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 loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma.

Oncogene - 16 Jan 2003

Li Wen-Jun, Hu Nan, Su Hua, Wang Chaoyu, Goldstein Alisa M, Wang Yuan, Emmert-Buck Michael R, Roth Mark J, Guo Wen-Jie, Taylor Philip R

Abstract excerpt

Previous studies have shown frequent allelic loss on chromosome 13 in esophageal squamous cell carcinoma (ESCC). We assessed the frequency of allelic loss on chromosome 13q14 and mutations of deleted in cancer 1 (DICE1) (also found on 13q14) in ESCC patients to determine if this candidate tumor suppressor gene has a role in the development of ESCC, and whether this gene was an inactivation target for allelic loss...

Read the complete abstract on PubMed

Topics

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

Share to Carcinoma, Squamous Cell
Share to Chromosomes, Human, Pair 13

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Esophageal Neoplasms

Share to Loss of Heterozygosity

Share to Polymorphism, Single-Stranded Conformational

Share to Ribosomal Proteins

Share to RNA-Binding Proteins

Share to RNA Helicases

Source

Identifiers

PMID: 12527901
DOI: 10.1038/sj.onc.1206098

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma.PMID 12527901Read ↗

Evidence for a familial esophageal cancer susceptibility gene on chromosome 13.Semantic proximity Read ↗

Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history.Semantic proximity Read ↗

Lymph node metastasis is associated with allelic loss on chromosome 13q12-13 in esophageal squamous cell carcinoma.Semantic proximity Read ↗

Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma.Semantic proximity Read ↗

Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China.Semantic proximity Read ↗

Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array.Semantic proximity Read ↗

Genetic alterations on chromosomes 3 and 9 of esophageal cancer tissues from China.Semantic proximity Read ↗

Genetic mechanisms in esophageal carcinogenesis: frequent deletion of 3p and 17p in premalignant lesions.Semantic proximity Read ↗

Microsatellite alterations in esophageal dysplasia and squamous cell carcinoma from laser capture microdissected endoscopic biopsies.Semantic proximity Read ↗

Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer.Semantic proximity Read ↗

Polymorphism and allelic loss at the AS3 locus on 13q12-13 in esophageal squamous cell carcinoma.Semantic proximity Read ↗

Clinicopathological significance of loss of heterozygosity on chromosome 13q in hepatocellular carcinoma.Semantic proximity Read ↗

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