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Links from GEO DataSets

Items: 20

1.

DNA methylome signatures of prenatal exposure to synthetic glucocorticoids in hippocampus and peripheral whole blood of female guinea pigs in early life

(Submitter supplied) We examined the hypothesis that prenatal synthetic glucocorticoids (sGC) administration alters DNA methylation signatures in Guinea pig offspring hippocampus and whole blood. Guinea pigs were treated with sGC or saline in late gestation. Genome-wide modifications of DNA methylation were analyzed using reduced representation bisulfite sequencing in juvenile female offspring.
Organism:
Cavia porcellus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL29163
24 Samples
Download data: TXT
Series
Accession:
GSE163447
ID:
200163447
2.

The Transgenerational Effects of Prenatal Synthetic Glucocorticoids on the Hippocampus Cortex

(Submitter supplied) First generation animals (F1) were exposed to multiple courses of synthetic glucocorticoids in utero. Animals were then bred to produce second (F2) and third (F3) generation offspring. These animals underwent behavioural assessmenets before sacrifice. In this experiment the prefrontal cortex for F1, F2, and F3 female animals, as well as F1 males (Control and sGC) have been extracted via micro-punch and RNA has been extracted.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL22346
72 Samples
Download data: TXT
Series
Accession:
GSE109765
ID:
200109765
3.

miRNA levels in F1-F3 male germ cells and female F2 PFC following prenatal exposure to sGC in guinea pigs

(Submitter supplied) Stress and glucocorticoid exposure during pregnancy alters neurodevelopment and behavior in offspring, and these effects extend multiple generations through a paternal lineage. The epigenetic mechanisms that govern this transgenerational transmission are unclear. We hypothesized that maternal exposure to multiple courses of sGC in late pregnancy would result in altered miRNA levels in germs cells of male guinea pigs across three generations. more...
Organism:
Cavia porcellus; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL21572
49 Samples
Download data: CEL
Series
Accession:
GSE250055
ID:
200250055
4.

Glucocorticoid Exposure During Hippocampal Neurogenesis Primes Future Stress Response by Inducing Long-Lasting Changes in DNA Methylation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by genome tiling array
Platforms:
GPL10558 GPL13534
122 Samples
Download data: IDAT
Series
Accession:
GSE119847
ID:
200119847
5.

Glucocorticoid Exposure During Hippocampal Neurogenesis Primes Future Stress Response by Inducing Long-Lasting Changes in DNA Methylation [methylation]

(Submitter supplied) Prenatal stress exposure is associated with the risk for psychiatric disorders later in life. This may be mediated via enhanced exposure to glucocorticoids (GCs), known to impact neurogenesis. We aimed to identify molecular mediators of these effects, focusing on long-lasting epigenetic changes. In a human hippocampal progenitor cell (HPC) line, we assessed the short- and long-term effects of GC exposure during neurogenesis on mRNA expression and DNA methylation (DNAm) profiles. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
60 Samples
Download data: IDAT
Series
Accession:
GSE119846
ID:
200119846
6.

Glucocorticoid Exposure During Hippocampal Neurogenesis Primes Future Stress Response by Inducing Long-Lasting Changes in DNA Methylation [expression_acute]

(Submitter supplied) Prenatal stress exposure is associated with the risk for psychiatric disorders later in life. This may be mediated via enhanced exposure to glucocorticoids (GCs), known to impact neurogenesis. We aimed to identify molecular mediators of these effects, focusing on long-lasting epigenetic changes. In a human hippocampal progenitor cell (HPC) line, we assessed the short- and long-term effects of GC exposure during neurogenesis on mRNA expression and DNA methylation (DNAm) profiles. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
15 Samples
Download data: IDAT, TXT
Series
Accession:
GSE119843
ID:
200119843
7.

Glucocorticoid Exposure During Hippocampal Neurogenesis Primes Future Stress Response by Inducing Long-Lasting Changes in DNA Methylation [expression]

(Submitter supplied) Prenatal stress exposure is associated with the risk for psychiatric disorders later in life. This may be mediated via enhanced exposure to glucocorticoids (GCs), known to impact neurogenesis. We aimed to identify molecular mediators of these effects, focusing on long-lasting epigenetic changes. In a human hippocampal progenitor cell (HPC) line, we assessed the short- and long-term effects of GC exposure during neurogenesis on mRNA expression and DNA methylation (DNAm) profiles. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
47 Samples
Download data: TXT
Series
Accession:
GSE119842
ID:
200119842
8.

The Transgenerational Effects of Prenatal Synthetic Glucocorticoids

(Submitter supplied) First generation animals (F1) were exposed to multiple courses of synthetic glucocorticoids in utero. Animals were then bred to produce second (F2) and third (F3) generation offspring. These animals underwent behavioural assessmenets before sacrifice. In this experiment the paraventricular nucleus of the hypothalamus fo F1, F2, and F3 female anmials (Beta and Control) have been extracted via micro-punch and RNA has been extracted.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22346
34 Samples
Download data: TXT
Series
Accession:
GSE85822
ID:
200085822
9.

Perinatal exposure to nicotine alters spermatozoal DNA methylation near genes controlling nicotine action

(Submitter supplied) Perinatal smoke/nicotine exposure alters lung development and causes asthma in exposed offspring, transmitted transgenerationally. The mechanism underlying the transgenerational inheritance of perinatal smoke/nicotine-induced asthma remains unknown, but germline epigenetic modulations may play a role. Using a well-established rat model of perinatal nicotine-induced asthma, we determined the DNA methylation pattern of spermatozoa of F1 rats exposed perinatally to nicotine in F0 gestation. more...
Organism:
Rattus norvegicus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20084
20 Samples
Download data: COV
Series
Accession:
GSE173898
ID:
200173898
10.

Prenatal stress-induced programming of genome-wide promoter DNA methylation in 5-Htt deficient mice

(Submitter supplied) The serotonin transporter (5-HTT) gene-linked polymorphic region has been suggested to play a modulatory role in mediating the effects of early-life stress on psychopathology rendering carriers of the low-expression short (s)-allele more vulnerable to environmental adversity in later life. Here we analyzed the effects of prenatal stress (PS), 5-Htt genotype, and an interactin of both on DNA methylation in the hippocampi of female C57BL/6 mice. more...
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL5811
22 Samples
Download data: BED, BEDGRAPH, CEL
Series
Accession:
GSE51634
ID:
200051634
11.

Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-related Stress

(Submitter supplied) Prenatal adversity or stress can have long-term consequences on developmental trajec-tories and health outcomes. Although the biological mechanisms underlying these effects are poorly understood, epigenetic modifications, such as DNA methylation, have the potential to link early-life environments to alterations in physiological systems, with long-term functional impli-cations. We investigated the consequences of two prenatal insults, prenatal alcohol exposure (PAE) and food-related stress, on DNA methylation profiles of the rat brain during early devel-opment. more...
Organism:
Rattus norvegicus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL14844
30 Samples
Download data: TXT
Series
Accession:
GSE186840
ID:
200186840
12.

Epigenetic signatures of gestational diabetes mellitus on ATP5A1, PRKCH, SLC17A4 and HIF3A cord blood methylation

(Submitter supplied) Background: Intrauterine exposure to gestational diabetes mellitus (GDM) confers a lifelong increased risk for metabolic and other complex disorders to the offspring. GDM-induced epigenetic modifications modulating gene regulation and persisting into later life are generally assumed to mediate these increased disease risks. To identify candidate genes for fetal programming, we compared genome-wide methylation patterns of fetal cord bloods (FCBs) from GDM and control pregnancies. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
132 Samples
Download data: TXT
Series
Accession:
GSE88929
ID:
200088929
13.

Epigenetic changes in the adult brain following exposure to prenatal maternal immune activation and dietary intervention

(Submitter supplied) Epigenetic changes such as DNA cytosine methylation modulate gene function across brain and are implicated in the pathophysiology of neurodevelopmental disorders including schizophrenia and autism. Epigenetic changes can be caused by environmental exposures such as inflammation, and may at least partly explain why prenatal exposure to inflammation increase risk of neurodevelopmental disorders. We used an MIA mouse model to investigate the postnatal epigenetic changes associated with exposure to the viral analogue PolyI:C. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
24 Samples
Download data: TXT
Series
Accession:
GSE102942
ID:
200102942
14.

GR mutation in mice changes the genome-wide epigenome of frontal cortex in a highly sex-specific manner

(Submitter supplied) We found that the GR mutation leads to a changes of the DNA methylation landscape in frontal cortex of c57/bl6n male mice
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: BEDGRAPH
Series
Accession:
GSE123460
ID:
200123460
15.

GR mutation in mice changes the genome-wide epigenome of placental tissue in a highly sex-specific manner

(Submitter supplied) We found that the GR mutation leads to a complete change of the DNA methylation landscape in fetal placenta of c57/bl6n mice in a highly sex-specific manner. The genome-wide capture-sequencing analysis revealed enrichments in genes related to a broad range of biological functions associated with basic signaling pathways and neurological development, but also with diseases like diabetes and dementia. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE123188
ID:
200123188
16.

In utero heat stress alters the offspring epigenome [methylation]

(Submitter supplied) Exposure to intrauterine heat stress during late gestation affects offspring performance into adulthood. However, underlying mechanistic links between thermal insult in fetal life and postnatal outcomes are not completely understood. Utilizing Reduced Representation Bisulfite Sequencing, this study evaluated DNA methylation of liver and mammary gland of bull calves and heifers that were gestated under maternal conditions of heat stress or cooling, i.e., in utero heat stressed (HT) vs. more...
Organism:
Bos taurus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL23295
15 Samples
Download data: TXT
Series
Accession:
GSE119445
ID:
200119445
17.

In utero heat stress alters the offspring epigenome

(Submitter supplied) Exposure to intrauterine heat stress during late gestation affects offspring performance into adulthood. However, underlying mechanistic links between thermal insult in fetal life and postnatal outcomes are not completely understood. Utilizing RNA Sequencing, this study characterized the mammary gland transcriptome of heifers that were gestated under maternal conditions of heat stress or cooling, i.e., in utero heat stressed (HT) vs. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21659
6 Samples
Download data: TXT
Series
Accession:
GSE119216
ID:
200119216
18.

DNA methylome modifications in ME/CFS

(Submitter supplied) Examination of DNA methylome patterns in a larger cohort of ME/CFS samples using the Illumina Infinium HumanMethylation450 Beadchip Array
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
75 Samples
Download data: IDAT, TXT
Series
Accession:
GSE93266
ID:
200093266
19.

Genome wide effects of maternal undernutrition

(Submitter supplied) DNA methylation profiles of the livers of 1 day old rats from mothers fed with three different diets during gestation. The first animal group was fed with a normal diet (c=control); second group received much less protein than normal and slighlty more carbs (p=low protein, or programmed); third group diet was same as low protein but with extra folic acid (f=low protein+folate). All diets were matched for energy.
Organism:
Rattus norvegicus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL10287
3 Samples
Download data: BED, WIG
Series
Accession:
GSE50935
ID:
200050935
20.

Genome-wide effects of maternal undernutrition

(Submitter supplied) A comparison of the liver transcriptomes of 1 day old rats that are born to mothers fed with three different diets during gestation. The first animal group was fed with a normal diet (control); second group received much less protein than normal and slightly more carbs (low protein); third group diet was same as low protein but with an extra dosage of folic acid (lowp.+f). All diets were matched for energy.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
12 Samples
Download data: TXT
Series
Accession:
GSE50799
ID:
200050799
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