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Links from GEO DataSets

Items: 20

1.

RNA-sequencing of healthy human skeletal myocytes

(Submitter supplied) Skeletal myocytes are metabolically active and susceptible to insulin resistance, thus implicated in type 2 diabetes (T2D). This complex disease involves systemic metabolic changes and their elucidation at the systems level requires genome-wide data and biological networks. Genome-scale metabolic models (GEMs) provide a network-context to integrate high-throughput data. We generated myocyte-specific RNA-seq data and investigated their correlation with proteome data. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL16791
6 Samples
Download data: TXT
2.

RNA-sequencing of human skeletal myocytes from healthy, obese, and type 2 diabetic subjects

(Submitter supplied) Skeletal muscle is one of the primary tissues involved in the development of type 2 diabetes (T2D). Obesity is tightly associated with T2D, making it challenging to isolate specific effects attributed to the disease alone. By using an in vitro myocyte model system we were able to isolate the inherent properties retained in myocytes originating from donor muscle precursor cells, without being confounded by varying extracellular factors present in the in vivo environment of the donor. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL16791 GPL11154
90 Samples
Download data: TXT
3.

Transcription profiling of myotubes from patients with type 2 diabetes

(Submitter supplied) Microarray-based studies of skeletal muscle from patients with type 2 diabetes and high-risk individuals have demonstrated that insulin resistance and reduced mitochondrial biogenesis co-exist early in the pathogenesis of type 2 diabetes independent of hyperglycaemia and obesity. It is unknown whether reduced mitochondrial biogenesis or other transcriptional alterations co-exist with impaired insulin-responsiveness in primary human muscle cells from patients with type 2 diabetes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3681
Platform:
GPL8300
20 Samples
Download data: CEL
Series
Accession:
GSE12643
ID:
200012643
4.
Full record GDS3681

Type 2 diabetes: myotube

Analysis of myotube cell lines established from type 2 diabetes (T2D) subjects. Insulin resistance and reduced mitochondrial biogenesis coexist early in T2D pathogenesis independent of hyperglycemia and obesity. Results provide insight into the effect of T2D on developing skeletal muscle cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL8300
Series:
GSE12643
20 Samples
Download data: CEL
DataSet
Accession:
GDS3681
ID:
3681
5.

Transcriptomic study of heart tissue from diabetic cardiomyopathy mice

(Submitter supplied) To explore the key genes involved in spontaneous diabetic cardiomyopathy, db/db and BKS mice were used to examine the differently expressed genes in the related progresses. Briely, the heart transcriptome of db/db and BKS mice was correlated with the heart function, cardiomyocyte ultrastructure and histopathology characters.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
10 Samples
Download data: CSV
Series
Accession:
GSE161931
ID:
200161931
6.

Skeletal muscle enhancer interactions identify genes controlling whole body metabolism in humans

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other; Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154
43 Samples
Download data
Series
Accession:
GSE126102
ID:
200126102
7.

Skeletal muscle enhancer interactions identify genes controlling whole body metabolism in humans [RNA-seq]

(Submitter supplied) Obesity and type 2 diabetes (T2D) are metabolic disorders influenced by lifestyle and genetic factors, and characterized by insulin resistance in skeletal muscle, a prominent site of glucose disposal. Numerous genetic variants have been associated with obesity and T2D, of which the majority is located in non-coding DNA regions. This suggest that most variants mediate their effect by altering the activity of gene-regulatory elements, including enhancers. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: CSV
8.

Skeletal muscle enhancer interactions identify genes controlling whole body metabolism in humans [cHiC-seq]

(Submitter supplied) Obesity and type 2 diabetes (T2D) are metabolic disorders influenced by lifestyle and genetic factors, and characterized by insulin resistance in skeletal muscle, a prominent site of glucose disposal. Numerous genetic variants have been associated with obesity and T2D, of which the majority is located in non-coding DNA regions. This suggest that most variants mediate their effect by altering the activity of gene-regulatory elements, including enhancers. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
6 Samples
Download data: CSV
Series
Accession:
GSE126100
ID:
200126100
9.

Skeletal muscle enhancer interactions identify genes controlling whole body metabolism in humans [ChIP-seq]

(Submitter supplied) Obesity and type 2 diabetes (T2D) are metabolic disorders influenced by lifestyle and genetic factors, and characterized by insulin resistance in skeletal muscle, a prominent site of glucose disposal. Numerous genetic variants have been associated with obesity and T2D, of which the majority is located in non-coding DNA regions. This suggest that most variants mediate their effect by altering the activity of gene-regulatory elements, including enhancers. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
25 Samples
Download data: BED, BW, CSV
Series
Accession:
GSE126099
ID:
200126099
10.

Multi-Omic Integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in type 2 diabetic obesity [Methylation data]

(Submitter supplied) Analysis of skeletal muscle DNA methylation from type 2 diabetic volunteers before and after 16 weeks of chronic exercise training (two groups, one undergoing aerobic excercise and the other resistance training exercise)
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
34 Samples
Download data: TXT
Series
Accession:
GSE58280
ID:
200058280
11.

Multi-Omic Integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in type 2 diabetic obesity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array; Expression profiling by array; Methylation profiling by array
Platforms:
GPL13534 GPL14613 GPL10558
102 Samples
Download data: CEL, CHP
Series
Accession:
GSE58250
ID:
200058250
12.

Multi-Omic Integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in type 2 diabetic obesity [mRNA data]

(Submitter supplied) Analysis of skeletal muscle gene expression from type 2 diabetic volunteers before and after 16 weeks of chronic exercise training (two groups, one undergoing aerobic ecercise and the other resistance training exercise)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
34 Samples
Download data: TXT
Series
Accession:
GSE58249
ID:
200058249
13.

Multi-Omic Integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in type 2 diabetic obesity [miRNA data]

(Submitter supplied) Analysis of skeletal muscle miRNA expression from type 2 diabetic volunteers before and after 16 weeks of chronic exercise training (two groups, one undergoing aerobic ecercise and the other resistance training exercise)
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL14613
34 Samples
Download data: CEL, CHP
Series
Accession:
GSE58248
ID:
200058248
14.

Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures

(Submitter supplied) We have previously reported that providing a control diet to obese and diabetic mice during the periconceptional/gestation/lactation period, led to a drastic sex-specific shift from susceptibility to resistance to high fat feeding (HFD) in the female offspring. In the present study, we aimed to characterize exhaustively the metabolic phenotype of F1 and F2 sensitive (S1, S2) and resistant (R1, R2) mice and underscore in the liver, muscle and adipose tissue, the transcriptional and epigenetic mechanisms supporting the response to HFD, the trait of resistance/susceptibility and the adaptation across generations. more...
Organism:
Mus musculus; Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL13688
19 Samples
Download data: GPR, TXT
Series
Accession:
GSE30085
ID:
200030085
15.

FTO: gene expression and function in skeletal muscle

(Submitter supplied) We identified the target genes of FTO ("fat mass and obesity associated") in primary cultures of human skeletal muscle cells using adenoviral vectors expressing FTO or GFP and oligonucleotide microarrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1456
4 Samples
Download data: GPR
Series
Accession:
GSE22857
ID:
200022857
16.

Methylated DNA Immunoprecipitation (MeDIP) using a custom type 2 diabetes and related phenotypes array

(Submitter supplied) Custom array designed to tile Linkage Disequilibrium Blocks of T2D GWAS SNPs, monogenic candidates for T2D and Obesity, and all plausible imprinted loci from human and mouse data.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL10113
60 Samples
Download data: PAIR
Series
Accession:
GSE20553
ID:
200020553
17.

Novel Transcriptome Profiling Analyses Demonstrate that Selective PPARg Modulators Display Attenuated and Selective Gene Regulatory Activity in Comparison with PPARg Full Agonists

(Submitter supplied) We conducted extensive transcriptome profiling studies to characterize 70 SPPARgMs and seven PPARg full agonists in 3T3-L1 adipocytes, and a subset of these ligands in adipose tissue of diabetic db/db mice. In both cases, the SPPARgMs generated attenuated gene regulatory responses, and their gene expression signatures were more enriched in metabolic pathways that are likely to mediate anti-diabetic efficacy than those of PPARg full agonists. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13717
331 Samples
Download data
Series
Accession:
GSE31222
ID:
200031222
18.

Gene expression in PBMCs from children with diabetes

(Submitter supplied) Objective: We hypothesized that type 1 diabetes (T1D) is accompanied by changes in gene expression in peripheral blood mononuclear cells (PBMCs) due to dysregulation of adaptive and innate immunity, counterregulatory responses to immune dysregulation, insulin deficiency and hyperglycemia. Research Design and Methods: Microarray analysis was performed on PBMCs from 43 patients with newly diagnosed T1D, 12 patients with newly diagnosed type 2 diabetes (T2D) and 24 healthy controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS3874 GDS3875
Platforms:
GPL97 GPL96
234 Samples
Download data: CEL
Series
Accession:
GSE9006
ID:
200009006
19.
Full record GDS3875

Diabetic children: peripheral blood mononuclear cells (U133B)

Analysis of PBMCs from children (2-18 years) with newly diagnosed type 1 or 2 diabetes (T1D or T2D). One and 4 month samples were obtained from 20 of the T1D patients. Results provide insight into molecular mechanisms that distinguish T1D and T2D and those that are common to both forms of diabetes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state, 2 gender, 4 time sets
Platform:
GPL97
Series:
GSE9006
117 Samples
Download data: CEL
DataSet
Accession:
GDS3875
ID:
3875
20.
Full record GDS3874

Diabetic children: peripheral blood mononuclear cells (U133A)

Analysis of PBMCs from children (2-18 years) with newly diagnosed type 1 or 2 diabetes (T1D or T2D). One and 4 month samples were obtained from 20 of the T1D patients. Results provide insight into molecular mechanisms that distinguish T1D and T2D and those that are common to both forms of diabetes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state, 2 gender, 4 time sets
Platform:
GPL96
Series:
GSE9006
117 Samples
Download data: CEL
DataSet
Accession:
GDS3874
ID:
3874
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