Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome (Q64458922)

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11 October 2019

title

Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome (English)

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11 October 2019

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3

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11 October 2019

author name string

A Santos

1

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11 October 2019

L Osorio-Almeida

2

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11 October 2019

J M Silva

4

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11 October 2019

M G Boavida

5

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11 October 2019

J Cowell

6

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11 October 2019

publication date

1 August 1993

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11 October 2019

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11 October 2019

volume

92

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11 October 2019

issue

1

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11 October 2019

page(s)

83-86

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https://scigraph.springernature.com/pub.10.1007/bf00216151

11 October 2019

exact match

0 references

cites work

Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome

1 reference

12 December 2020

Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families

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The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.

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

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Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT

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

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The candidate Wilms' tumour gene is involved in genitourinary development

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Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome

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Incidence of malignant tumors in U.S. children

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Development of homozygosity for chromosome 11p markers in Wilms' tumour

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Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

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12 December 2020

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

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12 December 2020

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

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Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

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12 December 2020

A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm

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12 December 2020

Definition of the limits of the Wilms tumor locus on human chromosome 11p13.

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12 December 2020

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

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

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12 December 2020

The genomic organization and expression of the WT1 gene

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12 December 2020

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

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Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing

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Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci

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Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

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12 December 2020

Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient

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12 December 2020

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

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12 December 2020

Mutation and cancer: a model for Wilms' tumor of the kidney

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12 December 2020

Structural rearrangements of the WT1 gene in Wilms' tumour cells

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12 December 2020

Intragenic homozygous deletion of the WT1 gene in Wilms' tumor

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12 December 2020

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

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12 December 2020

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1 reference

12 December 2020