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

A one centimorgan deletion unit on chromosome Xq12 is commonly lost in borderline and invasive epithelial ovarian tumors.

Oncogene - 15 Jan 1998

Edelson M I, Lau C C, Colitti C V, Welch W R, Bell D A, Berkowitz R S, Mok S C

Abstract excerpt

We have used polymerase chain reaction (PCR) amplification of tandem repeats to study the pattern of allelic loss on chromosome X11.2-q12 in borderline and invasive epithelial ovarian tumors. Using eight microsatellite markers spanning Xq11.2-q12, 41 borderline and 65 invasive ovarian tumors, together with their corresponding normal tissues, were analysed. The highest percentage of loss of heterozygosity (LOH)...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Loss of Heterozygosity
Share to Ovarian Neoplasms

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

Share to X Chromosome

Source

Identifiers

PMID: 9464537
DOI: 10.1038/sj.onc.1201479

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

A one centimorgan deletion unit on chromosome Xq12 is commonly lost in borderline and invasive epithelial ovarian tumors.PMID 9464537Read ↗

Loss of heterozygosity on chromosome XP22.2-p22.13 and Xq26.1-q27.1 in human breast carcinomas.Semantic proximity Read ↗

Detailed deletion mapping of chromosome 6q in borderline epithelial ovarian tumors.Semantic proximity Read ↗

Identification of allelic losses in benign, borderline, and invasive epithelial ovarian tumors and correlation with clinical outcome.Semantic proximity Read ↗

Frequent loss of heterozygosity targeting the inactive X chromosome in melanoma.Semantic proximity Read ↗

Association Between Nonrandom X-Chromosome Inactivation and BRCA1 Mutation in Germline DNA of Patients With Ovarian CancerSemantic proximity Read ↗

Refinement of two chromosome 11q regions of loss of heterozygosity in ovarian cancer.Semantic proximity Read ↗

Loss of Heterozygosity Analysis and DNA Copy Number Measurement on 8p in Bladder Cancer Reveals Two Mechanisms of Allelic LossSemantic proximity Read ↗

The frequency and mechanism of loss of heterozygosity on chromosome 11q in breast cancer.Semantic proximity Read ↗

Potential role of the inactivated X chromosome in ovarian epithelial tumor development.Semantic proximity Read ↗

Allelic deletions at chromosome 11q22-q23.1 and 11q25-qterm are frequent in sporadic breast but not colorectal cancers.Semantic proximity Read ↗

Allele loss on chromosome 1p36 in epithelial ovarian cancers.Semantic proximity Read ↗

Frequent loss Xq25 on the inactive X chromosome in primary breast carcinomas is associated with tumor grade and axillary lymph node metastasis.Semantic proximity Read ↗

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