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Links from GEO DataSets

Items: 20

1.

Comparison of target genes from the pregnane X receptor (Pxr) in the liver vs the intestine

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
63 Samples
Download data: TXT
Series
Accession:
GSE123804
ID:
200123804
2.

Comparison of target genes from the pregnane X receptor (Pxr) in the liver vs the intestine [colon]

(Submitter supplied) We performed a transcriptomic comparison of the Pxr-regulated genes in the liver and intestine (ileum and colon) using microarrays in adult wild-type (WT) vs Pxr-/- C57Bl6/J male mice treated with the rodent specific Pxr ligand pregnenolone 16α-carbonitrile (PCN) (100 mg/kg i.p. once daily for 4 days).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
17 Samples
Download data: TXT
Series
Accession:
GSE123963
ID:
200123963
3.

Comparison of target genes from the pregnane X receptor (Pxr) in the liver vs the intestine [ileum]

(Submitter supplied) We performed a transcriptomic comparison of the Pxr-regulated genes in the liver and intestine (ileum and colon) using microarrays in adult wild-type (WT) vs Pxr-/- C57Bl6/J male mice treated with the rodent specific Pxr ligand pregnenolone 16α-carbonitrile (PCN) (100 mg/kg i.p. once daily for 4 days).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
23 Samples
Download data: TXT
Series
Accession:
GSE123803
ID:
200123803
4.

Comparison of target genes from the pregnane X receptor (Pxr) in the liver vs the intestine [liver]

(Submitter supplied) We performed a transcriptomic comparison of the Pxr-regulated genes in the liver and intestine (ileum and colon) using microarrays in adult wild-type (WT) vs Pxr-/- C57Bl6/J male mice treated with the rodent specific Pxr ligand pregnenolone 16α-carbonitrile (PCN) (100 mg/kg i.p. once daily for 4 days).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
23 Samples
Download data: TXT
Series
Accession:
GSE123802
ID:
200123802
5.

RNA-Seq Profiling of Pharmacological Activation of PXR and CAR Mice

(Submitter supplied) This study aimed to quantify and compare the mRNA abundance of major xenobiotic processing genes in liver following activation of PXR and CAR using RNA-Seq
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
9 Samples
Download data: ZIP
Series
Accession:
GSE104734
ID:
200104734
6.

Genome wide comparison of the inducible transcriptomes of CAR, PXR and PPARα in primary human hepatocytes

(Submitter supplied) To identify the CAR-, PXR- and PPARα-specific genome-wide expression changes, hepatocyte cultures from six individual donors were treated with the prototypical ligands for CAR (CITCO), PXR (rifampicin) and PPARα (WY14,643) as well as DMSO (vehicle control). Afterwards, the mRNA expression in these samples was determined utilizing Affymetrix® microarrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
24 Samples
Download data: CEL
Series
Accession:
GSE76148
ID:
200076148
7.

The effect of PCN on gene expression in mouse primary hepatocytes

(Submitter supplied) The effect of prototypical pregnane receptor X (PXR) agonist (pregnenolone 16α-carbonitrile) PCN on hepatic gene expression was studied in mice primary hepatocytes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL9746
2 Samples
Download data: CEL
Series
Accession:
GSE106293
ID:
200106293
8.

The effects of perfluorooctanoate on high fat diet induced non-alcoholic fatty liver disease in mice

(Submitter supplied) We reported the hepatic gene expression profiling in mice treated by perfluorooctanoate (PFOA) and high fat diet (HFD). Chronic HFD treatment was associated with gene expression changes in cholesterol biosynthetic process, lipid metabolic process, extracellular matrix, and inflammatory response pathways. Many chemokine related genes including Ccl2, Ccr2, Ccl3l3, Cx3cl1, Cx3cr1, Cxcl14, and toll-like receptor (TLR) related genes including Tlr2, Tlr7, Tlr8, Tlr13 were all significant upregulated comparing vehicle-treated HFD-fed mice to control diet (CD)-fed mice, suggesting their roles in the development of steatohepatitis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
16 Samples
Download data: TXT
Series
Accession:
GSE119441
ID:
200119441
9.

Liver transcriptomic response to fasting, high glucose or a high fructose challenges in wild-type C57Bl/6J male mice

(Submitter supplied) Microarrays experiment was performed to detail the global programme of gene expression in liver of WT male mice in response to fasting (for 24h) or challenged with high glucose or high fructose compared to mice fed ad libitum.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
24 Samples
Download data: TXT
Series
Accession:
GSE92502
ID:
200092502
10.

JNK-mediated control of gene expression in liver

(Submitter supplied) RNAseq analysis of gene expression in Liver of Control and JNK deficient mice fed a control or a High fat diet
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
24 Samples
Download data: TXT
Series
Accession:
GSE55190
ID:
200055190
11.

The effect pregnane receptor X (PXR) agonist PCN on hepatic gene expression in mouse liver with and without glucose

(Submitter supplied) The mice were treated i.p. with pregnenolone-16-α-carbonitrile (PCN, 50mg/kg dissolved in DMSO-corn oil 1:3) or vehicle (DMSO-corn oil 1:3) once daily for four days. The mice were fasted for four hours and then administered glucose (2g/kg) by oral gavage or further kept on fasting. The mice were sacrificed 1 hour after glucose administration.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21278
12 Samples
Download data: TXT
Series
Accession:
GSE125695
ID:
200125695
12.

Fibroblast growth factor 21 reflects liver fat accumulation and dysregulation of signalling pathways in the liver of C57BL/6J mice

(Submitter supplied) Fibroblast growth factor 21 (Fgf21) has emerged as a potential plasma marker to diagnose non-alcoholic fatty liver disease (NAFLD). To study the molecular processes underlying the association of plasma Fgf21 with NAFLD, we explored the liver transcriptome data of a mild NAFLD model of aging C57BL/6J mice at 12, 24, and 28 months of age. The plasma Fgf21 level significantly correlated with intrahepatic triglyceride content. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
78 Samples
Download data: CEL
Series
Accession:
GSE84495
ID:
200084495
13.

Effect of PCN on CAR and PXR regulated genes involved in circadian rhythm, drug metabolism and cholesterol homeostasis

(Submitter supplied) The nuclear receptor PXR (Pregnane X rreceptor) mediates the effects of pregnenolone-16alpha-carbonitrile (PCN) on gene transcription. The relative role of PXR and also CAR to the induction response by PCN was studied on cDNA arrays containing 320 (Steroltalk V2) genes (genes involved in cyrcadian rhythm, drug metabolism, cholesterol biosynthesis, sterol synthesis/transport, heme synthesis). Samples from livers of wild type and CAR-/-, PXR-/- or CAR/PXR-/- knockout mice were tested after treatment with PCN for gene expression within the European Framework V program “Steroltalk” (www.steroltalk.net). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7190
24 Samples
Download data: TXT
Series
Accession:
GSE12537
ID:
200012537
14.

Phenobarbital and TCPOBOP effects on CAR and PXR regulated genes involved in drug metabolism and cholesterol homeostasis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7138
44 Samples
Download data: TXT
Series
Accession:
GSE12529
ID:
200012529
15.

Effect of TCPOBOP on CAR and PXR regulated genes involved in drug metabolism and cholesterol homeostasis

(Submitter supplied) The nuclear receptor CAR (constitutive androstane receptor) mediates the effects of 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene (TCPOBOP) on gene transcription. To investigate the relative role of CAR and also PXR in the induction response, cDNA arrays were generated containing 120 (Sterolgene V1) genes which are known to be regulated with these or related nuclear receptors (genes involved in drug metabolism, cholesterol biosynthesis, sterol synthesis/transport, heme synthesis). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7138
20 Samples
Download data: TXT
Series
Accession:
GSE12509
ID:
200012509
16.

Effect of phenobarbital on CAR and PXR regulated genes involved in drug metabolism and cholesterol homeostasis

(Submitter supplied) The nuclear receptors CAR (constitutive androstane receptor) and PXR (pregnane X receptor) mediate the effects of phenobarbital (PB) on gene transcription. To investigate the relative role of CAR and PXR in the induction response, cDNA arrays were generated containing 120 genes which are known to be regulated with these or related nuclear receptors (genes involved in drug metabolism, cholesterol biosynthesis, sterol synthesis/transport, heme synthesis). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7138
24 Samples
Download data: TXT
Series
Accession:
GSE12489
ID:
200012489
17.

Global hepatic gene expression data from PPARa liver-specific KO and PPARa liver wild-type male mice fed ad libitum

(Submitter supplied) To identify genes whose expression is under the strict dependence of hepatocyte PPARa activity, we used a mouse strain of PPARa-specific deletion in hepatocyte (albumin-Cre+/- Pparaflox/flox or LKO) and we compared them to their liver WT littermates (albumin-Cre-/- Pparaflox/flox or LWT) fed ad libitum or fasted for 24 hours.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21810
24 Samples
Download data: TXT
Series
Accession:
GSE96559
ID:
200096559
18.

Transcriptional profiling of PPARα-/- and CREB3L3-/- livers reveals disparate regulation of hepatoproliferative and metabolic functions of PPARα

(Submitter supplied) Peroxisome Proliferator-Activated receptor α (PPARα) and cAMP-Responsive Element Binding Protein 3-Like 3 (CREB3L3) are transcription factors involved in the regulation of lipid metabolism in the liver. The aim of the present study was to characterize the interrelationship between PPARα and CREB3L3 in regulating hepatic gene expression. Male wildtype, PPARα-/-, CREB3L3-/- and combined PPARα/CREB3L3-/- mice were subjected to a 16-hour fast or 4 days of ketogenic diet. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
30 Samples
Download data: CEL
Series
Accession:
GSE121096
ID:
200121096
19.

Xenobiotic-responsive Nuclear Receptors in Transcriptional Effects Upon Perfluoroalkyl Acid Exposure in Diverse Species

(Submitter supplied) Humans and ecological species have been found to have detectable body burdens of a number of perfluorinated alkyl acids (PFAA) including perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). In mouse and rat liver these compounds elicit transcriptional and phenotypic effects similar to peroxisome proliferator chemicals (PPC) that work through the nuclear receptor peroxisome proliferator activated receptor alpha (PPARalpha). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platforms:
GPL85 GPL341 GPL1355
129 Samples
Download data: CEL
Series
Accession:
GSE14712
ID:
200014712
20.

Hepatic transcriptome of rats treated with vehicle or fipronil (3 mg/kg/d per os for 14 days)

(Submitter supplied) Fipronil (CAS #: 120068-37-3), a widely used insecticide, has been described as a thyroid disruptor in rat inducing a marked increase in thyroxine (T4) clearance resulting in a decrease in T4 plasma concentration. These effects seem to require the bioactivation of fipronil via its biotransformation into fipronil sulfone by cytochromes P450 (CYP). Here, we hypothesized that fipronil-induced thyroid disruption may, at least in part, result from the induction of hepatic enzymes involved in the metabolism of thyroid hormones. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
15 Samples
Download data: TXT
Series
Accession:
GSE39378
ID:
200039378
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