 5752-5756
-
-
May, W.A.1
Gishizky, M.L.2
Lessnick, S.L.3
Lunsford, L.B.4
Lewis, B.C.5
Delattre, O.6
-
113
-
-
0027438827
-
Combinatorial generation of variable fusion proteins in the ewing family of tumours
-
J. Zucman, T. Melot, C. Desmaze, J. Ghysdael, B. Plougastel, M. Peter et al. , Combinatorial generation of variable fusion proteins in the Ewing family of tumours, Embo J 12 (1993), 4481-4487.
-
(1993)
Embo. J.
, vol.12
, pp. 4481-4487
-
-
Zucman, J.1
Melot, T.2
Desmaze, C.3
Ghysdael, J.4
Plougastel, B.5
Peter, M.6
-
114
-
-
0028903089
-
A variant ewings sarcoma translocation 7;22 fuses the ews gene to the ets gene etv1
-
I. S. Jeon, J. N. Davis, B. S. Braun, J. E. Sublett, M. F. Roussel, C. T. Denny et al. , A variant Ewing's sarcoma translocation (7;22) fuses the EWS gene to the ETS gene ETV1, Oncogene 10 (1995), 1229-1234.
-
(1995)
Oncogene
, vol.10
, pp. 1229-1234
-
-
Jeon, I.S.1
Davis, J.N.2
Braun, B.S.3
Sublett, J.E.4
Roussel, M.F.5
Denny, C.T.6
-
115
-
-
34548775691
-
Ewing sarcoma with novel translocation t2;16 producing an in-frame fusion of fus and fev
-
T. L. Ng, M. J. O'Sullivan, C. J. Pallen, M. Hayes, P. W. Clarkson, M. Winstanley et al. , Ewing sarcoma with novel translocation t(2;16) producing an in-frame fusion of FUS and FEV, J Mol Diagn 9 (2007), 459-463.
-
(2007)
J. Mol. Diagn.
, vol.9
, pp. 459-463
-
-
Ng, T.L.1
Van, M.J.O.2
Pallen, C.J.3
Hayes, M.4
Clarkson, P.W.5
Winstanley, M.6
-
116
-
-
0030975975
-
A new member of the ets family fused to ews in ewing tumors
-
M. Peter, J. Couturier, H. Pacquement, J. Michon, G. Thomas, H. Magdelenat et al. , A new member of the ETS family fused to EWS in Ewing tumors, Oncogene 14 (1997), 1159-1164.
-
(1997)
Oncogene
, vol.14
, pp. 1159-1164
-
-
Peter, M.1
Couturier, J.2
Pacquement, H.3
Michon, J.4
Thomas, G.5
Magdelenat, H.6
-
117
-
-
34548806398
-
Undifferentiated small round cell sarcomas with rare ews gene fusions: Identification of a novel ewssp3 fusion and of additional cases with the ews-etv1 and ews-fev fusions
-
L. Wang, R. Bhargava, T. Zheng, L. Wexler, M. H. Collins, D. Roulston et al. , Undifferentiated small round cell sarcomas with rare EWS gene fusions: identification of a novel EWSSP3 fusion and of additional cases with the EWS-ETV1 and EWS-FEV fusions, J Mol Diagn 9 (2007), 498-509.
-
(2007)
J. Mol. Diagn.
, vol.9
, pp. 498-509
-
-
Wang, L.1
Bhargava, R.2
Zheng, T.3
Wexler, L.4
Collins, M.H.5
Roulston, D.6
-
118
-
-
0030707948
-
EWS/fli1-induced manic fringe renders nih 3t3 cells tumorigenic
-
W. A. May, A. Arvand, A. D. Thompson, B. S. Braun, M. Wright and C. T. Denny, EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic, Nat Genet 17 (1997), 495-497.
-
(1997)
Nat. Genet.
, vol.17
, pp. 495-497
-
-
May, W.A.1
Arvand, A.2
Thompson, A.D.3
Braun, B.S.4
Wright, M.5
Denny, C.T.6
-
119
-
-
0035866778
-
The Ewing's sarcoma gene product functions as a transcriptional activator
-
K. L. Rossow and R. Janknecht, The Ewing's sarcoma gene product functions as a transcriptional activator, Cancer Res 61 (2001), 2690-2695.
-
(2001)
Cancer Res.
, vol.61
, pp. 2690-2695
-
-
Rossow, K.L.1
Janknecht, R.2
-
120
-
-
0035839938
-
Biology of ews/ets fusions in ewing's family tumors
-
A. Arvand and C. T. Denny, Biology of EWS/ETS fusions in Ewing's family tumors, Oncogene 20 (2001), 5747-5754.
-
(2001)
Oncogene.
, vol.20
, pp. 5747-5754
-
-
Arvand, A.1
Denny, C.T.2
-
121
-
-
0036560740
-
The Ewings sarcoma oncoprotein EWS/FLI induces a p53-dependent growth arrest in primary human fibroblasts
-
S. L. Lessnick, C. S. Dacwag and T. R. Golub, The Ewing's sarcoma oncoprotein EWS/FLI induces a p53-dependent growth arrest in primary human fibroblasts, Cancer Cell 1 (2002), 393-401.
-
(2002)
Cancer Cell
, vol.1
, pp. 393-401
-
-
Lessnick, S.L.1
Dacwag, C.S.2
Golub, T.R.3
-
122
-
-
0037569709
-
PIM3 proto-oncogene kinase is a common transcriptional target of divergent ews/ets oncoproteins
-
B. Deneen, S. M. Welford, T. Ho, F. Hernandez, I. Kurland and C. T. Denny, PIM3 proto-oncogene kinase is a common transcriptional target of divergent EWS/ETS oncoproteins, Mol Cell Biol 23 (2003), 3897-3908.
-
(2003)
Mol. Cell Biol.
, vol.23
, pp. 3897-3908
-
-
Deneen, B.1
Welford, S.M.2
Ho, T.3
Hernandez, F.4
Kurland, I.5
Denny, C.T.6
-
123
-
-
10744231438
-
EWS/ets fusions activate telomerase in ewing's tumors
-
A. Takahashi, F. Higashino, M. Aoyagi, K. Yoshida, M. Itoh, S. Kyo et al. , EWS/ETS fusions activate telomerase in Ewing's tumors, Cancer Res 63 (2003), 8338-8344.
-
(2003)
Cancer Res.
, vol.63
, pp. 8338-8344
-
-
Takahashi, A.1
Higashino, F.2
Aoyagi, M.3
Yoshida, K.4
Itoh, M.5
Kyo, S.6
-
124
-
-
3543151418
-
Wnt/Frizzled signaling in Ewing sarcoma
-
A. Uren, V. Wolf, Y. F. Sun, A. Azari, J. S. Rubin and J. A. Toretsky, Wnt/Frizzled signaling in Ewing sarcoma, Pediatr Blood Cancer 43 (2004), 243-249.
-
(2004)
Pediatr. Blood Cancer
, vol.43
, pp. 243-249
-
-
Uren, A.1
Wolf, V.2
Sun, Y.F.3
Azari, A.4
Rubin, J.S.5
Toretsky, J.A.6
-
125
-
-
20044367805
-
Ewing sarcomas with p53 mutation or p16/p14ARF homozygous deletion: A highly lethal subset associated with poor chemoresponse
-
H. Y. Huang, P. B. Illei, Z. Zhao, M. Mazumdar, A. G. Huvos, J. H. Healey et al. , Ewing sarcomas with p53 mutation or p16/p14ARF homozygous deletion: a highly lethal subset associated with poor chemoresponse, J Clin Oncol 23 (2005), 548-558.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 548-558
-
-
Huang, H.Y.1
Illei, P.B.2
Zhao, Z.3
Mazumdar, M.4
Huvos, A.G.5
Healey, J.H.6
-
126
-
-
8544237013
-
DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets
-
M. S. Staege, C. Hutter, I. Neumann, S. Foja, U. E. Hattenhorst, G. Hansen et al. , DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets, Cancer Res 64 (2004), 8213-8221.
-
(2004)
Cancer Res.
, vol.64
, pp. 8213-8221
-
-
Staege, M.S.1
Hutter, C.2
Neumann, I.3
Foja, S.4
Hattenhorst, U.E.5
Hansen, G.6
-
127
-
-
0036517835
-
Expression analysis of pediatric solid tumor cell lines using oligonucleotide microarrays
-
D. H. Wai, K. L. Schaefer, A. Schramm, E. Korsching, F. Van Valen, T. Ozaki et al. , Expression analysis of pediatric solid tumor cell lines using oligonucleotide microarrays, Int J Oncol 20 (2002), 441-451.
-
(2002)
Int. J. Oncol.
, vol.20
, pp. 441-451
-
-
Wai, D.H.1
Schaefer, K.L.2
Schramm, A.3
Korsching, E.4
Van Valen, F.5
Ozaki, T.6
-
128
-
-
10644251887
-
Prediction of high risk Ewings sarcoma by gene expression profiling
-
A. Ohali, S. Avigad, R. Zaizov, R. Ophir, S. Horn-Saban, I. J. Cohen et al. , Prediction of high risk Ewing's sarcoma by gene expression profiling, Oncogene 23 (2004), 8997-9006.
-
(2004)
Oncogene.
, vol.23
, pp. 8997-9006
-
-
Ohali, A.1
Avigad, S.2
Zaizov, R.3
Ophir, R.4
Horn-Saban, S.5
Cohen, I.J.6
-
129
-
-
0027365309
-
Mutations of the p53 gene are involved in Ewings sarcomas but not in neuroblastomas
-
H. Komuro, Y. Hayashi, M. Kawamura, K. Hayashi, Y. Kaneko, S. Kamoshita et al. , Mutations of the p53 gene are involved in Ewing's sarcomas but not in neuroblastomas, Cancer Res 53 (1993), 5284-5288.
-
(1993)
Cancer Res.
, vol.53
, pp. 5284-5288
-
-
Komuro, H.1
Hayashi, Y.2
Kawamura, M.3
Hayashi, K.4
Kaneko, Y.5
Kamoshita, S.6
-
130
-
-
0028179992
-
P53 mutations in human tumors with chimeric EWS/FLI-1 genes
-
R. Hamelin, J. Zucman, T. Melot, O. Delattre and G. Thomas, p53 mutations in human tumors with chimeric EWS/FLI-1 genes, Int J Cancer 57 (1994), 336-340.
-
(1994)
Int. J. Cancer
, vol.57
, pp. 336-340
-
-
Hamelin, R.1
Zucman, J.2
Melot, T.3
Delattre, O.4
Thomas, G.5
-
131
-
-
0030060750
-
Molecular and immunohistochemical identification of p53 alterations in bone and soft tissue sarcomas
-
S. Mousses, L. McAuley, R. S. Bell, R. Kandel and I. L. Andrulis, Molecular and immunohistochemical identification of p53 alterations in bone and soft tissue sarcomas, Mod Pathol 9 (1996), 1-6.
-
(1996)
Mod. Pathol.
, vol.9
, pp. 1-6
-
-
Mousses, S.1
McAuley, L.2
Bell, R.S.3
Kandel, R.4
Andrulis, I.L.5
-
132
-
-
0031421683
-
Molecular alterations of the RB1 TP53 and MDM2 genes in primary and xenografted human osteosarcomas
-
A. Pellin, J. Boix-Ferrero, D. Carpio, D. Lopez-Terrada, C. Carda, S. Navarro et al. , Molecular alterations of the RB1, TP53, and MDM2 genes in primary and xenografted human osteosarcomas, Diagn Mol Pathol 6 (1997), 333-341.
-
(1997)
Diagn. Mol. Pathol.
, vol.6
, pp. 333-341
-
-
Pellin, A.1
Boix-Ferrero, J.2
Carpio, D.3
Lopez-Terrada, D.4
Carda, C.5
Navarro, S.6
-
133
-
-
4344708374
-
Selective usage of D-Type cyclins by Ewings tumors and rhabdomyosarcomas
-
J. Zhang, S. Hu, D. E. Schofield, P. H. Sorensen and T. J. Triche, Selective usage of D-Type cyclins by Ewing's tumors and rhabdomyosarcomas, Cancer Res 64 (2004), 6026-6034.
-
(2004)
Cancer Res.
, vol.64
, pp. 6026-6034
-
-
Zhang, J.1
Hu, S.2
Schofield, D.E.3
Sorensen, P.H.4
Triche, T.J.5
-
134
-
-
0027179611
-
Reverse transcriptase pcr amplification of ews/fli-1 fusion transcripts as a diagnostic test for peripheral primitive neuroectodermal tumors of childhood
-
P. H. Sorensen, X. F. Liu, O. Delattre, J. M. Rowland, C. A. Biggs, G. Thomas et al. , Reverse transcriptase PCR amplification of EWS/FLI-1 fusion transcripts as a diagnostic test for peripheral primitive neuroectodermal tumors of childhood, Diagn Mol Pathol 2 (1993), 147-157.
-
(1993)
Diagn. Mol. Pathol.
, vol.2
, pp. 147-157
-
-
Sorensen, P.H.1
Liu, X.F.2
Delattre, O.3
Rowland, J.M.4
Biggs, C.A.5
Thomas, G.6
-
135
-
-
0028711912
-
Detection of ews- /fli-1 gene fusion transcripts by rt-pcr as a tool in the diagnosis of tumors of the ewing sarcoma group
-
B. Dockhorn-Dworniczak, K. L. Schafer, R. Dantcheva, S. Blasius, F. van Valen, S. Burdach et al. , [Detection of EWS- /FLI-1 gene fusion transcripts by RT-PCR as a tool in the diagnosis of tumors of the Ewing sarcoma group], Verh Dtsch Ges Pathol 78 (1994), 214-219.
-
(1994)
Verh. Dtsch. Ges. Pathol.
, vol.78
, pp. 214-219
-
-
Dockhorn-Dworniczak, B.1
Schafer, K.L.2
Dantcheva, R.3
Blasius, S.4
Van Valen, F.5
Burdach, S.6
-
136
-
-
0029618877
-
A consensus polymerase chain reaction-oligonucleotide hybridization approach for the detection of chromosomal translocations in pediatric bone and soft tissue sarcomas
-
F. G. Barr, Q. B. Xiong and K. Kelly, A consensus polymerase chain reaction-oligonucleotide hybridization approach for the detection of chromosomal translocations in pediatric bone and soft tissue sarcomas, Am J Clin Pathol 104 (1995), 627-633.
-
(1995)
Am. J. Clin. Pathol.
, vol.104
, pp. 627-633
-
-
Barr, F.G.1
Xiong, Q.B.2
Kelly, K.3
-
137
-
-
0036328614
-
Practical application of molecular genetic testing as an aid to the surgical pathologic diagnosis of sarcomas: A rospective study
-
D. A. Hill, M. J. O'Sullivan, X. Zhu, R. T. Vollmer, P. A. Humphrey, L. P. Dehner et al. , Practical application of molecular genetic testing as an aid to the surgical pathologic diagnosis of sarcomas: a rospective study, Am J Surg Pathol 26 (2002), 965-977.
-
(2002)
Am. J. Surg. Pathol.
, vol.26
, pp. 965-977
-
-
Hill, D.A.1
O'sullivan, M.J.2
Zhu, X.3
Vollmer, R.T.4
Humphrey, P.A.5
Dehner, L.P.6
-
138
-
-
32844474047
-
Molecular diagnosis of Ewing sarcoma/primitive neuroectodermal tumor in routinely processed tissue: A comparison of two fish strategies and rt-pcr in malignant round cell tumors
-
R. S. Bridge, V. Rajaram, L. P. Dehner, J. D. Pfeifer and J. D. Perry, Molecular diagnosis of Ewing sarcoma/primitive neuroectodermal tumor in routinely processed tissue: a comparison of two FISH strategies and RT-PCR in malignant round cell tumors, Mod Pathol 19 (2006), 1-8.
-
(2006)
Mod. Pathol.
, vol.19
, pp. 1-8
-
-
Bridge, R.S.1
Rajaram, V.2
Dehner, L.P.3
Pfeifer, J.D.4
Perry, J.D.5
-
139
-
-
0028277974
-
Interphase molecular cytogenetics of ewings sarcoma and peripheral neuroepithelioma t 11;22 with flanking and overlapping cosmid probes
-
C. Desmaze, J. Zucman, O. Delattre, T. Melot, G. Thomas and A. Aurias, Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes, Cancer Genet Cytogenet 74 (1994), 13-18.
-
(1994)
Cancer Genet. Cytogenet.
, vol.74
, pp. 13-18
-
-
Desmaze, C.1
Zucman, J.2
Delattre, O.3
Melot, T.4
Thomas, G.5
Aurias, A.6
-
140
-
-
0032979365
-
Detection of ews-fli-1 fusion in ewing's sarcoma/peripheral primitive neuroectodermal tumor by fluorescence in situ hybridization using formalin-fixed paraffinembedded tissue
-
S. Kumar, S. Pack, D. Kumar, R. Walker, M. Quezado, Z. Zhuang et al. , Detection of EWS-FLI-1 fusion in Ewing's sarcoma/peripheral primitive neuroectodermal tumor by fluorescence in situ hybridization using formalin-fixed paraffinembedded tissue, Hum Pathol 30 (1999), 324-330.
-
(1999)
Hum. Pathol.
, vol.30
, pp. 324-330
-
-
Kumar, S.1
Pack, S.2
Kumar, D.3
Walker, R.4
Quezado, M.5
Zhuang, Z.6
-
141
-
-
0032979531
-
Documentation of ews gene rearrangements by fluorescence in-situ hybridization fish in frozen sections of ewings sarcoma-peripheral primitive neuroectodermal tumor
-
H. Monforte-Munoz, D. Lopez-Terrada, H. Affendie, J. M. Rowland and T. J. Triche, Documentation of EWS gene rearrangements by fluorescence in-situ hybridization (FISH) in frozen sections of Ewing's sarcoma-peripheral primitive neuroectodermal tumor, Am J Surg Pathol 23 (1999), 309-315.
-
(1999)
Am. J. Surg. Pathol.
, vol.23
, pp. 309-315
-
-
Monforte-Munoz, H.1
Lopez-Terrada, D.2
Affendie, H.3
Rowland, J.M.4
Triche, T.J.5
-
142
-
-
0029026614
-
Sensitive detection of occult ewings cells by the reverse transcriptase-polymerase chain reaction
-
M. Peter, H. Magdelenat, J. Michon, T. Melot, O. Oberlin, J. M. Zucker et al. , Sensitive detection of occult Ewing's cells by the reverse transcriptase-polymerase chain reaction, Br J Cancer 72 (1995), 96-100.
-
(1995)
Br. J. Cancer
, vol.72
, pp. 96-100
-
-
Peter, M.1
Magdelenat, H.2
Michon, J.3
Melot, T.4
Oberlin, O.5
Zucker, J.M.6
-
143
-
-
0028913950
-
Detection of 11;22 q24;q12 translocation-bearing cells in peripheral blood progenitor cells of patients with Ewings sarcoma family of tumors
-
J. A. Toretsky, L. Neckers and L. H. Wexler, Detection of (11;22)(q24;q12) translocation-bearing cells in peripheral blood progenitor cells of patients with Ewing's sarcoma family of tumors, J Natl Cancer Inst 87 (1995), 385-386.
-
(1995)
J. Natl. Cancer Inst.
, vol.87
, pp. 385-386
-
-
Toretsky, J.A.1
Neckers, L.2
Wexler, L.H.3
-
144
-
-
0031756456
-
Ewing family tumors: Potential prognostic value of reverse-transcriptase polymerase chain reaction detection ofminimal residual disease in peripheral blood samples
-
E. de Alava, M. D. Lozano, A. Patino, L. Sierrasesumaga and F. J. Pardo-Mindan, Ewing family tumors: potential prognostic value of reverse-transcriptase polymerase chain reaction detection ofminimal residual disease in peripheral blood samples, Diagn Mol Pathol 7 (1998), 152-157.
-
(1998)
Diagn. Mol. Pathol.
, vol.7
, pp. 152-157
-
-
De Alava, E.1
Lozano, M.D.2
Patino, A.3
Sierrasesumaga, L.4
Pardo-Mindan, F.J.5
-
145
-
-
0029869130
-
Mobilization of tumour cells during biopsy in an infant with ewing sarcoma
-
A. Zoubek, H. Kovar, M. Kronberger, G. Amann, R. Windhager, B. Gruber et al. , Mobilization of tumour cells during biopsy in an infant with Ewing sarcoma, Eur J Pediatr 155 (1996), 373-376.
-
(1996)
Eur. J. Pediatr.
, vol.155
, pp. 373-376
-
-
Zoubek, A.1
Kovar, H.2
Kronberger, M.3
Amann, G.4
Windhager, R.5
Gruber, B.6
-
146
-
-
10744233322
-
The predictive potential of molecular detection in the nonmetastatic ewing family of tumors
-
S. Avigad, I. J. Cohen, J. Zilberstein, E. Liberzon, Y. Goshen, S. Ash et al. , The predictive potential of molecular detection in the nonmetastatic Ewing family of tumors, Cancer 100 (2004), 1053-1058.
-
(2004)
Cancer
, vol.100
, pp. 1053-1058
-
-
Avigad, S.1
Cohen, I.J.2
Zilberstein, J.3
Liberzon, E.4
Goshen, Y.5
Ash, S.6
-
147
-
-
0033119006
-
Differential transactivation by alternative ews-fli1 fusion proteins correlates with clinical heterogeneity in ewing's sarcoma
-
P. P. Lin, R. I. Brody, A. C. Hamelin, J. E. Bradner, J. H. Healey and M. Ladanyi, Differential transactivation by alternative EWS-FLI1 fusion proteins correlates with clinical heterogeneity in Ewing's sarcoma, Cancer Res 59 (1999), 1428-1432.
-
(1999)
Cancer Res.
, vol.59
, pp. 1428-1432
-
-
Lin, P.P.1
Brody, R.I.2
Hamelin, A.C.3
Bradner, J.E.4
Healey, J.H.5
Ladanyi, M.6
-
148
-
-
0142074314
-
Oligonucleotides targeted against a junction oncogene are made efficient by nanotechnologies
-
A. Maksimenko, C. Malvy, G. Lambert, J. R. Bertrand, E. Fattal, J. Maccario et al. , Oligonucleotides targeted against a junction oncogene are made efficient by nanotechnologies, Pharm Res 20 (2003), 1565-1567.
-
(2003)
Pharm. Res.
, vol.20
, pp. 1565-1567
-
-
Maksimenko, A.1
Malvy, C.2
Lambert, G.3
Bertrand, J.R.4
Fattal, E.5
MacCario, J.6
-
149
-
-
2942622488
-
Targeting of ews/fli-1 by rna interference attenuates the tumor phenotype of ewings sarcoma cells in vitro
-
H. A. Chansky, F. Barahmand-Pour, Q. Mei, W. Kahn- Farooqi, A. Zielinska-Kwiatkowska, M. Blackburn et al. , Targeting of EWS/FLI-1 by RNA interference attenuates the tumor phenotype of Ewing's sarcoma cells in vitro, J Orthop Res 22 (2004), 910-917.
-
(2004)
J. Orthop. Res.
, vol.22
, pp. 910-917
-
-
Chansky, H.A.1
Barahmand-Pour, F.2
Mei, Q.3
Kahn- Farooqi, W.4
Zielinska-Kwiatkowska, A.5
Blackburn, M.6
-
150
-
-
20944448531
-
RNA-based nanoparticle treatment shows promise in ewing's sarcoma model
-
M. Hede, RNA-based nanoparticle treatment shows promise in Ewing's sarcoma model, J Natl Cancer Inst 97 (2005), 627.
-
(2005)
J. Natl. Cancer Inst.
, vol.97
, pp. 627
-
-
Hede, M.1
-
151
-
-
17644403503
-
A small interfering RNA targeting vascular endothelial growth factor inhibits ewings sarcoma growth in a xenograft mouse model
-
H. Guan, Z. Zhou, H. Wang, S. F. Jia,W. Liu and E. S. Kleinerman, A small interfering RNA targeting vascular endothelial growth factor inhibits Ewing's sarcoma growth in a xenograft mouse model, Clin Cancer Res 11 (2005), 2662-2669.
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 2662-2669
-
-
Guan, H.1
Zhou, Z.2
Wang, S.F.3
Jiaw, L.H.4
Kleinerman, E.S.5
-
152
-
-
0034722888
-
The rapamycin-sensitive signal transduction pathway as a target for cancer therapy
-
M. Hidalgo and E. K. Rowinsky, The rapamycin-sensitive signal transduction pathway as a target for cancer therapy, Oncogene 19 (2000), 6680-6686.
-
(2000)
Oncogene.
, vol.19
, pp. 6680-6686
-
-
Hidalgo, M.1
Rowinsky, E.K.2
-
153
-
-
0344825088
-
Ewing's sarcoma: A miracle drug waiting to happen
-
R. Longtin, Ewing's sarcoma: a miracle drug waiting to happen? J Natl Cancer Inst 95 (2003), 1574-1576.
-
(2003)
J. Natl. Cancer Inst.
, vol.95
, pp. 1574-1576
-
-
Longtin, R.1
-
154
-
-
1642540093
-
Rapamycin induces the fusion-type independent downregulation of the ews/fli-1 proteins and inhibits ewings sarcoma cell proliferation
-
S. Mateo-Lozano, O. M. Tirado and V. Notario, Rapamycin induces the fusion-type independent downregulation of the EWS/FLI-1 proteins and inhibits Ewing's sarcoma cell proliferation, Oncogene 22 (2003), 9282-9287.
-
(2003)
Oncogene.
, vol.22
, pp. 9282-9287
-
-
Mateo-Lozano, S.1
Tirado, O.M.2
Notario, V.3
-
155
-
-
82955197047
-
-
P. A. Pizzo andD. G. Poplack eds Philadelphia: Lippincott Williams and Wilkins
-
J. S. Dome, E. J. Perlman,M. L. Ritchey, M. J. Coppes, J. Karapurakal and P. E. Grundy, Renal Tumors, in: Principles and Practice of Pediatric Oncology, P. A. Pizzo andD. G. Poplack, eds, Philadelphia: Lippincott Williams and Wilkins, 2006.
-
(2006)
Renal Tumors Principles and Practice of Pediatric Oncology
-
-
Dome, J.S.1
Perlmanm, L.2
Ritchey, E.J.3
Coppes, M.J.4
Karapurakal, J.5
Grundy, P.E.6
-
156
-
-
0028059816
-
Genetic events in the development ofWilms tumor
-
M. J. Coppes, D. A. Haber and P. E. Grundy, Genetic events in the development ofWilms' tumor, N Engl JMed 331 (1994), 586-590.
-
(1994)
N. Engl. J. Med.
, vol.331
, pp. 586-590
-
-
Coppes, M.J.1
Haber, D.A.2
Grundy, P.E.3
-
157
-
-
34247579714
-
A tumor suppressor and oncogene: The WT1 story
-
L. Yang, Y. Han, F. Suarez Saiz and M. D. Minden, A tumor suppressor and oncogene: the WT1 story, Leukemia 21 (2007), 868-876.
-
(2007)
Leukemia
, vol.21
, pp. 868-876
-
-
Yang, L.1
Han, Y.2
Suarez Saiz, F.3
Minden, M.D.4
-
158
-
-
0025992044
-
Alternative splicing and genomic structure of the Wilms tumor gene WT1
-
U S A
-
D. A. Haber, R. L. Sohn, A. J. Buckler, J. Pelletier, K. M. Call and D. E. Housman, Alternative splicing and genomic structure of the Wilms tumor gene WT1, Proc Natl Acad Sci U S A 88 (1991), 9618-9622.
-
(1991)
Proc. Natl. Acad. Sci.
, vol.88
, pp. 9618-9622
-
-
Haber, D.A.1
Sohn, R.L.2
Buckler, A.J.3
Pelletier, J.4
Call, K.M.5
Housman, D.E.6
-
159
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11Wilms tumor locus
-
K. M. Call, T. Glaser, C. Y. Ito, A. J. Buckler, J. Pelletier, D. A. Haber et al. , Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11Wilms' tumor locus, Cell 60 (1990), 509-520.
-
(1990)
Cell
, vol.60
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
Buckler, A.J.4
Pelletier, J.5
Haber, D.A.6
-
160
-
-
33751251698
-
Wilms tumor 1-associating protein regulates g2/m transition through stabilization of cyclin a2 mrna
-
U S A
-
K. Horiuchi, M. Umetani, T. Minami, H. Okayama, S. Takada, M. Yamamoto et al. , Wilms' tumor 1-associating protein regulates G2/M transition through stabilization of cyclin A2 mRNA, Proc Natl Acad Sci U S A 103 (2006), 17278-17283.
-
(2006)
Proc. Natl. Acad. Sci.
, vol.103
, pp. 17278-17283
-
-
Horiuchi, K.1
Umetani, M.2
Minami, T.3
Okayama, H.4
Takada, S.5
Yamamoto, M.6
-
161
-
-
0031686142
-
Microdissecting the genetic events in nephrogenic rests and Wilms tumor development
-
A. K. Charles, K. W. Brown and P. J. Berry, Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development, Am J Pathol 153 (1998), 991-1000.
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 991-1000
-
-
Charles, A.K.1
Brown, K.W.2
Berry, P.J.3
-
162
-
-
0027453021
-
Homozygous somaticWt1 point mutations in sporadic unilateral Wilms tumor
-
U S A
-
M. J. Coppes, G. J. Liefers, P. Paul, H. Yeger and B. R. Williams, Homozygous somaticWt1 point mutations in sporadic unilateral Wilms tumor, Proc Natl Acad Sci U S A 90 (1993), 1416-1419.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 1416-1419
-
-
Coppes, M.J.1
Liefers, G.J.2
Paul, P.3
Yeger, H.4
Williams, B.R.5
-
163
-
-
0024505754
-
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms tumor cells
-
A. E. Reeve, S. A. Sih, A. M. Raizis and A. P. Feinberg, Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells, Mol Cell Biol 9 (1989), 1799-1803.
-
(1989)
Mol. Cell Biol.
, vol.9
, pp. 1799-1803
-
-
Reeve, A.E.1
Sih, S.A.2
Raizis, A.M.3
Feinberg, A.P.4
-
164
-
-
0034024407
-
Genetics of Beckwith-Wiedemann syndrome-associated tumors: Common genetic pathways
-
M. Steenman, A. Westerveld and A. Mannens, Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways, Genes Chromosomes Cancer 28 (2000), 1-13.
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 1-13
-
-
Steenman, M.1
Westerveld, A.2
Mannens, A.3
-
165
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
-
E. R. Maher and W. Reik, Beckwith-Wiedemann syndrome: imprinting in clusters revisited, J Clin Invest 105 (2000), 247-252.
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
166
-
-
33846846526
-
An X chromosome gene WTX, is commonly inactivated in Wilms tumor
-
M. N. Rivera, W. J. Kim, J. Wells, D. R. Driscoll, B. W. Brannigan, M. Han et al. , An X chromosome gene, WTX, is commonly inactivated in Wilms tumor, Science 315 (2007), 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
Han, M.6
-
167
-
-
34249061491
-
Wilms tumor suppressor wtx negatively regulates wnt/beta-catenin signaling
-
M. B. Major, N. D. Camp, J. D. Berndt, X. Yi, S. J. Goldenberg, C. Hubbert et al. , Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling, Science 316 (2007), 1043-1046.
-
(2007)
Science
, vol.316
, pp. 1043-1046
-
-
Major, M.B.1
Camp, N.D.2
Berndt, J.D.3
Yi, X.4
Goldenberg, S.J.5
Hubbert, C.6
-
168
-
-
31444451325
-
Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorablehistology Wilms tumor: A report from the national wilms tumor study group
-
P. E. Grundy, N. E. Breslow, S. Li, E. Perlman, J. B. Beckwith, M. L. Ritchey et al. , Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorablehistology Wilms tumor: a report from the National Wilms Tumor Study Group, J Clin Oncol 23 (2005), 7312-7321.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 7312-7321
-
-
Grundy, P.E.1
Breslow, N.E.2
Li, S.3
Perlman, E.4
Beckwith, J.B.5
Ritchey, M.L.6
-
169
-
-
0031299355
-
Molecular basis of Wilms tumor
-
P. Grundy, Molecular basis of Wilms' tumor, Cancer Treat Res 92 (1997), 101-123.
-
(1997)
Cancer Treat. Res.
, vol.92
, pp. 101-123
-
-
Grundy, P.1
-
170
-
-
0035061543
-
Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours
-
D. Perotti, M. A. Testi, P. Mondini, S. Pilotti, E. D. Green, A. Pession et al. , Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours, Genes Chromosomes Cancer 31 (2001), 42-47.
-
(2001)
Genes. Chromosomes Cancer
, vol.31
, pp. 42-47
-
-
Perotti, D.1
Testi, M.A.2
Mondini, P.3
Pilotti, S.4
Green, E.D.5
Pession, A.6
-
171
-
-
0035219944
-
P53 expression in Wilms' tumor: A possible role as prognostic factor
-
A. J. Beniers, T. Efferth, L. Fuzesi, B. Granzen, R. Mertens and R. Jakse, p53 expression in Wilms' tumor: a possible role as prognostic factor, Int J Oncol 18 (2001), 133-139.
-
(2001)
Int. J. Oncol.
, vol.18
, pp. 133-139
-
-
Beniers, A.J.1
Efferth, T.2
Fuzesi, L.3
Granzen, B.4
Mertens, R.5
Jakse, R.6
-
172
-
-
0033677022
-
Frequent association of beta-catenin and WT1 mutations in Wilms tumors
-
S. Maiti, R. Alam, C. I. Amos and V. Huff, Frequent association of beta-catenin and WT1 mutations in Wilms tumors, Cancer Res 60 (2000), 6288-6292.
-
(2000)
Cancer Res.
, vol.60
, pp. 6288-6292
-
-
Maiti, S.1
Alam, R.2
Amos, C.I.3
Huff, V.4
-
173
-
-
36049006224
-
C-KIT overexpression without gene amplification and mutation in paediatric renal tumours
-
C. Jones, M. Rodriguez-Pinilla, M. Lambros, D. Bax, B. Messahel, G. M. Vujanic et al. , c-KIT overexpression, without gene amplification and mutation, in paediatric renal tumours, J Clin Pathol 60 (2007), 1226-1231.
-
(2007)
J. Clin. Pathol.
, vol.60
, pp. 1226-1231
-
-
Jones, C.1
Rodriguez-Pinilla, M.2
Lambros, M.3
Bax, D.4
Messahel, B.5
Vujanic, G.M.6
-
174
-
-
0033198499
-
High telomerase reverse transcriptase htertmessenger rna level correlates with tumor recurrence in patients with favorable histology Wilms tumor
-
J. S. Dome, S. Chung, T. Bergemann, C. B. Umbricht, M. Saji, L. A. Carey et al. , High telomerase reverse transcriptase (hTERT)messenger RNA level correlates with tumor recurrence in patients with favorable histology Wilms' tumor, Cancer Res 59 (1999), 4301-4307.
-
(1999)
Cancer Res.
, vol.59
, pp. 4301-4307
-
-
Dome, J.S.1
Chung, S.2
Bergemann, T.3
Umbricht, C.B.4
Saji, M.5
Carey, L.A.6
-
175
-
-
0035253655
-
Expression of the neurotrophin receptor trkb is associated with unfavorable outcome in wilms tumor
-
A. Eggert, M. A. Grotzer, N. Ikegaki, H. Zhao, A. Cnaan, G. M. Brodeur et al. , Expression of the neurotrophin receptor TrkB is associated with unfavorable outcome in Wilms' tumor, J Clin Oncol 19 (2001), 689-696.
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 689-696
-
-
Eggert, A.1
Grotzer, M.A.2
Ikegaki, N.3
Zhao, H.4
Cnaan, A.5
Brodeur, G.M.6
-
176
-
-
0035158304
-
The survivin:fas ratio in pediatric renal tumors
-
S. Takamizawa, D. Scott, J. Wen, P. Grundy, W. Bishop, K. Kimura et al. , The survivin:fas ratio in pediatric renal tumors, J Pediatr Surg 36 (2001), 37-42.
-
(2001)
J. Pediatr. Surg.
, vol.36
, pp. 37-42
-
-
Takamizawa, S.1
Scott, D.2
Wen, J.3
Grundy, P.4
Bishop, W.5
Kimura, K.6
-
177
-
-
0033855507
-
Decreased expression of the ink4 family of cyclin-dependent kinase inhibitors in wilms tumor
-
M. Y. Arcellana-Panlilio, R. M. Egeler, E. Ujack, A. Pinto, D. J. Demetrick, S. M. Robbins et al. , Decreased expression of the INK4 family of cyclin-dependent kinase inhibitors in Wilms tumor, Genes Chromosomes Cancer 29 (2000), 63-69.
-
(2000)
Genes. Chromosomes Cancer
, vol.29
, pp. 63-69
-
-
Arcellana-Panlilio, M.Y.1
Egeler, R.M.2
Ujack, E.3
Pinto, A.4
Demetrick, D.J.5
Robbins, S.M.6
-
178
-
-
36749050382
-
Defective chromosome segregation and telomere dysfunction in aggressive wilms tumors
-
Y. Stewenius, Y. Jin, I. Ora, J. de Kraker, J. Bras, A. Frigyesi et al. , Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors, Clin Cancer Res 13 (2007), 6593-6602.
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 6593-6602
-
-
Stewenius, Y.1
Jin, Y.2
Ora, I.3
De Kraker, J.4
Bras, J.5
Frigyesi, A.6
-
180
-
-
0031736957
-
Confirmation of FWT1 as a wilms' tumour susceptibility gene and phenotypic characteristics of wilms' tumour attributable to fwt1
-
N. Rahman, F. Abidi, D. Ford, L. Arbour, E. Rapley, P. Tonin et al. , Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1, Hum Genet 103 (1998), 547-556.
-
(1998)
Hum. Genet.
, vol.103
, pp. 547-556
-
-
Rahman, N.1
Abidi, F.2
Ford, D.3
Arbour, L.4
Rapley, E.5
Tonin, P.6
-
181
-
-
0032053822
-
Linkage of familial Wilms tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors
-
J. M. McDonald, E. C. Douglass, R. Fisher, C. F. Geiser, C. E. Krill, L. C. Strong et al. , Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors, Cancer Res 58 (1998), 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
-
182
-
-
0029765587
-
Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization
-
R. A. Altura, M. Valentine, H. Li, J. M. Boyett, P. Shearer, P. Grundy et al. , Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization, Cancer Res 56 (1996), 3837-3841.
-
(1996)
Cancer Res.
, vol.56
, pp. 3837-3841
-
-
Altura, R.A.1
Valentine, M.2
Li, H.3
Boyett, J.M.4
Shearer, P.5
Grundy, P.6
-
183
-
-
33749266701
-
Syndromes and constitutional chromosomal abnormalities associated withWilms tumour
-
R. H. Scott, C. A. Stiller, L. Walker and N. Rahman, Syndromes and constitutional chromosomal abnormalities associated withWilms tumour, JMedGenet 43 (2006), 705-715.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 705-715
-
-
Scott, R.H.1
Stiller, C.A.2
Walker, L.3
Rahman, N.4
-
184
-
-
0018668497
-
Aniridia-Wilms tumor association: Evidence for specific deletion of 11p13
-
U. Francke, L. B. Holmes, L. Atkins and V. M. Riccardi, Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13, Cytogenet Cell Genet 24 (1979), 185-192.
-
(1979)
Cytogenet. Cell Genet.
, vol.24
, pp. 185-192
-
-
Francke, U.1
Holmes, L.B.2
Atkins, L.3
Riccardi, V.M.4
-
185
-
-
0026907525
-
Constitutional mutations in the wt1 gene in patients with denys-drash syndrome
-
P. N. Baird, A. Santos, N. Groves, L. Jadresic and J. K. Cowell, Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome, Hum Mol Genet 1 (1992), 301-305.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 301-305
-
-
Baird, P.N.1
Santos, A.2
Groves, N.3
Jadresic, L.4
Cowell, J.K.5
-
186
-
-
0026457966
-
Inherited wt1 mutation in denys-drash syndrome
-
M. J. Coppes, G. J. Liefers, M. Higuchi, A. B. Zinn, J. W. Balfe and B. R. Williams, Inherited WT1 mutation in Denys-Drash syndrome, Cancer Res 52 (1992), 6125-6128.
-
(1992)
Cancer Res.
, vol.52
, pp. 6125-6128
-
-
Coppes, M.J.1
Liefers, G.J.2
Higuchi, M.3
Zinn, A.B.4
Balfe, J.W.5
Williams, B.R.6
-
187
-
-
0027175810
-
Evidence that wt1 mutations in denys-drash syndrome patients may act in a dominantnegative fashion
-
M. H. Little, K. A. Williamson, M. Mannens, A. Kelsey, C. Gosden, N. D. Hastie et al. , Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominantnegative fashion, Hum Mol Genet 2 (1993), 259-264.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 259-264
-
-
Little, M.H.1
Williamson, K.A.2
Mannens, M.3
Kelsey, A.4
Gosden, C.5
Hastie, N.D.6
-
188
-
-
17444381939
-
Translocation carcinomas of the kidney
-
P. Argani and P. Ladanyi, Translocation carcinomas of the kidney, Clin Lab Med 25 (2005), 363-378.
-
(2005)
Clin. Lab. Med.
, vol.25
, pp. 363-378
-
-
Argani, P.1
Ladanyi, P.2
-
189
-
-
0010346928
-
Primary renal neoplasms with the aspl-tfe3 gene fusion of alveolar soft part sarcoma: A distinctive tumor entity previously included among renal cell carcinomas of children and adolescents
-
P. Argani, C. R. Antonescu, P. B. Illei, M. Y. Lui, C. F. Timmons, R. Newbury et al. , Primary renal neoplasms with the ASPL-TFE3 gene fusion of alveolar soft part sarcoma: a distinctive tumor entity previously included among renal cell carcinomas of children and adolescents, Am J Pathol 159 (2001), 179-192.
-
(2001)
Am. J. Pathol.
, vol.159
, pp. 179-192
-
-
Argani, P.1
Antonescu, C.R.2
Illei, P.B.3
Lui, M.Y.4
Timmons, C.F.5
Newbury, R.6
-
190
-
-
0037230146
-
Renal cell carcinoma with t X;17: Singular pediatric neoplasm with specific phenotype/ genotype features
-
E. Zambrano and M. Reyes-Mugica, Renal cell carcinoma with t(X;17): singular pediatric neoplasm with specific phenotype/ genotype features, Pediatr Dev Pathol 6 (2003), 84-87.
-
(2003)
Pediatr. Dev. Pathol.
, vol.6
, pp. 84-87
-
-
Zambrano, E.1
Reyes-Mugica, M.2
-
191
-
-
0037716678
-
Five new cases of juvenile renal cell carcinoma with translocations involving Xp11. 2: A cytogenetic andmorphologic study
-
C. Perot, L. Boccon-Gibod, R. Bouvier, F. Doz, J. C. Fournet, P. Freneaux et al. , Five new cases of juvenile renal cell carcinoma with translocations involving Xp11. 2: a cytogenetic andmorphologic study, Cancer Genet Cytogenet 143 (2003), 93-99.
-
(2003)
Cancer Genet. Cytogenet.
, vol.143
, pp. 93-99
-
-
Perot, C.1
Boccon-Gibod, L.2
Bouvier, R.3
Doz, F.4
Fournet, J.C.5
Freneaux, P.6
-
192
-
-
3442875929
-
Morphologic and molecular characterization of renal cell carcinoma in children and young adults
-
E. Bruder, O. Passera, D. Harms, I. Leuschner, M. Ladanyi, P. Argani et al. , Morphologic and molecular characterization of renal cell carcinoma in children and young adults, Am J Surg Pathol 28 (2004), 1117-1132.
-
(2004)
Am. J. Surg. Pathol.
, vol.28
, pp. 1117-1132
-
-
Bruder, E.1
Passera, O.2
Harms, D.3
Leuschner, I.4
Ladanyi, M.5
Argani, P.6
-
193
-
-
10144257193
-
The t x;1 p11. 2;q21. 2 translocation in papillary renal cell carcinoma fuses a novel gene prcc to the tfe3 transcription factor gene
-
S. K. Sidhar, J. Clark, S. Gill, S. Hamoudi, A. J. Crew, R. Gwilliam et al. , The t(X;1)(p11. 2;q21. 2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene, Hum Mol Genet 5 (1996), 1333-1338.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1333-1338
-
-
Sidhar, S.K.1
Clark, J.2
Gill, S.3
Hamoudi, S.4
Crew, A.J.5
Gwilliam, R.6
-
194
-
-
0030463172
-
Fusion of the transcription factor tfe3 gene to a novel gene prcc in t x;1 p11;q21-positive papillary renal cell carcinomas
-
U S A
-
M. A. Weterman, M. Wilbrink and A. Geurts van Kessel, Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)- positive papillary renal cell carcinomas, Proc Natl Acad Sci U S A 93 (1996), 15294-15298.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 15294-15298
-
-
Weterman, M.A.1
Wilbrink, M.2
Kessel Van A.Geurts3
-
195
-
-
0034975421
-
A distinctive pediatric renal neoplasm characterized by epithelioid morphology basement membrane production focal hmb45 immunoreactivity and t 6;11 p21. 1;q12 chromosome translocation
-
P. Argani, A. Hawkins, C. A. Griffin, J. D. Goldstein, M. Haas, J. B. Beckwith et al. , A distinctive pediatric renal neoplasm characterized by epithelioid morphology, basement membrane production, focal HMB45 immunoreactivity, and t(6;11)(p21. 1;q12) chromosome translocation, Am J Pathol 158 (2001), 2089-2096.
-
(2001)
Am. J. Pathol.
, vol.158
, pp. 2089-2096
-
-
Argani, P.1
Hawkins, A.2
Griffin, C.A.3
Goldstein, J.D.4
Haas, M.5
Beckwith, J.B.6
-
196
-
-
19944433827
-
Renal carcinomas with the t 6;11 p21;q12: Clinicopathologic features and demonstration of the specific alpha-tfeb gene fusion by immunohistochemistry rt-pcr and dna pcr
-
P. Argani, M. Lae, B. Hutchinson, V. E. Reuter, M. H. Collins, J. Perentesis et al. , Renal carcinomas with the t(6;11)(p21;q12): clinicopathologic features and demonstration of the specific alpha-TFEB gene fusion by immunohistochemistry, RT-PCR, and DNA PCR, Am J Surg Pathol 29 (2005), 230-240.
-
(2005)
Am. J. Surg. Pathol.
, vol.29
, pp. 230-240
-
-
Argani, P.1
Lae, M.2
Hutchinson, B.3
Reuter, V.E.4
Collins, M.H.5
Perentesis, J.6
-
197
-
-
33645985526
-
Expression of etv6- ntrk in classical, cellular andmixed subtypes of congenital mesoblastic nephroma
-
J. Anderson, S. Gibson andN. J. Sebire, Expression of ETV6- NTRK in classical, cellular andmixed subtypes of congenital mesoblastic nephroma, Histopathology 48 (2006), 748-753.
-
(2006)
Histopathology
, vol.48
, pp. 748-753
-
-
Anderson, J.1
Gibson, S.2
Sebire, N.J.3
-
198
-
-
0032533497
-
ETV6-ntrk3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma
-
S. R. Knezevich, M. J. Garnett, T. J. Pysher, J. B. Beckwith, P. E. Grundy and P. H. Sorensen, ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma, Cancer Res 58 (1998), 5046-5048.
-
(1998)
Cancer Res.
, vol.58
, pp. 5046-5048
-
-
Knezevich, S.R.1
Garnett, M.J.2
Pysher, T.J.3
Beckwith, J.B.4
Grundy, P.E.5
Sorensen, P.H.6
-
199
-
-
2642647094
-
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
-
I. Versteege, N. Sevenet, J. Lange, M. F. Rousseau-Merck, P. Ambros, R. Handgretinger et al. , Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer, Nature 394 (1998), 203-206.
-
(1998)
Nature
, vol.394
, pp. 203-206
-
-
Versteege, I.1
Sevenet, N.2
Lange, J.3
Rousseau-Merck, M.F.4
Ambros, P.5
Handgretinger, R.6
-
200
-
-
0031680298
-
Atypical teratoid/rhabdoid tumor of the central nervous system: A highly malignant tumor of infancyand childhood requently mistaken for medulloblastoma: A pediatriconcology group study
-
P. C. Burger, I. T. Yu, T. Tihan, H. S. Friedman, D. R. Strother, J. L. Kepner et al. , Atypical teratoid/rhabdoid tumor of the central nervous system: a highly malignant tumor of infancyand childhood requently mistaken for medulloblastoma: a PediatricOncology Group study, AmJ Surg Pathol 22 (1998), 1083-1092.
-
(1998)
Am. J. Surg. Pathol.
, vol.22
, pp. 1083-1092
-
-
Burger, P.C.1
Yu, I.T.2
Tihan, T.3
Friedman, H.S.4
Strother, D.R.5
Kepner, J.L.6
-
201
-
-
0027401232
-
Uniparental origin of i 12p in human germ cell tumors
-
R. J. Sinke, R. F. Suijkerbuijk, B. de Jong, J. W. Oosterhuis and A. Geurts van Kessel, Uniparental origin of i(12p) in human germ cell tumors, Genes Chromosomes Cancer 6 (1993), 161-165.
-
(1993)
Genes. Chromosomes Cancer
, vol.6
, pp. 161-165
-
-
Sinke, R.J.1
Suijkerbuijk, R.F.2
De Jong, B.3
Oosterhuis, J.W.4
Kessel Van A.Geurts5
-
202
-
-
0027368745
-
Molecular cytogenetic analysis of i 12p-negative human male germ cell tumors
-
E. Rodriguez, J. Houldsworth, V. E. Reuter, P. Meltzer, J. Zhang, J. M. Trent et al. , Molecular cytogenetic analysis of i(12p)-negative human male germ cell tumors, Genes Chromosomes Cancer 8 (1993), 230-236.
-
(1993)
Genes. Chromosomes Cancer
, vol.8
, pp. 230-236
-
-
Rodriguez, E.1
Houldsworth, J.2
Reuter, V.E.3
Meltzer, P.4
Zhang, J.5
Trent, J.M.6
-
203
-
-
0027526407
-
In situ numeric analysis of centromeric regions of chromosomes 1 12 and 15 of seminomas, nonseminomatous germ cell tumors and carcinoma in situ of human testis
-
L. H. Looijenga, A. J. Gillis, W. L. Van Putten and J. W. Oosterhuis, In situ numeric analysis of centromeric regions of chromosomes 1, 12, and 15 of seminomas, nonseminomatous germ cell tumors, and carcinoma in situ of human testis, Lab Invest 68 (1993), 211-219.
-
(1993)
Lab. Invest.
, vol.68
, pp. 211-219
-
-
Looijenga, L.H.1
Gillis, A.J.2
Van Putten, W.L.3
Oosterhuis, J.W.4
-
204
-
-
10544251842
-
Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization
-
W. M. Korn, D. E. Oide Weghuis, R. F. Suijkerbuijk, U. Schmidt, T. Otto, S. du Manoir et al. , Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization, Genes Chromosomes Cancer 17 (1996), 78-87.
-
(1996)
Genes Chromosomes Cancer
, vol.17
, pp. 78-87
-
-
Korn, W.M.1
Oide Weghuis, D.E.2
Suijkerbuijk, R.F.3
Schmidt, U.4
Otto, T.5
Du Manoir, S.6
-
205
-
-
0028046406
-
Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
-
S. Mathew, V. V. Murty, G. J. Bosl and R. S. Chaganti, Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors, Cancer Res 54 (1994), 6265-6269.
-
(1994)
Cancer Res.
, vol.54
, pp. 6265-6269
-
-
Mathew, S.1
Murty, V.V.2
Bosl, G.J.3
Chaganti, R.S.4
-
206
-
-
0025273871
-
Detection of preferentialNRASmutations in human male germ cell tumors by the polymerase chain reaction
-
S. Ganguly, V. V. Murty, F. Samaniego, V. E. Reuter, G. J. Bosl andR. S. Chaganti, Detection of preferentialNRASmutations in human male germ cell tumors by the polymerase chain reaction, Genes Chromosomes Cancer 1 (1990), 228-232.
-
(1990)
Genes. Chromosomes Cancer
, vol.1
, pp. 228-232
-
-
Ganguly, S.1
Murty, V.V.2
Samaniego, F.3
Reuter, V.E.4
Bosl, G.J.5
Chaganti, R.S.6
-
207
-
-
0028210523
-
Differential expression of protooncogenes in human germ cell tumors of the testis
-
T. Shuin, H. Misaki, Y. Kubota, M. Yao and M. Hosaka, Differential expression of protooncogenes in human germ cell tumors of the testis, Cancer 73 (1994), 1721-1727.
-
(1994)
Cancer
, vol.73
, pp. 1721-1727
-
-
Shuin, T.1
Misaki, H.2
Kubota, Y.3
Yao, M.4
Hosaka, M.5
-
208
-
-
0027243180
-
Frequent loss of 11p13 and 11p15 loci in male germ cell tumours
-
R. A. Lothe, N. Hastie, K. Heimdal, S. D. Fossa, A. E. Stenwig and A. L. Borresen, Frequent loss of 11p13 and 11p15 loci in male germ cell tumours, Genes Chromosomes Cancer 7 (1993), 96-101.
-
(1993)
Genes Chromosomes Cancer
, vol.7
, pp. 96-101
-
-
Lothe, R.A.1
Hastie, N.2
Heimdal, K.3
Fossa, S.D.4
Stenwig, A.E.5
Borresen, A.L.6
-
209
-
-
0027944119
-
Frequent allelic deletions and loss of expression characterize the dcc gene in male germ cell tumors
-
V. V. Murty, R. G. Li, J. Houldsworth, D. L. Bronson, V. E. Reuter, G. J. Bosl et al. , Frequent allelic deletions and loss of expression characterize the DCC gene in male germ cell tumors, Oncogene 9 (1994), 3227-3231.
-
(1994)
Oncogene
, vol.9
, pp. 3227-3231
-
-
Murty, V.V.1
Li, R.G.2
Houldsworth, J.3
Bronson, D.L.4
Reuter, V.E.5
Bosl, G.J.6
-
210
-
-
33644668607
-
Ovarian germ cell tumors in children: A clinical study of 66 patients
-
A. De Backer, G. C. Madern, J. W. Oosterhuis, F. G. Hakvoort- Cammel and F. W. Hazebroek, Ovarian germ cell tumors in children: a clinical study of 66 patients, Pediatr Blood Cancer 46 (2006), 459-464.
-
(2006)
Pediatr. Blood Cancer
, vol.46
, pp. 459-464
-
-
De Backer, A.1
Madern, G.C.2
Oosterhuis, J.W.3
Hakvoort- Cammel, F.G.4
Hazebroek, F.W.5
-
211
-
-
0025092775
-
Genetics and biology of human ovarian teratomas i cytogenetic analysis and mechanism of origin
-
U. Surti, L. Hoffner, A. Chakravarti and R. E. Ferrell, Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin, Am J Hum Genet 47 (1990), 635-643.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 635-643
-
-
Surti, U.1
Hoffner, L.2
Chakravarti, A.3
Ferrell, R.E.4
-
212
-
-
0032527910
-
Genetic analysis of ovarian germ cell tumors by comparative genomic hybridization
-
M. A. Riopel, A. Spellerberg, C. A. Griffin and E. J. Perlman, Genetic analysis of ovarian germ cell tumors by comparative genomic hybridization, Cancer Res 58 (1998), 3105-3110.
-
(1998)
Cancer Res.
, vol.58
, pp. 3105-3110
-
-
Riopel, M.A.1
Spellerberg, A.2
Griffin, C.A.3
Perlman, E.J.4
-
213
-
-
0036203138
-
Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents
-
D. T. Schneider, A. E. Schuster, M. K. Fritsch, G. Calaminus, U. Gobel, D. Harms et al. , Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents, Genes Chromosomes Cancer 34 (2002), 115-125.
-
(2002)
Genes. Chromosomes Cancer
, vol.34
, pp. 115-125
-
-
Schneider, D.T.1
Schuster, A.E.2
Fritsch, M.K.3
Calaminus, G.4
Gobel, U.5
Harms, D.6
-
214
-
-
0025181655
-
Cytogenetic and immunohistochemical evidence for the germcell origin of a subset of acute leukemias associated with mediastinal germ cell tumors
-
M. Ladanyi, F. Samaniego, V. E. Reuter, R. J. Motzer, S. C. Jhanwar, G. J. Bosl et al. , Cytogenetic and immunohistochemical evidence for the germcell origin of a subset of acute leukemias associated with mediastinal germ cell tumors, J Natl Cancer Inst 82 (1990), 221-227.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 221-227
-
-
Ladanyi, M.1
Samaniego, F.2
Reuter, V.E.3
Motzer, R.J.4
Jhanwar, S.C.5
Bosl, G.J.6
-
215
-
-
0028961918
-
Numerical sex chromosomal abnormalities in pineal teratomas by cytogenetic analysis and fluorescence in situ hybridization
-
I. T. Yu, C. A. Griffin, P. C. Phillips, L. C. Strauss and E. J. Perlman, Numerical sex chromosomal abnormalities in pineal teratomas by cytogenetic analysis and fluorescence in situ hybridization, Lab Invest 72 (1995), 419-423.
-
(1995)
Lab Invest
, vol.72
, pp. 419-423
-
-
Yu, I.T.1
Griffin, C.A.2
Phillips, P.C.3
Strauss, L.C.4
Perlman, E.J.5
-
216
-
-
0032961983
-
Chromosome abnormalities of eighty-one pediatric germ cell tumors: Sex- age- site- and histopathology-related differences - A childrens cancer group study
-
K. J. Bussey, H. J. Lawce, S. B. Olson, D. C. Arthur, D. K. Kalousek, M. Krailo et al. , Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences - a Children's Cancer Group study, Genes Chromosomes Cancer 25 (1999), 134-146.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 134-146
-
-
Bussey, K.J.1
Lawce, H.J.2
Olson, S.B.3
Arthur, D.C.4
Kalousek, D.K.5
Krailo, M.6
-
217
-
-
0028142538
-
Cytogenetic analysis of childhood endodermal sinus tumors: A pediatric oncology group study
-
E. J. Perlman, B. Cushing, E. Hawkins and C. A. Griffin, Cytogenetic analysis of childhood endodermal sinus tumors: a Pediatric Oncology Group study, Pediatr Pathol 14 (1994), 695-708.
-
(1994)
Pediatr. Pathol.
, vol.14
, pp. 695-708
-
-
Perlman, E.J.1
Cushing, B.2
Hawkins, E.3
Griffin, C.A.4
-
218
-
-
0034455638
-
Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization
-
E. J. Perlman, J. Hu, D. Ho, B. Cushing, S. Lauer and R. P. Castleberry, Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization, J Pediatr Hematol Oncol 22 (2000), 100-105.
-
(2000)
J. Pediatr. Hematol. Oncol.
, vol.22
, pp. 100-105
-
-
Perlman, E.J.1
Hu, J.2
Ho, D.3
Cushing, B.4
Lauer, S.5
Castleberry, R.P.6
-
219
-
-
0020634258
-
The distribution of chromosomal genotypes associated with Turner's syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism
-
E. B. Hook and D. Warburton, The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism, Hum Genet 64 (1983), 24-27.
-
(1983)
Hum. Genet.
, vol.64
, pp. 24-27
-
-
Hook, E.B.1
Warburton, D.2
-
220
-
-
0033365196
-
Gonadoblastoma, testicular and prostate cancers and the tspy gene
-
Y. F. Lau, Gonadoblastoma, testicular and prostate cancers, and the TSPY gene, Am J Hum Genet 64 (1999), 921-927.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 921-927
-
-
Lau, Y.F.1
-
221
-
-
0023392352
-
Klinefelters syndrome associated with mediastinal germ cell neoplasms
-
C. R. Nichols, N. A. Heerema, C. Palmer, P. J. Sr. Loehrer, S. D. Williams and L. H. Einhorn, Klinefelter's syndrome associated with mediastinal germ cell neoplasms, J Clin Oncol 5 (1987), 1290-1294.
-
(1987)
J. Clin. Oncol.
, vol.5
, pp. 1290-1294
-
-
Nichols, C.R.1
Heerema, N.A.2
Palmer, C.3
Loehrer Sr., P.J.4
Williams, S.D.5
Einhorn, L.H.6
-
222
-
-
25844442348
-
IGF2/h19 imprinting analysis of human germ cell tumors gcts using the methylationsensitive single-nucleotide primer extension method reflects the origin of gcts in different stages of primordial germ cell development
-
S. Sievers, K. Alemazkour, S. Zahn, E. J. Perlman, A. J. Gillis, L. H. Looijenga et al. , IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylationsensitive single-nucleotide primer extension method reflects the origin of GCTs in different stages of primordial germ cell development, Genes Chromosomes Cancer 44 (2005), 256-264.
-
(2005)
Genes. Chromosomes Cancer
, vol.44
, pp. 256-264
-
-
Sievers, S.1
Alemazkour, K.2
Zahn, S.3
Perlman, E.J.4
Gillis, A.J.5
Looijenga, L.H.6
-
223
-
-
67449089704
-
Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes
-
S. Furukawa, M. Haruta, Y. Arai, S. Honda, J. Ohshima, W. Sugawara et al. , Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes, Cancer Sci 100 (2009), 698-708.
-
(2009)
Cancer Sci.
, vol.100
, pp. 698-708
-
-
Furukawa, S.1
Haruta, M.2
Arai, Y.3
Honda, S.4
Ohshima, J.5
Sugawara, W.6
-
224
-
-
0023767249
-
Identification of germline and somatic mutations affecting the retinoblastoma gene
-
J. M. Dunn, R. A. Phillips, A. J. Becker and B. L. Gallie, Identification of germline and somatic mutations affecting the retinoblastoma gene, Science 241 (1988), 1797-1800.
-
(1988)
Science
, vol.241
, pp. 1797-1800
-
-
Dunn, J.M.1
Phillips, R.A.2
Becker, A.J.3
Gallie, B.L.4
-
225
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
U S A
-
A. G. Jr. Knudson, Mutation and cancer: statistical study of retinoblastoma, Proc Natl Acad Sci U S A 68 (1971), 820-823.
-
(1971)
Proc. Natl. Acad. Sci.
, vol.68
, pp. 820-823
-
-
Knudson Jr., A.G.1
-
226
-
-
3342996653
-
Retinoblastoma: Revisiting the model prototype of inherited cancer
-
D. R. Lohmann and B. L. Gallie, Retinoblastoma: revisiting the model prototype of inherited cancer, Am J Med Genet C Semin Med Genet 129C (2004), 23-28.
-
(2004)
Am. J. Med. Genet. C Semin Med. Genet.
, vol.C
, pp. 23-28
-
-
Lohmann, D.R.1
Gallie, B.L.2
-
227
-
-
0024339365
-
Parental origin of mutations of the retinoblastoma gene
-
T. P. Dryja, S. Mukai, R. Petersen, J. M. Rapaport, D. Walton and D. W. Yandell, Parental origin of mutations of the retinoblastoma gene, Nature 339 (1989), 556-558.
-
(1989)
Nature
, vol.339
, pp. 556-558
-
-
Dryja, T.P.1
Mukai, S.2
Petersen, R.3
Rapaport, J.M.4
Walton, D.5
Yandell, D.W.6
-
228
-
-
0024382804
-
Preferential germline mutation of the paternal allele in retinoblastoma
-
X. P. Zhu, J. M. Dunn, R. A. Phillips, A. D. Goddard, K. E. Paton, A. Becker et al. , Preferential germline mutation of the paternal allele in retinoblastoma, Nature 340 (1989), 312-313.
-
(1989)
Nature
, vol.340
, pp. 312-313
-
-
Zhu, X.P.1
Dunn, J.M.2
Phillips, R.A.3
Goddard, A.D.4
Paton, K.E.5
Becker, A.6
-
229
-
-
0033786378
-
Rb function in cell-cycle regulation and apoptosis
-
J. W. Harbour and D. C. Dean, Rb function in cell-cycle regulation and apoptosis, Nat Cell Biol 2 (2000), E65-67.
-
(2000)
Nat. Cell Biol.
, vol.2
-
-
Harbour, J.W.1
Dean, D.C.2
-
231
-
-
33748870748
-
Hereditary cancer predisposition in children: Genetic basis and clinical implications
-
B. Strahm and D. Malkin, Hereditary cancer predisposition in children: genetic basis and clinical implications, Int J Cancer 119 (2006), 2001-2006.
-
(2006)
Int. J. Cancer
, vol.119
, pp. 2001-2006
-
-
Strahm, B.1
Malkin, D.2
-
232
-
-
1542318327
-
Lifetime risks of common cancers amongretinoblastoma survivors
-
O. Fletcher, D. Easton, K. Anderson, C. Gilham, M. Jay and M. Peto, Lifetime risks of common cancers amongretinoblastoma survivors, J Natl Cancer Inst 96 (2004), 357-363.
-
(2004)
J. Natl. Cancer Inst.
, vol.96
, pp. 357-363
-
-
Fletcher, O.1
Easton, D.2
Anderson, K.3
Gilham, C.4
Jay, M.5
Peto, M.6
-
233
-
-
0023106062
-
Human retinoblastoma susceptibility gene: Cloning Identification and sequence
-
W. H. Lee, R. Bookstein, F. Hong, L. J. Young, J. Y. Shew and E. Y. Lee, Human retinoblastoma susceptibility gene: cloning, identification, and sequence, Science 235 (1987), 1394-1399.
-
(1987)
Science
, vol.235
, pp. 1394-1399
-
-
Lee, W.H.1
Bookstein, R.2
Hong, F.3
Young, L.J.4
Shew, J.Y.5
Lee, E.Y.6
-
234
-
-
0036884829
-
The retinoblastoma tumour suppressor in development and cancer
-
M. Classon and E. Harlow, The retinoblastoma tumour suppressor in development and cancer, Nat Rev Cancer 2 (2002), 910-917.
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 910-917
-
-
Classon, M.1
Harlow, E.2
-
235
-
-
0031737407
-
Overview of RB gene mutations in patients with retinoblastoma implications for clinical genetic screening
-
J. W. Harbour, Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening, Ophthalmology 105 (1998), 1442-1447.
-
(1998)
Ophthalmology
, vol.105
, pp. 1442-1447
-
-
Harbour, J.W.1
-
236
-
-
0030925099
-
Extensive dna methylation spanning the rb promoter in retinoblastoma tumors
-
C. Stirzaker, D. S. Millar, C. L. Paul, P. M. Warnecke, J. Harrison, P. C. Vincent et al. , Extensive DNA methylation spanning the Rb promoter in retinoblastoma tumors, Cancer Res 57 (1997), 2229-2237.
-
(1997)
Cancer Res.
, vol.57
, pp. 2229-2237
-
-
Stirzaker, C.1
Millar, D.S.2
Paul, C.L.3
Warnecke, P.M.4
Harrison, J.5
Vincent, P.C.6
-
237
-
-
66149083996
-
High incidence of allelic loss at 16q12. 2 region spanning rbl2/p130 gene in retinoblastoma
-
K. Priya, S. R. Jada, B. L. Quah, T. C. Quah and P. S. Lai, High incidence of allelic loss at 16q12. 2 region spanning RBL2/p130 gene in retinoblastoma, Cancer Biol Ther 8 (2009), 714-717.
-
(2009)
Cancer Biol. Ther.
, vol.8
, pp. 714-717
-
-
Priya, K.1
Jada, S.R.2
Quah, B.L.3
Quah, T.C.4
Lai, P.S.5
-
238
-
-
34547457538
-
Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis
-
S. Chakraborty, S. Khare, S. K. Dorairaj, V. C. Prabhakaran, D. R. Prakash and D. R. Kumar, Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis, Genomics 90 (2007), 344-353.
-
(2007)
Genomics
, vol.90
, pp. 344-353
-
-
Chakraborty, S.1
Khare, S.2
Dorairaj, S.K.3
Prabhakaran, V.C.4
Prakash, D.R.5
Kumar, D.R.6
-
239
-
-
33750488365
-
-
5th ed. D. G. Poplack PAPa ed. Philadelphia: Lippincott Williams and Wilkins
-
BL-T, D. Mueller and M. J. Finegold, Tumors of the liver, in: Principles and Practice of Pediatric Oncology, (5th ed. ), D. G. Poplack PAPa, ed. , Philadelphia: Lippincott Williams and Wilkins; 2006, pp. 887-904.
-
(2006)
Tumors of the Liver Principles and Practice of Pediatric Oncology
, pp. 887-904
-
-
Mueller, B.D.1
Finegold, M.J.2
-
240
-
-
0042824128
-
Epidemiology of primary hepatic malignancies in U. S. children
-
A. Darbari, K. M. Sabin, C. N. Shapiro and K. B. Schwarz, Epidemiology of primary hepatic malignancies in U. S. children, Hepatology 38 (2003), 560-566.
-
(2003)
Hepatology
, vol.38
, pp. 560-566
-
-
Darbari, A.1
Sabin, K.M.2
Shapiro, C.N.3
Schwarz, K.B.4
-
241
-
-
0008878205
-
Primary hepatic tumors of childhood
-
A. G. Weinberg and M. J. Finegold, Primary hepatic tumors of childhood, Hum Pathol 14 (1983), 512-537.
-
(1983)
Hum. Pathol.
, vol.14
, pp. 512-537
-
-
Weinberg, A.G.1
Finegold, M.J.2
-
242
-
-
0027270242
-
Liver tumors in childhood: Epidemiology and clinics
-
F. F. Bellani and M. Massimino, Liver tumors in childhood: epidemiology and clinics, J Surg Oncol Suppl 3 (1993), 119-121.
-
(1993)
J. Surg. Oncol. Suppl.
, vol.3
, pp. 119-121
-
-
Bellani, F.F.1
Massimino, M.2
-
243
-
-
71049119486
-
Predictive power of pretreatment prognostic factors in children with hepatoblastoma: A report from the children's oncology group
-
R. L. Meyers, J. R. Rowland, M. Krailo, Z. Chen, H. M. Katzenstein and M. H. Malogolowkin, Predictive power of pretreatment prognostic factors in children with hepatoblastoma: a report from the Children's Oncology Group, Pediatr Blood Cancer 53 (2009), 1016-1022.
-
(2009)
Pediatr. Blood Cancer
, vol.53
, pp. 1016-1022
-
-
Meyers, R.L.1
Rowland, J.R.2
Krailo, M.3
Chen, Z.4
Katzenstein, H.M.5
Malogolowkin, M.H.6
-
244
-
-
24944469682
-
Cytogenetic evaluation of a large series of hepatoblastomas: Numerical abnormalities with recurring aberrations involving 1q12-q21
-
G. E. Tomlinson, E. C. Douglass, B. H. Pollock, M. J. Finegold and N. R. Schneider, Cytogenetic evaluation of a large series of hepatoblastomas: numerical abnormalities with recurring aberrations involving 1q12-q21, Genes Chromosomes Cancer 44 (2005), 177-184.
-
(2005)
Genes Chromosomes Cancer 44
, pp. 177-184
-
-
Tomlinson, G.E.1
Douglass, E.C.2
Pollock, B.H.3
Finegold, M.J.4
Schneider, N.R.5
-
245
-
-
0033900096
-
Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome
-
R. G. Weber, T. Pietsch, D. von Schweinitz and D. Lichter, Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome, Am J Pathol 157 (2000), 571-578.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 571-578
-
-
Weber, R.G.1
Pietsch, T.2
Von Schweinitz, D.3
Lichter, D.4
-
246
-
-
0035735788
-
Genetic abnormalities in a pre and postchemotherapy hepatoblastoma
-
M. Mullarkey, C. J. Breen, M. McDermott, A. O'Meara and R. L. Stallings, Genetic abnormalities in a pre and postchemotherapy hepatoblastoma, Cytogenet Cell Genet 95 (2001), 9-11.
-
(2001)
Cytogenet. Cell Genet.
, vol.95
, pp. 9-11
-
-
Mullarkey, M.1
Breen, C.J.2
McDermott, M.3
O'meara, A.4
Stallings, R.L.5
-
247
-
-
0025844921
-
Consistent cytogenetic aberrations in hepatoblastoma: A common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies
-
J. A. Fletcher, H. P. Kozakewich, K. Pavelka, H. E. Grier, R. C. Shamberger, B. Korf et al. , Consistent cytogenetic aberrations in hepatoblastoma: a common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies? Genes Chromosomes Cancer 3 (1991), 37-43.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 37-43
-
-
Fletcher, J.A.1
Kozakewich, H.P.2
Pavelka, K.3
Grier, H.E.4
Shamberger, R.C.5
Korf, B.6
-
248
-
-
0025953113
-
Abnormalities of 2q: A common genetic link between rhabdomyosarcoma and hepatoblastoma
-
E. Rodriguez, V. E. Reuter, C. Mies, G. J. Bosl and R. S. Chaganti, Abnormalities of 2q: a common genetic link between rhabdomyosarcoma and hepatoblastoma? Genes Chromosomes Cancer 3 (1991), 122-127.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 122-127
-
-
Rodriguez, E.1
Reuter, V.E.2
Mies, C.3
Bosl, G.J.4
Chaganti, R.S.5
-
249
-
-
0021932813
-
Loss of heterozygosity in threeembryonal tumours suggests a common pathogenetic mechanism
-
A. Koufos,M. F. Hansen, N. G. Copeland, N. A. Jenkins, B. C. Lampkin and W. K. Cavenee, Loss of heterozygosity in threeembryonal tumours suggests a common pathogenetic mechanism, Nature 316 (1985), 330-334.
-
(1985)
Nature
, vol.316
, pp. 330-334
-
-
Koufosm. F Hansen, A.1
Copeland, N.G.2
Jenkins, N.A.3
Lampkin, B.C.4
Cavenee, W.K.5
-
250
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
I. Hatada, H. Ohashi, Y. Fukushima, Y. Kaneko, M. Inoue, Y. Komoto et al. , An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome, Nat Genet 14 (1996), 171-173.
-
(1996)
Nat. Genet.
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
-
251
-
-
0030610260
-
Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors
-
D. O'Keefe, D. Dao, L. Zhao, R. Sanderson, D. Warburton, L. Weiss et al. , Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors, Am J Hum Genet 61 (1997), 295-303.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 295-303
-
-
O'keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Weiss, L.6
-
252
-
-
0030610261
-
Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome
-
M. P. Lee, M. DeBaun, G. Randhawa, B. A. Reichard, S. J. Elledge and A. P. Feinberg, Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome, Am J Hum Genet 61 (1997), 304-309.
-
(1997)
Am. J. Hum. Genet. 61
, pp. 304-309
-
-
Lee, M.P.1
Debaun, M.2
Randhawa, G.3
Reichard, B.A.4
Elledge, S.J.5
Feinberg, A.P.6
-
253
-
-
0032790193
-
Major hepatectomy for hepatocellular carcinoma in patients with an unsatisfactory indocyanine green clearance test
-
C. M. Lam, S. T. Fan, C. M. Lo and J. Wong, Major hepatectomy for hepatocellular carcinoma in patients with an unsatisfactory indocyanine green clearance test, Br J Surg 86 (1999), 1012-1017.
-
(1999)
Br. J. Surg.
, vol.86
, pp. 1012-1017
-
-
Lam, C.M.1
Fan, S.T.2
Lo, C.M.3
Wong, J.4
-
254
-
-
0033815532
-
P57 KIP2 is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57 KIP2 IGF2, and H19
-
W. Hartmann, A. Waha, A. Koch, C. G. Goodyer, S. Albrecht, D. von Schweinitz et al. , p57(KIP2) is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57(KIP2), IGF2, and H19, Am J Pathol 157 (2000), 1393-1403.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 1393-1403
-
-
Hartmann, W.1
Waha, A.2
Koch, A.3
Goodyer, C.G.4
Albrecht, S.5
Von Schweinitz, D.6
-
255
-
-
0028126475
-
Loss of maternal alleles on chromosome arm 11p in hepatoblastoma
-
S. Albrecht, D. von Schweinitz, A. Waha, J. A. Kraus, A. von Deimling and T. Pietsch, Loss of maternal alleles on chromosome arm 11p in hepatoblastoma, Cancer Res 54 (1994), 5041-5044.
-
(1994)
Cancer Res.
, vol.54
, pp. 5041-5044
-
-
Albrecht, S.1
Von Schweinitz, D.2
Waha, A.3
Kraus, J.A.4
Von Deimling, A.5
Pietsch, T.6
-
256
-
-
0035886696
-
Methylation changes in the human igf2 p3 promoter parallel igf2 expression in the primary tumor established cell line and xenograft of a human hepatoblastoma
-
T. Eriksson, T. Frisk, S. G. Gray, D. von Schweinitz, T. Pietsch, C. Larsson et al. , Methylation changes in the human IGF2 p3 promoter parallel IGF2 expression in the primary tumor, established cell line, and xenograft of a human hepatoblastoma, Exp Cell Res 270 (2001), 88-95.
-
(2001)
Exp. Cell Res.
, vol.270
, pp. 88-95
-
-
Eriksson, T.1
Frisk, T.2
Gray, S.G.3
Von Schweinitz, D.4
Pietsch, T.5
Larsson, C.6
-
257
-
-
0035199390
-
Glypican-3 expression in Wilms tumor and hepatoblastoma
-
J. A. Toretsky, N. L. Zitomersky, A. E. Eskenazi, R. W. Voigt, E. D. Strauch, C. C. Sun et al. , Glypican-3 expression in Wilms tumor and hepatoblastoma, J Pediatr Hematol Oncol 23 (2001), 496-499.
-
(2001)
J. Pediatr. Hematol. Oncol.
, vol.23
, pp. 496-499
-
-
Toretsky, J.A.1
Zitomersky, N.L.2
Eskenazi, A.E.3
Voigt, R.W.4
Strauch, E.D.5
Sun, C.C.6
-
258
-
-
0035951687
-
Expression levels of insulin-like growth factor binding proteins and insulin receptor isoforms in hepatoblastomas
-
H. von Horn, M. Tally, K. Hall, T. Eriksson, T. J. Ekstrom and S. G. Gray, Expression levels of insulin-like growth factor binding proteins and insulin receptor isoforms in hepatoblastomas, Cancer Lett 162 (2001), 253-260.
-
(2001)
Cancer Lett.
, vol.162
, pp. 253-260
-
-
Von Horn, H.1
Tally, M.2
Hall, K.3
Eriksson, T.4
Ekstrom, T.J.5
Gray, S.G.6
-
259
-
-
0031757172
-
Overexpression of cyclin D1 and cdk4 in tumorigenesis of sporadic hepatoblastomas
-
H. Kim, E. K. Ham, Y. I. Kim, J. G. Chi, H. S. Lee, S. H. Park et al. , Overexpression of cyclin D1 and cdk4 in tumorigenesis of sporadic hepatoblastomas, Cancer Lett 131 (1998), 177-183.
-
(1998)
Cancer Lett.
, vol.131
, pp. 177-183
-
-
Kim, H.1
Ham, E.K.2
Kim, Y.I.3
Chi, J.G.4
Lee, H.S.5
Park, S.H.6
-
260
-
-
0031923034
-
Analysis of cdkn2a cdkn2b cdkn2c and cyclin ds gene status in hepatoblastoma
-
A. Iolascon, L. Giordani, A. Moretti, G. Basso, G. Borriello and F. Della Ragione, Analysis of CDKN2A, CDKN2B, CDKN2C, and cyclin Ds gene status in hepatoblastoma, Hepatology 27 (1998), 989-995.
-
(1998)
Hepatology
, vol.27
, pp. 989-995
-
-
Iolascon, A.1
Giordani, L.2
Moretti, A.3
Basso, G.4
Borriello, G.5
Della Ragione, F.6
-
261
-
-
2942750364
-
CCND1 polymorphism and age of onset of hepatoblastoma
-
S. Pakakasama, T. T. Chen, W. Frawley, C. Y. Muller, E. C. Douglass, E. C. Lee et al. , CCND1 polymorphism and age of onset of hepatoblastoma, Oncogene 23 (2004), 4789-4792.
-
(2004)
Oncogene
, vol.23
, pp. 4789-4792
-
-
Pakakasama, S.1
Chen, T.T.2
Frawley, W.3
Muller, C.Y.4
Douglass, E.C.5
Lee, E.C.6
-
262
-
-
0038146961
-
Hypermethylation of the p16 gene and lack of p16 expression in hepatoblastoma
-
Y. H. Shim, H. J. Park, M. S. Choi, J. S. Kim, H. Kim, J. J. Kim et al. , Hypermethylation of the p16 gene and lack of p16 expression in hepatoblastoma, Mod Pathol 16 (2003), 430-436.
-
(2003)
Mod. Pathol.
, vol.16
, pp. 430-436
-
-
Shim, Y.H.1
Park, H.J.2
Choi, M.S.3
Kim, J.S.4
Kim, H.5
Kim, J.J.6
-
263
-
-
0036220817
-
Distinct patterns of p27/KIP 1 gene expression in hepatoblastoma and prognostic implications with correlation before and after chemotherapy
-
M. Brotto and M. J. Finegold, Distinct patterns of p27/KIP 1 gene expression in hepatoblastoma and prognostic implications with correlation before and after chemotherapy, Hum Pathol 33 (2002), 198-205.
-
(2002)
Hum. Pathol.
, vol.33
, pp. 198-205
-
-
Brotto, M.1
Finegold, M.J.2
-
264
-
-
0031841285
-
Expression of transforming growth factor-alpha in hepatoblastoma
-
A. Kiss, A. Szepesi, G. Lotz, P. Nagy and P. Schaff, Expression of transforming growth factor-alpha in hepatoblastoma, Cancer 83 (1998), 690-697.
-
(1998)
Cancer
, vol.83
, pp. 690-697
-
-
Kiss, A.1
Szepesi, A.2
Lotz, G.3
Nagy, P.4
Schaff, P.5
-
265
-
-
4644297399
-
High expression of telomerase is an independent prognostic indicator of poor outcome in hepatoblastoma
-
E. Hiyama, H. Yamaoka, T. Matsunaga, Y. Hayashi, H. Ando, S. Suita et al. , High expression of telomerase is an independent prognostic indicator of poor outcome in hepatoblastoma, Br J Cancer 91 (2004), 972-979.
-
(2004)
Br. J. Cancer
, vol.91
, pp. 972-979
-
-
Hiyama, E.1
Yamaoka, H.2
Matsunaga, T.3
Hayashi, Y.4
Ando, H.5
Suita, S.6
-
267
-
-
0034906471
-
Frequent deletions and mutations of the beta-catenin gene are associated with overexpression of cyclin d1 and fibronectin and poorly differentiated histology in childhood hepatoblastoma
-
H. Takayasu, H. Horie, E. Hiyama, T. Matsunaga, Y. Hayashi, Y. Watanabe et al. , Frequent deletions and mutations of the beta-catenin gene are associated with overexpression of cyclin D1 and fibronectin and poorly differentiated histology in childhood hepatoblastoma, Clin Cancer Res 7 (2001), 901-908.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 901-908
-
-
Takayasu, H.1
Horie, H.2
Hiyama, E.3
Matsunaga, T.4
Hayashi, Y.5
Watanabe, Y.6
-
268
-
-
0035066173
-
Nuclear localization of beta-catenin is an important prognostic factor in hepatoblastoma
-
W. S. Park, R. R. Oh, J. Y. Park, P. J. Kim, M. S. Shin, J. H. Lee et al. , Nuclear localization of beta-catenin is an important prognostic factor in hepatoblastoma, J Pathol 193 (2001), 483-490.
-
(2001)
J. Pathol.
, vol.193
, pp. 483-490
-
-
Park, W.S.1
Oh, R.R.2
Park, J.Y.3
Kim, P.J.4
Shin, M.S.5
Lee, J.H.6
-
269
-
-
67349272856
-
Histologic subtypes of hepatoblastoma are characterized by differential canonical Wnt andNotch pathway activation inDLK+ precursors
-
D. Lopez-Terrada, P. H. Gunaratne, A. M. Adesina, J. Pulliam, D. M. Hoang, Y. Nguyen et al. , Histologic subtypes of hepatoblastoma are characterized by differential canonical Wnt andNotch pathway activation inDLK+ precursors, Hum Pathol 40 (2009), 783-794.
-
(2009)
Hum. Pathol.
, vol.40
, pp. 783-794
-
-
Lopez-Terrada, D.1
Gunaratne, P.H.2
Adesina, A.M.3
Pulliam, J.4
Hoang, D.M.5
Nguyen, Y.6
-
270
-
-
0029979793
-
Somatic mutations of the apc gene in sporadic hepatoblastomas
-
H. Oda, Y. Imai, Y. Nakatsuru, J. Hata and J. Ishikawa, Somatic mutations of the APC gene in sporadic hepatoblastomas, Cancer Res 56 (1996), 3320-3323.
-
(1996)
Cancer Res.
, vol.56
, pp. 3320-3323
-
-
Oda, H.1
Imai, Y.2
Nakatsuru, Y.3
Hata, J.4
Ishikawa, J.5
-
271
-
-
0037130449
-
Mutational spectrum of beta-catenin AXIN1 and AXIN2 in hepatocellular carcinomas and hepatoblastomas
-
K. Taniguchi, L. R. Roberts, I. N. Aderca, X. Dong, C. Qian, L. M. Murphy et al. , Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas, Oncogene 21 (2002), 4863-4871.
-
(2002)
Oncogene
, vol.21
, pp. 4863-4871
-
-
Taniguchi, K.1
Roberts, L.R.2
Aderca, I.N.3
Dong, X.4
Qian, C.5
Murphy, L.M.6
-
272
-
-
20444466479
-
Elevated expression of Wnt antagonists is a common event in hepatoblastomas
-
A. Koch, A. Waha, W. Hartmann, A. Hrychyk, U. Schuller, U. Waha et al. , Elevated expression of Wnt antagonists is a common event in hepatoblastomas, Clin Cancer Res 11 (2005), 4295-4304.
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 4295-4304
-
-
Koch, A.1
Waha, A.2
Hartmann, W.3
Hrychyk, A.4
Schuller, U.5
Waha, U.6
-
273
-
-
57049182539
-
Hepatic stem-like phenotype and interplay of Wnt/beta-catenin and Myc signaling in aggressive childhood liver cancer
-
S. Cairo, C. Armengol, A. De Reynies, Y. Wei, E. Thomas, C. A. Renard et al. , Hepatic stem-like phenotype and interplay of Wnt/beta-catenin and Myc signaling in aggressive childhood liver cancer, Cancer Cell 14 (2008), 471-484.
-
(2008)
Cancer Cell
, vol.14
, pp. 471-484
-
-
Cairo, S.1
Armengol, C.2
De Reynies, A.3
Wei, Y.4
Thomas, E.5
Renard, C.A.6
|