Molecular genetic analysis of chromosome 11p in familial Wilms tumour (Q35979181)

11 August 2017

Molecular genetic analysis of chromosome 11p in familial Wilms tumour (English)

1 reference

11 August 2017

1 reference

Baird PN

1

1 reference

11 August 2017

Pritchard J

series ordinal

2

1 reference

11 August 2017

Cowell JK

series ordinal

3

1 reference

11 August 2017

language of work or name

English

0 references

publication date

1 June 1994

1 reference

British Journal of Cancer

11 August 2017

1 reference

11 August 2017

69

1 reference

11 August 2017

6

1 reference

11 August 2017

1072-1077

1 reference

FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Wilms' tumor and other renal tumors of childhood: A selective review from the National Wilms' Tumor Study Pathology Center

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Parental imprinting of the mouse H19 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Alternative splicing and genomic structure of the Wilms tumor gene WT1

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Intragenic homozygous deletion of the WT1 gene in Wilms' tumor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Genetics and epidemiology of Wilms' tumor: The French Wilms' tumor study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Parental imprinting of the mouse insulin-like growth factor II gene.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

High frequency mutagenesis by a DNA methyltransferase

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Inherited WT1 mutation in Denys-Drash syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Relaxation of imprinted genes in human cancer.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1969446

Rapid and quantitative preparation of cytoplasmic RNA from small numbers of cells

24 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Structural rearrangements of the WT1 gene in Wilms' tumour cells

1 reference

12 December 2020

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

1 reference

12 December 2020

A third Wilms' tumor locus on chromosome 16q

1 reference

12 December 2020

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

1 reference

12 December 2020

Nonlinkage of 16q markers to familial predisposition to Wilms' tumor

1 reference

12 December 2020

Hypomethylation of ras oncogenes in primary human cancers

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1038/BJC.1994.210

1 reference

Dimensions Publication ID

11 August 2017

0 references

1 reference

11 August 2017

PubMed publication ID

7911030

1 reference