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

Comparative genomic hybridization detects frequent overrepresentation of chromosomal material from 3q26, 8q24, and 20q13 in human ovarian carcinomas

1 Dec 1997

Abstract excerpt

We used comparative genomic hybridization (CGH) to identify recurrent chromosomal imbalances in tumor DNA from 25 malignant ovarian carcinomas and two ovarian tumors of low malignant potential (LMP). Many of the carcinoma specimens displayed numerous imbalances. The most common sites of copy number increases, in order of frequency, were 8q24.1, 20q13.2-qter, 3q26.3-qter, 1q32, 20p, 9p21-pter, and 12p. DNA...

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 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: 9408747
DOI: 10.1002/(sici)1098-2264(199712)20:4<320::aid-gcc2>3.0.co;2-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Comparative genomic hybridization detects frequent overrepresentation of chromosomal material from 3q26, 8q24, and 20q13 in human ovarian carcinomasPMID 9408747Read ↗

Detection of DNA gains and losses in primary endometrial carcinomas by comparative genomic hybridization.Semantic proximity Read ↗

Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiationSemantic proximity Read ↗

Copy Number Analysis Identifies Novel Interactions Between Genomic Loci in Ovarian CancerSemantic proximity Read ↗

Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISHSemantic 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 ↗

High-resolution analysis of DNA copy number alterations in colorectal cancer by array-based comparative genomic hybridization.Semantic proximity Read ↗

Genetic imbalances in precursor lesions of endometrial cancer detected by comparative genomic hybridization.Semantic proximity Read ↗

Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome.Semantic proximity Read ↗

Distinct Chromosomal Bias of Gene Expression Signatures in the Progression of Hepatocellular CarcinomaSemantic proximity Read ↗

Chromosome abnormalities in ovarian adenocarcinoma: I. nonrandom chromosome abnormalities from 244 casesSemantic proximity Read ↗

Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative genomic hybridizationSemantic proximity Read ↗

Evidence for divergence of DNA copy number changes in serous, mucinous and endometrioid ovarian carcinomas.Semantic proximity Read ↗

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