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

Deletion mapping on chromosome 10q25-q26 in human endometrial cancer.

British journal of cancer - 1 Dec 1996

Nagase S, Sato S, Tezuka F, Wada Y, Yajima A, Horii A

Abstract excerpt

To understand genetic events which play a role in the development and/or progression of human endometrial cancer, we studied allelotypes on all autosomal chromosomes, as well as chromosome X, with 42 microsatellite markers and 56 endometrial cancers. The most frequent loss of heterozygosity (LOH) was observed on the long arm of chromosome 10 (14 of 30, 47%), which was commonly detected in grade 1 cancer. We...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 10

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

Share to DNA Replication

Share to Gene Deletion

Share to Heterozygote

Share to Mutation

Share to Neoplasm Staging

Source

Open in PubMed Open full text

Identifiers

PMID: 8980400
DOI: 10.1038/bjc.1996.663
PMCID: PMC2074818

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

Deletion mapping on chromosome 10q25-q26 in human endometrial cancer.PMID 8980400Read ↗

Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers.Semantic proximity Read ↗

Identification of a 0.4 Kb deletion region in 10q26 associated with endometrial carcinoma.Semantic proximity Read ↗

Identification of a 790-kilobase region of common allelic loss in chromosome 10q25-q26 in human endometrial cancer.Semantic proximity Read ↗

Allelotype of endometrial carcinoma.Semantic proximity Read ↗

Allelotype of human bladder cancer.Semantic proximity Read ↗

Identification of a novel candidate gene, CASC2, in a region of common allelic loss at chromosome 10q26 in human endometrial cancer.Semantic proximity Read ↗

Cluster of allele losses within a 2.5 cM region of chromosome 10 in high-grade invasive bladder cancer.Semantic proximity Read ↗

Allelotype of uterine cancer by analysis of RFLP and microsatellite polymorphisms: frequent loss of heterozygosity on chromosome arms 3p, 9q, 10q, and 17p.Semantic proximity Read ↗

Polymerase chain reaction allelotyping of human ovarian cancer.Semantic proximity Read ↗

Loss of heterozygosity from the short arm of chromosome 8 is an early event in breast cancersSemantic proximity Read ↗

Allelotype analysis of uterine leiomyoma: localization of a potential tumor suppressor gene to a 4-cM region of chromosome 7q.Semantic proximity Read ↗

Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer.Semantic proximity Read ↗

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