DataSet Record GDS5090: Expression Profiles Data Analysis Tools Sample Subsets
Title: Cystatin B knockout model of progressive myoclonus epilepsy: postnatal day 30 cerebellum
Cluster AnalysisGDS5090 Cluster Image
Summary: Analysis of cerebella from symptomatic, postnatal day 30 cystatin B (CSTB)-deficient mice. Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is a neurodegenerative disease caused by mutations in the CSTB gene. Results provide insight into the molecular basis of EPM1 pathogenesis.
Organism: Mus musculus
Platform: GPL1261: [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
  • Joensuu T, Tegelberg S, Reinmaa E, Segerstråle M et al. Gene expression alterations in the cerebellum and granule neurons of Cstb(-/-) mouse are associated with early synaptic changes and inflammation. PLoS One 2014;9(2):e89321. PMID: 24586687
Reference Series: GSE47516 Sample count: 6
Value type: transformed count Series published: 2014/03/03