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

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

Cancer research - 1 Oct 2005

Teh Muy-Teck, Blaydon Diana, Chaplin Tracy, Foot Nicola J, Skoulakis Spyros, Raghavan Manoj, Harwood Catherine A, Proby Charlotte M, Philpott Michael P, Young Bryan D, Kelsell David P

Abstract excerpt

Basal cell carcinoma is the most common human cancer with increasing incidence reported worldwide. Despite the aberrant signaling role of the Hedgehog pathway, little is known about the genetic mechanisms underlying basal cell carcinomas. Towards a better understanding of global genetic events, we have employed the Affymetrix Mapping 10K single nucleotide polymorphism (SNP) microarray technique for...

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 Carcinoma, Basal Cell

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Neoplasm

Share to Loss of Heterozygosity

Share to Patched-1 Receptor

Share to Patched Receptors

Share to Receptors, Cell Surface

Share to Skin Neoplasms

Source

Identifiers

PMID: 16204023
DOI: 10.1158/0008-5472.CAN-05-0842

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

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.PMID 16204023Read ↗

Genome-Wide Profiling of Acquired Uniparental Disomy Reveals Prognostic Factors in Head and Neck Squamous Cell Carcinoma.Semantic proximity Read ↗

Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis.Semantic proximity Read ↗

Pathogenesis and consequences of uniparental disomy in cancer.Semantic proximity Read ↗

Genetic losses in breast cancer: toward an integrated molecular cytogenetic map.Semantic proximity Read ↗

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.Semantic proximity Read ↗

Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays.Semantic proximity Read ↗

Genetics of basal cell carcinoma.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 ↗

Single nucleotide polymorphism microarray analysis in cortisol-secreting adrenocortical adenomas identifies new candidate genes and pathways.Semantic proximity Read ↗

Allele-specific imbalance mapping identifies HDAC9 as a candidate gene for cutaneous squamous cell carcinoma.Semantic proximity Read ↗

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.Semantic proximity Read ↗

Novel pheochromocytoma susceptibility loci identified by integrative genomics.Semantic proximity Read ↗

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