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Series GSE208396 Query DataSets for GSE208396
Status Public on Jun 30, 2023
Title GLUT1 is redundant in hypoxic and glycolytic nucleus pulposus cells of the intervertebral disc
Organism Mus musculus
Experiment type Expression profiling by array
Summary Glucose is critical to the development, homeostasis, and survival of nucleus pulposus cells. GLUT1 is a major glucose transporter, a NP phenotypic cell marker, and highly expressed in nucleus pulposus (NP) cells, however its level of importance in NP cell development and homeostasis is unknown.
We used microarrays to explore the transcriptomics of differentially expressed genes between wildtype and Glut1 cKO NP cells in 9-month-old mice.
 
Overall design NP tissue were dissected from discs from control (n=6) and K19Cre; Glut1 cKO mice (n=6). Mice were injected with Tamoxifen at 3-months-old and aged until they became 9-months-old. RNA extraction was prefomed and hybridization on Affymetrix microarrays.
 
Contributor(s) Johnston SN, Silagi E, Madhu V, Shapiro I, Risbud MV
Citation(s) 36917198
Submission date Jul 18, 2022
Last update date Sep 07, 2023
Contact name Shira N Johnston
E-mail(s) snj007@students.jefferson.edu
Organization name Thomas Jefferson University
Street address 1025 Walnut St., Suite 511 College Bldg.
City Philadelphia
State/province PA
ZIP/Postal code 19107
Country USA
 
Platforms (1)
GPL23038 [Clariom_S_Mouse] Affymetrix Clariom S Assay, Mouse (Includes Pico Assay)
Samples (12)
GSM6345558 9M WT, NP 1
GSM6345559 9M WT, NP 2
GSM6345560 9M WT, NP 3
Relations
BioProject PRJNA859800

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
GSE208396_K19Glut1cKO_vs_WT_FOLD2_FDRPval0.05.txt.gz 350 b (ftp)(http) TXT
GSE208396_K19Glut1cKO_vs_WT_FOLD2_Pval0.05.txt.gz 2.1 Kb (ftp)(http) TXT
GSE208396_RAW.tar 13.0 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table
Processed data are available on Series record

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