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Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation

Human molecular genetics, 2014-01, Vol.23 (2), p.333-341

2014

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Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors

Genes chromosomes & cancer, 2008-06, Vol.47 (6), p.461-470

2008

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Children's Oncology Group's 2013 blueprint for research: Renal tumors

Pediatric blood & cancer, 2013-06, Vol.60 (6), p.994-1000

2013

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Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional target

Experimental cell research, 2013-03, Vol.319 (5), p.612-622

2013

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Race disparities in peptide profiles of North American and Kenyan Wilms tumor specimens

Journal of the American College of Surgeons, 2014-04, Vol.218 (4), p.707

2014

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Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

American journal of medical genetics, 2004-06, Vol.127A (3), p.249-257

2004

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Generation of a Wt1 conditional deletion, nuclear red fluorescent protein reporter allele in the mouse

Differentiation (London), 2024-07, Vol.138, p.100791, Article 100791

2024

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Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour

Journal of medical genetics, 2016-06, Vol.53 (6), p.385-388

2016

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Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation

The Journal of clinical investigation, 2011-01, Vol.121 (1), p.174-183

2011

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Wilms tumor 1 (WT1) regulates KRAS-driven oncogenesis and senescence in mouse and human models

The Journal of clinical investigation, 2010-11, Vol.120 (11), p.3940-3952

2010

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Left-sided cryptorchidism in mice with Wilms' tumour 1 gene deletion in gubernaculum testis

The Journal of pathology, 2013-05, Vol.230 (1), p.39-47

2013

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Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumor using whole genome sequencing

Journal of medical genetics, 2015-11, Vol.53 (6), p.385-388

2015

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Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

The Journal of pediatrics, 1993-11, Vol.123 (5), p.673-678

1993

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Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5

Annals of surgery, 2010-03, Vol.251 (3), p.555-558

2010

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Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study

The Journal of pathology, 2012-09, Vol.228 (1), p.119-130

2012

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Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome

Pediatric blood & cancer, 2009-12, Vol.53 (7), p.1349-1351

2009

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Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Oncogene, 2003-06, Vol.22 (24), p.3821-3826

2003

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Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors

Genes chromosomes & cancer, 2005-06, Vol.43 (2), p.172-180

2005

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Universal Nephroblastomatosis with Bilateral Hyperplastic Nephromegaly in Siblings

Pediatric and developmental pathology, 2009-01, Vol.12 (1), p.47-52

2009

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Pleuropulmonary blastoma: A marker for familial disease

The Journal of pediatrics, 1996-02, Vol.128 (2), p.220-224

1996

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UNIVERSAL NEPHROBLASTOMATOSIS WITH BILATERAL HYPERPLASTIC NEPHROMEGALY IN SIBLINGS

Pediatric and developmental pathology, 2006, Vol.preprint (2008), p.1

2006

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Mutation in the PAX6 gene in twenty patients with aniridia

Human mutation, 2000-01, Vol.15 (4), p.332-339

2000

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Genome-wide loss of heterozygosity analysis ofWT1-wild-type andWT1-mutant Wilms tumors

Genes chromosomes & cancer, 2005, Vol.43 (2), p.172-180

2005

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Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation

Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors

Children's Oncology Group's 2013 blueprint for research: Renal tumors

Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional target

Race disparities in peptide profiles of North American and Kenyan Wilms tumor specimens

Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

Generation of a Wt1 conditional deletion, nuclear red fluorescent protein reporter allele in the mouse

Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour

Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation

Wilms tumor 1 (WT1) regulates KRAS-driven oncogenesis and senescence in mouse and human models

Left-sided cryptorchidism in mice with Wilms' tumour 1 gene deletion in gubernaculum testis

Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumor using whole genome sequencing

Hallmark discoveries in the biology of Wilms tumour

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5

Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study

Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: A report from the National Wilms Tumor Study Group

Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome

Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors

Universal Nephroblastomatosis with Bilateral Hyperplastic Nephromegaly in Siblings

Pleuropulmonary blastoma: A marker for familial disease

UNIVERSAL NEPHROBLASTOMATOSIS WITH BILATERAL HYPERPLASTIC NEPHROMEGALY IN SIBLINGS

Mutation in the PAX6 gene in twenty patients with aniridia

Genome-wide loss of heterozygosity analysis ofWT1-wild-type andWT1-mutant Wilms tumors

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