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Links from GEO DataSets

Items: 15

1.
Full record GDS2292

Atherogenic diet effect on the liver: time course

Analysis of livers of animals fed an atherogenic diet with either a 14% or 60% fat content for 6 or 24 weeks. Results provide insight into the molecular basis of atherogenic diet-induced liver injury.
Organism:
Mus musculus
Type:
Expression profiling by array, log10 ratio, 2 protocol, 2 time sets
Platform:
GPL1292
Series:
GSE5852
4 Samples
Download data
DataSet
Accession:
GDS2292
ID:
2292
2.

Livers of mice fed an atherogenic diet for 6 or 24 weeks

(Submitter supplied) To address the molecular basis for atherogenic diet-induced liver injury, we performed microarray analysis using livers at early (6 weeks) and pre-cirrhosis stages (24 weeks) in the development of steatohepatitis. The Atherogenic diet up-regulated the gene expression for fatty acid synthesis, inflammatory cytokines, oxidative stress, and fibrosis, and with down-regulation of fatty acid beta-oxidation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2292
Platform:
GPL1292
4 Samples
Download data
Series
Accession:
GSE5852
ID:
200005852
3.

Transcriptome Analysis from non-alcoholic steatohepatitis (NASH)

(Submitter supplied) The mechanisms underlying the progression of non-alcoholic steatohepatitis (NASH) are not completely elucidated. In this study we have integrated gene expression profiling of liver biopsies of NASH patients with translational studies in a mouse model of steatohepatitis and with pharmacological interventions in isolated hepatocytes to identify a novel mechanism implicated in the pathogenesis of NASH. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14877
15 Samples
Download data: CEL
Series
Accession:
GSE37031
ID:
200037031
4.

Mouse livers: control vs miR-155 transgenic mice

(Submitter supplied) Transcriptional profiling of mouse livers comparing control mice with miR-155 transgenic mice that overexpression of miR-155 in the liver
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13509
6 Samples
Download data: LSR, XLS
Series
Accession:
GSE64255
ID:
200064255
5.

Gene expression Tet-mev-1 mouse fed either normal diet or high fat high sucrose diet compared with wild type mouse

(Submitter supplied) To assess the effect of steatosis and oxidative stress on progression of liver fibrosis, we have employed whole genome microarray expression profiling as a discovery platform to identify genes that are related with oxidative stress- and steatosis-induced hepatic fibrogenesis. When wild type mice were fed high-fat/high-sucrose diet for 24 weeks, expression of 69 genes was changed more than 10-fold compared with wild type animals fed normal diet, 11 of which were categorized to lipid metabolic process. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
8 Samples
Download data: TXT
Series
Accession:
GSE68632
ID:
200068632
6.

Effects of low and high doses of bisphenol A on mouse liver transcriptome

(Submitter supplied) Bisphenol A (BPA) is used in the plastic industry as the monomer of polycarbonates and epoxy resins. Heat and changes in pH conditions lead to its leakage from the plastics in which it is incorporated. This largely contributes to the widespread exposure of the general population to this environmental contaminant. The exposure levels in humans are likely below the Tolerable Daily Intake (TDI: 50 µg/kg/day) and well below the No Observable Adverse Effect Level (NOAEL: 5000 µg/kg/day) defined from reprotoxicity studies. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7042
18 Samples
Download data: TXT
Series
Accession:
GSE26728
ID:
200026728
7.

Increased expression of c-Jun in nonalcoholic fatty liver disease

(Submitter supplied) Background & Aims: Overnutrition is one of the major causes of non-alcoholic fatty liver disease (NAFLD) and its advanced form non-alcoholic steatohepatitis (NASH). Besides the quantity of consumed calories, distinct dietary components are increasingly recognized as important contributor to the pathogenesis of NASH. We aimed to develop and characterize a hitherto missing murine model which resembles both the pathology and nutritional situation of NASH-patients in Western societies. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17997
8 Samples
Download data: CEL, TXT
Series
Accession:
GSE52748
ID:
200052748
8.

Liver mRNA microarray study for mice treated with various diets

(Submitter supplied) The goal of this study was to investigate the effects of vairous diets on the expression of genes involved in intermediary metabolism in liver. Adult wild type male mice (3 for each group) were fed with the corresponding diet for two weeks, and then liver samples were collected. Total RNA was isolated by the RNAzol B reagent, and pellet was disolved in DEPC-treated water. Total RNA was isolated using RNA Bee reagent (Tel-Test Inc., Friendswood, TX) per the manufacturers protocol. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
27 Samples
Download data: CEL
Series
Accession:
GSE51885
ID:
200051885
9.

Atherogenic diet supplemented with oil palm phenolics effect on liver, spleen, and heart

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6422
41 Samples
Download data
Series
Accession:
GSE30908
ID:
200030908
10.

Microarray analysis on livers, spleens and hearts of mice fed an atherogenic diet and supplemented with either oil palm phenolics (OPP) or distilled water

(Submitter supplied) OPP (1500 ppm gallic acid equivalent (GAE)) was supplemented to BALB/c mice given an atherogenic diet for six weeks to observe for possible anti-atherogenic effects. The control group received distilled water instead of OPP. Livers, spleens and hearts were harvested six weeks after the feeding regimen for gene expression studies. Results from the separate microarray data analysis carried out on the different organs show that OPP attenuated the effects of the atherogenic diet in the organs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6422
19 Samples
Download data: TXT
Series
Accession:
GSE30907
ID:
200030907
11.

Microarray analysis on livers, spleens and hearts of mice given distilled water fed with either a normal diet or an atherogenic diet

(Submitter supplied) BALB/c mice were given an atherogenic diet and compared to those given a normal diet to observe for gene expression changes caused by the atherogenic diet. Both groups of mice received distilled water as drinks ad libitum. Livers, spleens and hearts were harvested six weeks after the feeding regimen for gene expression studies. Results from the separate microarray data analysis carried out on the different organs show that the atherogenic diet caused oxidative stress and inflammation in the organs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6422
22 Samples
Download data: TXT
Series
Accession:
GSE30905
ID:
200030905
12.

Novartis 12 Strain Diet Sex Survey

(Submitter supplied) High-fat diets are associated with increased obesity and metabolic disease in mice and humans. Here we used analysis of variance (ANOVA) to scrutinize a microarray data set consisting of 10 inbred strains of mice from both sexes fed atherogenic high-fat and control chow diets. An overall F-test was applied to the 40 unique groups of strain-diet-sex to identify 15,288 genes with altered transcription. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
144 Samples
Download data: CEL
Series
Accession:
GSE10493
ID:
200010493
13.

Loss of SNORA73 reprograms cellular metabolism and protects against steatohepatitis

(Submitter supplied) Dyslipidemia and resulting lipotoxicity are pathologic signatures of metabolic syndrome and type 2 diabetes. Excess lipid causes cell dysfunction and induces cell death through pleiotropic mechanisms that link to oxidative stress. However, pathways that regulate the response to metabolic stress are not well understood. Herein, we show that disruption of the box H/ACA SNORA73 small nucleolar RNAs encoded within the small nucleolar RNA hosting gene 3 (Snhg3) causes resistance to lipid-induced cell death and general oxidative stress in cultured cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24247
20 Samples
Download data: CSV
Series
Accession:
GSE179228
ID:
200179228
14.

Vertical sleeve gastrectomy reverses diet-induced gene-regulatory changes impacting lipid metabolism

(Submitter supplied) Vertical sleeve gastrectomy (VSG) produces sustainable weight loss, remission of type 2 diabetes (T2D), and improvement of nonalcoholic fatty liver disease (NAFLD). However, the molecular mechanisms underlying the metabolic benefits of VSG have remained elusive. We have previously demonstrated that diet-induced obesity leads to chromatin modifications in the liver of mice. We demonstrate here that VSG in C57BL/6J wild-type male mice can reverse these chromatin modifications and thereby impact the expression of key metabolic genes. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: BED, BW, NARROWPEAK, TXT
Series
Accession:
GSE94842
ID:
200094842
15.

Effects of diet and age on canine liver gene expression

(Submitter supplied) The liver is the central organ in the regulation of nutrient metabolism, xenobiotic metabolism, and detoxification. Aging leads to a marked change in liver structure and function, characterized by a decline in weight, blood flow, regeneration rate, and detoxification. However, the mechanisms that contribute to these changes are poorly described. Global gene expression profiles of aged versus young adult dogs have not been compared previously. more...
Organism:
Canis lupus familiaris
Type:
Expression profiling by array
Platform:
GPL3979
12 Samples
Download data: CEL
Series
Accession:
GSE22945
ID:
200022945
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