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

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.

Cancer genetics and cytogenetics - 1 Jul 2008

Faussillon Marine, Murakami Ichiro, Bichat Magalie, Telvi Louise, Jeanpierre Cécile, Nezelof Christian, Jaubert Francis, Gogusev Jean

Abstract excerpt

The novel continuous cell line WT-Pe.1 was established in vitro from Wilms tumor with histological features of diffuse anaplasia. The cultures grew as poorly differentiated epithelial-like cells with pleomorphic polygonal shapes and formation of typical monolayers. WT-Pe.1 cells were immunoreactive for cytokeratin, vimentin, laminin, villin, CD10, and CD24 proteins. Conventional cytogenetic analysis by...

Read the complete abstract on PubMed

Topics

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

Share to Cell Line
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to Immunohistochemistry

Share to In Situ Hybridization, Fluorescence

Share to Mice, Nude

Share to Wilms Tumor

Source

Identifiers

PMID: 18558285
DOI: 10.1016/j.cancergencyto.2008.02.018

Genes

CCND2
CDK4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.PMID 18558285Read ↗

Retrospective analysis of FFPE based Wilms' Tumor samples through copy number and somatic mutation related Molecular Inversion Probe Based Array.Semantic proximity Read ↗

Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.Semantic proximity Read ↗

Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumorsSemantic proximity Read ↗

Molecular profiling reveals frequent gain of MYCN and anaplasia-specific loss of 4q and 14q in Wilms tumor.Semantic proximity Read ↗

High-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.Semantic proximity Read ↗

Extrarenal Anaplastic Wilms Tumor: A Case Report With Genomic Analysis and Tumor Models.Semantic proximity Read ↗

A Gradual Transition Toward Anaplasia in Wilms Tumor Through Tolerance to Genetic Damage.Semantic proximity Read ↗

Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screeningSemantic proximity Read ↗

TP53 mutational status is a potential marker for risk stratification in Wilms tumour with diffuse anaplasia.Semantic proximity Read ↗

High-risk blastemal Wilms tumor can be modeled by 3D spheroid cultures in vitroSemantic proximity Read ↗

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

Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm.Semantic proximity Read ↗

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