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Series GSE72073 Query DataSets for GSE72073
Status Public on Aug 15, 2015
Title Expression data from lung tissues of IPF patients and Normal Control
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Idiopathic pulmonary fibrosis (IPF) is a progressive lethal interstitial lung disease of unkown etiology with limited effective therapies. The pathogenic mechanisms of IPF remain unkown. Emerging evidences indicate that abnormal behaviors of fibroblasts in IPF are associated with a variety of genetic alterations and aberrant reactivation of developmental signaling pathways.
We compared gene expression profiles in fibrotic lung tissues from IPF patients and normal lung tissues from patients with primary spontaneous pneumothorax using cDNA microarray to examine the mechnisms involved in the pathogenesis of IPF.
 
Overall design Lung tissues were obtained from 5 IPF patients and 3 normal control subjects (patients with primary spontaneous pneumothorax). Gene expression profiling was performed using GeneChip Human Transcriptome Array 2.0.
 
Contributor(s) Geng J, Dai H
Citation(s) 26453058
Submission date Aug 14, 2015
Last update date Oct 29, 2019
Contact name Huaping Dai
E-mail(s) daihuaping@ccmu.edu.cn
Organization name Beijing Chao-Yang Hospital-Beijing Institute of Respiratory Medicine, Capital Medical University
Street address No. 8 Gongren Tiyuchang South Road
City Beijing
ZIP/Postal code 100020
Country China
 
Platforms (1)
GPL17586 [HTA-2_0] Affymetrix Human Transcriptome Array 2.0 [transcript (gene) version]
Samples (8)
GSM1854182 IPF patient 1
GSM1854183 IPF patient 2
GSM1854184 IPF patient 3
Relations
BioProject PRJNA292870

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
GSE72073_RAW.tar 191.5 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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