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Links from GEO DataSets

Items: 8

1.

Short-term effects of Elastase inhibition on human islets protein phosphorylation

(Submitter supplied) To evaluate the short-term effect of elastase inhibition using telaprevir or sivelestat or DMSO on human islets
Organism:
Homo sapiens
Type:
Protein profiling by protein array
Platform:
GPL26730
24 Samples
Download data: XLSX
Series
Accession:
GSE189986
ID:
200189986
2.

Long-term effects of Elastase inhibition on human islets at single-cell resolution

(Submitter supplied) To evaluate the long-term effect of elastase inhibition using telaprevir, sivelestat, or DMSO on human islet cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
12 Samples
Download data: CSV
Series
Accession:
GSE190447
ID:
200190447
3.

Abnormal exocrine-endocrine cell crosstalk promotes β-cell dysfunction and loss in MODY8

(Submitter supplied) MODY8 (maturity-onset diabetes of the young, type 8) is a dominantly inherited monogenic form of diabetes associated with frameshift mutations in the carboxyl ester lipase (CEL) gene expressed by pancreatic acinar cells. Patients carrying the mutation develop childhood-onset exocrine pancreas dysfunction followed by the manifestation of diabetes during adulthood. However, it is unclear how CEL mutations cause diabetes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
29 Samples
Download data: CSV
Series
Accession:
GSE185430
ID:
200185430
4.

Gene expression in 832/13 INS1 beta-cells transduced with lentiviral vector conferring expression of GFP or Pax5

(Submitter supplied) We found PAX5 to be overexpressed in human pancreatic islets of donors from donors with type 2 diabetes compared to islets from non-diabetic individuals. Functional follow-up showed that Pax5 overexpression in rat clonal beta-cells (832/13 INS1) results in impaired insulin secretion. Microarrays were used to investigate if overexpression of Pax5 alters the gene expression profile of 832/13 INS1 beta-cells.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL23040
16 Samples
Download data: CEL
Series
Accession:
GSE211310
ID:
200211310
5.

Modeling pancreatic beta cell senescence by induction of DNA double-strand breaks

(Submitter supplied) Pancreatic beta cell senescence occurs during the development of Type 1 Diabetes. To model the transcriptional responses of islet cells to DNA damage, we previously developed a human islet culture model in which the DNA damage response and senescence can be induced via double strand-breaks with the agent bleomycin. Here, we report the transcriptome-wide changes in human pancreatic islet cells following bleomycin exposure.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: XLSX
6.

Genome-wide RNA sequencing of B6 mouse islets

(Submitter supplied) Isoform quantification results for B6 mouse using Bowtie and RSEM.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
1 Sample
Download data: TSV
Series
Accession:
GSE76477
ID:
200076477
7.

Genome-wide RNA-sequencing of mouse islets 48 hour after transduction with adenoviruses expressing either GFP (control), or constitutively active forms of the transcription factors, Nfatc1 or Nfatc2.

(Submitter supplied) Genetic variation at ~160 gene loci is associated with type 2 diabetes (T2D). Using an F2 mouse intercross segregating for T2D, we searched for a driver of GWAS gene expression and found that ~40% of the GWAS genes are regulated in trans by a locus on chromosome 2 in islets. We identified Nfatc2 as a candidate driver of GWAS gene expression. Overexpression of Nfatc2 induced β-cell proliferation in mouse and human islets. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
15 Samples
Download data: XLSX
Series
Accession:
GSE73697
ID:
200073697
8.

Global gene expression profile of hIAPP-Tg mice, BACE2-KO mice and hIAPP-TgxBACE2-KO mice

(Submitter supplied) 12 weeks old wild type, hIAPP transgenic, BACE2 deficient and both overexpressing hIAPP and lacking BACE2 mice were taken for the study. Pancreatic islets were isolated at sacrifice. RNA was extracted and hybridized on Affymetrix microarrays. We used microarrays to determine gene expression changes in pancreatic islets from mice overexepressing hIAPP, mice with a functional deletion in BACE2, mice with both of these modifications and wild type mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
12 Samples
Download data: CEL
Series
Accession:
GSE94672
ID:
200094672
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