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

Genomic Markers for Ovarian Cancer at Chromosomes 1, 8 and 17 Revealed by Array CGH Analysis

1 May 2009

Abstract excerpt

AIMS AND BACKGROUND: The literature data show that the most frequently affected chromosomes in ovarian carcinogenesis are 1, 8 and 17. In the present study we aimed to define more precisely at a high resolution the genomic imbalances of these chromosomes in ovarian cancer and to determine genomic markers separating tumors of different histological types and stages. METHODS: Array comparative genomic hybridization...

Read the complete abstract on PubMed

Topics

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

Share to Chromatin Remodeling and Cancer
Share to Genomic variations and chromosomal abnormalities
Share to Ovarian cancer diagnosis and treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19688977
DOI: 10.1177/030089160909500315

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic Markers for Ovarian Cancer at Chromosomes 1, 8 and 17 Revealed by Array CGH AnalysisPMID 19688977Read ↗

CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.Semantic proximity Read ↗

17q21-q25 aberrations in breast cancer: combined allelotyping and CGH analysis reveals 5 regions of allelic imbalance among which two correspond to DNA amplification.Semantic proximity Read ↗

Molecular genetic changes in human epithelial ovarian malignancies.Semantic proximity Read ↗

Genetic profile of hepatocellular carcinoma revealed by array-based comparative genomic hybridization: identification of genetic indicators to predict patient outcome.Semantic proximity Read ↗

Allele loss from large regions of chromosome 17 is common only in certain histological subtypes of ovarian carcinomas.Semantic proximity Read ↗

Loss, mutation and deregulation of L3MBTL4 in breast cancers.Semantic proximity Read ↗

High-density genetic map of the BRCA1 region of chromosome 17q12-q21.Semantic proximity Read ↗

Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis.Semantic proximity Read ↗

Aberrations of Chromosomes 1 and 16 in Breast Cancer: A Framework for Cooperation of Transcriptionally Dysregulated GenesSemantic proximity Read ↗

The important molecular markers on chromosome 17 and their clinical impact in breast cancer.Semantic proximity Read ↗

Chromosome-breakage genomic instability and chromothripsis in breast cancer.Semantic proximity Read ↗

Genomic imbalances detected by comparative genomic hybridization are prognostic markers in invasive ductal breast carcinomasSemantic proximity Read ↗

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