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Links from GEO DataSets

Items: 13

1.

Fetal liver development

(Submitter supplied) Hepatoblasts emerging at E8.5 from the foregut endoderm proliferate vigorously and differentiate to hepatocytes and biliary epithelial cells. To find genes important for hepatocyte differentiation during development, we compared gene expression profiles of hepatoblasts/immature hepatocytes at E12.5 and E17.5. As Dlk, also known as Pref-1, is expressed in hepatoblasts/immature hepatocytes, we performed a microarray analysis of the Dlk+ cells isolated from livers at E12.5 and E17.5. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7533
1 Sample
Download data: TXT
Series
Accession:
GSE13363
ID:
200013363
2.

The basic helix-loop-helix transcription factor Mist1 overexpression in mouse fetal hepatoblast culture

(Submitter supplied) To identify the molecular mechanism of Mist1 during hepatoblasts differentiation, we performed gene expression analysis in Mist1 over-expressed cells. Dlk+ hepatoblasts derived from E13 fetal livers were purified. Purification of Dlk+ cells were performed using anti-Dlk antibody after hematopoietic cells were removed. Cells were infected with mock or Mist1-overexpressing retroviruses and cultured for 3days with oncostatin M.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
6 Samples
Download data: TXT
Series
Accession:
GSE67406
ID:
200067406
3.

FS001: Aberrant gene expression in dogs with portosystemic shunts

(Submitter supplied) Background: Congenital portosystemic shunts are developmental anomalies of the vascular system that cause portal blood to bypass the liver. Large-breed dogs are reported to have a predisposition for intrahepatic portosystemic shunts (IHPSS) and small-breed dogs a predisposition for extrahepatic portosystemic shunts (EHPSS). While the physiological consequences of the two types of shunt are identical, the metabolic pathways involved are probably different. more...
Organism:
Canis lupus familiaris
Type:
Expression profiling by array
Platform:
GPL15184
92 Samples
Download data: TXT
Series
Accession:
GSE39005
ID:
200039005
4.

C/EBPa Regulates Protease/anti-protease Balance and Mediates Bronchiolar Cell Recovery After Injury

(Submitter supplied) In the present study, we hypothesized that C/EBPa (CCAAT/enhancer-binding protein alpha) plays a role in cell regeneration in response to bronchiolar epithelial cell injury. C/EBPa mediated ciliated cell regeneration after naphthalene bronchiolar epithelial cell injury in vivo. Furthermore, we demonstrated that C/EBPa regulates protease/anti-protease balance after lung injury, and intratracheal treatment with anti-protease (BPTI) restored ciliated cell regeneration after naphthalene injury in CebpaD/D mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
18 Samples
Download data: CEL
Series
Accession:
GSE29285
ID:
200029285
5.

profiling of C/EBP targets

(Submitter supplied) The zinc-inducible C/EBP expression vectors pMTa, pMTb, pMTd and pMTe were constructed by cloning the human C/EBPa, C/EBPb, C/EBPd and C/EBPe cDNAs, respectively, into the pMTCB6+ vector. NIH 3T3 cells were transfected with zinc-inducible C/EBP vectors as well as control empty vector using the GenePORTER™ transfection Reagent (GTS Inc.). Multiple polyclonal clones were obtained by selection with G418 (700 mg/ml). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1872
Platform:
GPL81
15 Samples
Download data
Series
Accession:
GSE2188
ID:
200002188
6.
Full record GDS1872

CCAAT/enhancer-binding proteins C/EBP alpha, beta, delta, and epsilon induction

Analysis of NIH 3T3 cells following induction of CCAAT/enhancer-binding protein (C/EBP) alpha, beta, delta, or epsilon from zinc inducible expression vectors. The C/EBP family of transcription factors regulate growth and differentiation in numerous cell types. Results identify C/EBP targets.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 agent sets
Platform:
GPL81
Series:
GSE2188
15 Samples
Download data
7.

C/EBPa mediates the growth inhibitory effect of progestins on breast cancer cells

(Submitter supplied) Steroid hormones are key gene regulators in breast cancer cells. While estrogens stimulate cell proliferation, progestins activate a single cell cycle followed by proliferation arrest. Here, we use biochemical and genome wide approaches to show that progestins achieve this effect via a functional crosstalk with C/EBPα. Using ChIP-seq, we identify around 1,000 sites where C/EBPα binding precedes and helps binding of Progesterone Receptor (PR) in response to hormone. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
30 Samples
Download data: BW, TXT
Series
Accession:
GSE132649
ID:
200132649
8.

Temporal mapping of C/EBPα and –β binding during liver regeneration

(Submitter supplied) Temporal mapping of C/EBPα and –β binding during liver regeneration reveals dynamic occupancy and specific regulatory codes for homeostatic and cell cycle gene batteries.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11002
26 Samples
Download data: BED
Series
Accession:
GSE42321
ID:
200042321
9.

Bookmarking by “non-pioneer” transcription factors during liver development establishes competence for future gene activation

(Submitter supplied) Transcription factor binding to enhancer and promoter regions is critical for gene activation. To understand how cell-specific gene expression patterns are generated, we studied the developmental timing of association of two prominent hepatic transcription factors with gene regulatory regions. We found that most individual binding events displayed extraordinarily high temporal variations during liver development. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
4 related Platforms
48 Samples
Download data: BED, BIGWIG, TXT
Series
Accession:
GSE137066
ID:
200137066
10.

Whole genome gene expression profiles of migratory cells in the Drosophila ovary

(Submitter supplied) Cell migration contributes to normal development and homeostasis as well as to pathological processes such as inflammation and tumor metastasis. Previous genetic screens have revealed a few major signaling pathways that govern follicle cell migrations in the Drosophila ovary, several of which elicit transcriptional responses. However few downstream targets of the critical transcriptional regulators, such as the C/EBP homolog SLBO, have been identified. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Dataset:
GDS1877
Platform:
GPL72
12 Samples
Download data: CEL
Series
Accession:
GSE4235
ID:
200004235
11.
Full record GDS1877

slbo mutant migratory cells of the ovary

Analysis of slbo mutant border and centripetal migratory cells in the ovary. SLBO, a C/EBP family transcriptional activator, is required for the switch from stationary to migratory behavior. Results identify genes involved in cell migration and downstream targets of SLBO.
Organism:
Drosophila melanogaster
Type:
Expression profiling by array, count, 2 cell type, 2 genotype/variation sets
Platform:
GPL72
Series:
GSE4235
12 Samples
Download data: CEL
DataSet
Accession:
GDS1877
ID:
1877
12.

Transcriptional ontogeny of the developing liver

(Submitter supplied) We characterized gene expression changes in the developing mouse liver at gestational days (GD) 11.5, 12.5, 13.5, 14.5, 16.5, and 19.5 and in the neonate (postnatal day (PND) 7 and 30) using full-genome microarrays and compared these changes to that in the adult liver. The fetal liver, and to a lesser extent the neonatal liver, exhibited dramatic differences in gene expression compared to adults. Canonical pathway analysis of the fetal liver signature demonstrated increases in functions important in cell replication and DNA fidelity whereas most metabolic pathways of intermediary metabolism were suppressed. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
16 Samples
Download data: CEL
Series
Accession:
GSE21224
ID:
200021224
13.

Multi-stage analysis of gene expression in C57/B6 mouse liver development

(Submitter supplied) The liver performs a number of essential functions for life. The development of such a complex organ relies on finely regulated gene expression profiles which change over time in the development and determine the phenotype and function of the liver. We used high-density oligonucleotide microarrays to study the gene expression and transcription regulation at 14 time points across the C57/B6 mouse liver development, which include E11.5 (embryonic day 11.5), E12.5, E13.5, E14.5, E15.5, E16.5, E17.5, E18.5, Day0 (the day of birth), Day3, Day7, Day14, Day21, and normal adult liver. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
25 Samples
Download data: CEL
Series
Accession:
GSE13149
ID:
200013149
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