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

Identification of a Novel, Recurrent <scp>SLC44A1‐PRKCA</scp> Fusion in Papillary Glioneuronal Tumor

22 Jun 2012

Abstract excerpt

Mixed neuronal-glial tumors are rare and challenging to subclassify. One recently recognized variant, papillary glioneuronal tumor (PGNT), is characterized by prominent pseudopapillary structures and glioneuronal elements. We identified a novel translocation, t(9;17)(q31;q24), as the sole karyotypic anomaly in two PGNTs. A fluorescence in situ hybridization (FISH)-based positional cloning strategy revealed...

Read the complete abstract on PubMed

Topics

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

Share to Cell Adhesion Molecules Research
Share to Chromatin Remodeling and Cancer
Share to Glioma Diagnosis and Treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 22725730
DOI: 10.1111/j.1750-3639.2012.00612.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

Identification of a Novel, Recurrent <scp>SLC44A1‐PRKCA</scp> Fusion in Papillary Glioneuronal TumorPMID 22725730Read ↗

Papillary glioneuronal tumors: histological and molecular characteristics and diagnostic value of SLC44A1-PRKCA fusion.Semantic proximity Read ↗

EWSR1‐PATZ1 gene fusion may define a new glioneuronal tumor entitySemantic proximity Read ↗

Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma.Semantic proximity Read ↗

PIK3CA mutation in a mixed dysembryoplastic neuroepithelial tumor and rosette forming glioneuronal tumor, a case report and literature review.Semantic proximity Read ↗

Molecular Profiling of a Rare Rosette-Forming Glioneuronal Tumor Arising in the Spinal CordSemantic proximity Read ↗

Clinical-Pathological, Immunohistochemical, and Genetic Characterization of a Series of Posterior Pituitary Tumors.Semantic proximity Read ↗

Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genes.Semantic proximity Read ↗

Clinical, radiological, and pathological features of 16 papillary glioneuronal tumors.Semantic proximity Read ↗

Alterations in<i>PTPN11</i>and other RAS-/MAP-Kinase pathway genes define ganglioglioma with adverse clinical outcome and atypic histopathological featuresSemantic proximity Read ↗

Recurrent copy number alterations in low-grade and anaplastic pleomorphic xanthoastrocytoma with and without BRAF V600E mutation.Semantic proximity Read ↗

Papillary Tumor of the Pineal Region: A Distinct Molecular Entity.Semantic proximity Read ↗

Case Report: A Unique Case of Pediatric Central Nervous System Embryonal Tumor Harboring the CIC–LEUTX Fusion, Germline NBN Variant and Somatic TSC2 Mutation: Expanding the Spectrum of CIC-Rearranged NeoplasiaSemantic proximity Read ↗

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