(Q42550921)

English

Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation

scientific article published on June 2007

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scholarly article

1 reference

Europe PubMed Central

2 November 2017

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Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation (English)

1 reference

Europe PubMed Central

2 November 2017

1 reference

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inferred from title

Brigitte Royer-Pokora

6

object named as

Brigitte Royer-Pokora

0 references

author name string

Constanze Uschkereit

1

1 reference

Europe PubMed Central

2 November 2017

Noelia Perez

2

1 reference

Europe PubMed Central

2 November 2017

Carmen de Torres

3

1 reference

Europe PubMed Central

2 November 2017

Maike Küff

4

1 reference

Europe PubMed Central

2 November 2017

Jaume Mora

5

1 reference

Europe PubMed Central

2 November 2017

language of work or name

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publication date

1 June 2007

1 reference

Europe PubMed Central

2 November 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

2 November 2017

44

1 reference

Europe PubMed Central

2 November 2017

6

1 reference

Europe PubMed Central

2 November 2017

393-396

1 reference

Europe PubMed Central

2 November 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

A clinical overview of WT1 gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

WT-1 is required for early kidney development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

28 May 2018

Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

16 August 2018

Codon 45 of the beta-catenin gene, a specific mutational target site of Wilms' tumor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

16 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740887

3 November 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17551084

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2006.047530

1 reference

Europe PubMed Central

2 November 2017

1 reference

Europe PubMed Central

2 November 2017

1 reference

Europe PubMed Central

2 November 2017

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