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Links from GEO DataSets

Items: 20

1.

Gene expression of mouse colon organoids treated with inflammatory reagents.

(Submitter supplied) Microarray analysis of mouse colon organoids after treatment with the mixture of inflammatory reagents.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
9 Samples
Download data: TXT
Series
Accession:
GSE153176
ID:
200153176
2.

Mouse colon organoids treated with inflammatory reagents.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL10787 GPL21810
15 Samples
Download data: TXT
Series
Accession:
GSE153178
ID:
200153178
3.

Gene expression of mouse colon organoids after the removal of inflammatory reagents.

(Submitter supplied) Microarray analysis of mouse colon organoids after the removal of inflammatory reagents following long-term treatment with inflammatory reagents.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21810
6 Samples
Download data: TXT
Series
Accession:
GSE153175
ID:
200153175
4.

Gene expression of UC organoids and UC model organoids (long-term inflammation model) derived from human colonic organoids

(Submitter supplied) Gene expression changes of human colon orgnaoids by 60weeks of inflammatory stimulation in vitro (long-term inflammed organoids) and after 10weeks from the removal of stimulation (inflammation-removed organoids). GSEA analysis was performed about RNA1-9 (Organoids #1). For the reproducibility of the analysis, GSEA was performed in triplicate. The key molecule for long-term inflammation was extracted from RNA10-12 (Organoids #2). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20844
15 Samples
Download data: TXT
Series
Accession:
GSE156806
ID:
200156806
5.

Expression data from intestinal epithelial cells (IECs)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6246 GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE57642
ID:
200057642
6.

Expression data from intestinal epithelial cells (IECs) [Mouse430_2 array]

(Submitter supplied) Polycomb group (PcG) proteins are epigenetic silencers whose dysregulation is frequently linked to cancer via mechanisms that remain unclear. Using conditional knock-out mice in a colitis-associated colorectal cancer (CAC) model, we found that Bmi1 and Mel18 are important initiation and maintenance factors during CAC tumorigenesis. Epithelial depletion of both Bmi1 and Mel18, but not either gene alone, significantly reduces tumor growth and multiplicity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE57641
ID:
200057641
7.

Expression data from intestinal epithelial cells (IECs) [MoGene-1_0-st array]

(Submitter supplied) Polycomb group (PcG) proteins are epigenetic silencers whose dysregulation is frequently linked to cancer via mechanisms that remain unclear. Using conditional knock-out mice in a colitis-associated colorectal cancer (CAC) model, we found that Bmi1 and Mel18 are important initiation and maintenance factors during CAC tumorigenesis. Epithelial depletion of both Bmi1 and Mel18, but not either gene alone, significantly reduces tumor growth and multiplicity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL
Series
Accession:
GSE57640
ID:
200057640
8.

Pathological activation of canonical nuclear-factor kB by synergy of tumor necrosis factor alpha and TNF-like weak inducer of apoptosis in mouse acute colitis

(Submitter supplied) To test the efficacy of TNFR-Fc and anti-TWEAK mAb treatment alone and in combination Tumor necrosis factor (TNF)-alpha is a major effector in various inflammatory conditions. TNF-like weak inducer of apoptosis (TWEAK) is a member of the TNF superfamily that promotes inflammatory tissue damage through its receptor, FGF-inducible molecule 14 (Fn14). Since both TWEAK and TNF-alpha have been shown to mediate pathological responses through inter-dependent or independent pathways by in vitro, the potential interplay of these pathways was investigated in a mouse colitis model. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
72 Samples
Download data: CEL
Series
Accession:
GSE53835
ID:
200053835
9.

Gene expression changes by telomere shortening in human colonic organoids

(Submitter supplied) Gene expression changes of UC-model organoids derive from human colon indcued by telomere enlongation was assessed by Madecassoside treatemt (telomerase activator). Gene expression changes of human colon organoids induced by telomere shortening was assessd by MST-312 treatment (telomerase inhibitor).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20844
8 Samples
Download data: TXT, XLSX
Series
Accession:
GSE175994
ID:
200175994
10.

RNA-sequencing study on DSS-induced ulcerative colitis in mice of wild type and intestinal epithelial cell-sepific NCoR1 deletion.

(Submitter supplied) Purpose: The goal of this study is to investigate the role of NCoR1 in protecting colon from ulcerative colitis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
16 Samples
Download data: XLSX
Series
Accession:
GSE136153
ID:
200136153
11.

Pattern of miR-31 knockout mouse colon gene expression

(Submitter supplied) To further understand different gene expression of miR-31 knockout mouse colon and normal colon, we have employed colonic epithelium microarray expression profiling as a discovery platform to identify different genes with miR-31 knockout mouse colon and normal colon.comparision with normal colonic epithelium,upgene is 285 and downgene is 178 in knockout group.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
6 Samples
Download data: TXT
Series
Accession:
GSE123556
ID:
200123556
12.

Gene Expression Changes in Non-Dysplastic Mucosa from Patients with Ulcerative Colitis Harboring Remote Neoplastic Lesions

(Submitter supplied) Background and Aims: Individuals with ulcerative colitis (UC) are at increased risk for colorectal cancer, although underlying mechanisms are incompletely understood. We sought to identify a potential gene expression signature in non-dysplastic distal mucosa that as a “genetic field effect” could be a marker for remote neoplastic lesions. Results: 468 genes were significantly up-regulated and 541 genes were significantly down-regulated >2-fold in UC patients with neoplasia compared to UC patients without neoplasia. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
20 Samples
Download data: CEL
Series
Accession:
GSE37283
ID:
200037283
13.

miRNome of colonic crypt stem cells from DSS-induced colitis mice

(Submitter supplied) To identify potential unique miRs that contribute to shaping the intestinal stemness in colitis, we analyzed the miRNome of colonic crypt stem cells from DSS-induced colitis mice.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL21265
6 Samples
Download data: TXT
Series
Accession:
GSE137892
ID:
200137892
14.

Effect of miR-494-3p on LPS-treated intestinal epithelial cells isolated from C57BL/6 mice

(Submitter supplied) The microenvironment of injured mucosa has important effects on intestinal stem cell self-renewal and reconstruction of epithelial barrier function in inflammatory bowel disease (IBD). However, the precise status of the interactions between intestinal epithelial cell (IEC) injury, particularly intestinal crypt absence, and microenvironment in IBD is not completely understood. We identified miR-494-3p as important for protection of colonic stemness in intestinal inflammation colonic organoid culture. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
2 Samples
Download data: XLS
Series
Accession:
GSE137890
ID:
200137890
15.

Effect of miR-494 deficiency on colonic crypt stem cells isolated from dextran sulfate sodium-induced colitis mice

(Submitter supplied) The microenvironment of injured mucosa has important effects on intestinal stem cell self-renewal and reconstruction of epithelial barrier function in inflammatory bowel disease (IBD). However, the precise status of the interactions between intestinal epithelial cell (IEC) injury, particularly intestinal crypt absence, and microenvironment in IBD is not completely understood. We identified miR-494-3p as important for protection of colonic stemness in intestinal inflammation colonic organoid culture. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: XLS
Series
Accession:
GSE137889
ID:
200137889
16.

RNAseq for the identification of genes induced upon TGR5 stimulation in intestinal stem cells

(Submitter supplied) Purpose: Transcriptomic exploration for the identification of genes induced upon TGR5 stimulation in intestinal stem cells Methods: For each biological replicate, GFPhi cells were isolated by FACS from intestines from 4 pooled Lgr5-eGFP-IRES-CreERT2 mice. About 200.000 GFPhi cells were then embedded in Matrigel (20.000 per well in 10µL Matrigel drop) and after 4 hours were treated with INT-777 (30µM) or DMSO as control. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
6 Samples
Download data: TAB
Series
Accession:
GSE140554
ID:
200140554
17.

Mouse colon expression in wild type and STAT5b deficient mice

(Submitter supplied) Regulation of epithelial barrier function is dependent upon precise control of cell survival and activation of inflammatory pathways in response to the enteric flora. These experiments tested differential colon gene expression relative to these pathways in wild type and STAT5b deficient mice. Keywords: Single time point in wild type and STAT5b deficient mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3385
Platform:
GPL5759
8 Samples
Download data: CEL
Series
Accession:
GSE8942
ID:
200008942
18.
Full record GDS3385

Transcription factor STAT5b deficiency effect on the colon

Analysis of colons of animals lacking the Signal Transducers and Activators of Transcription member STAT5b. STAT5b mutants are more susceptible to experimental colitis, associated with intestinal barrier function defects. Results provide insight into the role of STAT5b in colonic barrier function.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL5759
Series:
GSE8942
8 Samples
Download data: CEL
19.

Transcriptional Responses of Human Intestinal Organoids to Interferon Types I, II, and III

(Submitter supplied) RNAseq of intestinal epithelial cell (IEC) organoids derived from biopsy of ileum or colon from healthy subjects and treated with type I interferon (IFN beta), type II interferon (IFN gamma), or type III interferon (IFN lambda 2).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
35 Samples
Download data: TXT
20.

Spatiotemporally resolved ex vivo colorectal cancer development in engineered mini-colons (RNA-Seq Gpx2 KD)

(Submitter supplied) Here we developed topobiologically complex mini-colons able to undergo tumorigenesis ex vivo by integrating microfabrication, optogenetic, and tissue engineering approaches. With this system, tumorigenic transformation can be spatiotemporally controlled by directing oncogenic activation through blue-light exposure, and emerging colon tumors can be tracked in real-time with single-cell resolution for several weeks without breaking the culture. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: TXT
Series
Accession:
GSE246568
ID:
200246568
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