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Stratification of Wilms tumor by genetic and epigenetic analysis

Stratification of Wilms tumor by genetic and epigenetic analysis

http://www.wikidata.org/entity/Q35987087

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Is Wilms tumor a candidate neoplasia for treatment with WNT/β-catenin pathway modulators?--A report from the renal tumors biology-driven drug development workshop Wilms' tumor: biology, diagnosis and treatment Realizing the promise of cancer predisposition genes.Nuclear β-Catenin Expression is Frequent in Sinonasal Hemangiopericytoma and Its Mimics.Methylome analysis identifies a Wilms tumor epigenetic biomarker detectable in blood.Comparative methylome analysis identifies new tumour subtypes and biomarkers for transformation of nephrogenic rests into Wilms tumour A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan, and the penetrance rates in children with WT1 germline mutation Genetic and chromosomal alterations in Kenyan Wilms Tumor.Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors.Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review Biomarkers to detect Wilms tumors in pediatric patients: where are we now?An update on genomic-guided therapies for pediatric solid tumors.Bilateral Wilms tumour: a review of clinical and molecular features.The genetic factors contributing to the development of Wilm's tumor and their clinical utility in its diagnosis and prognosis.Long non-coding RNAs and complex diseases: from experimental results to computational models.Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients.The IGF signalling pathway in Wilms tumours--a report from the ENCCA Renal Tumours Biology-driven drug development workshop.Biallelic DICER1 mutations occur in Wilms tumours.Association between long interspersed nuclear element-1 methylation levels and relapse in Wilms tumors.Racial and Ethnic Disparities in the Incidence of Pediatric Extracranial Embryonal Tumors.Paediatrics: Integrating genomics to dig deeper into Wilms tumour biology.Activation of the Wnt/β-catenin pathway is common in wilms tumor, but rarely through β-catenin mutation and APC promoter methylation.Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of in Wilms tumour susceptibility Genomics of adult and pediatric solid tumors

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Stratification of Wilms tumor by genetic and epigenetic analysis

http://www.wikidata.org/entity/Q35987087

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Stratification of Wilms tumor by genetic and epigenetic analysis

@ast

Stratification of Wilms tumor by genetic and epigenetic analysis

@en

type

label

Stratification of Wilms tumor by genetic and epigenetic analysis

@ast

Stratification of Wilms tumor by genetic and epigenetic analysis

@en

prefLabel

Stratification of Wilms tumor by genetic and epigenetic analysis

@ast

Stratification of Wilms tumor by genetic and epigenetic analysis

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Stratification of Wilms tumor by genetic and epigenetic analysis

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Anna Kelsey

http://www.w3.org/2001/XMLSchema#string

Anne Murray

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Barry Pizer

http://www.w3.org/2001/XMLSchema#string

Charles A Stiller

http://www.w3.org/2001/XMLSchema#string

Chey Loveday

http://www.w3.org/2001/XMLSchema#string

Denise Williams

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Fin Breatnach

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Gill A Levitt

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Gordan M Vujanic

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Heidi Traunecker

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P2860

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

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

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

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

Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors.

Epidemiology of Wilms tumor.

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.

International variations in the incidence of childhood renal tumours.

Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.

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327-335

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scholarly article

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10.18632/ONCOTARGET.468

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3

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3

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Kathy Pritchard-Jones

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2012-03-01T00:00:00Z

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223982791

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22470196

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3359888

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