(Q41235668)

28 September 2017

title

A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. (English)

1 reference

embryonal rhabdomyosarcoma

28 September 2017

main subject

1 reference

1 reference

C Besnard-Guérin

1

1 reference

28 September 2017

I Newsham

series ordinal

2

1 reference

28 September 2017

R Winqvist

series ordinal

3

1 reference

28 September 2017

W K Cavenee

series ordinal

4

1 reference

28 September 2017

publication date

1 February 1996

1 reference

28 September 2017

1 reference

28 September 2017

volume

97

1 reference

28 September 2017

issue

2

1 reference

28 September 2017

page(s)

163-170

1 reference

https://scigraph.springernature.com/pub.10.1007/bf02265259

28 September 2017

exact match

0 references

cites work

Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02265259

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02265259

Integrated human genome-wide maps constructed using the CEPH reference panel.

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression

1 reference

12 December 2020

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

12 December 2020

PCR detection of 9 polymorphisms in the WT1 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

12 December 2020

A second-generation linkage map of the human genome

1 reference

12 December 2020

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

1 reference

12 December 2020

Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors

1 reference

12 December 2020

Dinucleotide repeat polymorphisms at the D11S439 and HBB loci

1 reference

12 December 2020

Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor

1 reference

12 December 2020

Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

12 December 2020

Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the D11S860 locus

1 reference

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A microsatellite-based index map of human chromosome 11

1 reference

12 December 2020

Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)

1 reference

12 December 2020

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

1 reference

12 December 2020

Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

1 reference

12 December 2020

A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors

1 reference

12 December 2020

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

1 reference

12 December 2020

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

1 reference

12 December 2020

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

1 reference

12 December 2020

Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

1 reference

12 December 2020

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

1 reference

12 December 2020

A third Wilms' tumor locus on chromosome 16q

1 reference

12 December 2020

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

12 December 2020

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

1 reference

12 December 2020

The genomic organization and expression of the WT1 gene

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

Hypervariable polymorphism in the APOC3 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor

1 reference

12 December 2020

Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors

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

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

1 reference

12 December 2020

Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts

1 reference

12 December 2020

The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney.

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of genes on the short arm of chromosome 11 in bladder cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02265259

1 reference

Dimensions Publication ID

28 September 2017

1022180133

0 references

1 reference