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Loss of Heterozygosity for Chromosomes 1p and 16q Is an Adverse Prognostic Factor in Favorable-Histology Wilms Tumor: A Report From the National Wilms Tumor Study Group

Journal of clinical oncology, 2005-10, Vol.23 (29), p.7312-7321

2005

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Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

The Journal of pathology, 2006-09, Vol.210 (1), p.49-58

2006

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CTNNB1 Mutations and Overexpression of Wnt/β-Catenin Target Genes in WT1 -Mutant Wilms' Tumors

The American journal of pathology, 2004-12, Vol.165 (6), p.1943-1953

2004

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ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma

Cancer research (Chicago, Ill.), 1998-11, Vol.58 (22), p.5046-5048

1998

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Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter its DNA-binding specificity

Cancer research (Chicago, Ill.), 2002, Vol.62 (1), p.48-52

2002

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Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney

Human molecular genetics, 2004-09, Vol.13 (18), p.2061-2074

2004

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Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour

The Journal of pathology, 2007-01, Vol.211 (1), p.52-59

2007

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Relaxation of imprinted genes in human cancer

Nature (London), 1993-04, Vol.362 (6422), p.747-749

1993

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Comparison between single-dose and divided-dose administration of dactinomycin and doxorubicin for patients with Wilms' tumor: a report from the National Wilms' Tumor Study Group

Journal of clinical oncology, 1998-01, Vol.16 (1), p.237-245

1998

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Effect of Duration of Treatment on Treatment Outcome for Patients With Clear-Cell Sarcoma of the Kidney: A Report From the National Wilms' Tumor Study Group

Journal of clinical oncology, 2004-02, Vol.22 (3), p.468-473

2004

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Treatment With Nephrectomy Only for Small, Stage I/Favorable Histology Wilms’ Tumor: A Report From the National Wilms’ Tumor Study Group

Journal of clinical oncology, 2001-09, Vol.19 (17), p.3719-3724

2001

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Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Cancer research (Chicago, Ill.), 1994-05, Vol.54 (9), p.2331-2333

1994

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Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor

American journal of human genetics, 2005-11, Vol.77 (5), p.887-891

2005

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Decrease in LDL receptor-related protein expression and function correlates with advanced stages of Wilms tumors

Pediatric blood & cancer, 2006-01, Vol.46 (1), p.40-49

2006

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High telomerase reverse transcriptase (hTERT) messenger RNA level correlates with tumor recurrence in patients with favorable histology Wilms' tumor

Cancer research (Chicago, Ill.), 1999-09, Vol.59 (17), p.4301-4307

1999

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Genetic Events in the Development of Wilms' Tumor

The New England journal of medicine, 1994-09, Vol.331 (9), p.586-590

1994

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Fine mapping of Wilms' tumors with 16q loss of heterozygosity localizes the putative tumor suppressor gene to a region of 6.7 megabases

Annals of surgical oncology, 2003-03, Vol.10 (2), p.136-143

2003

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Protocol for the examination of specimens from patients with Wilms tumor (nephroblastoma) or other renal tumors of childhood

Archives of pathology & laboratory medicine (1976), 2003-10, Vol.127 (10), p.1280-1289

2003

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Decreased E-cadherin expression correlates with higher stage of Wilms' tumors

Journal of pediatric surgery, 2005-02, Vol.40 (2), p.341-348

2005

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Increased microvascular density predicts relapse in Wilms' tumor

Journal of pediatric surgery, 2003-03, Vol.38 (3), p.325-330

2003

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Cytotoxicity of 2‐chlorodeoxyadenosine and arabinosylcytosine in leukaemic lymphoblasts from paediatric patients: significance of cellular nucleoside transporter content

British journal of haematology, 2002-03, Vol.116 (3), p.528-537

2002

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The Simpson-Golabi-Behmel gene, GPC3, is not involved in sporadic Wilms tumorigenesis

American journal of medical genetics, 2003-09, Vol.122A (1), p.30-36

2003

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Prognostic value of quantifying apoptosis factor expression in favorable histology wilms tumors

Journal of pediatric hematology/oncology, 2005-01, Vol.27 (1), p.11-14

2005

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16q loss of heterozygosity and microsatellite instability in Wilms' tumor

Journal of pediatric surgery, 2000-06, Vol.35 (6), p.891-897

2000

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Wilms tumor

CA: a cancer journal for clinicians, 1996-01, Vol.46 (1), p.46-63

1996

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Loss of Heterozygosity for Chromosomes 1p and 16q Is an Adverse Prognostic Factor in Favorable-Histology Wilms Tumor: A Report From the National Wilms Tumor Study Group

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

CTNNB1 Mutations and Overexpression of Wnt/β-Catenin Target Genes in WT1 -Mutant Wilms' Tumors

ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma

Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter its DNA-binding specificity

Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney

Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour

Relaxation of imprinted genes in human cancer

Comparison between single-dose and divided-dose administration of dactinomycin and doxorubicin for patients with Wilms' tumor: a report from the National Wilms' Tumor Study Group

Effect of Duration of Treatment on Treatment Outcome for Patients With Clear-Cell Sarcoma of the Kidney: A Report From the National Wilms' Tumor Study Group

Treatment With Nephrectomy Only for Small, Stage I/Favorable Histology Wilms’ Tumor: A Report From the National Wilms’ Tumor Study Group

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor

Decrease in LDL receptor-related protein expression and function correlates with advanced stages of Wilms tumors

High telomerase reverse transcriptase (hTERT) messenger RNA level correlates with tumor recurrence in patients with favorable histology Wilms' tumor

Genetic Events in the Development of Wilms' Tumor

Fine mapping of Wilms' tumors with 16q loss of heterozygosity localizes the putative tumor suppressor gene to a region of 6.7 megabases

Protocol for the examination of specimens from patients with Wilms tumor (nephroblastoma) or other renal tumors of childhood

Decreased E-cadherin expression correlates with higher stage of Wilms' tumors

Increased microvascular density predicts relapse in Wilms' tumor

Cytotoxicity of 2‐chlorodeoxyadenosine and arabinosylcytosine in leukaemic lymphoblasts from paediatric patients: significance of cellular nucleoside transporter content

The Simpson-Golabi-Behmel gene, GPC3, is not involved in sporadic Wilms tumorigenesis

Prognostic value of quantifying apoptosis factor expression in favorable histology wilms tumors

16q loss of heterozygosity and microsatellite instability in Wilms' tumor

Wilms tumor

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