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Links from GEO DataSets

Items: 17

1.
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
2.

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
3.

Microarray analysis of colonic mucosa gene expression in wild type and foxo4 knock out mice

(Submitter supplied) Analysis of mechano-regulation of tenocyte metabolism at gene expression level. The hypothesis tested in the present study was that cyclic tensile strain influence the balance of anabolism/catabolism of tenocytes. Forkhead box O (FoxO) proteins are a family of transcription factors implicated in many biological processes including immune regulation. In this study, we found that mice null for Foxo4, a member of the FoxO family, are more susceptible to 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis than wild type controls. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6105
6 Samples
Download data: TXT
Series
Accession:
GSE16033
ID:
200016033
4.

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
5.

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
6.

The Molecular Mechanism for EZH2 Function in DSS-induced Colitis

(Submitter supplied) Here we employed the genetically engineered mice models (GEM) to uncover the role of gut epithelial EZH2 in the pathogenesis of colitis. To dissect the underlying mechanism, Chip-Seq analysis is used for mechanistic study. From the result we find EZH2 mainly targeted in the TSS region. As we have known TNF-alpha pathway can be regulated by EZH2, we try and find TRAF2/5 may be the key point for EZH2 to regulated TNF-alpha pathway. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
2 Samples
Download data: BW
Series
Accession:
GSE84858
ID:
200084858
7.

The Role of Epithelium EZH2 in Experimental Colitis

(Submitter supplied) Despite recent progress, the contribution of epigenetic mechanisms to govern Inflammatory bowel disease (IBD) pathogenesis remains elusive. Here we show that epithelial EZH2, the catalytic subunit of PRC2 is critical for experimental colitis. Depletion of EZH2 in intestinal epithelial cells sensitized the cells to DSS-induced colitis in mice. To dissect underlying mechanism, we conducted gene expression profile analysis (RNA-Seq) by using primary Intestinal epithelial cells (IECs) isolated from EZH2 WT and KO mice to gain molecular insights into the affected biological processes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
4 Samples
Download data: TXT
Series
Accession:
GSE84857
ID:
200084857
8.

Sex-dependent and STAT5b-dependent Liver Gene Expression

(Submitter supplied) A series of dual-channel gene expression profiles obtained using Rosetta/Merck Mouse TOE 75k microarrays was used to examine the sex-dependent and STAT5b-dependent differences in gene expression in adult mouse liver. This series is comprised of 4 pools of 3 randomly chosen independent wildtype male and female mouse liver cDNA samples and 4 pools of 3 randomly chosen independent STAT5b-deficient male and female mouse liver cDNA samples, totaling 16 pools. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3562
12 Samples
Download data
Series
Accession:
GSE5072
ID:
200005072
9.

Murine Liver Cells: Control B6 males vs. little (GH-deficient) and Tfm (AR-null) males

(Submitter supplied) Transcriptional profiling of mouse whole liver comparing control WT B6 mice with B6 growth hormone-deficient little, B6 androgen receptor-null Tfm mice, and STAT5b KOs normalized to WT on B6 and BALB/c backgrounds. All animals were 10-week-old males initiated with DEN. Oberley et al. Molecular carcinogenesis 2014 May 17. doi: 10.1002/mc.22165.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
21 Samples
Download data: TXT
Series
Accession:
GSE60253
ID:
200060253
10.

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
11.

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
12.

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
13.

Sex-dependent and strain-dependent gene liver gene expression

(Submitter supplied) A series of dual-channel gene expression profiles obtained using Agilent Mouse TOE 75k microarrays was used to examine the sex-dependent differences in gene expression across three outbred mouse strains, 129J x Black Swiss, 129J x BALB/c, and ICR. This series is comprised of samples obtained from 3 pools of randomly chosen independent cDNA samples of male and female 129Jx BALB/c mice and 3 randomly chosen independent cDNA samples of male and female 129J x Black Swiss mice and 5 randomly chosen independent cDNA samples of male and female ICR mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3562
10 Samples
Download data: TXT
Series
Accession:
GSE7170
ID:
200007170
14.

Sex-dependent and STAT5a-dependent Liver Gene Expression

(Submitter supplied) A series of dual-channel gene expression profiles obtained using Agilent Mouse TOE 75k microarrays was used to examine the sex-dependent and STAT5a-dependent differences in gene expression in adult mouse liver. This series is comprised of 3 randomly chosen independent male and female wildtype mouse liver cDNA samples and 3 randomly chosen independent male and female STAT5a-deficient mouse liver cDNA samples, totalling 12 samples. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3562
12 Samples
Download data: TXT
Series
Accession:
GSE7169
ID:
200007169
15.

m6A mRNA modification is a rheostat to maintain colonic epithelial cell homeostasis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21273 GPL19057
6 Samples
Download data
Series
Accession:
GSE171423
ID:
200171423
16.

m6A mRNA modification is a rheostat to maintain colonic epithelial cell homeostasis [scRNA-seq]

(Submitter supplied) The function of m6A modification in colonic epithelial cells has been validated in our study that depletion of METTL14 in colonic epithelial cells triggers cell death. To further explore the biological effects of m6A deficiency in colonic epithelial cell heterogeneity, we performed single cell RNA-seq of colonic epithelial cells form 2-week-old Mettl14-KO and WT control mice
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
2 Samples
Download data: TXT
Series
Accession:
GSE171422
ID:
200171422
17.

m6A mRNA modification is a rheostat to maintain colonic epithelial cell homeostasis [bulkRNA-seq]

(Submitter supplied) The function of m6A modification in colonic epithelial cells has been validated in our study that depletion of METTL14 in colonic epithelial cells triggers cell death. To further explore the biological effects of m6A deficiency in colonic epithelial cells, we performed RNA sequencing analysis of colonic epithelial cells form 2-week-old Mettl14-KO and WT control mice.The bioinformatic analysis revealed that METTL14 depletion increased the mRNA expression of NF-kB inhibitor Nfkbia, which favored TNF-induced cell death.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
4 Samples
Download data: TXT
Series
Accession:
GSE171421
ID:
200171421
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