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Items: 1 to 20 of 81

1.

Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing

(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 genome tiling array
Platforms:
GPL7408 GPL9115 GPL11154
20 Samples
Download data: GFF, PAIR
Series
Accession:
GSE59365
ID:
200059365
2.

Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing [ChIP-chip]

(Submitter supplied) Dendritic-cell (DC) maturation involves substantial remodeling of their gene-expression program. Most research has focused on inducible gene-expression networks promoting the acquisition of new functions, such as cytokine production and enhanced T-cell-stimulatory capacity. In contrast, mechanisms that modulate DC-function by inducing gene silencing remain poorly understood. Here we describe a novel primary epigenetic-silencing response that makes major contributions to the DC-maturation process. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
6 Samples
Download data: GFF, PAIR
Series
Accession:
GSE58961
ID:
200058961
3.

H3Cit26 ChIP-chip from MCF-7 cells

(Submitter supplied) Estrogen receptor α (ER), a member of the nuclear hormone receptor superfamily, regulates transcriptional activity by ligand-dependent recruitment of cofactors which, in turn, locally alter chromatin structure. It is generally believed that co-factor activity at target promoters leads to a more open, transcriptionally permissive chromatin structure, however, these mechanisms remain to be fully established. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
4 Samples
Download data: PAIR
Series
Accession:
GSE32599
ID:
200032599
4.

Role of MXD3 in DAOY cell proliferation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL6104 GPL7408
10 Samples
Download data: PAIR
Series
Accession:
GSE34101
ID:
200034101
5.

ChIP-chip from DAOY cells stably expressing HA-MXD3 with anti-HA

(Submitter supplied) A subset of medulloblastomas, the most common brain tumor in children, is hypothesized to originate from granule neuron precursors (GNPs) in which the sonic hedgehog (SHH) pathway is over-activated. MXD3, a basic helix-look-helix zipper transcription factor of the MAD family, has been reported to be upregulated during postnatal cerebellar development and to promote GNP proliferation and MYCN expression. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
2 Samples
Download data: PAIR
Series
Accession:
GSE34050
ID:
200034050
6.

Profiles of Epigenetic Histone Post-translational Modifications at Type 1 Diabetes Susceptible Genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL6244 GPL7408 GPL7583
25 Samples
Download data: CEL, GFF, PAIR
Series
Accession:
GSE36403
ID:
200036403
7.

ChIP-chip of lymphocytes using H3K9Ac, H3K4me3, H3K9me3, H3K27me3 and H4K16Ac antibodies

(Submitter supplied) Both genetic and environmental factors are implicated in Type 1 Diabetes (T1D). Since environmental factors can trigger epigenetic changes, we hypothesized that variations in histone posttranslational modifications (PTMs) at the promoter/enhancer regions of T1D susceptible genes may be associated with T1D. We therefore evaluated histone PTM variations at known T1D susceptible genes in blood cells from T1D patients versus healthy non-diabetic controls, and explored their connections to T1D. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
10 Samples
Download data: GFF, PAIR
Series
Accession:
GSE36402
ID:
200036402
8.

PADI4 ChIP-chip from MCF-7 cells

(Submitter supplied) Peptidylarginine deiminase IV (PADI4) catalyzes the conversion of positively charged arginine and methylarginine residues to neutrally charged citrulline residues on histone tails. This activity has been linked to the repression of gene transcription on a limited number of genes. To broaden our knowledge of the regulatory potential of PADI4, we utilized chromatin immunoprecipitation coupled with promoter tiling array (ChIP-chip) to more comprehensively investigate the range of PADI4 target genes across the genome in MCF-7 cells. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
2 Samples
Download data: PAIR
Series
Accession:
GSE18755
ID:
200018755
9.

H3K9K14ac ChIP-chip in lung cancer cells treated with histone deacetylase inhibitor

(Submitter supplied) Lung cancer is the leading cause of cancer mortality worldwide, yet the therapeutic strategy for advanced non-small cell lung cancer (NSCLC) is limitedly effective. In addition, validated histone deacetylase (HDAC) inhibitors for the treatment of solid tumors remain to be developed. Here, we propose a novel HDAC inhibitor, OSU-HDAC-44, as a chemotherapeutic drug for NSCLC. OSU-HDAC-44 was a pan-HDAC inhibitor and exhibits 3-4 times more effectiveness than suberoylanilide hydroxamic acid (SAHA) in suppressing cell viability in various NSCLC cell lines. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
6 Samples
Download data: PAIR, TXT
Series
Accession:
GSE20304
ID:
200020304
10.

DNA methylation in progenitor cells

(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:
GPL7408 GPL7363
23 Samples
Download data: PAIR
Series
Accession:
GSE19795
ID:
200019795
11.

DNA methylation in progenitor cells: MeDIP study

(Submitter supplied) We surveyed DNA methylation profiles of all human RefSeq promoters in relation to gene expression and differentiation in adipose tissue, bone marrow and muscle mesenchymal progenitors, as well as in bone marrow-derived hematopoietic progenitors. We unravel strongly overlapping DNA methylation profiles between adipose stem cells (ASCs), bone marrow mesenchymal stem cells (BMMSCs) and muscle progenitor cells (MPCs), while hematopoietic progenitor cells (HPCs) are more epigenetically distant from MSCs seen as a whole. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL7408
12 Samples
Download data: PAIR
Series
Accession:
GSE19794
ID:
200019794
12.

Epigenetic environment of histone H3.3 on promoters revealed by integration of imaging, ChIP-chip, and MeDIP-chip data

(Submitter supplied) Epigenetic environment of histone H3.3 on promoters revealed by integration of imaging and genome-scale chromatin and methyl-DNA immunoprecipitation information. Chromatin regions with different transcriptional outputs are distinguished by the deposition of histone variants. Histone H3.3 is incorporated into chromatin in a replication-independent manner; yet the relationship between H3.3 deposition, chromatin environment is incompletely understood. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array; Methylation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL7408 GPL7363
18 Samples
Download data: PAIR, TXT
Series
Accession:
GSE17053
ID:
200017053
13.

ChIP-chip from the follicular lymphoma cell line RL with H3K4me3, H3K37me3 and Suz12

(Submitter supplied) We conducted genome-wide bisulfite sequencing analysis of the follicular lymphoma cell line RL and found that a large amount of methylated genes are polycomb target genes in ES cells. We therefore conducted a ChIP-chip experiment to determine the methylated genes that are bound by the polycomb protein Suz12. Although 28% of MRIs are PRC2 target genes in ES cells, our ChIP-on-Chip analysis showed that only 13% of MRIs are associated with H3K27Me3 marks and only 5% of the MRIs are bound by Suz12 in RL cells in vivo.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
3 Samples
Download data: PAIR
Series
Accession:
GSE20019
ID:
200020019
14.

MLL and Pol2 Chip-chip in interphase and mitotic arrested cells

(Submitter supplied) Mixed Lineage Leukemia (MLL) and its metazoan Trithorax orthologs have been linked with the epigenetic maintenance of transcriptional activity. To identify mechanisms by which MLL perpetuates active transcription in dividing cells, we investigated its role during M-phase of the cell cycle. Unlike other chromatin modifying enzymes examined, we found that MLL associates with gene promoters packaged within condensed mitotic chromosomes. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
4 Samples
Download data: GFF, PAIR
Series
Accession:
GSE19155
ID:
200019155
15.

Postrecruitment Regulation of RNA Pol II Directs Rapid Signaling Responses at the Promoters of Estrogen Target Genes

(Submitter supplied) Under current models for signal-dependent transcription in eukaryotes, DNA-binding activator proteins regulate the recruitment of RNA polymerase II (Pol II) to a set of target promoters. Yet, recent studies, as well as our results herein, show that Pol II is widely distributed (i.e., "preloaded") at the promoters of many genes prior to specific signaling events. How Pol II recruitment and Pol II preloading fit within a unified model of gene regulation is unclear. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7408
6 Samples
Download data: TXT
Series
Accession:
GSE13051
ID:
200013051
16.

Nimblegen HG18 RefSeq promoter array

(Submitter supplied) 2006-07-18_HG18_RefSeq_promoter Promoter design based only on normal RefSeq genes (NM_) for human (HG18; NCBI Build 36). Includes 2200 bp upstream of transcriptional start and 500 bp downstream. Isothermal probes using dual tm/cycle restriction:, 50-75 bp, tm 76, 148 cycles, 15-mer frequency of 50. Interval spacing of 100 bp.
Organism:
Homo sapiens
15 Series
65 Samples
Download data: NDF, POS
Platform
Accession:
GPL7408
ID:
100007408
17.

Mo-DC H4Ac LPS 1 hour rep 3.2

Organism:
Homo sapiens
Source name:
H4Ac ChIP DNA from immature DC (channel 1) H4Ac ChIP DNA from 1h LPS DC (channel 2)
Platform:
GPL7408
Series:
GSE58961 GSE59365
Download data: GFF, PAIR
Sample
Accession:
GSM1423107
ID:
301423107
18.

Mo-DC H4Ac LPS 1 hour rep 3.1

Organism:
Homo sapiens
Source name:
H4Ac ChIP DNA from immature DC (channel 1) H4Ac ChIP DNA from 1h LPS DC (channel 2)
Platform:
GPL7408
Series:
GSE58961 GSE59365
Download data: GFF, PAIR
Sample
Accession:
GSM1423106
ID:
301423106
19.

Mo-DC H4Ac LPS 1 hour rep 2.2

Organism:
Homo sapiens
Source name:
H4Ac ChIP DNA from immature DC (channel 1) H4Ac ChIP DNA from 1h LPS DC (channel 2)
Platform:
GPL7408
Series:
GSE58961 GSE59365
Download data: GFF, PAIR
Sample
Accession:
GSM1423105
ID:
301423105
20.

Mo-DC H4Ac LPS 1 hour rep 2.1

Organism:
Homo sapiens
Source name:
H4Ac ChIP DNA from immature DC (channel 1) H4Ac ChIP DNA from 1h LPS DC (channel 2)
Platform:
GPL7408
Series:
GSE58961 GSE59365
Download data: GFF, PAIR
Sample
Accession:
GSM1423104
ID:
301423104
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