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Series GSE174020 Query DataSets for GSE174020
Status Public on May 07, 2021
Title An integrated transcriptomic approach to identify molecular markers of calcineurin inhibitor nephrotoxicity in pediatric kidney transplant recipients
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Calcineurin inhibitor nephrotoxicity (CNIT) has been associated with the development of chronic renal allograft dysfunction and decreased graft survival. This study evaluated 37 formalin-fixed paraffin-embedded biopsies from pediatric kidney transplant recipients using gene expression profiling.
Oxidative phosphorylation and mitochondrial dysfunction were the top molecular pathways as-sociated with overexpressed genes in CNIT samples. Decreased ATP synthesis was identified as a significant biological function in CNIT, while key toxicology pathways included NRF2-mediated oxidative stress response and increased permeability transition of mitochondria.
 
Overall design To identify a unique molecular signature for accurate pediatric CNIT diagnosis.
 
Contributor(s) Mas V, Dumur CI, Maluf D
Citation(s) 34063776
Submission date May 06, 2021
Last update date Jun 28, 2021
Contact name Catherine Dumur
Organization name Sonic Healthcare USA
Department Anatomic Pathology
Lab Bernhardt
Street address 5008 Mustang Rd
City Jacksonville
State/province FL
ZIP/Postal code 32216
Country USA
 
Platforms (1)
GPL571 [HG-U133A_2] Affymetrix Human Genome U133A 2.0 Array
Samples (37)
GSM5284715 CNIT_Pt01
GSM5284716 CNIT_Pt02
GSM5284717 CNIT_Pt03
Relations
BioProject PRJNA728193

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
GSE174020_RAW.tar 64.0 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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