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Links from GEO DataSets

Items: 16

1.

Aging and obesity prime the methylome and transcriptome of adipose stem cells for disease and dysfunction [RNA-seq]

(Submitter supplied) The epigenome of stem cells occupies a critical interface between genes and environment, serving to regulate expression through modification by intrinsic and extrinsic factors. We hypothesized that aging and obesity, which represent major risk factors for a variety of diseases, synergistically modify the epigenome of adult adipose stem cells (ASCs). Using integrated RNA- and targeted bisulfite-sequencing in murine ASCs from lean and obese mice at 5- and 12-months of age, we identified global DNA hypomethylation with either aging or obesity, and a synergistic effect of aging combined with obesity. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
30 Samples
Download data: TXT
Series
Accession:
GSE251721
ID:
200251721
2.

Aging and obesity prime the methylome and transcriptome of adipose stem cells for disease and dysfunction

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL17021
53 Samples
Download data: BEDGRAPH
Series
Accession:
GSE251722
ID:
200251722
3.

Aging and obesity prime the methylome and transcriptome of adipose stem cells for disease and dysfunction [Methyl-seq]

(Submitter supplied) The epigenome of stem cells occupies a critical interface between genes and environment, serving to regulate expression through modification by intrinsic and extrinsic factors. We hypothesized that aging and obesity, which represent major risk factors for a variety of diseases, synergistically modify the epigenome of adult adipose stem cells (ASCs). Using integrated RNA- and targeted bisulfite-sequencing in murine ASCs from lean and obese mice at 5- and 12-months of age, we identified global DNA hypomethylation with either aging or obesity, and a synergistic effect of aging combined with obesity. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL17021
23 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE251720
ID:
200251720
4.

Adipose derived stem cells (ASCs) methylation differences between lean and obese individuals

(Submitter supplied) Pathological expansion of adipose tissue (AT) in obesity is supported by adipocyte precursors, termed adipose-derived stromal/stem cells (ASCs). Elucidation of mechanisms underlying ASC function may lead to therapeutic interventions to treat fat mass accumulation. Using epigenome-wide association studies, we explored the impact of obesity on the methylation signature of human ASCs.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
12 Samples
Download data: CSV, IDAT
Series
Accession:
GSE111632
ID:
200111632
5.

Transcriptome and DNA methylome of mouse Müller glia

(Submitter supplied) Müller cells are the primary glia of the neural retina and play crucial roles in maintaining the structural and functional homeostasis of the retina. Müller cells also possess certain levels of retinal regeneration capacity, especially in lower vertebrates. In this study, we deep sequenced the transcriptomes and methylomes of mouse Müller cells and early retinal progenitor cells (RPCs), as well as Müller cells from injured retinas and aged retinas, which will help to reveal molecular mechanisms governing Müller cells development, physiological functions and regeneration activities.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL21273
22 Samples
Download data: TXT
Series
Accession:
GSE124532
ID:
200124532
6.

Early Chronological Aging in Human Adipose-Derived Stem Cells Marked by Distinct Transcriptional Regulation Compared to Differentiated Cells

(Submitter supplied) Aging is a complex process characterized by a progressive decline in physiological integrity that leads to impaired cellular and tissue function. Adult stem cells play a critical role in organismal health and aging. Their age-related deterioration contributes to a reduced homeostatic and regenerative capacity. Notably, most studies of stem cell aging focus on the mechanisms of replicative aging in stem cells with high cellular turnover. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
40 Samples
Download data: TXT
7.

Skeletal glucocorticoid signaling determines aging-related leptin resistance and obesity

(Submitter supplied) Aging contributes to many chronic conditions, including central obesity, insulin resistance and osteoporosis, which are also critical features of glucocorticoid excess. To investigate tissue-specific sites of glucocorticoid (GC) action during aging, we disrupted GC signalling in mouse osteoblasts via transgenic overexpression of the GC-inactivating enzyme, 11β-hydroxysteroid-dehydrogenase type 2 (11β-HSD2). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
24 Samples
Download data: CEL
Series
Accession:
GSE141448
ID:
200141448
8.

The diurnal rhythm of adipose tissue gene expression is reduced in obese patients with type 2 diabetes

(Submitter supplied) Animal studies have linked disturbed adipose tissue clock gene rhythms to the pathophysiology of the metabolic syndrome. However, data on molecular clock rhythms in human patients are limited. Therefore, in a standardized real life setting, we compared diurnal gene expression profiles in subcutaneous adipose tissue between obese patients with type 2 diabetes and age-matched healthy lean control subjects, using RNA sequencing. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16558
48 Samples
Download data: TXT, XLSX
Series
Accession:
GSE104674
ID:
200104674
9.

Genome-wide lung transcriptional profiling of mouse models for pneumonia given human adipose-derived mesenchymal stem cells treatment or Prekallikrein

(Submitter supplied) Adult mesenchymal stem cells exert immunomodulatory effects that might improve the host response during sepsis. Knowledge on the effect of adipocyte-derived mesenchymal stem cells (ASCs) in sepsis is limited. Klebsiella (K.) pneumoniae is a common cause of gram-negative pneumonia and sepsis. The aim of this study was to determine the effect of human ASCs on the host response during pneumosepsis in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL24242
47 Samples
Download data: CEL
Series
Accession:
GSE121970
ID:
200121970
10.

RNA-seq analysis of abdominal and gulteofemoral adipose derived stem cells isolated form PCOS and control women

(Submitter supplied) RNA-seq experiments revealed an ABD-and GF-ASC selective gene expression signature between PCOS and control women.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
16 Samples
Download data: TXT
Series
Accession:
GSE193812
ID:
200193812
11.

Human and feline adipose-derived mesenchymal stem cells have comparable immunomodulatory functions

(Submitter supplied) Adipose-derived mesenchymal stem cells (ASCs) are a promising cell therapy to treat inflammatory and immune-mediated diseases. Development of appropriate pre-clinical animal models is critical to determine safety and attain early efficacy data for the most promising therapeutic candidates. Naturally occurring diseases in cats already serve as valuable models to inform human clinical trials in oncologic, cardiovascular and genetic diseases. more...
Organism:
Felis catus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23056
3 Samples
Download data: TXT
Series
Accession:
GSE94773
ID:
200094773
12.

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
13.

Novel Alterations in Chromatin Structure during Aging Reveal Cell-Specific Differential Expression of SUMO Proteins

(Submitter supplied) We investigated the chromatin accessibility of primary human adipose-derived stem cells (ASCs) and fibroblasts during chronological aging using ATAC-seq technology. our data suggest a significant role for nucleosome positioning in sumoylation pathway regulation in response to stress during aging of adult stem cells.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
21 Samples
Download data: BIGWIG
Series
Accession:
GSE105077
ID:
200105077
14.

RNA sequencing of brown adipose tissue of lean and obese mice

(Submitter supplied) We report differential expressed genes in brown adipose tissue of mice fed with a low-fat diet or a high-fat diet.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE112740
ID:
200112740
15.

Genome-wide analysis of gene expression in adipose tissue of female mice after continuous high fat diet feeding

(Submitter supplied) Analysis of gene expression in adipose tissue of female mice after continuous high fat diet (HFD) feeding for three generations. The hypothesis in this study is that continuous HFD feeding has transgenerational amplification effects to the offspring. Results provide important information on the impacts of over-nutrition over one generation on the offspring, such as transgenerational up-regulated or down-regulated genes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
4 Samples
Download data: TXT
Series
Accession:
GSE37238
ID:
200037238
16.

Transcriptome analysis of metabolic tissues in young and aged mice

(Submitter supplied) Studies on aging have largely included one or two OMICS layers, which may not necessarily reflect the signatures of other layers. Moreover, most aging studies have often compared very young (4-5 wks) mice with old (24 months) mice which does not reflect the aging transition after the attainment of adulthood. Therefore, we aimed to study and compared muti-OMICS aging signatures across key metabolic tissues of mature adults (6 months) and old (24 months) C57BL/6J mice (the most commonly used mouse strain). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6246 GPL20258
28 Samples
Download data: CEL
Series
Accession:
GSE120290
ID:
200120290
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