Infrequent mutation of theWT1 gene in 77 Wilms' tumors (Q58298619)

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23 October 2019

title

Infrequent mutation of the WT1 gene in 77 Wilms' Tumors (English)

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23 October 2019

1

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23 October 2019

Craig Peters

7

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23 October 2019

author name string

König A

2

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23 October 2019

Arden K

3

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23 October 2019

Grundy P

4

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23 October 2019

Orkin S

5

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23 October 2019

Sallan S

6

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23 October 2019

Ruyle S

8

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23 October 2019

Mandell J

9

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23 October 2019

Li F

10

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23 October 2019

publication date

1 January 1994

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23 October 2019

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23 October 2019

volume

3

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23 October 2019

issue

3

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23 October 2019

page(s)

212-222

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Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

23 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Genetic mosaicism in normal tissues of Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Abnormalities of chromosomes 1 and 11 in Wilms' tumor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

A physical map around the WAGR complex on the short arm of chromosome 11

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

The genomic organization and expression of the WT1 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Zinc finger point mutations within the WT1 gene in Wilms tumor patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Transcriptional repression mediated by the WT1 Wilms tumor gene product

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Familial predisposition to Wilms tumor does not segregate with the WT1 gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Cytogenetics and molecular genetics of Wilms' tumor of childhood

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030307

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380030307

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

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