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

The EP300:BCOR fusion extends the genetic alteration spectrum defining the new tumoral entity of “CNS tumors with BCOR internal tandem duplication”

2 Nov 2020

Abstract excerpt

International audience

Read the complete abstract on PubMed

Topics

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

Share to Cancer Genomics and Diagnostics
Share to Chromatin Remodeling and Cancer
Share to Glioma Diagnosis and Treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33138864
DOI: 10.1186/s40478-020-01064-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The EP300:BCOR fusion extends the genetic alteration spectrum defining the new tumoral entity of “CNS tumors with BCOR internal tandem duplication”PMID 33138864Read ↗

CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors.Semantic proximity Read ↗

Recurrent EP300-BCOR Fusions in Pediatric Gliomas With Distinct Clinicopathologic FeaturesSemantic proximity Read ↗

Fusions involving BCOR and CREBBP are rare events in infiltrating gliomaSemantic proximity Read ↗

Intra‐ and extra‐cranial <scp><i>BCOR‐</i>ITD</scp> tumours are separate entities within the <scp><i>BCOR</i></scp>‐rearranged familySemantic proximity Read ↗

Primary intracranial sarcoma associated with DICER1 mutant: a case report and preclinical investigationSemantic proximity Read ↗

Multifocal Neuroblastoma in Rubinstein-Taybi Syndrome Harboring a Novel CREBBP Variant Identified by Paired Whole Genome Sequencing.Semantic proximity Read ↗

Benign and malignant tumors in Rubinstein-Taybi syndrome.Semantic proximity Read ↗

Rubinstein-Taybi because of a novel EP300 mutation with novel clinical findings.Semantic proximity Read ↗

A single supratentorial high-grade neuroepithelial tumor with two distinct BCOR mutations, exceptionally long complete remission and survival.Semantic proximity Read ↗

Bladder malignant granular cell tumor with EP300 gene mutation: a case report and literature reviewSemantic proximity Read ↗

Novel somatic and germline mutations in intracranial germ cell tumours.Semantic proximity Read ↗

BCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidney.Semantic proximity Read ↗

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