Dataset: Expression profiles of the hippocampus of Rsk2-KO mice
Coffin–Lowry Syndrome (CLS) is a syndromic form of mental retardation caused by loss of function mutations in the X-linked RPS6KA3 gene,...
Coffin–Lowry Syndrome (CLS) is a syndromic form of mental retardation caused by loss of function mutations in the X-linked RPS6KA3 gene, which encodes Rsk2, a serine/threonine kinase involved in spatial memory. We analyzed hippocampal gene expression profiles in Rsk2-KO mice to identify changes in molecular pathways. Total RNA was extracted from hippocampi from 6 KO and 6 WT (littermates) 2-month-old male mice. For each genotype, equivalent amounts of RNA from 2 mice were pooled and processed for hybridization to the genome wide oligonucleotide microarray (Murine 430A 2.0 Affymetrix, 22.000 probe sets). Thus, 3 independent pooled samples were hybridized for each genotype. We compared hippocampal gene expression profiles from rsk2-KO and normal littermate mice to identify changes in molecular pathways
- Species:
- mouse
- Samples:
- 6
- Source:
- E-GEOD-22137
- PubMed:
- 21116650
- Updated:
- Dec.12, 2014
- Registered:
- Nov.24, 2014
Sample | GENOTYPE/VARIATION |
---|---|
GSM550617 | Rsk2-KO |
GSM550617 | Rsk2-KO |
GSM550617 | Rsk2-KO |
GSM550620 | wild type |
GSM550620 | wild type |
GSM550620 | wild type |