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Article

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.

Genomics - 1 Jan 2005

Bittel Douglas C, Kibiryeva Nataliya, Talebizadeh Zohreh, Driscoll Daniel J, Butler Merlin G

Abstract excerpt

Angelman syndrome (AS) is a neurodevelopmental disorder due to a functional deficit, usually a deletion, of the UBE3A gene located in the 15q11-q13 chromosome region. We report the first microarray analysis of gene expression in AS using a custom cDNA microarray to compare expression patterns from lymphoblastoid cell lines from control males and AS subjects with a 15q deletion or uniparental paternal disomy 15....

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Topics

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Share to Angelman Syndrome
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Expression Profiling

Share to Microarray Analysis

Share to Transcription, Genetic

Share to Ubiquitin-Protein Ligases

Share to Uniparental Disomy

Source

Open in PubMed Open full text

Identifiers

PMID: 15607424
DOI: 10.1016/j.ygeno.2004.10.010
PMCID: PMC6800218

Genes

GABRA5
GABRB3

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.

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