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Links from GEO DataSets

Items: 20

1.

Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures

(Submitter supplied) We have previously reported that providing a control diet to obese and diabetic mice during the periconceptional/gestation/lactation period, led to a drastic sex-specific shift from susceptibility to resistance to high fat feeding (HFD) in the female offspring. In the present study, we aimed to characterize exhaustively the metabolic phenotype of F1 and F2 sensitive (S1, S2) and resistant (R1, R2) mice and underscore in the liver, muscle and adipose tissue, the transcriptional and epigenetic mechanisms supporting the response to HFD, the trait of resistance/susceptibility and the adaptation across generations. more...
Organism:
Rattus norvegicus; Mus musculus
Type:
Expression profiling by array
Platform:
GPL13688
19 Samples
Download data: GPR, TXT
Series
Accession:
GSE30085
ID:
200030085
2.

Genome-wide analysis of gene expression in adipose tissue of female mice after continuous high fat diet feeding

(Submitter supplied) Analysis of gene expression in adipose tissue of female mice after continuous high fat diet (HFD) feeding for three generations. The hypothesis in this study is that continuous HFD feeding has transgenerational amplification effects to the offspring. Results provide important information on the impacts of over-nutrition over one generation on the offspring, such as transgenerational up-regulated or down-regulated genes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
4 Samples
Download data: TXT
Series
Accession:
GSE37238
ID:
200037238
3.

Gene expression in the liver, effect of maternal high-fat diet during or prior to pregnancy

(Submitter supplied) The present study aimed to examine the effect of high-fat diet prior to pregnancy on the liver of mouse offspring. Female C57BL/6J mice were fed a normal chow (15.2% fat by energy) (CTR and CTR-PP groups) or a high-fat chow (31.2% fat by energy) (HFD and HFD-PP groups) for 3−4 weeks and then mated with male C57BL/6J mice fed normal chow. Some mothers continued on the same diet until pups reached 21 days of age (CTR and HFD), and others were fed the different chows from gestational day 0 (CTR-PP and HFD-PP) to determine the effects of a high-fat diet during the pre-pregnancy period in HFD-PP/CTR and HFD/CTR-PP comparisons.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
10 Samples
Download data: CSV
Series
Accession:
GSE48014
ID:
200048014
4.

Effect of high fat diet versus low fat diet on histone distribution in sperm of male mice

(Submitter supplied) Several studies have described phenotypic changes in offspring of mice exposed to environmental factors including diet, but the effect of diet on sperm chromatin remains unclear. We used a high fat diet (HFD) induced obesity mouse model, and examined chromatin of paternal spermatozoa. We performed chromatin immunoprecipitation followed by high throughput sequencing using specific H3 antibodies or specific H3K4me1antibodies.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
10 Samples
Download data: WIG
Series
Accession:
GSE72211
ID:
200072211
5.

Rat Adipose Tissue

(Submitter supplied) Male 130 day old rat adipose tissue from control and obese rats Keywords: ordered
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS880
Platform:
GPL341
4 Samples
Download data
Series
Accession:
GSE1813
ID:
200001813
6.
Full record GDS880

Visceral adiposity resulting from poor fetal nutrition

Expression profiling of visceral adipose tissue of 130 day old adult male Wistars that had been subjected to poor nutrition during fetal development caused by maternal protein restriction. Results indicate that poor fetal nutrition predisposes to visceral obesity.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 growth protocol sets
Platform:
GPL341
Series:
GSE1813
4 Samples
Download data
DataSet
Accession:
GDS880
ID:
880
7.

Folic acid supplementation alters the DNA methylation profile and improves insulin resistance in high-fat-diet-fed mice

(Submitter supplied) Folic acid (FA) supplementation may protect from obesity and insulin resistance, the effects and mechanism of FA on chronic high-fat-diet-induced obesity-related metabolic disorders are not well elucidated. We adopted a genome-wide approach to directly examine whether FA supplementation affects the DNA methylation profile of mouse adipose tissue and identify the functional consequences of these changes. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL17021
3 Samples
Download data: BED
Series
Accession:
GSE97576
ID:
200097576
8.

Female Mice Lacking p47phox Have Altered Adipose Tissue Gene Expression and are Protected against High Fat-Induced Obesity and Metabolic Syndrome

(Submitter supplied) Oxidative stress in adipose tissue and liver has been linked to the development of obesity. NADPH oxidases (NOX) enzymes are a major source of reactive oxygen species (ROS). The current study was designed to determine if NOX2-generated ROS play a role in development of obesity and metabolic syndrome after high fat feeding. Wild type (WT) mice and mice lacking the cytosolic NOX2 activated protein p47phox (P47KO) were fed AIN-93G diets or high fat diets (HFD) containing 45% fat and 0.5% cholesterol for 13 weeks from weaning. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE41932
ID:
200041932
9.

Hepatic gene expression profiles after long-term high-fat diet feeding in wild type and Nrf2 knock-out mice.

(Submitter supplied) To assess the role of the transcription factor NFE2 related factor 2 like 2 ( Nrf2) in the development of high-fat diet (HFD)-induced obesity and non-alcoholic HFD-induced fatty liver disease, 8 wild type (WT) and 8 Nrf2 knock-out (Nrf2-KO) C57BL6J male mice (obtained from Riken BRC, Tsukuba, Japan and originally developed by Prof. M. Yamamoto) were fed an HFD (60 kcal % fat) for 180 days. Whole genome microarray expression profiling was performed in pooled liver samples of WT and Nrf2-KO mice to identify genes that are differentially expressed between WT and Nrf2-KO mice under the stress conditions of HFD-induced obesity.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
8 Samples
Download data: TXT
Series
Accession:
GSE33575
ID:
200033575
10.

Liver transcriptome comparison of divergently selected Lean and Fat mouse lines in cholesterol homeostasis, bile acids, glucose and lipoprotein metabolism

(Submitter supplied) This study aimed to identify molecular basis of obesity-resistant mechanisms in the Lean line with the emphasis on lipid homeostasis. Expression profiling using custom Steroltalk v2 microarray demonstrated that Lean mice exhibit a higher hepatic expression of cholesterol synthesis genes compared to the Fat line. A significant difference between the strains was also found in the bile acid metabolism. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7190
17 Samples
Download data: TXT
Series
Accession:
GSE24967
ID:
200024967
11.

Transcriptome Analyses of LncRNA Metabolic Regulators from High Fat Diet Induced T2DM Mouse Adipose Tissue

(Submitter supplied) To search long noncoding RNAs (lncRNAs) which regulating energy metabolism in high fat diet induced T2DM mouse, we performed transcriptome analyses to simultaneously profile mRNAs and lncRNAs in epididymal adipose tissue in normal and high fat diet induced mouse. Combining genome-wide screens, bioinformatics function predictions, and cell-based analyses, we developed an integrative roadmap to identify lncRNA metabolic regulators in epididymal adipose tissue under high fat diet induced T2DM mouse.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL20258
6 Samples
Download data: CEL
Series
Accession:
GSE100028
ID:
200100028
12.

Primate fetal hepatic response to maternal obesity: epigenetic signaling pathways and lipid accumulation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Papio hamadryas; Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL15440 GPL6947
22 Samples
Download data
Series
Accession:
GSE99718
ID:
200099718
13.

Primate fetal hepatic response to maternal obesity: epigenetic signaling pathways and lipid accumulation [miRNA-seq]

(Submitter supplied) The liver is a major site for synthesis, storage and redistribution of carbohydrates, proteins and lipids. In addition, it is well-known that maternal obesity (MO) increases risk of offspring cardiovascular disease (CVD), diabetes and obesity. However, the mechanisms by which the MO intrauterine environment predisposes offspring to CVD and metabolic dysregulation are unknown. The goal of this study was to assess the impact of MO on primate fetal liver and identify underlying molecular mechanisms by which MO increases disease risk. more...
Organism:
Papio hamadryas
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15440
11 Samples
Download data: FA, XLSX
Series
Accession:
GSE99717
ID:
200099717
14.

Primate fetal hepatic response to maternal obesity: epigenetic signaling pathways and lipid accumulation [gene expression]

(Submitter supplied) The liver is a major site for synthesis, storage and redistribution of carbohydrates, proteins and lipids. In addition, it is well-known that maternal obesity (MO) increases risk of offspring cardiovascular disease (CVD), diabetes and obesity. However, the mechanisms by which the MO intrauterine environment predisposes offspring to CVD and metabolic dysregulation are unknown. The goal of this study was to assess the impact of MO on primate fetal liver and identify underlying molecular mechanisms by which MO increases disease risk. more...
Organism:
Homo sapiens; Papio hamadryas
Type:
Expression profiling by array
Platform:
GPL6947
11 Samples
Download data: TXT
Series
Accession:
GSE97554
ID:
200097554
15.

Efect of neonatal nutrition on adipose tissue remodeling genes during early development and in adult mice

(Submitter supplied) While the phenomenon linking the early nutritional environment to disease susceptibility exists in many mammalian species, the underlying mechanisms are unknown. We hypothesized that nutritional programming is a variable quantitative state of gene expression, fixed by the state of energy balance in the neonate, that waxes and wanes in the adult animal in response to changes in energy balance. We tested this hypothesis with an experiment, based upon global gene expression, to identify networks of genes in which expression patterns in inguinal fat of mice have been altered by the nutritional environment during early post-natal development. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2995
45 Samples
Download data: TXT
Series
Accession:
GSE19809
ID:
200019809
16.

Maternal Nutrition Induces Pervasive Gene Expression Changes but no Detectable DNA Methylation Differences in the Liver of Adult Offspring

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
80 Samples
Download data
Series
Accession:
GSE52268
ID:
200052268
17.

Maternal Nutrition Induces Pervasive Gene Expression Changes but no Detectable DNA Methylation Differences in the Liver of Adult Offspring [selected loci]

(Submitter supplied) Aims: Epidemiological and animal studies have shown that maternal diet can influence metabolism in adult offspring. However, the molecular mechanisms underlying these changes remain poorly understood. Here, we aim to explore phenotypes induced by maternal obesity in a mouse model and examine gene expression and epigenetic alterations in adulthood induced by maternal diet. Methods: We analyzed genetically identical male mice born from dams fed a high- or low-fat diet throughout pregnancy and until day 21 postpartum. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
40 Samples
Download data: TXT
Series
Accession:
GSE52267
ID:
200052267
18.

Maternal Nutrition Induces Pervasive Gene Expression Changes but no Detectable DNA Methylation Differences in the Liver of Adult Offspring [RRBS]

(Submitter supplied) Aims: Epidemiological and animal studies have shown that maternal diet can influence metabolism in adult offspring. However, the molecular mechanisms underlying these changes remain poorly understood. Here, we aim to explore phenotypes induced by maternal obesity in a mouse model and examine gene expression and epigenetic alterations in adulthood induced by maternal diet. Methods: We analyzed genetically identical male mice born from dams fed a high- or low-fat diet throughout pregnancy and until day 21 postpartum. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
40 Samples
Download data: TXT
Series
Accession:
GSE52266
ID:
200052266
19.

Genome-wide analysis of expression in various tissues in response to maternal diet

(Submitter supplied) Note: non-normalized values and associated raw data cannot be located by the submitter This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
236 Samples
Download data
Series
Accession:
GSE40903
ID:
200040903
20.

Genome-wide analysis of white adipose tissue gene expression induced by maternal diet

(Submitter supplied) The aim of this study is to characterize transcriptional changes induced by maternal diet in several adult tissues and to test whether differences in DNA methylation or microRNA expression could explain these changes. -------------------------- Note: non-normalized values and associated raw data cannot be located by the submitter
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
40 Samples
Download data
Series
Accession:
GSE40902
ID:
200040902
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