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Links from GEO DataSets

Items: 16

1.

Profiling of Gene Expression in Idiopathic Pulmonary Fibrosis

(Submitter supplied) Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic, progressive fibrosing interstitial disease of unknown cause. It remains impractical to conduct early diagnosis and predict IPF progression just based on gene expression information. Moreover, the relationship between gene expression and quantitative phenotypic value in IPF keeps controversial. To identify biomarkers to predict survival in IPF, we profiled protein-coding gene expression in peripheral blood mononuclear cells (PBMCs). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
115 Samples
Download data: CEL
Series
Accession:
GSE38958
ID:
200038958
2.

Knockout LYCAT modulates altered gene expression profile in H2122 cells

(Submitter supplied) We present the set of gene expression in in H2122 cells with transfection of control shRNA vs H2122 cells with transfection of LYCAT shRNA. Methods: Cell mRNA profiles of H2122 control cells and H2122 LYCAT KO cells were generated by deep sequencing, in triplicate, using Illumina GAIIx. The sequence reads that passed quality filters were analyzed at the transcript isoform level with two way ANOVA (ANOVA).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
3.

IPF versus Control

(Submitter supplied) Archived lung tissues of patients with IPF were obtained from the tissue bank of the Department of Pathology at the University of Pittsburgh. The diagnosis of IPF was confirmed by open lung biopsy. All patients fulfilled the criteria of the American Thoracic Society and European Respiratory Society for the diagnosis of IPF. Normal histology lung tissues resected from patients with lung cancer were used as controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1252
Platform:
GPL1739
26 Samples
Download data
Series
Accession:
GSE2052
ID:
200002052
4.
Full record GDS1252

Idiopathic pulmonary fibrosis

Expression profiling of lung tissues from patients with idiopathic pulmonary fibrosis (IPF), a progressive and lethal disorder characterized by the abnormal formation of fibrous scar tissue in the lungs. Results provide insight into the pathogenesis of IPF.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 disease state sets
Platform:
GPL1739
Series:
GSE2052
26 Samples
Download data
5.

Defining the Activated Fibroblast Population in Lung Fibrosis Using Single Cell Sequencing

(Submitter supplied) In brief, we have applied a novel and unbiased approach to identify distinct and dynamic cell populations, including an in-depth analysis of the fibroblast population, in lung fibrosis. We found that while fibroblast number did not increase after injury, a population of activated fibroblasts can be identified in the fibrotic mouse lung. Using expression profiles of 1,945 lung fibroblasts we redefine the molecular characteristics of activated fibroblasts, finding that they are not a separate population but rather exhibit a similar, yet amplified, gene expression pattern to non-activated cells.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
11 Samples
Download data: MTX, TSV
Series
Accession:
GSE129605
ID:
200129605
6.

miR-29 targets in human fetal lung fibroblast IMR-90 cells

(Submitter supplied) TGFβ is one of most intensively studied regulators of extracellular matrix formation, and has been implicated in the development of pulmonary fibrosis in different models. However, little is know about the role of miRNAs in TGFβ mediated fibrogenic gene regulation. By using miRNA qRT-PCR array, we have identified miRNAs whose expression are regulated by TGFβ in IMR-90 cells. Among those down-regulated miRNAs are miR-29 family members. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
9 Samples
Download data: CEL
Series
Accession:
GSE18651
ID:
200018651
7.

Translation value of the bleomycin rat model for the treatment of patients with Idiopathic Pulmonary Fibrosis (IPF)

(Submitter supplied) Intratracheal application of bleomycin is known to induce inflammatory and fibrotic reactions in the lung within a short period of time and histological features include infiltration of inflammatory cells, collagen deposition and obliteration of alveolar spaces. Because some of these features are found in patients with idiopathic pulmonary fibrosis (IPF), the bleomycin-induced lung fibrosis animal model is commonly used. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
72 Samples
Download data: TXT
Series
Accession:
GSE48455
ID:
200048455
8.

MMP1 and MMP7 as potential peripheral blood biomarkers in Idiopathic Pulmonary Fibrosis

(Submitter supplied) Idiopathic pulmonary fibrosis (IPF) is a chronic progressive fibrotic lung disease associated with significant morbidity and mortality. We identified a combinatorial signature of 5 proteins that was sufficient to distinguish IPF patients from controls; of these proteins MMP7 and MMP1 exhibited significantly higher values in both peripheral blood concentrations and lung tissue gene expression, suggesting their role as true biomarkers. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
46 Samples
Download data: TXT
Series
Accession:
GSE10667
ID:
200010667
9.

Tetraspanin CD151 protects against pulmonary fibrosis by maintaining epithelial integrity

(Submitter supplied) Comparison of gene expressions between the lungs of CD9KO and CD151KO mice A microarray study identified an enrichment of genes involved in connective tissue disorders in the lungs of CD151 KO mice, but not in CD9 KO mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE159236
ID:
200159236
10.

Alveolar Macrophage Gene Expression in Human Pulmonary Fibrosis

(Submitter supplied) Gene expression profiles for patients affected with Sporadic and Familial Pulmonary Fibrosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
84 Samples
Download data: CEL
Series
Accession:
GSE49072
ID:
200049072
11.

Bleomycin induces molecular changes directly relevant to idiopathic pulmonary fibrosis: A model for “active” disease

(Submitter supplied) Genomic profiling of RNA from cultured human fibroblasts of donor samples in the 10-14th passage was carried out to determine expression changes in the fibroblasts of individual with different degrees of pulmonary fibrosis. Donors consisted of individuals with rapid progressing pulmonary fibrosis, slow progressing pulmonary fibrosis, or no fibrosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4580
Platform:
GPL570
14 Samples
Download data: CEL
Series
Accession:
GSE44723
ID:
200044723
12.

Bleomycin induces molecular changes directly relevant to idiopathic pulmonary fibrosis: A model for “active” disease.

(Submitter supplied) Genomic profiling of bleomycin- and saline-treated mice across 7 timepoints (1, 2, 7, 14, 21, 28, 35 days post treatment) was carried out in C57BL6/J mice to determine the phases of response to bleomycin treatment which correspond to onset of active pulmonary fibrosis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
111 Samples
Download data: CEL
Series
Accession:
GSE40151
ID:
200040151
13.
Full record GDS4580

Idiopathic pulmonary fibrosis: cultured lung fibroblasts

Analysis of lung fibroblasts from individuals with rapid or slow progressing idiopathic pulmonary fibrosis (IPF). Results provide insight into molecular mechanisms underlying the different degrees of
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state sets
Platform:
GPL570
Series:
GSE44723
14 Samples
Download data: CEL
14.

miRNA expression data in idiopathic pulmonary fibrosis

(Submitter supplied) Idiopathic pulmonary fibrosis (IPF) is an untreatable fibrotic lung disease characterized by fibroblast proliferation and epithelial mesenchymal transition. The expression and role of microRNAs (miRNA) has not been studied in IPF. Using miRNA expression microarrays we identified 46 differentially expressed miRNA in IPF lungs which included let-7d and the miR-30 family. Keywords: miRNA expression
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL6955
20 Samples
Download data: TXT
Series
Accession:
GSE13316
ID:
200013316
15.

microRNA expression profiles in Idiopathic Pulmonary Fibrosis (IPF)

(Submitter supplied) Idiopathic pulmonary fibrosis (IPF) is a lethal fibrotic lung disease characterized by enhanced fibroblast proliferation, collagen synthesis, extracellular matrix deposition. We obtained 28 IPF patient lung tissue samples from the Lung Tissue Research Consortium (LTRC). Here we determined the miRNA expression profiles in these IPF lung samples.
Organism:
Homo sapiens; Mus musculus; Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL26371
29 Samples
Download data: GPR
Series
Accession:
GSE129126
ID:
200129126
16.

Gene expression profiling of chronic lung disease for the Lung Genomics Research Consortium

(Submitter supplied) Microarray data from total RNA extracted from whole lung homogenate from subjects undergoing thoracic surgery. These subjects were diagnosed as being controls or having interstitial lung disease or COPD as determined by clinical history, CT scan, and surgical pathology. There was no intervention, these are cross-sectional data. All samples are from the Lung Tissue Research Consorium (LTRC and are indexed by their LTRC tissue label).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6480 GPL14550
582 Samples
Download data: TXT
Series
Accession:
GSE47460
ID:
200047460
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