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Links from GEO DataSets

Items: 18

1.

Arsenic is more potent than cadmium or manganese in disrupting the INS-1 beta cell microRNA landscape

(Submitter supplied) Diabetes is a metabolic disorder characterized by fasting hyperglycemia and impaired glucose tolerance. Laboratory and population studies have shown that inorganic arsenic (iAs) can impair these pathways. Other metals including cadmium (Cd) and manganese (Mn) have also been linked to diabetes phenotypes. MicroRNAs, short non-coding RNAs that regulate gene expression, have emerged as potential drivers of metabolic dysfunction. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL18694 GPL22396
21 Samples
Download data: CSV
Series
Accession:
GSE131544
ID:
200131544
2.

MicroRNAs and histone deacetylase inhibition-mediated protection against inflammatory β-cell damage

(Submitter supplied) Inflammatory b-cell failure contributes to type 1 and type 2 diabetes pathogenesis. Proinflammatory cytokines cause b-cell dysfunction and apoptosis, and lysine deacetylase inhibitors (KDACi) prevent b-cell failure in vitro and in vivo, in part by reducing NFkB transcriptional activity. Here we investigated the hypothesis that the protective effect of KDACi involves transcriptional regulation of microRNAs (miRs), potential new targets in diabetes treatment. more...
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL22760
24 Samples
Download data: TXT
Series
Accession:
GSE117451
ID:
200117451
3.

Next Generation Sequencing of langerhans islets of miR-17-92/106b KO vs control

(Submitter supplied) NGS was used in order to discover novel downstream targets of the miR-17-92/106b clusters.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: XLSX
Series
Accession:
GSE126516
ID:
200126516
4.

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
5.

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
6.

Molecular and Metabolic Analysis of Arsenic-Exposed Humanized AS3MT Mice

(Submitter supplied) Background: Chronic exposure to inorganic arsenic (iAs) has been associated with type 2 diabetes (T2D). However, potential sex divergence and the underlying mechanisms remain understudied. iAs is not metabolized uniformly across species, which is a limitation of typical exposure studies in rodent models. The development of a new “humanized” mouse model overcomes this limitation. In this study, we leverage this model to study sex differences in the context of iAs exposure. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL19057 GPL21493
64 Samples
Download data: CSV, XLSX
Series
Accession:
GSE236059
ID:
200236059
7.

sRNA sequencing of miRNAs in primary human islets

(Submitter supplied) miRNAs are exported to high density lipoproteins (HDL). This study aimed to understand what miRNAs are present in primary human islets from 1 donor
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: CSV
Series
Accession:
GSE125137
ID:
200125137
8.

sRNA sequencing of miRNAs exported to HDL from primary human islets

(Submitter supplied) miRNAs are exported to high density lipoproteins (HDL). This study aimed to understand what miRNAs are exported from primary islets to HDL in vitro.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: CSV
Series
Accession:
GSE125136
ID:
200125136
9.

sRNA sequencing of miRNAs exported to HDL from INS-1 rat insulinoma cells

(Submitter supplied) miRNAs are exported to high density lipoproteins (HDL). This study aimed to understand what miRNAs are exported from INS-1 cells to HDL in vitro.
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18694
2 Samples
Download data: CSV
Series
Accession:
GSE125135
ID:
200125135
10.

sRNA sequencing of HDL from human donors

(Submitter supplied) miRNAs and other small RNAs have been found associated with high-density lipoproteins (HDL). The aim of this study was to investigate the miRNA signature on human HDL from 10 donors.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
10 Samples
Download data: TXT
Series
Accession:
GSE124559
ID:
200124559
11.

Beta cell 5’-shifted isomiRs are candidate regulatory hubs in type 2 diabetes

(Submitter supplied) We performed deep sequencing of small RNA from mouse insulinoma (MIN6) cells cultured in 25mM glucose. We then developed and implemented an in-house short-read mapping strategy to analyze isomiR diversity.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BED
Series
Accession:
GSE44262
ID:
200044262
12.

Insights from long non-coding RNAs profiling of beta cells undergoing high glucose/palmitate -induced glucolipotoxicity

(Submitter supplied) RNA-Seq was performed to compare the control INS-1 cells (rat beta cell line)with the high glucose/palmitate-treated INS-1 cells. According to the expression profiling data, 264 significantly dysregulated lncRNAs were identified with a set filter (fold-change ≥2.0, p < 0.05) in the HG/PA-treated INS-1 cells: 153 were up-regulated, while 111 were down-regulated.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
6 Samples
Download data: TXT
Series
Accession:
GSE124833
ID:
200124833
13.

Effect of paternal inorganic arsenic exposure on transcriptional profilings of F1-male liver in mouse

(Submitter supplied) Adult male mice (F0) were exposed to 250 ppb inorganic arsenic (iAs) in drinking water before mating with unexposed female mice to generate male F1 offspring (iAsF1-M). Unexposed male mice were bred simultaneously to generate male controls (conF1-M). Both iAsF1-M and conF1-M mice drank normal water without iAs. Adult iAsF1-M and conF1-M mice were harvested to collect liver samples to do RNA-seq.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: XLSX
Series
Accession:
GSE205355
ID:
200205355
14.

RNA-seq of the liver tissue from female F1 generation with parternal exposure to arsenic in drinking water

(Submitter supplied) We treated C56BL/6 male mice with 0.25 ppm iAs in drinking water before breeding with untreated females. GTT and other metabolic assaies were done on F1 offsprings. iAsF1-F showed significantly impared glucose intolerance than conF1-F. RNA-seq was thus applied to the liver samples of F1 generation to explore potential mechanism.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: XLSX
Series
Accession:
GSE154130
ID:
200154130
15.

Expression data from TK6 exposed to low-dose metals

(Submitter supplied) We are investigating the response of human lymphoblastoid cells to low-dose exposure of environmental metals We used microarrays to detail the global programme of gene expression upon response to low-dose metals Keywords: dose
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4915 GDS4916
Platform:
GPL6244
8 Samples
Download data: CEL
Series
Accession:
GSE20320
ID:
200020320
16.
Full record GDS4916

Lymphoblastoid cell response to low-dose cadmium exposure in vitro

Analysis of TK6 lymphoblastoid cells treated with 0.1 uM cadmium chloride for 24 hours. Results provide insight into the molecular impact resulting from exposure to an environmentally relevant dose of cadmium.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL6244
Series:
GSE20320
4 Samples
Download data: CEL
17.
Full record GDS4915

Lymphoblastoid cell response to low-dose arsenic exposure in vitro

Analysis of TK6 lymphoblastoid cells treated with 0.1 uM sodium arsenite for 24 hours. Results provide insight into the molecular impact resulting from exposure to an environmentally relevant dose of arsenic.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL6244
Series:
GSE20320
4 Samples
Download data: CEL
18.

RNA Sequencing Reveals Regulation of Marginal Zone B-Cell Differentiation by MicroRNA-146a

(Submitter supplied) Splenocytes were FACS-sorted from Wild-type and Mir146a-/- mice to isolate specific B-cell developmental stages. Utilizing high-throughput sequencing, we comparatively analyzed developmental stage-specific splenic B cell transcriptomes, including Transitional-1 (T1), Transitional-2 (T2), Marginal zone (MZ) and Follicular (FO) in both Wild-type and Mir146a-/- B cells. Two replicates of each developmental stage were submitted for high-throughput sequencing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
16 Samples
Download data: TXT
Series
Accession:
GSE93252
ID:
200093252
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