(Q35199262)

7 August 2017

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

1 reference

7 August 2017

1 reference

D D Dao

1

1 reference

7 August 2017

W T Schroeder

2

1 reference

7 August 2017

L Y Chao

3

1 reference

7 August 2017

H Kikuchi

4

1 reference

7 August 2017

L C Strong

5

1 reference

7 August 2017

V M Riccardi

6

1 reference

7 August 2017

S Pathak

7

1 reference

7 August 2017

W W Nichols

8

1 reference

7 August 2017

W H Lewis

9

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7 August 2017

G F Saunders

10

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7 August 2017

language of work or name

English

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publication date

1 August 1987

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

41

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7 August 2017

202-217

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7 August 2017

2

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Chromosome preparations of leukocytes cultured from human peripheral blood

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Isolation of a transforming sequence from a human bladder carcinoma cell line

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Rhabdoid tumors of the kidney contain mesenchymal specific and epithelial specific intermediate filament proteins

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Genetic origin of mutations predisposing to retinoblastoma

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Structure of the human gene encoding the invariant gamma-chain of class II histocompatibility antigens

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Recent amplification of an alpha satellite DNA in humans

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

An RFLP associated with the human catalase gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

The ovalbumin gene: Alleles created by mutations in the intervening sequences of the natural gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Fetal rhabdomyomatous nephroblastoma—A variant of Wilms' tumor

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Chromosome banding techniques

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Clinical aspects of the rhabdoid tumor of the kidney: A report of the national wilms' tumor study group

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684225

Multiple cytogenetic aberrations in neurofibrosarcomas complicating neurofibromatosis

26 September 2018

1 reference

12 December 2020

Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization

1 reference

12 December 2020

Rhabdomyogenesis in renal neoplasia of childhood

1 reference

12 December 2020

Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study

1 reference

12 December 2020

Homozygosity of chromosome 13 in retinoblastoma

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

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

Genetics of Wilms' tumor

1 reference

12 December 2020

The cytogenetics of Wilms' tumor

1 reference

12 December 2020

A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individuals

1 reference

12 December 2020

The Perlman familial nephroblastomatosis syndrome

1 reference

12 December 2020

Identifiers

PMCID

1684225

1 reference

7 August 2017

1 reference