A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. (Q41235668)

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scientific article published on February 1996

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English	A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.	scientific article published on February 1996

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

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)

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Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

main subject

embryonal rhabdomyosarcoma

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inferred from title

heterozygosity

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based on heuristic

inferred from title

author name string

C Besnard-Guérin

series ordinal

1

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Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

I Newsham

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

R Winqvist

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

W K Cavenee

series ordinal

4

1 reference

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Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

publication date

1 February 1996

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

volume

97

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stated in

Europe PubMed Central

PubMed publication ID

8566947

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28 September 2017

issue

2

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stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

page(s)

163-170

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stated in

Europe PubMed Central

PubMed publication ID

8566947

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28 September 2017

cites work

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

1 reference

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Crossref

reference URL

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

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

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

retrieved

21 January 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCR detection of 9 polymorphisms in the WT1 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphisms at the D11S439 and HBB loci

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the D11S860 locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A microsatellite-based index map of human chromosome 11

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A third Wilms' tumor locus on chromosome 16q

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genomic organization and expression of the WT1 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypervariable polymorphism in the APOC3 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8566947

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF02265259

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

Dimensions Publication ID

1022180133

0 references

PubMed publication ID

8566947

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8566947

retrieved

28 September 2017

 

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