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Series GSE50225 Query DataSets for GSE50225
Status Public on Jan 22, 2016
Title Wild-type and Mecp2 -/y callosal projection neurons
Organism Mus musculus
Experiment type Expression profiling by array
Summary Mutations of the transcriptional regulator Mecp2 cause the X-linked autism spectrum disorder Rett syndrome (RTT), and Mecp2 has been implicated in several other neurodevelopmental disorders. To identify potential target genes regulated directly or indirectly by MeCP2, we performed comparative gene expression analysis via oligonucleotide microarrays on Mecp2-/y (Mecp2-null) and wild-type CPN purified via fluorescence-activated cell sorting (FACS).
 
Overall design Independent RNA samples were collected from three independent FACS purifications for both wild-type and Mecp2 -/y callosal projection neurons.
 
Contributor(s) Kishi N, MacDonald JL, Ye J, Molyneaux BJ, Azim E, Macklis JD
Citation(s) 26821816
Submission date Aug 27, 2013
Last update date Feb 11, 2019
Contact name Noriyuki Kishi
E-mail(s) noriyukik@nifty.com
Organization name Keio Univ. School of Medicine
Department Department of Physiology
Lab Hideyuki Okano Lab
Street address 35 Shinanomachi
City Shinjuku-ku
State/province Tokyo
ZIP/Postal code 160-8582
Country Japan
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (6)
GSM1216096 CPN_P14_WT1
GSM1216097 CPN_P14_WT2
GSM1216098 CPN_P14_WT3
Relations
BioProject PRJNA217318

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE50225_RAW.tar 41.9 Mb (http)(custom) TAR (of CEL, CHP)
Processed data included within Sample table
Processed data provided as supplementary file

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