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 alterations in pancreatic endocrine tumors identified by genome-wide single nucleotide polymorphism analysis.

Endocrine-related cancer - 1 Jun 2007

Nagano Yasuhiko, Kim Do Ha, Zhang Li, White Jill A, Yao James C, Hamilton Stanley R, Rashid Asif

Abstract excerpt

Pancreatic endocrine tumors (PETs) are uncommon and the genetic alterations in these indolent tumors are not well characterized. Chromosomal imbalances are frequent in tumors but PETs have not been studied by high-density single nucleotide polymorphism (SNP) array. We used genome-wide high-density SNP array analysis to detect copy number alterations using matched tumor and non-neoplastic tissue samples from 15...

Read the complete abstract on PubMed

Topics

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

Share to Allelic Imbalance
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human

Share to Genome, Human

Share to Loss of Heterozygosity

Share to Neuroendocrine Tumors

Share to Oligonucleotide Array Sequence Analysis

Share to Pancreatic Neoplasms

Source

Identifiers

PMID: 17639061
DOI: 10.1677/ERC-06-0090

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

Allelic alterations in pancreatic endocrine tumors identified by genome-wide single nucleotide polymorphism analysis.PMID 17639061Read ↗

Allelic alterations in well-differentiated neuroendocrine tumors (carcinoid tumors) identified by genome-wide single nucleotide polymorphism analysis and comparison with pancreatic endocrine tumors.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 ↗

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.Semantic proximity Read ↗

Allelotype of pancreatic acinar cell carcinoma.Semantic proximity Read ↗

Localization of putative tumor suppressor loci by genome-wide allelotyping in human pancreatic endocrine tumors.Semantic proximity Read ↗

Association between genetic subgroups of pancreatic ductal adenocarcinoma defined by high density 500 K SNP-arrays and tumor histopathology.Semantic proximity Read ↗

Genome-wide genetic characterization of bladder cancer: a comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis.Semantic proximity Read ↗

Large-Scale Allelotype of Pancreaticobiliary Carcinoma Provides Quantitative Estimates of Genome-Wide Allelic LossSemantic proximity Read ↗

Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays.Semantic proximity Read ↗

Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell LinesSemantic proximity Read ↗

Genome-wide allelotypes of familial pancreatic adenocarcinomas and familial and sporadic intraductal papillary mucinous neoplasms.Semantic proximity Read ↗

Whole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors.Semantic proximity Read ↗

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