Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features

10 Nov 2009

Abstract excerpt

PURPOSE: Recent studies suggest that children <24 months with stage I favorable histology Wilms tumors <550 g [very low risk Wilms tumors (VLRWT)] have an excellent prognosis when treated with nephrectomy only, without adjuvant chemotherapy. The identification of risk categories within VLRWT may enable refinement of their definition and optimization of their therapy. EXPERIMENTAL DESIGN: To define biologically...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Renal and related cancers
Share to Renal cell carcinoma treatment
Share to Tuberous Sclerosis Complex Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19903788
DOI: 10.1158/1078-0432.ccr-09-0312

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical FeaturesPMID 19903788Read ↗

WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group study.Semantic proximity Read ↗

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study.Semantic proximity Read ↗

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 GroupSemantic proximity Read ↗

Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis.Semantic proximity Read ↗

Outcome and Prognostic Factors in Stage III Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group Study AREN0532.Semantic proximity Read ↗

Association of Chromosome 1q Gain With Inferior Survival in Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group.Semantic proximity Read ↗

Clinically and biologically relevant subgroups of Wilms tumour defined by genomic and epigenomic analyses.Semantic proximity Read ↗

A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group studySemantic proximity Read ↗

Two molecular subgroups of Wilms' tumors with or without WT1 mutations.Semantic proximity Read ↗

Advances in Wilms Tumor Treatment and Biology: Progress Through International Collaboration.Semantic proximity Read ↗

Association between long interspersed nuclear element-1 methylation levels and relapse in Wilms tumorsSemantic proximity Read ↗

Wilms TumorSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.