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Series GSE108484 Query DataSets for GSE108484
Status Public on Oct 29, 2018
Title Transcriptome analysis of Chrdl1-treated RGCs
Organism Rattus norvegicus
Experiment type Expression profiling by high throughput sequencing
Summary Chrdl1 treatment promotes formation of synapses and GluA2-AMPAR recruitment in Retinal ganglion cell (RGC) cultures. Analysis of the transcriptome of RGCs with or without Chrdl1 treatment let us determine potential alterations in the expression of genes related to BMP signaling, or genes involved in excitatory synaptogenesis and AMPAR trafficking.
 
Overall design RNA was isolated from RGC cultures treated for 12 hours with 1ug/ml Chrdl1, and compared to RNA isolated from buffer-treated (vehicle) RGCs as a control.
 
Contributor(s) Blanco-Suarez E, Shokhirev MN, Allen N
Citation(s) 30344043
Submission date Dec 23, 2017
Last update date Mar 28, 2022
Contact name April Elizabeth Williams
E-mail(s) apriljack06@gmail.com, awilliams@salk.edu
Phone 7345461645
Organization name Salk Institute for Biological Studies
Department IGC
Street address 10010 N Torrey Pines Rd
City San Diego
State/province California
ZIP/Postal code 92037
Country USA
 
Platforms (1)
GPL18694 Illumina HiSeq 2500 (Rattus norvegicus)
Samples (6)
GSM2901408 RGCControl052416
GSM2901409 RGCControl092016
GSM2901410 RGCControl092716
Relations
BioProject PRJNA427397
SRA SRP127490

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

Supplementary file Size Download File type/resource
GSE108484_fpkm_rat.txt.gz 770.3 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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