(Q71601023)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504520%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

title

Low frequency of mutations in the WT1 coding region in Wilms' tumor (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504520%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

author name string

Brown KW

1

1 reference

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19 October 2019

Wilmore HP

2

1 reference

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19 October 2019

Watson JE

3

1 reference

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19 October 2019

Mott MG

4

1 reference

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19 October 2019

Berry PJ

5

1 reference

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19 October 2019

Maitland NJ

6

1 reference

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19 October 2019

publication date

1 October 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504520%20AND%20SRC:MED&resulttype=core&format=json

Genes, Chromosomes and Cancer

19 October 2019

published in

1 reference

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19 October 2019

volume

8

1 reference

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19 October 2019

issue

2

1 reference

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19 October 2019

page(s)

74-79

1 reference

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Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

19 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Loss of chromosome 11p alleles in cultured cells derived from Wilms' tumours

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

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%2FGCC.2870080203

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%2FGCC.2870080203

7 January 2021

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

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%2FGCC.2870080203

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%2FGCC.2870080203

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%2FGCC.2870080203

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%2FGCC.2870080203

7 January 2021

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Wilms' tumour and a de novo (1;7) translocation in a child with bilateral radial aplasia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Transcriptional repression mediated by the WT1 Wilms tumor gene product

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

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%2FGCC.2870080203

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%2FGCC.2870080203

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

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%2FGCC.2870080203

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Protocols for an improved detection of point mutations by SSCP

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

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%2FGCC.2870080203

7 January 2021

Wilms' tumour: reconciling genetics and biology

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080203

7 January 2021

Identifiers

DOI

10.1002/GCC.2870080203

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504520%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference