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

Delineation of commonly deleted chromosomal regions in meningiomas by high-density single nucleotide polymorphism genotyping arrays.

Genes, chromosomes & cancer - 1 Jun 2012

Tabernero Maria Dolores, Maíllo Angel, Nieto Ana Belen, Diez-Tascón Cristina, Lara Mónica, Sousa Pablo, Otero Alvaro, Castrillo Abel, Patino-Alonso Maria del Carmen, Espinosa Ana, Mackintosh Carlos, de Alava Enrique, Orfao Alberto

Abstract excerpt

Despite recent advances in the identification of the cytogenetic profiles of meningiomas, a significant group of tumors still show normal karyotypes or few chromosomal changes. The authors analyzed the cytogenetic profile of 50 meningiomas using fluorescence in situ hybridization and high-density (500 K) single nucleotide polymorphism (SNP) arrays. Our results confirm that del(22q) (52%) and del(1p) (16%) (common...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Meningeal Neoplasms

Share to Meningioma

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

Share to Signal Transduction

Source

Identifiers

PMID: 22371336
DOI: 10.1002/gcc.21948

Genes

CASP3
HDAC1
MYC
TERT

Provenance

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Delineation of commonly deleted chromosomal regions in meningiomas by high-density single nucleotide polymorphism genotyping arrays.PMID 22371336Read ↗

Genomic landscape of meningiomas.Semantic proximity Read ↗

High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas.Semantic proximity Read ↗

Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.Semantic proximity Read ↗

Genomic Profiling of Atypical Meningiomas Associates Gain of 1q With Poor Clinical OutcomeSemantic proximity Read ↗

Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics.Semantic proximity Read ↗

[MOLECULAR PATHOLOGY OF MENINGIOMAS].Semantic proximity Read ↗

Genomic landscape of intracranial meningiomas.Semantic proximity Read ↗

Increased mRNA expression of CDKN2A is a transcriptomic marker of clinically aggressive meningiomasSemantic proximity Read ↗

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.Semantic proximity Read ↗

A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression.Semantic proximity Read ↗

Genomic and transcriptome analysis revealing an oncogenic functional module in meningiomasSemantic proximity Read ↗

Genomic and Epigenomic Landscape in Meningioma.Semantic proximity Read ↗

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