Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors (Q34010180)

30 July 2017

Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors (English)

1 reference

30 July 2017

1 reference

3

Vicki Huff

1 reference

PubMed ID

18311776

30 July 2017

E. Cristy Ruteshouser

series ordinal

1

object named as

E Cristy Ruteshouser

1 reference

30 July 2017

Stephen M Robinson

2

1 reference

30 July 2017

1 June 2008

1 reference

Genes, Chromosomes and Cancer

30 July 2017

1 reference

30 July 2017

47

1 reference

30 July 2017

6

1 reference

30 July 2017

461-470

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Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

The many ways of Wnt in cancer

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

An X chromosome gene, WTX, is commonly inactivated in Wilms tumor

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Sequential WT1 and CTNNB1 mutations and alterations of beta-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Frequent association of beta-catenin and WT1 mutations in Wilms tumors.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Rapid detection of VHL exon deletions using real-time quantitative PCR.

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGCC.20553

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Mutational activation of the beta-catenin proto-oncogene is a common event in the development of Wilms' tumors

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Relaxation of imprinted genes in human cancer.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332772

Chromosome analysis of 31 Wilms' tumors

29 October 2018

1 reference

12 December 2020

Treatment of Wilms' tumor. Results of the Third National Wilms' Tumor Study

1 reference

12 December 2020

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

12 December 2020

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

1 reference

12 December 2020

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

1 reference

12 December 2020

A third Wilms' tumor locus on chromosome 16q

1 reference

12 December 2020

Non-11p constitutional chromosome abnormalities in Wilms' tumor patients

1 reference

12 December 2020

Cytogenetic changes in Wilms' tumors

1 reference

12 December 2020

Identifiers

DOI

10.1002/GCC.20553

1 reference

30 July 2017

1 reference

30 July 2017

1 reference

PubMed ID

18311776