(Q34841380)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544195%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

title

Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization (English)

1 reference

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30 January 2020

1

1 reference

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30 January 2020

John K. Cowell

series ordinal

2

1 reference

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30 January 2020

author name string

Lesleyann Hawthorn

series ordinal

1

1 reference

PubMed publication ID

21544195

4 August 2017

John K Cowell

series ordinal

2

1 reference

PubMed publication ID

21544195

4 August 2017

language of work or name

English

0 references

publication date

22 April 2011

1 reference

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30 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544195%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544195%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

issue

4

1 reference

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30 January 2020

page(s)

e18941

1 reference

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Creative Commons Attribution 4.0 International

30 January 2020

copyright license

start time

22 April 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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8 July 2018

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Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) Study

8 July 2018

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Ploidy status and copy number aberrations in primary glioblastomas defined by integrated analysis of allelic ratios, signal ratios and loss of heterozygosity using 500K SNP Mapping Arrays

8 July 2018

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Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.

8 July 2018

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aCGHViewer: a generic visualization tool for aCGH data

8 July 2018

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The application of microarray technology to the analysis of the cancer genome

8 July 2018

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Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour

8 July 2018

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Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group

8 July 2018

1 reference

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High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genome hybridization

8 July 2018

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FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

8 July 2018

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Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors

8 July 2018

1 reference

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Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation

8 July 2018

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Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.

8 July 2018

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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WT-1 is required for early kidney development

8 July 2018

1 reference

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

8 July 2018

1 reference

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Mutation and cancer: statistical study of retinoblastoma

8 July 2018

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

8 July 2018

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A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

8 July 2018

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Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism

8 July 2018

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International variations in the incidence of childhood renal tumours.

8 July 2018

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3081321

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour

8 July 2018

1 reference

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Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome

8 July 2018

1 reference

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Cytogenetics and molecular genetics of Wilms' tumor of childhood

8 July 2018

1 reference

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

8 July 2018

1 reference

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Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

8 July 2018

1 reference

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Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

Mutational activation of the beta-catenin proto-oncogene is a common event in the development of Wilms' tumors

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3081321

Bilateral Wilms' tumor: long-term survival and some epidemiological features

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3081321

Loss of 11q and 16q in Wilms tumors is associated with anaplasia, tumor recurrence, and poor prognosis

26 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0018941

Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour

21 January 2018

1 reference

12 December 2020

Familial Wilms' tumor: a descriptive study

1 reference

12 December 2020

Comparative genomic hybridization and its application to Wilms' tumorigenesis

1 reference

12 December 2020

Fine mapping of Wilms' tumors with 16q loss of heterozygosity localizes the putative tumor suppressor gene to a region of 6.7 megabases

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

Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors

1 reference

12 December 2020

A third Wilms' tumor locus on chromosome 16q

1 reference

12 December 2020

Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations

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

Cytogenetic abnormalities and clinical outcome in Wilms tumor: a study by the U.K. cancer cytogenetics group and the U.K. Children's Cancer Study Group

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

Cytogenetic changes in Wilms' tumors

1 reference

12 December 2020

Structural rearrangements of the WT1 gene in Wilms' tumour cells

1 reference

12 December 2020

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0018941

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544195%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

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Fatcat

https://api.fatcat.wiki/v0/release/hmhzlj5kk5abbhk6yzvplv42ii

24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544195%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

PubMed publication ID

21544195

1 reference