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Items: 1 to 20 of 9602

1.

Direct neuronal reprogramming of mouse astrocytes is associated with multiscale epigenome remodeling and requires Yy1

(Submitter supplied) Direct neuronal reprogramming is a promising approach to regenerate neurons from local glial cells. However, mechanisms of epigenome remodeling and co-factors facilitating this process are unclear. Here, we combine single-cell multiomics with genome-wide profiling of 3D nuclear architecture and DNA methylation in mouse astrocyte-to-neuron reprogramming mediated by Neurogenin2 (Ngn2) and its phosphorylation-resistant form (PmutNgn2), respectively. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Other
Platforms:
GPL24247 GPL18480 GPL32159
64 Samples
Download data: BED, BEDGRAPH, BW, MTX, NARROWPEAK, TAB, TSV, TXT, XLSX
Series
Accession:
GSE208742
ID:
200208742
2.

Influence of DNA-methylation at multiple stages of limb chondrogenesis

(Submitter supplied) Limb development is a well-established model for understanding cell fate decisions, and the formation of skeletal elements is coordinated through a sequence of events that control chondrogenesis spatiotemporally. It has been established that epigenetic control participates in cartilage maturation. Our research has shown for the first time that the inhibition of DNA methylation in interdigital tissue with 5-azacytidine results in the formation of an ectopic digit. more...
Organism:
Gallus gallus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL26853
4 Samples
Download data: TXT
Series
Accession:
GSE266119
ID:
200266119
3.

Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity [human WGBS]

(Submitter supplied) Isocitrate Dehydrogenase 1 (IDH1) is the most commonly mutated metabolic gene across human cancers. Mutant IDH1 (mIDH1) generates the oncometabolite (R)-2-hydroxyglutarate, disrupting enzymes involved in epigenetics and other processes. A hallmark of IDH1-mutant solid tumors is T cell exclusion, whereas mIDH1 inhibition in preclinical models restores anti-tumor immunity. Here, we define a cell-autonomous mechanism of mIDH1-driven immune evasion. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: COV
Series
Accession:
GSE265854
ID:
200265854
4.

Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity [mouse WGBS]

(Submitter supplied) Isocitrate Dehydrogenase 1 (IDH1) is the most commonly mutated metabolic gene across human cancers. Mutant IDH1 (mIDH1) generates the oncometabolite (R)-2-hydroxyglutarate, disrupting enzymes involved in epigenetics and other processes. A hallmark of IDH1-mutant solid tumors is T cell exclusion, whereas mIDH1 inhibition in preclinical models restores anti-tumor immunity. Here, we define a cell-autonomous mechanism of mIDH1-driven immune evasion. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24247
16 Samples
Download data: COV
Series
Accession:
GSE265806
ID:
200265806
5.

Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL24676 GPL24247 GPL18573
127 Samples
Download data: COV
Series
Accession:
GSE264730
ID:
200264730
6.

Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity [RRBS]

(Submitter supplied) Isocitrate Dehydrogenase 1 (IDH1) is the most commonly mutated metabolic gene across human cancers. Mutant IDH1 (mIDH1) generates the oncometabolite (R)-2-hydroxyglutarate, disrupting enzymes involved in epigenetics and other processes. A hallmark of IDH1-mutant solid tumors is T cell exclusion, whereas mIDH1 inhibition in preclinical models restores anti-tumor immunity. Here, we define a cell-autonomous mechanism of mIDH1-driven immune evasion. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL18573
15 Samples
Download data: COV
Series
Accession:
GSE264722
ID:
200264722
7.

Illumina Infinium MethylationEPIC BeadChip (850k) analysis of growing teratoma tissues

(Submitter supplied) Illumina Infinium MethylationEPIC BeadChip (850k) array analysis of DNA methylation of 12 different growing teratoma tissues. Samples were subgrouped based on growth speed into GTSslow to GTSrapid (see corresponding publication).
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL23976
12 Samples
Download data: IDAT
Series
Accession:
GSE240091
ID:
200240091
8.

The prenatal nicotine exposure leads to epigenetic alterations in nervous system signaling genes in the rat

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL32190 GPL22396
13 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE253596
ID:
200253596
9.

The prenatal nicotine exposure leads to epigenetic alterations in nervous system signaling genes in the rat [MeDIP]

(Submitter supplied) Background. Prenatal exposure to nicotine has been documented to impose numerous deleterious effects on fetal development. However, the epigenetic changes promoted by nicotine exposure on germ cell are still not well understood. Objectives. In this study, we focused on elucidating the impact of prenatal nicotine exposure on regulatory epigenetic mechanisms important for the germ cells development. s important for the germ cells development
Organism:
Rattus norvegicus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL32190
7 Samples
Download data: BEDGRAPH
Series
Accession:
GSE253594
ID:
200253594
10.

MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301
66 Samples
Download data: BW, TXT
Series
Accession:
GSE230716
ID:
200230716
11.

MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons [WGBS]

(Submitter supplied) Mutations in the methyl-DNA-binding protein MECP2 cause the neurodevelopmental disorder Rett syndrome (RTT). How MECP2 contributes to transcriptional regulation in normal and disease states is unresolved; it has been reported to be an activator and a repressor. We describe here the first integrated CUT&Tag, transcriptome, and proteome analyses using human neurons with wild-type and mutant MECP2 molecules. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20301
3 Samples
Download data: BW
Series
Accession:
GSE230715
ID:
200230715
12.

XIST dampens X chromosome activity in a SPEN-dependent manner during early human development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other; Methylation profiling by high throughput sequencing
Platforms:
GPL20301 GPL24676
123 Samples
Download data: BW, TXT
Series
Accession:
GSE246643
ID:
200246643
13.

XIST dampens X chromosome activity in a SPEN-dependent manner during early human development [MeD-seq]

(Submitter supplied) XIST long non-coding RNA is responsible for X chromosome inactivation (XCI) in placental mammals, yet it accumulates on both X chromosomes in human female pre-implantation embryos without triggering X chromosome silencing. The long non-coding RNA XACT co-accumulates with XIST on active Xs and may antagonize XIST function. Here we used human ES cells in a naïve state of pluripotency to assess the function of XIST and XACT in shaping the X chromosome chromatin and transcriptional landscapes during pre-implantation development. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL20301
3 Samples
Download data: TXT
Series
Accession:
GSE246640
ID:
200246640
14.

Skeletal muscle methylation signatures of obese high- and low- responders to endurance exercise training

(Submitter supplied) The participants performed 8 weeks of superised aerobic endurance exercise. Skeletal muscle biopsise were taken at rest before and after intervention and matched analysis was performed.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL21145
36 Samples
Download data: IDAT
Series
Accession:
GSE244359
ID:
200244359
15.

In vitro reconstitution of epigenetic reprogramming in the human germ line

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL24676 GPL18573
119 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE232078
ID:
200232078
16.

In vitro reconstitution of epigenetic reprogramming in the human germ line [EM-Seq]

(Submitter supplied) Epigenetic reprogramming resets parental epigenetic memories and differentiates primordial germ cells (PGCs) into mitotic pro-spermatogonia or oogonia, ensuring sexually dimorphic germ-cell development for totipotency. However, the mechanism of epigenetic reprogramming in humans remains unknown. Here, we establish a robust strategy for inducing epigenetic reprogramming and differentiation of pluripotent stem cell (PSC)-derived human PGC-like cells (hPGCLCs) into mitotic pro-spermatogonia or oogonia, coupled with their extensive amplification (~>10(10)-fold). more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24676
23 Samples
Download data: TXT
Series
Accession:
GSE231813
ID:
200231813
17.

Genome-wide methylation profile of mitochondrial DNA across bovine preimplantation development

(Submitter supplied) This study characterized variations in the methylation profile of mitochondrial DNA (mtDNA) during initial bovine embryo development and correlated the presence of methylation with mtDNA transcription. Bovine oocytes were obtained from abattoir ovaries and submitted to in vitro culture procedures. Oocytes and embryos were collected at various stages (immature oocyte, IM; mature oocyte, MII; zygote, ZY; 4-cells, 4C; 16-cells, 16C and blastocysts, BL). more...
Organism:
Bos taurus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL26012
18 Samples
Download data: TXT
Series
Accession:
GSE230476
ID:
200230476
18.

Trophectoderm biopsies of blastocysts for preimplantation genetic testing following in vitro fertilization and embryo culture increases epigenetic dysregulation in a mouse model

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array; Expression profiling by high throughput sequencing
Platforms:
GPL31191 GPL24247
158 Samples
Download data: IDAT
Series
Accession:
GSE225318
ID:
200225318
19.

Trophectoderm biopsies of blastocysts for preimplantation genetic testing following in vitro fertilization and embryo culture increases epigenetic dysregulation in a mouse model [array]

(Submitter supplied) Trophectoderm biopsy for preimplantation genetic testing (TEBx) impacts placental and embryonic health during early development, with some alterations resolving while others worsening later in development. We observed that at E12.5, IVF + TEBx had a worse outcome in terms of changes in DNA methylation and differential gene expression in placentas and whole embryos compared with IVF alone. These changes were reflected in alterations in placental morphology and blood vessel density. more...
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL31191
48 Samples
Download data: IDAT, XLSX
Series
Accession:
GSE224844
ID:
200224844
20.

Whole-Genome Methylation Profiling Reveals Regions Associated with Painful Temporomandibular Disorders and Active Recovery Processes

(Submitter supplied) Genome wide DNA methylation profiling of samples with/without chronic or acute Temporomandibular Disorders (TMD). The Illumina Infinium Human methylationEPIC Beadchip was used to obtain DNA methylation profiles across 1,051,943 CpGs in TMD samples. Samples included 452 non-TMD and 496 chronic TMD from OPPERA I, 36 healthy and 123 acute TMD from OPPERA II.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
1107 Samples
Download data: CSV, IDAT
Series
Accession:
GSE224124
ID:
200224124
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