(Q36621144)

15 August 2017

Loss of heterozygosity at 7p in Wilms' tumour development (English)

1 reference

15 August 2017

1 reference

Powlesland RM

1

1 reference

15 August 2017

Charles AK

2

1 reference

15 August 2017

Malik KT

3

1 reference

15 August 2017

Reynolds PA

4

1 reference

15 August 2017

Pires S

5

1 reference

15 August 2017

Boavida M

6

1 reference

15 August 2017

Brown KW

7

1 reference

15 August 2017

language of work or name

English

0 references

publication date

1 January 2000

1 reference

British Journal of Cancer

15 August 2017

1 reference

15 August 2017

82

1 reference

15 August 2017

2

1 reference

15 August 2017

323-329

1 reference

Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

A comprehensive genetic map of the human genome based on 5,264 microsatellites

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

The genetics of Wilms' tumor--a case of disrupted development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Detection of human papillomavirus DNA in biopsies of human oral tissue

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

A genetic model for colorectal tumorigenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266, and D16S267 loci.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Microsatellites for linkage analysis of genetic traits

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Mutations of the p53 tumor suppressor gene occur infrequently in Wilms' tumor

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Renal tumours of childhood

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

Relaxation of imprinted genes in human cancer.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363297

A third Wilms' tumor locus on chromosome 16q

20 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosome analysis of 31 Wilms' tumors

1 reference

12 December 2020

Translocation (7;7)(p13;q21) in a Wilms' tumor

1 reference

12 December 2020

Simplifying detection of microsatellite length polymorphisms

1 reference

12 December 2020

Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour

1 reference

12 December 2020

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

1 reference

12 December 2020

Germline and somatic abnormalities of chromosome 7 in Wilms' tumor

1 reference

12 December 2020

Involvement of chromosome 7 in Wilms tumor.

1 reference

12 December 2020

Constitutional mosaic t(2;7)(q33;p22) and other rearrangements in a girl with Wilms' tumor

1 reference

12 December 2020

Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11

1 reference

12 December 2020

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

1 reference

12 December 2020

Isochromosome 7q in adult Wilms' tumor

1 reference

12 December 2020

Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors

1 reference

12 December 2020

Comparative genomic hybridization analysis of Wilms tumors

1 reference

12 December 2020

Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour

1 reference

12 December 2020

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

1 reference

12 December 2020

Novel WT1 mutation, 11p LOH, and t(7;12) (p22;q22) chromosomal translocation identified in a Wilms' tumor case

1 reference

12 December 2020

Cytogenetic changes in Wilms' tumors

1 reference

12 December 2020

Identifiers

DOI

10.1054/BJOC.1999.0922

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

10646884

1 reference