-
1
-
-
39549123055
-
Wilms' tumor in children: An overview
-
Varan A. Wilms' tumor in children: an overview. Nephron Clin Pract. 2008;108:c83-c90.
-
(2008)
Nephron Clin Pract
, vol.108
-
-
Varan, A.1
-
3
-
-
55449104590
-
Perlman syndrome: Report prenatal findings and review
-
Alessandri JL, Cuillier F, Ramful D, et al. Perlman syndrome: report, prenatal findings and review. Am JMed Genet A. 2008;146A: 2532-2537.
-
(2008)
Am JMed Genet A
, vol.146 A
, pp. 2532-2537
-
-
Alessandri, J.L.1
Cuillier, F.2
Ramful, D.3
-
4
-
-
58149394124
-
Management of Wilms tumors in Drash and Frasier syndromes
-
Auber F, Jeanpierre C, Denamur E, et al. Management of Wilms tumors in Drash and Frasier syndromes. Pediatr Blood Cancer. 2009;52:55-59.
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 55-59
-
-
Auber, F.1
Jeanpierre, C.2
Denamur, E.3
-
5
-
-
43049102044
-
Different mechanisms cause imprinting Defects at the IGF2/H19 locus in Beckwith-WieDemann syndrome and Wilms' tumour
-
Cerrato F, Sparago A, VerDe G, et al. Different mechanisms cause imprinting Defects at the IGF2/H19 locus in Beckwith-WieDemann syndrome and Wilms' tumour. Hum Mol Genet. 2008;17:1427-1435.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1427-1435
-
-
Cerrato, F.1
Sparago, A.2
Verde, G.3
-
6
-
-
67349125403
-
A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor
-
Terenziani M, SarDella M, Gamba B, et al. A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor. Pediatr Nephrol. 2009;24:1413-1417.
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1413-1417
-
-
Terenziani, M.1
Sardella, M.2
Gamba, B.3
-
7
-
-
48249143175
-
Molecular eviDence of the inDepenDent origin of multiple Wilms tumors in a case of WAGR syndrome
-
Uccini S, Perotti D, Colarossi C, et al. Molecular eviDence of the inDepenDent origin of multiple Wilms tumors in a case of WAGR syndrome. Pediatr Blood Cancer. 2008;51:344-348.
-
(2008)
Pediatr Blood Cancer
, vol.51
, pp. 344-348
-
-
Uccini, S.1
Perotti, D.2
Colarossi, C.3
-
8
-
-
20444431941
-
Prognostic markers in nephroblastoma (Wilms' tumor)
-
Ghanem MA, Van Steenbrugge GJ, Nijman RJ, et al. Prognostic markers in nephroblastoma (Wilms' tumor). Urology. 2005;65: 1047-1054.
-
(2005)
Urology
, vol.65
, pp. 1047-1054
-
-
Ghanem, M.A.1
Van Steenbrugge, G.J.2
Nijman, R.J.3
-
9
-
-
43049157909
-
Wilms tumor genetics: Mutations in WT1 WTX and CTNNB1 account for only about one-third of tumors
-
Ruteshouser EC, Robinson SM, Huff V. Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors. Genes Chromosomes Cancer. 2008;47:461-470.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 461-470
-
-
Ruteshouser, E.C.1
Robinson, S.M.2
Huff, V.3
-
10
-
-
0035135573
-
Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors
-
Hing S, Lu YJ, Summersgill B, et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors. Am J Pathol. 2001;158:393-398.
-
(2001)
Am J Pathol
, vol.158
, pp. 393-398
-
-
Hing, S.1
Lu, Y.J.2
Summersgill, B.3
-
11
-
-
33846197915
-
Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour
-
Natrajan R, Little SE, Sodha N, et al. Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour. J Pathol. 2007;211:52-59.
-
(2007)
J Pathol
, vol.211
, pp. 52-59
-
-
Natrajan, R.1
Little, S.E.2
Sodha, N.3
-
12
-
-
41749091806
-
B7-H1 expression in Wilms tumor: Correlation with tumor biology and disease recurrence
-
discussion 1959-1960
-
Routh JC, Ashley RA, Sebo TJ, et al. B7-H1 expression in Wilms tumor: correlation with tumor biology and disease recurrence. J Urol. 2008;179:1954-1959; discussion 1959-1960.
-
(2008)
J Urol
, vol.179
, pp. 1954-1959
-
-
Routh, J.C.1
Ashley, R.A.2
Sebo, T.J.3
-
13
-
-
33845499657
-
Loss of 11q and 16q in Wilms tumors is associated with anaplasia, tumor recurrence, and poor prognosis
-
Wittmann S, Zirn B, Alkassar M, et al. Loss of 11q and 16q in Wilms tumors is associated with anaplasia, tumor recurrence, and poor prognosis. Genes Chromosomes Cancer. 2007;46:163-170.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 163-170
-
-
Wittmann, S.1
Zirn, B.2
Alkassar, M.3
-
14
-
-
33845454100
-
Array comparative genomic hybridization reveals unbalanced gain of the MYCN region in Wilms tumors
-
Schaub R, Burger A, Bausch D, et al. Array comparative genomic hybridization reveals unbalanced gain of the MYCN region in Wilms tumors. Cancer Genet Cytogenet. 2007;172:61-65.
-
(2007)
Cancer Genet Cytogenet
, vol.172
, pp. 61-65
-
-
Schaub, R.1
Burger, A.2
Bausch, D.3
-
15
-
-
44949232260
-
Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia
-
Faussillon M, Murakami I, Bichat M, et al. Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia. Cancer Genet Cytogenet. 2008;184:22-30.
-
(2008)
Cancer Genet Cytogenet
, vol.184
, pp. 22-30
-
-
Faussillon, M.1
Murakami, I.2
Bichat, M.3
-
16
-
-
41749111811
-
Screening for submicroscopic chromosomal rearrangements in Wilms tumor using wholegenome microarrays
-
Rassekh SR, Chan S, Harvard C, et al. Screening for submicroscopic chromosomal rearrangements in Wilms tumor using wholegenome microarrays. Cancer Genet Cytogenet. 2008;182:84-94.
-
(2008)
Cancer Genet Cytogenet
, vol.182
, pp. 84-94
-
-
Rassekh, S.R.1
Chan, S.2
Harvard, C.3
-
17
-
-
60549091924
-
Multiplex ligation-DepenDent probe amplification and its application
-
Zhou D, Ren Z. Multiplex ligation-DepenDent probe amplification and its application. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009; 26:45-49.
-
(2009)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.26
, pp. 45-49
-
-
Zhou, D.1
Ren, Z.2
-
18
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-DepenDent probe amplification
-
Schouten JP, McElgunn CJ, Waaijer R, et al. Relative quantification of 40 nucleic acid sequences by multiplex ligation-DepenDent probe amplification. Nucleic Acids Res. 2002;30:e57.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Schouten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
-
19
-
-
40749095333
-
Analysis of the CFTR gene in Iranian cystic fibrosis patients: IDentification of eight novel mutations
-
Alibakhshi R, Kianishirazi R, Cassiman JJ, et al. Analysis of the CFTR gene in Iranian cystic fibrosis patients: iDentification of eight novel mutations. J Cyst Fibros. 2008;7:102-109.
-
(2008)
J Cyst Fibros
, vol.7
, pp. 102-109
-
-
Alibakhshi, R.1
Kianishirazi, R.2
Cassiman, J.J.3
-
20
-
-
1042266541
-
Multiplex ligationDepenDent probe amplification (MLPA) Detects large Deletions in the MECP2 gene of Swedish Rett syndrome patients
-
Erlandson A, Samuelsson L, Hagberg B, et al. Multiplex ligationDepenDent probe amplification (MLPA) Detects large Deletions in the MECP2 gene of Swedish Rett syndrome patients. Genet Test. 2003; 7:329-332.
-
(2003)
Genet Test
, vol.7
, pp. 329-332
-
-
Erlandson, A.1
Samuelsson, L.2
Hagberg, B.3
-
21
-
-
0037380994
-
Large genomic Deletions and duplications in the BRCA1 gene iDentified by a novel quantitative method
-
Hogervorst FB, NeDerlof PM, Gille JJ, et al. Large genomic Deletions and duplications in the BRCA1 gene iDentified by a novel quantitative method. Cancer Res. 2003;63:1449-1453.
-
(2003)
Cancer Res
, vol.63
, pp. 1449-1453
-
-
Hogervorst, F.B.1
Nederlof, P.M.2
Gille, J.J.3
-
22
-
-
33745407500
-
Multiplex ligationDepenDent probe amplification: A diagnostic tool for simultaneous iDentification of different genetic markers in glial tumors
-
Jeuken J, Cornelissen S, Boots-Sprenger S, et al. Multiplex ligationDepenDent probe amplification: a diagnostic tool for simultaneous iDentification of different genetic markers in glial tumors. J Mol Diagn. 2006;8:433-443.
-
(2006)
J Mol Diagn
, vol.8
, pp. 433-443
-
-
Jeuken, J.1
Cornelissen, S.2
Boots-Sprenger, S.3
-
23
-
-
0142124795
-
IDentification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques
-
Nakagawa H, Hampel H, De la Chapelle A. IDentification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques. Hum Mutat. 2003;22:258.
-
(2003)
Hum Mutat
, vol.22
, pp. 258
-
-
Nakagawa, H.1
Hampel, H.2
De La Chapelle, A.3
-
24
-
-
48349140362
-
Comparison of different techniques for the Detection of genetic risk-iDentifying chromosomal gains and losses in neuroblastoma
-
Villamon E, Piqueras M, Mackintosh C, et al. Comparison of different techniques for the Detection of genetic risk-iDentifying chromosomal gains and losses in neuroblastoma. Virchows Arch. 2008;453:47-55.
-
(2008)
Virchows Arch
, vol.453
, pp. 47-55
-
-
Villamon, E.1
Piqueras, M.2
MacKintosh, C.3
-
25
-
-
40549140095
-
Detailed analysis of 22q11.2 with a high Density MLPA probe set
-
Jalali GR, Vorstman JA, Errami A, et al. Detailed analysis of 22q11.2 with a high Density MLPA probe set. Hum Mutat. 2008; 29:433-440.
-
(2008)
Hum Mutat
, vol.29
, pp. 433-440
-
-
Jalali, G.R.1
Vorstman, J.A.2
Errami, A.3
-
26
-
-
42649101672
-
MS-MLPA is a specific and sensitive technique for Detecting all chromosome 11p15.5 imprinting Defects of BWS and SRS in a single-tube experiment
-
Priolo M, Sparago A, Mammi C, et al. MS-MLPA is a specific and sensitive technique for Detecting all chromosome 11p15.5 imprinting Defects of BWS and SRS in a single-tube experiment. Eur J Hum Genet. 2008;16:565-571.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 565-571
-
-
Priolo, M.1
Sparago, A.2
Mammi, C.3
-
27
-
-
43949143824
-
Multiplex ligationDepenDent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorDers
-
ReDeker EJ, De Visser AS, Bergen AA, et al. Multiplex ligationDepenDent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorDers. Mol Vis. 2008;14: 836-840.
-
(2008)
Mol Vis
, vol.14
, pp. 836-840
-
-
Redeker, E.J.1
De Visser, A.S.2
Bergen, A.A.3
-
28
-
-
39149142187
-
Methylation-specific multiplex ligation-DepenDent probe amplification (MS-MLPA) robustly Detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation
-
Scott RH, Douglas J, Baskcomb L, et al. Methylation-specific multiplex ligation-DepenDent probe amplification (MS-MLPA) robustly Detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation. J Med Genet. 2008;45: 106-113.
-
(2008)
J Med Genet
, vol.45
, pp. 106-113
-
-
Scott, R.H.1
Douglas, J.2
Baskcomb, L.3
-
29
-
-
37249090241
-
Molecular diagnosis of 22q11.2 Deletion and duplication by multiplex ligation DepenDent probe amplification
-
Stachon AC, Baskin B, Smith AC, et al. Molecular diagnosis of 22q11.2 Deletion and duplication by multiplex ligation DepenDent probe amplification. Am J Med Genet A. 2007;143A: 2924-2930.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 2924-2930
-
-
Stachon, A.C.1
Baskin, B.2
Smith, A.C.3
-
30
-
-
39749173843
-
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia
-
Zeschnigk M, Albrecht B, Buiting K, et al. IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia. Eur J Hum Genet. 2008;16:328-334.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 328-334
-
-
Zeschnigk, M.1
Albrecht, B.2
Buiting, K.3
-
31
-
-
41349121558
-
New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumors
-
Wittmann S, WunDer C, Zirn B, et al. New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumors. Genes Chromosomes Cancer. 2008;47:386-395.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 386-395
-
-
Wittmann, S.1
Wunder, C.2
Zirn, B.3
-
32
-
-
33846846526
-
An X chromosome gene, WTX, is commonly inactivated in Wilms tumor
-
Rivera MN, Kim WJ, Wells J, et al. An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science. 2007;315: 642-645.
-
(2007)
Science
, vol.315
, pp. 642-645
-
-
Rivera, M.N.1
Kim, W.J.2
Wells, J.3
-
33
-
-
0035913171
-
Inhibition of Wilms' tumor growth by intramuscular administration of tissue inhibitor of metalloproteinases-4 plasmid DNA
-
Celiker MY, Wang M, Atsidaftos E, et al. Inhibition of Wilms' tumor growth by intramuscular administration of tissue inhibitor of metalloproteinases-4 plasmid DNA. Oncogene. 2001;20: 4337-4343.
-
(2001)
Oncogene
, vol.20
, pp. 4337-4343
-
-
Celiker, M.Y.1
Wang, M.2
Atsidaftos, E.3
-
34
-
-
0024238172
-
Growth characteristics of human Wilms' tumor in nuDe mice
-
Garvin AJ, Congleton L, Inabnett T, et al. Growth characteristics of human Wilms' tumor in nuDe mice. Pediatr Pathol. 1988;8: 599-615.
-
(1988)
Pediatr Pathol
, vol.8
, pp. 599-615
-
-
Garvin, A.J.1
Congleton, L.2
Inabnett, T.3
-
35
-
-
34347254640
-
Establishment of human tumor xenografts in immunoDeficient mice
-
Morton CL, Houghton PJ. Establishment of human tumor xenografts in immunoDeficient mice. Nat Protoc. 2007;2:247-250.
-
(2007)
Nat Protoc
, vol.2
, pp. 247-250
-
-
Morton, C.L.1
Houghton, P.J.2
-
36
-
-
33749000614
-
Prognostic value of the International Neuroblastoma Pathology Classification in Neuroblastoma (Schwannian stroma-poor) and comparison with other prognostic factors: A study of 182 cases from the Spanish Neuroblastoma Registry
-
Burgues O, Navarro S, Noguera R, et al. Prognostic value of the International Neuroblastoma Pathology Classification in Neuroblastoma (Schwannian stroma-poor) and comparison with other prognostic factors: a study of 182 cases from the Spanish Neuroblastoma Registry. Virchows Arch. 2006;449:410-420.
-
(2006)
Virchows Arch
, vol.449
, pp. 410-420
-
-
Burgues, O.1
Navarro, S.2
Noguera, R.3
-
37
-
-
65549156891
-
International consensus for neuroblastoma molecular diagnostics: Report from the International Neuroblastoma Risk Group (INRG) Biology Committee
-
Ambros PF, Ambros IM, BroDeur GM, et al. International consensus for neuroblastoma molecular diagnostics: report from the International Neuroblastoma Risk Group (INRG) Biology Committee. Br J Cancer. 2009;100:1471-1482.
-
(2009)
Br J Cancer
, vol.100
, pp. 1471-1482
-
-
Ambros, P.F.1
Ambros, I.M.2
Brodeur, G.M.3
-
38
-
-
59449084270
-
Analysis of biological prognostic factors using tissue microarrays in neuroblastic tumors
-
Piqueras M, Navarro S, Castel V, et al. Analysis of biological prognostic factors using tissue microarrays in neuroblastic tumors. Pediatr Blood Cancer. 2009;52:209-214.
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 209-214
-
-
Piqueras, M.1
Navarro, S.2
Castel, V.3
-
39
-
-
18844465839
-
Wilms tumors Develop through two distinct karyotypic pathways
-
Hoglund M, Gisselsson D, Hansen GB, et al. Wilms tumors Develop through two distinct karyotypic pathways. Cancer Genet Cytogenet. 2004;150:9-15.
-
(2004)
Cancer Genet Cytogenet
, vol.150
, pp. 9-15
-
-
Hoglund, M.1
Gisselsson, D.2
Hansen, G.B.3
-
40
-
-
0030825508
-
Chromosomal imbalance maps of malignant solid tumors: A cytogenetic survey of 3185 neoplasms
-
Mertens F, Johansson B, Hoglund M, et al. Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. Cancer Res. 1997;57:2765-2780.
-
(1997)
Cancer Res
, vol.57
, pp. 2765-2780
-
-
Mertens, F.1
Johansson, B.2
Hoglund, M.3
-
41
-
-
0036140003
-
Cytogenetic abnormalities and clinical outcome in Wilms tumor: A study by the UK cancer cytogenetics group and the UK Children's Cancer Study Group
-
Bown N, Cotterill SJ, Roberts P, et al. Cytogenetic abnormalities and clinical outcome in Wilms tumor: a study by the UK cancer cytogenetics group and the UK Children's Cancer Study Group. Med Pediatr Oncol. 2002;38:11-21.
-
(2002)
Med Pediatr Oncol
, vol.38
, pp. 11-21
-
-
Bown, N.1
Cotterill, S.J.2
Roberts, P.3
-
42
-
-
0026689597
-
Cytogenetics and molecular genetics of Wilms' tumor of childhood
-
Slater RM, Mannens MM. Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet Cytogenet. 1992;61: 111-121.
-
(1992)
Cancer Genet Cytogenet
, vol.61
, pp. 111-121
-
-
Slater, R.M.1
Mannens, M.M.2
-
43
-
-
0031747351
-
Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters
-
Klamt B, Schulze M, Thate C, et al. Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters. Genes Chromosomes Cancer. 1998;22:287-294.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 287-294
-
-
Klamt, B.1
Schulze, M.2
Thate, C.3
-
44
-
-
0031214256
-
Allelic imbalance at chromosome 1q21 in Wilms tumor
-
Law MH, Algar E, Little M. Allelic imbalance at chromosome 1q21 in Wilms tumor. Cancer Genet Cytogenet. 1997;97:54-59.
-
(1997)
Cancer Genet Cytogenet
, vol.97
, pp. 54-59
-
-
Law, M.H.1
Algar, E.2
Little, M.3
-
45
-
-
0033677022
-
Frequent association of betacatenin and WT1 mutations in Wilms tumors
-
Maiti S, Alam R, Amos CI, et al. Frequent association of betacatenin and WT1 mutations in Wilms tumors. Cancer Res. 2000; 60:6288-6292.
-
(2000)
Cancer Res
, vol.60
, pp. 6288-6292
-
-
Maiti, S.1
Alam, R.2
Amos, C.I.3
-
46
-
-
0033965743
-
Loss of heterozygosity at 7p in Wilms' tumour Development
-
Powlesland RM, Charles AK, Malik KT, et al. Loss of heterozygosity at 7p in Wilms' tumour Development. Br J Cancer. 2000; 82:323-329.
-
(2000)
Br J Cancer
, vol.82
, pp. 323-329
-
-
Powlesland, R.M.1
Charles, A.K.2
Malik, K.T.3
-
47
-
-
0041822121
-
Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18
-
AnDerson CE, Punnett HH, Huff V, et al. Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18. Am J Med Genet A. 2003;121A:52-55.
-
(2003)
Am J Med Genet A
, vol.121 A
, pp. 52-55
-
-
Anderson, C.E.1
Punnett, H.H.2
Huff, V.3
-
49
-
-
34548279275
-
Concomitant DDX1 and MYCN gain in neuroblastoma
-
Defferrari R, Tonini GP, Conte M, et al. Concomitant DDX1 and MYCN gain in neuroblastoma. Cancer Lett. 2007;256:56-63.
-
(2007)
Cancer Lett
, vol.256
, pp. 56-63
-
-
Defferrari, R.1
Tonini, G.P.2
Conte, M.3
-
50
-
-
0032422181
-
Comparative genomic hybridization and its application toWilms' tumorigenesis
-
Getman ME, Houseal TW, Miller GA, et al. Comparative genomic hybridization and its application toWilms' tumorigenesis. Cytogenet Cell Genet. 1998;82:284-290.
-
(1998)
Cytogenet Cell Genet
, vol.82
, pp. 284-290
-
-
Getman, M.E.1
Houseal, T.W.2
Miller, G.A.3
-
52
-
-
20444487719
-
Effects of chemotherapy on the cytogenetic constitution of Wilms' tumor
-
Schlomm T, Gunawan B, Schulten HJ, et al. Effects of chemotherapy on the cytogenetic constitution of Wilms' tumor. Clin Cancer Res. 2005;11:4382-4387.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 4382-4387
-
-
Schlomm, T.1
Gunawan, B.2
Schulten, H.J.3
-
53
-
-
0029121683
-
Duplication of N-MYC at its resiDent site 2p24 may be a mechanism of activation alternative to amplification in human neuroblastoma cells
-
Corvi R, Savelyeva L, Schwab M. Duplication of N-MYC at its resiDent site 2p24 may be a mechanism of activation alternative to amplification in human neuroblastoma cells. Cancer Res. 1995; 55:3471-3474.
-
(1995)
Cancer Res
, vol.55
, pp. 3471-3474
-
-
Corvi, R.1
Savelyeva, L.2
Schwab, M.3
-
54
-
-
0037601662
-
Quality assessment of genetic markers used for therapy stratification
-
Ambros IM, Benard J, Boavida M, et al. Quality assessment of genetic markers used for therapy stratification. J Clin Oncol. 2003; 21:2077-2084.
-
(2003)
J Clin Oncol
, vol.21
, pp. 2077-2084
-
-
Ambros, I.M.1
Benard, J.2
Boavida, M.3
-
55
-
-
9644278104
-
MYCN amplification remains prognostically strong 20 years after its "clinical Debut"
-
Cohn SL, Tweddle DA. MYCN amplification remains prognostically strong 20 years after its "clinical Debut". Eur J Cancer. 2004;40:2639-2642.
-
(2004)
Eur J Cancer
, vol.40
, pp. 2639-2642
-
-
Cohn, S.L.1
Tweddle, D.A.2
-
56
-
-
56249108694
-
Regulation of CRABP-II expression by MycN in Wilms tumor
-
Gupta A, Kessler P, Rawwas J, et al. Regulation of CRABP-II expression by MycN in Wilms tumor. Exp Cell Res. 2008;314: 3663-3668.
-
(2008)
Exp Cell Res
, vol.314
, pp. 3663-3668
-
-
Gupta, A.1
Kessler, P.2
Rawwas, J.3
-
57
-
-
0036500984
-
Morphologic features of neuroblastoma (Schwannian stroma-poor tumors) in clinically favorable and unfavorable groups
-
Ambros IM, Hata J, Joshi VV, et al. Morphologic features of neuroblastoma (Schwannian stroma-poor tumors) in clinically favorable and unfavorable groups. Cancer. 2002;94:1574-1583.
-
(2002)
Cancer
, vol.94
, pp. 1574-1583
-
-
Ambros, I.M.1
Hata, J.2
Joshi, V.V.3
-
58
-
-
33645065340
-
The MYCN enigma: Significance of MYCN expression in neuroblastoma
-
Tang XX, Zhao H, Kung B, et al. The MYCN enigma: significance of MYCN expression in neuroblastoma. Cancer Res. 2006;66: 2826-2833.
-
(2006)
Cancer Res
, vol.66
, pp. 2826-2833
-
-
Tang, X.X.1
Zhao, H.2
Kung, B.3
|