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Links from GEO DataSets

Items: 20

1.

Gene expression regulation of transporters and phase I/II metabolic enzymes in murine small intestine during fasting

(Submitter supplied) Gene expression regulation of transporters and phase I/II metabolic enzymes in murine small intestine during fasting Keywords: metabolic state analysis
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2934
Platform:
GPL339
12 Samples
Download data: CEL
Series
Accession:
GSE6864
ID:
200006864
2.
Full record GDS2934

PPARalpha deficient small intestine response to fasting

Analysis of PPARalpha deficient small intestines after a 24 hour fast. PPARalpha is a fatty acid-activated transcription factor. Results provide insight into transport function and phase I/II metabolism in the small intestine during fasting and the role of PPARalpha in the response to fasting.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 protocol sets
Platform:
GPL339
Series:
GSE6864
12 Samples
Download data: CEL
3.

PPARalpha-mediated effects of dietary lipids on intestinal barrier gene expression

(Submitter supplied) Background: The selective absorption of nutrients and other food constituents in the small intestine is mediated by a group of transport proteins and metabolic enzymes, often collectively called ‘intestinal barrier proteins’. An important receptor that mediates the effects of dietary lipids on gene expression is the peroxisome proliferator-activated receptor alpha (PPARα), which is abundantly expressed in enterocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
35 Samples
Download data: CEL
Series
Accession:
GSE9533
ID:
200009533
4.

Role of small intestine in the development of dietary fat-induced obesity and insulin resistance in C57BL/6J mice.

(Submitter supplied) Obesity and insulin resistance are two major risk factors underlying the metabolic syndrome. To gain more insight in the role of the small intestine in the etiology of these metabolic disorders, a microarray study was performed on small intestines (SI) of C57BL/6J mice that were fed a high fat diet mimicking the fatty acid composition of a Western-style human diet. The mice became obese and developed dietary fat-induced glucose intolerance. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3357
Platform:
GPL1261
18 Samples
Download data: CEL, EXP
Series
Accession:
GSE8582
ID:
200008582
5.
Full record GDS3357

High dietary fat effect on small intestine: time course

Analysis of small intestines of male C57BL/6J rodents fed a powdered high-fat purified diet for up to 8 weeks. Diet contributes to obesity and insulin resistance (IR) development. Results provide insight into the molecular mechanisms underlying dietary fat-induced obesity and IR pathogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 3 time, 3 tissue sets
Platform:
GPL1261
Series:
GSE8582
18 Samples
Download data: CEL, EXP
6.

Genomic profile of the mouse intestine

(Submitter supplied) 8 week-old male Hsd:ICR(CD-1) mice were fed ad libitum a standard chow (Harlan Teklad diet 2018S) and housed in groups of five. Animals were then divided into 3 pools (n=10) and sacrificed. The small intestine was extracted and divided into three sections, where the first 2-3 cm after the stomach comprised the duodenum, the middle third the jejunum, and the section before the ileo-ceco-colic junction comprised the ileum. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS521 GDS522 GDS524
Platforms:
GPL82 GPL81 GPL83
36 Samples
Download data
Series
Accession:
GSE849
ID:
200000849
7.
Full record GDS524

Intestinal tract gene expression (MG-U74C)

Analysis of regional differences in gene expression profiles along the intestinal tract. Duodenum, jejunum, ileum, and colon of 8 week-old male Hsd:ICR(CD-1) mice examined.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 tissue sets
Platform:
GPL83
Series:
GSE849
12 Samples
Download data
DataSet
Accession:
GDS524
ID:
524
8.
Full record GDS522

Intestinal tract gene expression (MG-U74B)

Analysis of regional differences in gene expression profiles along the intestinal tract. Duodenum, jejunum, ileum, and colon of 8 week-old male Hsd:ICR(CD-1) mice examined.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 tissue sets
Platform:
GPL82
Series:
GSE849
12 Samples
Download data
DataSet
Accession:
GDS522
ID:
522
9.
Full record GDS521

Intestinal tract gene expression (MG-U74A)

Analysis of regional differences in gene expression profiles along the intestinal tract. Duodenum, jejunum, ileum, and colon of 8 week-old male Hsd:ICR(CD-1) mice examined.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 tissue sets
Platform:
GPL81
Series:
GSE849
12 Samples
Download data
DataSet
Accession:
GDS521
ID:
521
10.

Genome-wide analysis of PPARα activation in murine small intestine

(Submitter supplied) The peroxisome proliferator-activated receptor alpha (PPARα) is a fatty acid-activated transcription factor that governs a variety of biological processes. Little is known about the role of PPARα in the small intestine. Since this organ is frequently exposed to high levels of PPARα ligands via the diet, we set out to characterize the function of PPARα in small intestine using functional genomics experiments and bioinformatics tools. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2886
Platform:
GPL339
12 Samples
Download data: CEL
Series
Accession:
GSE5475
ID:
200005475
11.
Full record GDS2886

PPARalpha activation effect on the small intestine

Analysis of small intestine of wild type and peroxisome proliferator-activated receptor alpha (PPARalpha) null animals after treatment with WY14643, an agonist of PPARalpha. PPARalpha is a fatty acid-activated transcription factor. Results provide insight into role of PPARalpha in small intestine.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 2 genotype/variation sets
Platform:
GPL339
Series:
GSE5475
12 Samples
Download data: CEL
DataSet
Accession:
GDS2886
ID:
2886
12.

Gestational Age-Dependent Changes in Gene Expression of Metabolic Enzymes and Transporters in Pregnant Mice

(Submitter supplied) Knowing the gene expression profiles of drug-metabolizing enzymes and transporters throughout gestation is important for understanding the mechanisms of pregnancy-induced changes in drug pharmacokinetics. In this study, we compared gene expression of drug-metabolizing enzymes and transporters in the maternal liver, kidney, small intestine, and placenta of pregnant mice throughout gestation by microarray analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
90 Samples
Download data: CEL
Series
Accession:
GSE41438
ID:
200041438
13.

The impact of PPARα activation on whole genome gene expression in human precision-cut liver slices

(Submitter supplied) Background: Studies in mice have shown that PPARα is an important regulator of lipid metabolism in liver and a key transcription factor involved in the adaptive response to fasting. However, much less is known about the role of PPARα in human liver. Here we set out to study the function of PPARα in human liver via analysis of whole genome gene regulation in human liver slices treated with the PPARα agonist Wy14643. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL11532
8 Samples
Download data: CEL
Series
Accession:
GSE71731
ID:
200071731
14.

Comparative analysis of gene regulation by the transcription factor PPARα_human

(Submitter supplied) Studies in mice have shown that PPARα is an important regulator of hepatic lipid metabolism and the acute phase response. However, little information is available on the role of PPARα in human liver. Here we set out to compare the function of PPARα in mouse and human hepatocytes via analysis of target gene regulation. Primary hepatocytes from 6 human and 6 mouse donors were treated with PPARα agonist Wy14643 and gene expression profiling was performed using Affymetrix GeneChips followed by a systems biology analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
24 Samples
Download data: CEL
Series
Accession:
GSE17251
ID:
200017251
15.

Fasting induces a biphasic adaptive metabolic response in murine small intestine

(Submitter supplied) Background The gut is a major energy consumer, but a comprehensive overview of the adaptive response to fasting is lacking. Gene-expression profiling, pathway analysis, and immunohistochemistry were therefore carried out on mouse small intestine after 0, 12, 24, and 72 hours of fasting. Results Intestinal weight declined to 50% of control, but this loss of tissue mass was distributed proportionally among the gut’s structural components, so that the microarrays’ tissue base remained unaffected. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL922
12 Samples
Download data: TIFF, TXT
Series
Accession:
GSE8019
ID:
200008019
16.

Mouse feeding experiment

(Submitter supplied) Mice used in this study were 129/sv males, 8-15 weeks of age, which were housed individually and received water ad libitum. Normal fed animals were fed before and during the 48h experiment with standard food ad libitum. Sugar fed animals were fed before the experiment with standard food ad libitum and during the 48h experiment with 50% (w/v) sugar solution (40% glucose, 10% sucrose). Mice were killed by CO2 asphyxiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL765
60 Samples
Download data
Series
Accession:
GSE858
ID:
200000858
17.

liver, 24h starved

(Submitter supplied) Mice used in this study were 129/sv males, 8-15 weeks of age, which were housed individually and received water ad libitum. Normal fed animals were fed before and during the 48h experiment with standard food ad libitum. Starved animals were fed before the experiment with standard food ad libitum and were starved during the 24h experiment. Mice were killed by CO2 asphyxiation. The livers were snap-frozen in liquid nitrogen and stored at -80 degrees C. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL765
24 Samples
Download data
Series
Accession:
GSE853
ID:
200000853
18.

liver, 48h starved

(Submitter supplied) Mice used in this study were 129/sv males, 8-15 weeks of age, which were housed individually and received water ad libitum. Normal fed animals were fed before and during the 48h experiment with standard food ad libitum. Starved animals were fed before the experiment with standard food ad libitum and were starved during the 48h experiment. Mice were killed by CO2 asphyxiation. The livers were snap-frozen in liquid nitrogen and stored at -80 degrees C. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL765
24 Samples
Download data
Series
Accession:
GSE852
ID:
200000852
19.

liver, 48h sugar

(Submitter supplied) Mice used in this study were 129/sv males, 8-15 weeks of age, which were housed individually and received water ad libitum. Normal fed animals were fed before and during the 48h experiment with standard food ad libitum. Sugar fed animals were fed before the experiment with standard food ad libitum and during the 48h experiment with 50% (w/v) sugar solution (40% glucose, 10% sucrose). Mice were killed by CO2 asphyxiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL765
12 Samples
Download data
Series
Accession:
GSE851
ID:
200000851
20.

MJArray Mus Musculus

(Submitter supplied) cDNA microarrays based on the Lion Bioscience (Heidelberg, Germany) clone collection Mouse ArrayTag(r) set A and B. Each microarray contains 43200 features within two seperate subarrays with each 21600 spots and 20188 spots containing gene probes. The ID is organized like this: Letter "A" or "B" to distiguish both subarrays from each other, followed by the # sign an a running index for each subarray (1 to 21600). more...
Organism:
Mus musculus
4 Series
60 Samples
Download data
Platform
Accession:
GPL765
ID:
100000765
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