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

Genome-wide copy number variation analysis identified ANO1 as a novel oncogene and prognostic biomarker in esophageal squamous cell cancer

22 Apr 2019

Abstract excerpt

Copy number variations (CNVs) represent one of the most common genomic alterations. This study aimed to evaluate the roles of genes within highly aberrant genome regions in the prognosis of esophageal squamous cell cancer (ESCC). Exome sequencing data from 81 paired ESCC tissues were used to screen aberrant genomic regions. The associations between CNVs and gene expression were evaluated using gene expression...

Read the complete abstract on PubMed

Topics

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

Share to Esophageal and GI Pathology
Share to Esophageal Cancer Research and Treatment
Share to Pancreatic and Hepatic Oncology Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31050728
DOI: 10.1093/carcin/bgz077

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide copy number variation analysis identified ANO1 as a novel oncogene and prognostic biomarker in esophageal squamous cell cancerPMID 31050728Read ↗

Consistent and Differential Genetic Aberrations between Esophageal Dysplasia and Squamous Cell Carcinoma Detected By Array Comparative Genomic HybridizationSemantic proximity Read ↗

Comprehensive genomic analysis of Oesophageal Squamous Cell Carcinoma reveals clinical relevance.Semantic proximity Read ↗

A comprehensive genomic characterization of esophageal squamous cell carcinoma: from prognostic analysis to in vivo assay.Semantic proximity Read ↗

Relationship between ENO1 and Metastasis Risk and Prognosis in Esophageal squamous cell carcinomaSemantic proximity Read ↗

Genome-wide analysis of esophageal adenocarcinoma yields specific copy number aberrations that correlate with prognosis.Semantic proximity Read ↗

Functional Role of a Novel Long Noncoding RNA TTN-AS1 in Esophageal Squamous Cell Carcinoma Progression and MetastasisSemantic proximity Read ↗

Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinomaSemantic proximity Read ↗

An Old Story Retold: Loss of G1 Control Defines A Distinct Genomic Subtype of Esophageal Squamous Cell Carcinoma.Semantic proximity Read ↗

Genomic Characterization of Esophageal Squamous Cell Carcinoma Reveals Critical Genes Underlying Tumorigenesis and Poor Prognosis.Semantic proximity Read ↗

ABCC4 copy number variation is associated with susceptibility to esophageal squamous cell carcinoma.Semantic proximity Read ↗

Identification of EXO1 as a potential biomarker associated with prognosis and tumor immune microenvironment for specific human cancers.Semantic proximity Read ↗

Prognostic biomarker study in patients with clinical stage I esophageal squamous cell carcinoma: JCOG0502-A1.Semantic proximity Read ↗

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