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

Prognostic significance of genetic alterations detected by high-density single nucleotide polymorphism array in gastric cancer.

Cancer science - 1 May 2010

Tada Motohisa, Kanai Fumihiko, Tanaka Yasuo, Sanada Masashi, Nannya Yasuhito, Tateishi Keisuke, Ohta Miki, Asaoka Yoshinari, Seto Motoko, Imazeki Fumio, Yoshida Haruhiko, Ogawa Seishi, Yokosuka Osamu, Omata Masao

Abstract excerpt

We sought to identify genomic changes that could be useful for clinical application, focusing on chromosomal instability and using a high-density single nucleotide polymorphism (SNP) array. We analyzed 34 gastric cancer cell lines for areas of DNA that exhibited copy number changes using the Affymetrix GeneChip Human Mapping 50 K Arrays. The results obtained with the cell lines were verified in 42 gastric cancer...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Cell Line, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to Gene Dosage

Share to Loss of Heterozygosity

Share to Polymorphism, Single Nucleotide

Share to Prognosis

Share to Stomach Neoplasms

Source

Open in PubMed Open full text

Identifiers

PMID: 20331625
DOI: 10.1111/j.1349-7006.2010.01500.x
PMCID: PMC11159782

Genes

MYC
PAK1
PTPRD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Prognostic significance of genetic alterations detected by high-density single nucleotide polymorphism array in gastric cancer.PMID 20331625Read ↗

Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays.Semantic proximity Read ↗

Genome-wide analysis of DNA copy number alterations and gene expression in gastric cancer.Semantic proximity Read ↗

Integrated analysis of copy number alterations and loss of heterozygosity in human pancreatic cancer using a high-resolution, single nucleotide polymorphism array.Semantic proximity Read ↗

Novel regions of chromosomal amplification at 6p21, 5p13, and 12q14 in gastric cancer identified by array comparative genomic hybridizationSemantic proximity Read ↗

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

High-Resolution Genomic and Expression Profiling Reveals 105 Putative Amplification Target Genes in Pancreatic CancerSemantic proximity Read ↗

Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.Semantic proximity Read ↗

Genome-wide analysis of genetic alterations in Barrett's adenocarcinoma using single nucleotide polymorphism arrays.Semantic proximity Read ↗

Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays.Semantic proximity Read ↗

Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.Semantic proximity Read ↗

Genomic Alterations in Primary Gastric Adenocarcinomas Correlate with Clinicopathological Characteristics and SurvivalSemantic proximity Read ↗

Array-Based Comparative Genomic Hybridization Identifies Localized DNA Amplifications and Homozygous Deletions in Pancreatic CancerSemantic proximity Read ↗

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