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Links from GEO DataSets

Items: 20

1.

Murine Hepatoblasts

(Submitter supplied) The homeobox transcription factor Prox1 is expressed in embryonic hepatoblasts and remains expressed in adult hepatocytes. Prox1-null mice show severe deficiencies of liver development, but the underlying mechanisms are unknown. We studied the effects of Prox1 on the transcriptional profile of embryonic day-14 (ED14) met-murine-hepatocytes (ED14-MMH). These immortalized murine hepatoblasts express numerous hepatoblast markers, but not Prox1. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2872
6 Samples
Download data: GPR
Series
Accession:
GSE7867
ID:
200007867
2.

Prox1 determines hepatocyte versus cholangiocyte cell fate in liver progenitors

(Submitter supplied) The mammalian liver, the largest solid organ in the body, accomplishes multiple critical roles necessary to preserve homeostasis. Human liver diseases are debilitating, costly and very often result in death. Uncovering developmental mechanisms that establish the complex architecture of the liver or generate the cellular diversity of this organ is necessary to develop more adequate methods to prevent, diagnose and cure liver diseases. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, CHP
Series
Accession:
GSE36583
ID:
200036583
3.

RLSC and MMH-D3 cell lines

(Submitter supplied) Increasing evidence provide support that the mammalian liver contains stem/progenitor cells, but their molecular phenotype, embryological derivation, cell biology as well as of their role in the liver cell turnover and regeneration remain to be further clarified. We report the isolation, characterization and reproducible establishment in line of a resident liver stem cell (RLSC) with immunophenotype and differentiative potential distinct from other previously reported liver precursor/stem cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3520
Platform:
GPL1261
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE7038
ID:
200007038
4.
Full record GDS3520

Resident liver stem cell lines

Analysis of the resident liver stem cell (RLSCs) lines MetE14/3 and WTE14/1. Results provide insight into the molecular phenotype of RLSCs.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 cell line, 2 cell type sets
Platform:
GPL1261
Series:
GSE7038
4 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS3520
ID:
3520
5.

Prox1 downregulation is a prerequisite for the maturation and expansion of postnatal murine beta cells

(Submitter supplied) Alterations in the expression of key transcription factors can be harmful for pancreatic beta cell homeostasis and could lead to diabetes. This study uncovered that Prox1 overexpression obstructs beta cell maturation and results in severe hyperglycemia. The function of β-cells is key for glucose homeostasis because they supply insulin to the entire body. Genetic or metabolic conditions that disrupt the complex physiology of β-cells can lead to diabetes mellitus, a prevalent life-threatening disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE68133
ID:
200068133
6.

Lgr5+ stem and progenitor cells reside at the apex of a heterogeneous embryonic hepatoblast pool

(Submitter supplied) During mouse embryogenesis, progenitors within the liver known as hepatoblasts give rise to adult hepatocytes and cholangiocytes. Hepatoblasts, which are specified at E8.5-E9.0, have been regarded as a homogeneous progenitor population that initiate differentiation from E13.5. Recently, scRNA-seq analysis has identified sub- populations of transcriptionally distinct hepatoblasts at E11.5. Here, we show that hepatoblasts are not only transcriptionally but also functionally heterogeneous, and that a subpopulation of E9.5-E10.0 hepatoblasts exhibit a previously unidentified early commitment to cholangiocyte fate. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
653 Samples
Download data: CSV
Series
Accession:
GSE123103
ID:
200123103
7.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Gallus gallus
Type:
Expression profiling by array
Platforms:
GPL3213 GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE106788
ID:
200106788
8.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord [chicken]

(Submitter supplied) The HMG-domain containing SoxC transcription factors Sox4 and Sox11 are expressed in the vertebrate central nervous system in neuronal precursors and neuroblasts. They are required during early stages of neurogenesis. Here we perform micorarray analysis to identify genes that are downstream of these SoxC proteins during spinal cord neurogenesis in chicken. The identified genes represent potential direct target genes of Sox4 and Sox11.
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
2 Samples
Download data: CEL
Series
Accession:
GSE106787
ID:
200106787
9.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord [mouse]

(Submitter supplied) The HMG-domain containing SoxC transcription factors Sox4 and Sox11 are expressed in the vertebrate central nervous system in neuronal precursors and neuroblasts. They are required during early stages of neurogenesis. Here we perform micorarray analysis to identify genes that are downstream of these SoxC proteins during spinal cord neurogenesis in mouse. The identified genes represent potential direct target genes of Sox4 and Sox11.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE106786
ID:
200106786
10.

Single cell changes in DBZ or DMSO treated cells derived from Apc-mutant organoid cultures

(Submitter supplied) We made intestinal organoid cultures from Villin-CreERT2;Apcflox/flox mice. Organoids were subjected to 4-OH-Tam treatment, whereafter Apc mutant organoids were selected in R-Spondin free medium. DBZ or DMSO treatment was started on day 3. On day 8, organoids were dissociated to obtain single cells and analyzed using the Chromium Single-cell 3'RNA-sequencing system
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
2 Samples
Download data: TXT
Series
Accession:
GSE118055
ID:
200118055
11.

Characterizing the gene expression profile of Prox1+ intestinal adenoma organoid cells

(Submitter supplied) We isolated and selected intestinal adenoma organoids from Apcmin/+; Rosa26LSL-TdTomato; Prox1-CreERT2 mice. After the selection procedure without growth factors, we induced CreERT2 activity and the transcription of tdTomato to label Prox1+ cells by 300 nM 4-hydroxytamoxifen for 16h. tdTomato+ (Prox1+) and tdTomato- cells (enriched for Prox1- cells) were FACS sorted and total RNA was isolated.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
6 Samples
Download data: TXT
Series
Accession:
GSE117981
ID:
200117981
12.

An HDAC3-PROX1 Corepressor Module Acts on HNF4α to Control Hepatic Triglycerides

(Submitter supplied) The histone deacetylase HDAC3 is a critical mediator of hepatic lipid metabolism, and liver-specific deletion of HDAC3 leads to fatty liver. To elucidate the underlying mechanism we developed a method of cross-linking followed by mass spectrometry to define a high-confidence HDAC3 interactome in vivo that includes the canonical NCoR/HDAC3 complex as well as Prospero-related homeobox 1 protein (PROX1). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL13112
34 Samples
Download data: BED, BIGWIG, XLSX
Series
Accession:
GSE90533
ID:
200090533
13.

Gene expression profiles of lymphatic endothelial cells after knockdown of Prox1 and/or NR2F2

(Submitter supplied) Gene expression profiles of primary lymphatic endothelial cells (LECs) isolated from human foreskin were analyzed after siRNA-mediated knockdown of control (firefly luciferase), Prox1, NR2F2 or Prox1/NR2F2 for 48 hours.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3534
Platform:
GPL570
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE12846
ID:
200012846
14.
Full record GDS3534

Lymphatic endothelial cell response to Prox1 and NR2F2 depletion

Analysis of lymphatic endothelial cells (LECs) depleted for Prox1, NR2F2, or both regulators. LECs are derived from venous endothelial cells (VECs). Prox1 and NR2F2 regulate LEC and VEC development, respectively. Results provide insight into the role of NR2F2 and Prox1 in maintaining LEC phenotypes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 protocol sets
Platform:
GPL570
Series:
GSE12846
4 Samples
Download data: CEL, CHP
15.

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
16.

Effect of Prox1 in tibialis anterior skeletal muscle

(Submitter supplied) We show that Prox1 overexpression induces slow muscle fiber type gene program in fast muscle and activates calcineurin signaling
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
6 Samples
Download data: TXT
Series
Accession:
GSE69199
ID:
200069199
17.

Genome-wide analysis of embryonic gene epression in the absence of Prox1 compared to wild type

(Submitter supplied) Overview: We report here that gene expression in E13.5 wild type (WT) mouse lenses differs from the lenses of mice that conditionally lack the Prox1 transcription factor in the lens of their eyes (Prox1 cKO) as assayed by high throughput RNA sequencing (RNAseq). The methodology outlined herein is similar to a previous RNAseq experiment from our lab (Manthey et al., 2014a)(Geo ascension: GSE 49949), and the filtering and processing criteria for this experiment was published as well.(Manthey et al., 2014b). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TXT
Series
Accession:
GSE69940
ID:
200069940
18.

Global transcript analysis of livers and/or jejunums of liver-specific Lrh-1 knockout as well as Lrh-1 K289R knockin mice

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL18741 GPL16570
44 Samples
Download data: CEL
Series
Accession:
GSE59333
ID:
200059333
19.

Global hepatic transcript data from LRH-1 hep+/+ and LRH-1 hep-/- livers

(Submitter supplied) Transcript data from LRH-1 hep+/+ and LRH-1 hep-/- livers from mice fed ad libitum and sacrificed at 7 am We used microarrays to detail the global programme of gene expression underlying hepatic function in ad libitum fed mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL18741
16 Samples
Download data: CEL
Series
Accession:
GSE59305
ID:
200059305
20.

Global hepatic transcript data from LRH-1 WT and LRH-1 K289R livers

(Submitter supplied) Transcript data from LRH-1 WT and LRH-1 K289R livers from mice fed ad libitum and sacrificed at 7 am We used microarrays to detail the global programme of gene expression underlying hepatic function in ad libitum fed mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL18741
14 Samples
Download data: CEL
Series
Accession:
GSE59304
ID:
200059304
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