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

Expression of ETV6‐NTRK in classical, cellular and mixed subtypes of congenital mesoblastic nephroma

24 Mar 2006

Abstract excerpt

AIM: Congenital mesoblastic nephroma (CMN) is the commonest renal tumour of infancy, with classical, cellular and mixed histological subtypes described. A specific ETV6-NTRK3 fusion-gene product is reported in association with the cellular variant. The aim was to investigate the relationship between the presence of this product and morphological phenotype using paraffin-embedded archival material. METHODS AND...

Read the complete abstract on PubMed

Topics

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

Share to Pediatric Urology and Nephrology Studies
Share to Renal and related cancers
Share to Renal cell carcinoma treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16681692
DOI: 10.1111/j.1365-2559.2006.02400.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Expression of ETV6‐NTRK in classical, cellular and mixed subtypes of congenital mesoblastic nephromaPMID 16681692Read ↗

Congenital mesoblastic nephroma is characterised by kinase mutations including EGFR internal tandem duplications, the ETV6-NTRK3 fusion, and the rare KLHL7-BRAF fusion.Semantic proximity Read ↗

ETV6–NTRK3 in congenital mesoblastic nephroma: A report of the SIOP/GPOH nephroblastoma studySemantic proximity Read ↗

Adjunctive diagnostic tool for histopathological classification in congenital mesoblastic nephromaSemantic proximity Read ↗

Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephromaSemantic proximity Read ↗

Non‐resectable congenital tumors with the <i>ETV6</i>–<i>NTRK3</i> gene fusion are highly responsive to chemotherapySemantic proximity Read ↗

Infantile fibrosarcoma with an EGFR kinase domain duplication: Underlining a close relationship with congenital mesoblastic nephroma and highlighting a similar morphological spectrumSemantic proximity Read ↗

ETV6 Rearrangements in Patients with Infantile Fibrosarcomas and Congenital Mesoblastic Nephromas by Fluorescence In Situ HybridizationSemantic proximity Read ↗

Paediatric and adult soft tissue sarcomas with NTRK1 gene fusions: a subset of spindle cell sarcomas unified by a prominent myopericytic/haemangiopericytic pattern.Semantic proximity Read ↗

Neonatal renal tumours.Semantic proximity Read ↗

Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type.Semantic proximity Read ↗

Evaluation of a Congenital Infantile Fibrosarcoma by Comprehensive Genomic Profiling Reveals an LMNA-NTRK1 Gene Fusion Responsive to CrizotinibSemantic proximity Read ↗

c-KIT overexpression, without gene amplification and mutation, in paediatric renal tumoursSemantic proximity Read ↗

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