(Q50108842)

English

Chromosome arm 16q in Wilms tumors: unbalanced chromosomal translocations, loss of heterozygosity, and assessment of the CTCF gene.

scientific article published in October 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Chromosome arm 16q in Wilms tumors: unbalanced chromosomal translocations, loss of heterozygosity, and assessment of the CTCF gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

1 reference

based on heuristic

inferred from title

author name string

Albert Yeh

1

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Michelle Wei

2

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Samuel B Golub

3

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Darrell J Yamashiro

4

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Vundavali V Murty

5

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Benjamin Tycko

6

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

publication date

1 October 2002

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

35

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

2

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

156-163

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Hyperdiploidy and chromosomal rearrangements define the anaplastic variant of Wilms' tumor.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Role of genomic imprinting in Wilms' tumour and overgrowth disorders

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Epigenetic gene silencing in cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

21 January 2018

Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Der(16)t(1;16)(q21;q13) in Wilms' tumor: friend or foe

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Hemizygous deletions of chromosome band 16q24 in Wilms tumor: detection by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic changes in Wilms' tumors

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic imprinting and cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10110

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.10110

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/12203779

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