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Links from GEO DataSets

Items: 8

1.
Full record GDS5167

Type 2 diabetic obese patients: visceral adipose tissue CD14+ cells

Analysis of visceral adipose tissue CD14+ cells isolated from obese, type 2 diabetic patients. Obesity is marked by changes in the immune cell composition of adipose tissue. Results provide insight into the molecular basis of proinflammatory cytokine production in obesity-linked type 2 diabetes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL10558
Series:
GSE54350
12 Samples
Download data
DataSet
Accession:
GDS5167
ID:
5167
2.

Genome wide analysis of Visceral adipose tissue CD14+ cells from Obese and obese diabetic subjects

(Submitter supplied) Identification of the inflammatory signature in visceral adipose tissue CD14+ cells (adipose tissue macrophage) Total RNA obtained from CD14+ cells (Immunoselcted cells from stromal adipose tissue cells)
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5167
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE54350
ID:
200054350
3.

Expression data of the BMDMs from GPS2 WT and MKO mice

(Submitter supplied) Obesity is a major risk factor for metabolic disorders like insulin resistance and diabetes. We previously identified GPS2 as a clinical relavant repressor of metaflammation. No animal KO models were used to study its physiological function in vivo. The role of GPS2 in macrophage activation and inflammation is also largely unknown. Here we developed a GPS2 myeloid specific KO mice to study the regulation of GPS2 in macrophage inflammation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
6 Samples
Download data: CEL
Series
Accession:
GSE66874
ID:
200066874
4.

GPS2 cistrome analysis in BMDMs and RAW264.7 cells and epigenome comparison between WT and GPS2-knockout BMDMs.

(Submitter supplied) GPS2 binding sites in BMDMs can be localized specially in enhancers (H3K27ac) and promoters (H3K27ac, H3K4me3). Upon GPS2 knock-out in BMDMs, de-repression of certain inflammatory genes occur, as accompanied by increased recruitment of H3K27ac and H3K4me3 marks.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
15 Samples
Download data: TXT
Series
Accession:
GSE66774
ID:
200066774
5.

IL-37 protects against obesity-induced inflammation and insulin resistance

(Submitter supplied) Cytokines of the IL-1 family are important modulators of obesity-induced inflammation and the development of systemic insulin resistance. Here, we report that IL-37, a newly-described antiinflammatory member of the IL-1 family, affects obesity-induced inflammation and insulin resistance. IL-37 transgenic mice (IL-37tg) did not develop an obese phenotype in response to a high-fat diet (HFD). Unlike WT mice, IL-37tg mice exhibited reduced numbers of adipose tissue macrophages and preserved glucose tolerance and insulin sensitivity after 16 weeks of HFD. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
8 Samples
Download data: CEL
Series
Accession:
GSE58952
ID:
200058952
6.

Transcriptome profile of subcutaneous adipocytes isolated from obese vs. lean postmenopausal women

(Submitter supplied) Adipocytes isolated from lean and obese postmenopausal women with no significant differences in metabolic syndrome parameters demonstrate changes in multiple inflammatory, metabolic and structural gene families.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
14 Samples
Download data: TXT
Series
Accession:
GSE44000
ID:
200044000
7.

Specific metabolic activation of adipose tissue macrophages during obesity promotes inflammatory responses

(Submitter supplied) Recent studies have identified intracellular metabolism as a fundamental determinant of macrophage function. In obesity, proinflammatory macrophages accumulate in adipose tissue and trigger chronic low-grade inflammation, that promotes the development of systemic insulin resistance, yet changes in their intracellular energy metabolism are currently unknown. We therefore set out to study metabolic signatures of adipose tissue macrophages (ATMs) in lean and obese conditions. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
8 Samples
Download data: CEL
Series
Accession:
GSE84000
ID:
200084000
8.

SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetes.

(Submitter supplied) Obesity induces macrophages to drive inflammation in adipose tissue, a crucial step towards the development of type 2 diabetes. The tricarboxylic acid (TCA) cycle intermediate succinate is released from cells under metabolic stress and has recently emerged as a metabolic signal induced by proinflammatory stimuli. We therefore investigated whether succinate receptor 1 (SUCNR1) could play a role in the development of adipose tissue inflammation and type 2 diabetes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
8 Samples
Download data: CEL
Series
Accession:
GSE64104
ID:
200064104
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Supplemental Content

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