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Links from GEO DataSets

Items: 10

1.
Full record GDS4942

Glucose effect on young pancreatic islets: dose response and time course

Analysis of islets isolated from young animals and cultured at 3mM glucose (G3) for 10 hr (T0) and then challenged with 11mM glucose for 1 hr (T1) and 4 hr (T4). Islets cultured at G3 for 2 days were also examined. Results provide insight into the kinetics of molecular response of islets to glucose.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 dose, 4 time sets
Platform:
GPL1261
Series:
GSE42591
8 Samples
Download data: CEL
DataSet
Accession:
GDS4942
ID:
4942
2.

Gene-expression profiles of primary cultures of cortical neurons and astrocytes.

(Submitter supplied) We used microarrays to compare the global programme of gene expression in primary cultures of neurons and astrocytes. These data sets were compared to the expression profiles of other tissues, including pancreatic islets, in order to identify a specific neuroendocrine program in pancreatic islets.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE42607
ID:
200042607
3.

Expression data from fresh and cultured islets at different glucose concentrations

(Submitter supplied) β-cell identity is determined by tightly regulated transcriptional networks that are modulated by extracellular cues, thereby ensuring β-cell adaptation to the organism’s insulin demands. We have observed in pancreatic islets that stimulatory glucose concentrations induced a gene profile that was similar to that of freshly isolated islets, indicating that glucose-elicited cues are involved in maintaining β-cell identity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS4939 GDS4942
Platform:
GPL1261
26 Samples
Download data: CEL
Series
Accession:
GSE42591
ID:
200042591
4.
Full record GDS4939

Glucose effect on young and aged pancreatic islets: dose response

Analysis of islets isolated from young and aged animals and cultured for 2 days at 3 to 16mM glucose (G3 to G16). Freshly-isolated islets were also examined. Ageing is associated with functional changes in beta cells. Results provide insight into the molecular response of aged islets to glucose.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 age, 5 dose, 2 protocol sets
Platform:
GPL1261
Series:
GSE42591
20 Samples
Download data: CEL
DataSet
Accession:
GDS4939
ID:
4939
5.

In vivo effects of short-term treatment with Bisphenol A (BPA) on mice pancreatic islets

(Submitter supplied) Bisphenol-A (BPA) is one of the most widespread endocrine disrupting chemicals (EDC) used as the base compound in the manufacture of polycarbonate plastics. Although evidence points to consider exposure to BPA as a risk factor for the development of Diabetes, its actions on whole body metabolism and on pancreatic beta cells are still unclear. The aim of this study was to study the in vivo effects of BPA on mice pancreatic islets, particularly on how it could regulate ion channels expression and function. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE126297
ID:
200126297
6.

Reduced insulin secretion in WFS1-deficient mice may be related to downregulation of Trpm5

(Submitter supplied) Wolfram syndrome, an autosomal recessive disorder characterized by juvenile-onset diabetes mellitus and optic atrophy, is caused by mutations in the WFS1 gene. WFS1 encodes an endoplasmic reticulum resident transmembrane protein. The Wfs1-null mice exhibit progressive insulin deficiency and diabetes. The aim of the present study was to describe the insulin secretion and transcriptome of pancreatic islets in WFS1-deficient mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15907
12 Samples
Download data: TXT
Series
Accession:
GSE65929
ID:
200065929
7.

Transcriptome analysis of islets from diabetes-resistant and diabetes-prone obese mice reveals novel gene regulatory networks involved in beta cell compensation and failure

(Submitter supplied) We carried out genome-wide transcriptome analysis of islets to investigate the gene expression landscape of ob/ob and db/db mouse models at 6 and 16 weeks of age. The purpose of this study is to determine the changes in the islet transcriptomic landscape that mediate the processes of beta cell compensation and failure in ob/ob and db/db mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL16570 GPL17400
18 Samples
Download data: CEL
Series
Accession:
GSE169275
ID:
200169275
8.

A Gene Expression Network Model of Type 2 Diabetes Links Cell Cycle

(Submitter supplied) Insulin resistance is necessary but not sufficient for the development of type 2 diabetes. Diabetes results when pancreatic beta-cells fail to compensate for insulin resistance by increasing insulin production through an expansion of beta-cell mass or increased insulin secretion. Communication between insulin target tissues and beta-cells may initiate this compensatory response. Correlated changes in gene expression between tissues can provide evidence for such intercellular communication. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3677
240 Samples
Download data
Series
Accession:
GSE10785
ID:
200010785
9.

Transcriptional analysis of islets of Langerhans from organ donors of different ages

(Submitter supplied) Islet function diminishes with age and as such the incidence of type 2 diabetes increases. The cause of this is unknown. In this study whole islets were extracted with laser capture microdissection from organ donors 1-81 years of age. Increasing age was associated with a downregulation of pathways associated with the cell cycle and increase in markers of senescence e.g. CDKN2A. Among novel genes increasing with age was SPP1.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24014
35 Samples
Download data: XLSX
Series
Accession:
GSE165121
ID:
200165121
10.

A histological and transcriptional characterization of the pancreatic acinar tissue in type 1 diabetes

(Submitter supplied) Despite reduced function and volume of the exocrine pancreas in type 1 diabetes, literature describing the histology and the molecular biological profile in this area is limited. Here, the density of acinar cells was examined adjacent to and at varying distances from islets and the transcriptome was analyzed on laser capture microdissected (LCM) tissue from organ donors with and without type 1 diabetes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24014
59 Samples
Download data: CSV, TXT
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