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

Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours.

Neuropathology and applied neurobiology - 1 Apr 2015

Nguyen Anh Tuan, Colin Carole, Nanni-Metellus Isabelle, Padovani Laetitia, Maurage Claude-Alain, Varlet Pascale, Miquel Catherine, Uro-Coste Emmanuelle, Godfraind Catherine, Lechapt-Zalcman Emmanuelle, Labrousse François, Gauchotte Guillaume, Silva Karen, Jouvet Anne, Figarella-Branger Dominique

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Brain Neoplasms
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Glioma

Share to Histones

Share to Infant

Share to Proto-Oncogene Proteins B-raf

Source

Identifiers

PMID: 25389051
DOI: 10.1111/nan.12196

Genes

BRAF

Variants

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

Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours.PMID 25389051Read ↗

Co-occurrence of histone H3 K27M and BRAF V600E mutations in paediatric midline grade I ganglioglioma.Semantic proximity Read ↗

A non-midline unclassified glioneuronal tumor with H3K27M mutation enlarging the spectrum of CNS tumors H3K27ME3-altered.Semantic proximity Read ↗

Diffuse midline gliomas with subclonal H3F3A K27M mutation and mosaic H3.3 K27M mutant protein expression.Semantic proximity Read ↗

Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic-pathological correlation.Semantic proximity Read ↗

Malignant gliomas with H3F3A G34R mutation or MYCN amplification in pediatric patients with Li Fraumeni syndrome.Semantic proximity Read ↗

FGFR1 N546K and H3F3A K27M mutations in a diffuse leptomeningeal tumour with glial and neuronal markers.Semantic proximity Read ↗

Gene of the month: H3F3A and H3F3B.Semantic proximity Read ↗

Evidence of H3 K27M mutations in posterior fossa ependymomas.Semantic proximity Read ↗

Mutations within FGFR1 are associated with superior outcome in a series of 83 diffuse midline gliomas with H3F3A K27M mutations.Semantic proximity Read ↗

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1Semantic proximity Read ↗

Malignant progression of a histone H3.3 K27M-mutated spinal pilocytic astrocytoma in an adult.Semantic proximity Read ↗

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.Semantic proximity Read ↗

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