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Article

The desmoplastic small round cell tumor t(11;22) translocation produces EWS/WT1 isoforms with differing oncogenic properties

16 Apr 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9591781
DOI: 10.1038/sj.onc.1201716

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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The desmoplastic small round cell tumor t(11;22) translocation produces EWS/WT1 isoforms with differing oncogenic propertiesPMID 9591781Read ↗

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Desmoplastic small round cell tumor is dependent on the EWS-WT1 transcription factorSemantic proximity Read ↗

Novel oncogenic mutations in the WT1 Wilms' tumor suppressor gene: a t(11;22) fuses the Ewing's sarcoma gene, EWS1, to WT1 in desmoplastic small round cell tumor.Semantic proximity Read ↗

Establishment of multiple novel patient-derived models of desmoplastic small round cell tumor enabling functional characterization of ERBB pathway signaling and pre-clinical evaluation of a novel targeted therapy approachSemantic proximity Read ↗

Comprehensive Transcriptomic Analysis of EWSR1::WT1 Targets Identifies CDK4/6 Inhibitors as an Effective Therapy for Desmoplastic Small Round Cell TumorsSemantic proximity Read ↗

EWS-WT1 fusion isoforms establish oncogenic programs and therapeutic vulnerabilities in desmoplastic small round cell tumorsSemantic proximity Read ↗

EWSR1-WT1 Target Genes and Therapeutic Options Identified in a Novel DSRCT In Vitro ModelSemantic proximity Read ↗

Variant EWS-WT1 chimeric product in the desmoplastic small round cell tumor.Semantic proximity Read ↗

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