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

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

Oncogene - 30 Jan 1997

Koreth J, Bakkenist C J, McGee J O

Abstract excerpt

We identified the chromosome 11q23 region as containing a putative tumour suppressor gene(s) frequently deleted in nonfamilial breast and other cancers. To define this region(s) further, we performed a systematic genetic analysis at chromosome 11q14-qterm in sporadic breast and colorectal cancer. Tumour and constitutional DNA from a panel of 81 cases (51 breast and 30 colorectal cancers) were analysed with...

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 Deletion
Share to Chromosome Mapping

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

Share to DNA, Neoplasm

Share to Gene Deletion

Share to Genetic Markers

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 9053840
DOI: 10.1038/sj.onc.1200847

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

Allelic deletions at chromosome 11q22-q23.1 and 11q25-qterm are frequent in sporadic breast but not colorectal cancers.PMID 9053840Read ↗

A region of deletion on chromosome 22q13 is common to human breast and colorectal cancers.Semantic proximity Read ↗

The BCSC-1 locus at chromosome 11q23-q24 is a candidate tumor suppressor gene.Semantic proximity Read ↗

Mutation at chromosome 11q23 in human non-familial breast cancer: a microdissection microsatellite analysis.Semantic proximity Read ↗

Loss of heterozygosity on chromosome 11 q in breast cancer.Semantic proximity Read ↗

Somatic mutations of the PPP2R1B candidate tumor suppressor gene at chromosome 11q23 are infrequent in ovarian carcinomas.Semantic proximity Read ↗

Identification of two distinct deletion targets at 11q23 in cutaneous malignant melanoma.Semantic proximity Read ↗

Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.Semantic proximity Read ↗

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

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

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25.Semantic proximity Read ↗

Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers.Semantic proximity Read ↗

Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas.Semantic proximity Read ↗

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