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Links from GEO DataSets

Items: 16

1.
Full record GDS5158

Ethanol effect on differentiated H1 embryonic stem cells

Analysis of H1 embryonic stem cells differentiated into neural rosettes and neural progenitor cells in the presence of 20mM EtOH. Results provide insight into the molecular effects of EtOH during neural differentiation of embryonic stem cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 3 cell type sets
Platform:
GPL570
Series:
GSE56906
10 Samples
Download data: CEL
2.

Effect of EtOH on neural stem cells derived from human embryonic stem cells

(Submitter supplied) We have performed gene expression microarray analysis to profile transcriptomic signatures affected by EtOH during neural differentiation of human embryonic stem cells
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5158
Platform:
GPL570
10 Samples
Download data: CEL
Series
Accession:
GSE56906
ID:
200056906
3.

20 mM EtOH on hESCs.

(Submitter supplied) We studied alcohol's effect on human embryonic stem cell line, H9. Our main objective was to delineate the molecular mechanisms that are involved in changing the differentiation potential of hESCs.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE45036
ID:
200045036
4.

Loss of non-coding RNA expression from the DLK1-DIO3 imprinted locus correlates with reduced neural differentiation potential in human embryonic stem cell lines

(Submitter supplied) Pluripotent stem cells are increasingly used for therapeutic models, including transplantation of neural progenitors derived from human embryonic stem cells (hESCs). Recently, long non-coding RNAs (lncRNAs), including Maternally Expressed Gene 3 (MEG3) that is derived from DLK1-DIO3 imprinted locus, were found to be expressed during neural developmental events. Their deregulations are associated with various neurological diseases. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE58809
ID:
200058809
5.

Expression of imprinted non-coding RNAs from the DLK1-DIO3 locus in human embryonic stem cells advantages neural lineage differentiation

(Submitter supplied) Pluripotent stem cells are increasingly used for therapeutic models, including transplantation of neural progenitors derived from human embryonic stem cells (hESCs). Recently, long non-coding RNAs (lncRNAs), including Maternally Expressed Gene 3 (MEG3) that is derived from DLK1-DIO3 imprinted locus, were found to be expressed during neural developmental events. Their deregulations are associated with various neurological diseases. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE58508
ID:
200058508
6.

Genome-wide map of SOX2 occupancy in human ES cells (hESCs) and hESC derived neural progenitor cells (hNPCs)

(Submitter supplied) To compare the genome wide binding profiles of SOX2 in hESCs and hNPCs, we carried out SOX2 ChIP-seq in the two cell types and dissected the the cell type and stage dependent regulatory groups of SOX2, thus providing important information for the mechanism underlying SOX2's dynamic functions in hESCs and hNPCs.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: BED, BW
Series
Accession:
GSE69479
ID:
200069479
7.

mRNA sequencing of the global effect of SOX2 on gene expression in hESC and hESC derived NPCs.

(Submitter supplied) Global transcriptome analysis reveals that SOX2 regulates a common group safeguarding stem cell identity in hESCs and hNPCs, and also distinct functional groups regulating diverse cell type dependent developmental processes in hESCs and hNPCs, sheding light on the mechanism underlying SOX2's dynamic function in the two related stem cell types.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
8.

Strain-dependent effects of alcohol on early mouse embryos

(Submitter supplied) EXPERIMENT: Microarray expression profiles derived from the cranial neural folds (headfold) of neurulation-stage mouse embryos 3.0h after maternal alcohol exposure on 8 d.p.c. ANIMAL MODEL: Pregnancies from 2 substrains of C57BL/6 mice that differ in relative risk of Fetal Alcohol Syndrome (FAS): C57BL/6J (B6J) high-risk condition, and C57BL/6NCrl (B6N) low-risk condition. EXPOSURE: Dams dosed with ethanol (EtOH) by intraperitoneal injection at 2.9 g EtOH per kg body weight. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL560
24 Samples
Download data: CEL, GPR
Series
Accession:
GSE1074
ID:
200001074
9.

Mouse Fetal Cortical-derived Neurosphere cultures transfected with null control or miRNA-153 mimetic

(Submitter supplied) The expression of the mciroRNA, miR-153 is significantly altered in neural stem cells (NSCs) following exposure to the teratogens, alcohol and nicotine (PMIDs:22458409, 17687032). To better understand how miR-153 may mediate teratogenesis, we first needed to identify miR153 targets in fetal NSCs. Gestational day 12.5 fetal mouse cortical neural epithelium was isolated and grown as neurospheres in defined medium for studies. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17548
12 Samples
Download data: TXT
Series
Accession:
GSE49684
ID:
200049684
10.

Effect of EtOH on transcriptome signatures in human dental pulp stem cells

(Submitter supplied) We have performed gene expression microarray analysis to profile transcriptomic signatures affected by EtOH in human dental pulp stem cells
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
24 Samples
Download data: CEL
Series
Accession:
GSE57255
ID:
200057255
11.

Comparative analysis between effects of thalidomide and environmental chemicals on neuronal differentiations in human sphere

(Submitter supplied) To develop molecular indicators of neurodevelopmental disorders related to the exposure to external chemicals, we have employed whole genome microarray expression profiling as a discovery platform to identify genes with the potential to influence neuronal differentiation from embryonic stem cells. Thalidomide (TMD), bisphenol A (BPA), 4-hydroxy-2,2',3,4',5,5',6-heptachlorobiphenyl (4OH-PCB187) and 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) were exposed to human embryonic stem (ES) cell-derived sphere on day 3 after starting sphere formation for 72 hours. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14550
8 Samples
Download data: TXT
Series
Accession:
GSE151239
ID:
200151239
12.

Nos3-/- iPSCs model concordant signatures of in utero cardiac pathogenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
43 Samples
Download data: CEL
Series
Accession:
GSE69317
ID:
200069317
13.

Nos3-/- iPSCs model concordant signatures of in utero cardiac pathogenesis [iPSCs]

(Submitter supplied) Through genome-wide transcriptional comparisons, this study interrogates the capacity of iPSCs to accurately model pathogenic signatures of structural cardiac defects. Herein, we studied the molecular etiology of structural cardiac defects in Nos3-/- mice via transcriptional analysis of stage-matched embryonic and iPSC-derived tissues. In vitro comparisons of differentiated embryoid bodies were calibrated to in utero benchmarks of health and disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
31 Samples
Download data: CEL
Series
Accession:
GSE69316
ID:
200069316
14.

Nos3-/- iPSCs model concordant signatures of in utero cardiac pathogenesis [tissue]

(Submitter supplied) Through genome-wide transcriptional comparisons, this study interrogates the capacity of iPSCs to accurately model pathogenic signatures of structural cardiac defects. Herein, we studied the molecular etiology of structural cardiac defects in Nos3-/- mice via transcriptional analysis of stage-matched embryonic and iPSC-derived tissues. In vitro comparisons of differentiated embryoid bodies were calibrated to in utero benchmarks of health and disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE69315
ID:
200069315
15.

Genome-wide anaylsis of histone acetylation during mouse ESC differentiation [ChIP-seq]

(Submitter supplied) Using acetylated histone H3 ChIP-seq, we reveal that the histone H3 acetylation level is gradually increased on the neural gene loci while decreased on the neural-inhibitory gene loci during mouse ESC neural differentiation. By overlapping with the targets of HDAC1 ChIP-seq, we identify Nodal as a target gene repressed by histone deacetylation. Thus, our study reveals an intrinsic mechanism that epigenetic histone deacetylation ensures neural fate commitment by restricting Nodal signaling.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL11002
8 Samples
Download data: BED, WIG
Series
Accession:
GSE66025
ID:
200066025
16.

Array CGH from mouse SFME cells and SFME cells differentiated with TGFB and FCS

(Submitter supplied) SFME cells (ATCC) were grown as spheres or differentiated with TGFß for 24 h or 10%FCS for 12 h. ArrayCGH experiments were performed on all three samples.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10989
3 Samples
Download data: PAIR, TXT
Series
Accession:
GSE35523
ID:
200035523
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