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Links from GEO DataSets

Items: 16

1.

A circular RNA generated from an intron of the insulin gene controls insulin secretion

(Submitter supplied) Fine-tuning of insulin release from pancreatic β-cells is essential to maintain blood glucose homeostasis. Here, we report that insulin secretion is regulated by a circular RNA containing the lariat sequence of the second intron of the insulin gene. Silencing of this intronic circular RNA in pancreatic islets leads to a decrease in the expression of key components of the secretory machinery of β-cells, resulting in impaired glucose- or KCl-induced insulin release and calcium signaling. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
6 Samples
Download data: XLSX
Series
Accession:
GSE134699
ID:
200134699
2.

Effects of circHIPK3 silencing on mRNA expression

(Submitter supplied) circHIPK3 silencing impairs ß-cell functions leading to a decrease in insulin secretion, proliferation, and survival. Therefore, we wanted to identify the mode of action of circHIPK3 by measuring gene expression changes upon circHIPK3 silencing in MIN6B1 cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
6 Samples
Download data: TXT
Series
Accession:
GSE105097
ID:
200105097
3.

Expression profiling of circular RNAs in human islet samples

(Submitter supplied) There is already strong evidence indicating that different types of non-coding RNAs, including microRNAs (miRNAs) and long non-coding RNAs, are key players in the regulation of β-cell functions and in the development of diabetes. However, the role of the newly discovered class of circular RNAs remains to be elucidated. We therefore analysed circular RNA expression in human islet samples.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19977
3 Samples
Download data: GPR, XLS, XLSX
Series
Accession:
GSE105096
ID:
200105096
4.

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and Diabetic db/db Mice Islets Transcriptomes

(Submitter supplied) Circular RNAs constitute an extensive fraction of the mammalian transcriptome.In this study, circular RNAs dysregulated in the islets of diabetic db/db mice were identified by high-throughput RNA sequencing. More than 5000 circRNAs were detected using RNA sequencing, indicating that circular transcripts were abundant in islets. Among them, we found that circ-Tulp4 showed significant downregulation in diabetic mouse islet cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: TXT
Series
Accession:
GSE138096
ID:
200138096
5.

Global transcriptomic analysis of human pancreatic islets reveals novel genes influencing glucose metabolism

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL6244 GPL11154
178 Samples
Download data: CEL
Series
Accession:
GSE50398
ID:
200050398
6.

Global transcriptomic analysis of human pancreatic islets reveals novel genes influencing glucose metabolism [expression array]

(Submitter supplied) Here we harnessed the potential of expression arrays in 89 human pancreatic islet donors (different levels of blood glucose (HbA1c)) to identify genes regulated in this relevant tissue for type 2 diabetes (T2D).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
89 Samples
Download data: CEL
Series
Accession:
GSE50397
ID:
200050397
7.

PIWI-interacting RNAs as novel regulators of pancreatic beta-cell function

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL22944
12 Samples
Download data: TXT, XLSX
Series
Accession:
GSE93792
ID:
200093792
8.

PIWI-interacting RNAs as novel regulators of pancreatic beta-cell function [GK, wistar samples]

(Submitter supplied) There is mounting evidence indicating that piRNAs are also present in somatic cells where they may accomplish additional regulatory tasks. The aim of this study was to identify the piRNAs expressed in pancreatic islets and to determine whether they are involved in the control of beta-cell activities. piRNA profiling of rat pancreatic islets was performed by microarray. We detected about 18’000 piRNAs in rat pancreatic islets, many of which were differentially expressed throughout islet of Goto-Kakizaki rats, a well-established model of Type 2 diabetes.
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL22944
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE93791
ID:
200093791
9.

PIWI-interacting RNAs as novel regulators of pancreatic beta-cell function [p10, adult samples]

(Submitter supplied) There is mounting evidence indicating that piRNAs are also present in somatic cells where they may accomplish additional regulatory tasks. The aim of this study was to identify the piRNAs expressed in pancreatic islets and to determine whether they are involved in the control of beta-cell activities. piRNA profiling of rat pancreatic islets was performed by microarray. We detected about 18’000 piRNAs in rat pancreatic islets, many of which were differentially expressed throughout islet postnatal development.
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL22944
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE93790
ID:
200093790
10.

The gene expression analysis of TDP knocked down MIN6 cells.

(Submitter supplied) TAR DNA-binding protein 43 kDa (TDP-43), encoded by TARDBP, is an RNA-binding protein, the nuclear depletion of which is the histopathological hallmark of amyotrophic lateral sclerosis (ALS). Here, we show that ALS subjects have reduced early-phase insulin secretion and that the nuclear localization of TDP-43 is lost in the islets of autopsied ALS pancreas. Loss of TDP-43 inhibits exocytosis, thereby reducing early-phase insulin secretion in a cultured β cell line (MIN6). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE125424
ID:
200125424
11.

Pancreatic Beta Cell Enhancers Regulate Rhythmic Transcription of Exocyst Triggering and Diabetes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL17021 GPL18573 GPL19057
68 Samples
Download data: TXT
Series
Accession:
GSE70961
ID:
200070961
12.

Pancreatic Beta-Cell Enhancers Regulate Rhythmic Transcription of Exocyst Triggering and Diabetes [ChIP-seq]

(Submitter supplied) The molecular clock is a transcriptional oscillator present in brain and peripheral cells that coordinates behavior and physiology with the solar cycle. Here we reveal that the clock gates insulin secretion through genome-wide transcriptional control of the pancreatic exocyst across species. Clock transcription factors bind to unique enhancer sites in cycling genes in beta cells that diverge from those in liver, revealing the dynamics of inter-tissue clock control of genomic and physiologic processes important in glucose homeostasis.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
8 Samples
Download data: TXT
Series
Accession:
GSE70960
ID:
200070960
13.

Genome-wide Circadian Control of Transcription at Active Enhancers Regulates Insulin Secretion and Diabetes Risk

(Submitter supplied) The molecular clock is a transcriptional oscillator present in brain and peripheral cells that coordinates behavior and physiology with the solar cycle. Here we reveal that the clock gates insulin secretion through genome-wide transcriptional control of the pancreatic exocyst across species. Clock transcription factors bind to unique enhancer sites in cycling genes in beta cells that diverge from those in liver, revealing the dynamics of inter-tissue clock control of genomic and physiologic processes important in glucose homeostasis.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL18573 GPL19057
60 Samples
Download data: TXT
Series
Accession:
GSE69889
ID:
200069889
14.

Tcf7 biology in mouse beta-cells

(Submitter supplied) We set out to identify differences in the transcriptome influenced by knockout of the transcription factor T-cell factor 7 (Tcf7) in mouse islets. Furthermore, we wanted to determine if metabolic stress (age,diet) influences these changes. Therefore, we compared the islet transcriptome from WT and Tcf7-/- mice both at a young age (8 weeks old) fed a low fat (10%) diet, versus WT and Tcf7-/- mice at an old age (20 weeks old) on a high-fat (45%) diet.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: XLS
Series
Accession:
GSE65361
ID:
200065361
15.

high-throughput sequencing analysis of NCD mice, HFD mice and db/db mice

(Submitter supplied) The goals of this study are to compare obese model mice islet transcriptome profiling (RNA-seq) to analyze the different lnc RNAs
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: TXT
Series
Accession:
GSE139991
ID:
200139991
16.

Free circular introns with an unusual branchpoint in neuronal projections

(Submitter supplied) In eukaryotic cells, most introns are degraded soon after splicing in the nucleus but some persist either due to lack of splicing (detained/retained introns) or because they contain important functional elements, for example, sno/scaRNAs. Few introns are detectable outside the nucleus. To hunt for interesting new phenomena in cytoplasmic introns and splicing, we conducted a multimodal study of total RNA within projections (axons, dendrites, glial projections) of rat hippocampal neurons and discovered a class of free circular introns enriched in distal projections.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL18694 GPL22396 GPL20084
22 Samples
Download data: BIGWIG, BW
Series
Accession:
GSE129924
ID:
200129924
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Supplemental Content

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