(Q35740193)

10 August 2017

title

Multiple mechanisms of MYCN dysregulation in Wilms tumour (English)

1 reference

10 August 2017

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Kathy Pritchard-Jones

15

Kathy Pritchard-Jones

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Marry M van den Heuvel-Eibrink

10 August 2017

9

Marry M van den Heuvel-Eibrink

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10 August 2017

10

Marcel Kool

1 reference

10 August 2017

Richard D Williams

1

1 reference

10 August 2017

Tasnim Chagtai

2

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10 August 2017

Marisa Alcaide-German

3

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10 August 2017

John Apps

4

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10 August 2017

Jenny Wegert

5

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10 August 2017

Sergey Popov

6

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10 August 2017

Gordan Vujanic

7

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10 August 2017

Harm van Tinteren

8

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10 August 2017

Jan de Kraker

11

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10 August 2017

David Gisselsson

12

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10 August 2017

Norbert Graf

13

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10 August 2017

Manfred Gessler

14

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10 August 2017

language of work or name

English

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publication date

1 March 2015

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10 August 2017

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10 August 2017

volume

6

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10 August 2017

issue

9

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10 August 2017

page(s)

7232-7243

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describes a project that uses

10 August 2017

limma

limma

2 references

22 June 2022

https://europepmc.org/article/PMC/4466681

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

minfi

minfi

1 reference

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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Subtype-specific FBXW7 mutation and MYCN copy number gain in Wilms' tumor.

27 July 2018

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27 July 2018

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

27 July 2018

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Analysis of gene expression data using BRB-ArrayTools.

27 July 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

27 July 2018

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Outcome prediction in pediatric medulloblastoma based on DNA copy-number aberrations of chromosomes 6q and 17q and the MYC and MYCN loci

27 July 2018

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An X chromosome gene, WTX, is commonly inactivated in Wilms tumor

27 July 2018

1 reference

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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

27 July 2018

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27 July 2018

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27 July 2018

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MYCC and MYCN oncogene amplification in medulloblastoma. A fluorescence in situ hybridization study on paraffin sections from the Children's Oncology Group

27 July 2018

1 reference

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Frequent association of beta-catenin and WT1 mutations in Wilms tumors.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

N-myc oncogene amplification in paediatric tumours

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Involvement of germline DDX1-MYCN duplication in inherited nephroblastoma.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Bilateral wilms tumor with TP53-related anaplasia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Dissecting the genomic complexity underlying medulloblastoma

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

A genome-wide association study identifies susceptibility loci for Wilms tumor

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

lumi: a pipeline for processing Illumina microarray

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumors.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Array comparative genomic hybridization reveals unbalanced gain of the MYCN region in Wilms tumors.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

Somatic glypican 3 (GPC3) mutations in Wilms' tumour

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4466681

N-myc amplification in Wilms' tumor

25 September 2018

1 reference

12 December 2020

Molecular profiling reveals frequent gain of MYCN and anaplasia-specific loss of 4q and 14q in wilms tumor

1 reference

12 December 2020

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

1 reference

12 December 2020

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

1 reference

12 December 2020

Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.18632/ONCOTARGET.3377

0 references

PMC publication ID

4466681

1 reference

10 August 2017

1 reference