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Links from GEO DataSets

Items: 12

1.
Full record GDS2757

Retinoblastoma protein deficiency effect on fetal livers

Analysis of embryonic day 12.5 livers from retinoblastoma protein (Rb)-null mutants. Rb-null embryos exhibit defective fetal liver erythropoiesis. Results provide insight into the molecular basis of the erythroblastic island defect in the Rb-null fetal liver.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE6787
6 Samples
Download data: CEL
2.

Expression data from wildtype and Rb-/- fetal liver at e12.5

(Submitter supplied) Rb null embryos exhibit defective fetal liver erythropoiesis. We used microarrays to compare Wt and Rb null fetal livers and to analyse gene expression differences which accompany and may underlie Rb null fetal liver degeneration, erythroid failure, and erythropoietic island dissolution. We used microarrays to compare Wt and Rb null fetal livers and analyse gene expression changes which accompany and may underlie fetal liver. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2757
Platform:
GPL81
6 Samples
Download data: CEL
Series
Accession:
GSE6787
ID:
200006787
3.

RNA-sequencing of murine wildtype and E2F-2 knockout hematopoietic progenitors and mature erythroblasts

(Submitter supplied) We identified a role for E2F-2 in the regulation of erythroblast nuclear condensation and enucleation. To help define the mechanism by which E2F-2 regulates these processes, we performed RNA-sequencing on undifferentiated hematopoietic cells and sorted, orthochromatic erythroblasts obtained from wildtype and E2F-2 knockout animals. In undifferentiated progenitor cells we find a limited number of differentially expressed genes associated with E2F-2-loss, likely due to compensation by other E2F family members. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16331
8 Samples
Download data: TXT
Series
Accession:
GSE87127
ID:
200087127
4.

Rb Intrinsically Promotes Erythropoiesis by Coupling Cell Cycle Exit with Mitochondrial Biogenesis

(Submitter supplied) Regulation of the cell cycle is intimately linked to erythroid differentiation, yet how these processes are coupled is not well understood. To gain insight into this coordinate regulation, we examined the role that the retinoblastoma protein (Rb), a central regulator of the cell cycle, plays in erythropoiesis. We found that Rb serves a cell-intrinsic role and its absence causes ineffective erythropoiesis, with a differentiation block at the transition from early to late erythroblasts. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE9717
ID:
200009717
5.

WT vs c-Maf KO fetal liver macrophage

(Submitter supplied) Homozygous disruption of c-Maf led to embryonic lethality and impaired erythroblastic island formation. c-Maf is expressed in the fetal liver macrophages. It suggests that macrophages are responsible for the lethality of c-Maf knock-out embryos. To search downstream genes of c-Maf, we surveyed genes associated with macrophage function by microarray analysis. keywords: c-Maf, macrophage, erythroblastic islands,
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, CHP
Series
Accession:
GSE23305
ID:
200023305
6.

Tmod3-/- mouse fetal liver compared with wild type

(Submitter supplied) Tropomodulins (Tmods) cap the pointed ends of actin filaments in erythroid and nonerythoid cell types. Targeted deletion of mouse Tmod3 leads to embryonic lethality at E14.5-E18.5, with anemia due to defects in definitive erythropoiesis in the fetal liver. BFU-E and CFU-E colony numbers are greatly reduced, indicating defects in progenitor populations. Flow-cytometry of fetal liver erythroblasts shows late stage populations are also decreased, including reduced percentages of enucleated cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4827
Platform:
GPL6246
6 Samples
Download data: CEL
Series
Accession:
GSE51960
ID:
200051960
7.
Full record GDS4827

Tropomodulin3 deficiency effect on the fetal liver

Analysis of at E14.5 fetal livers of Tropomodulin3 (Tmod3) deficient mutants. Tmod3 deletion leads to embryonic lethality at E14.5-E18.5, with anemia due to defects in definitive erythropoiesis in the fetal liver. Results provide insight into the role of Tmod3 in erythroid differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE51960
6 Samples
Download data: CEL
8.

Deletion of Stk40 impairs definitive erythropoiesis in the mouse fetal liver

(Submitter supplied) The serine threonine kinase Stk40 has been shown to involve in mouse embryonic stem cell differentiation, pulmonary maturation and adipocyte differentiation. Here we report that targeted deletion of Stk40 leads to fetal liver hypoplasia and anemia in the mouse embryos. The reduction of erythrocytes in the fetal liver is accompanied by increased apoptosis and compromised erythroid maturation. Stk40-/- fetal liver cells have significantly reduced colony forming units (CFUs) capable of erythroid differentiation, including burst forming unit-erythroid (BFU-E), colony forming unit-erythroid (CFU-E), and CFU-granulocyte, erythrocyte, megakaryocyte and macrophage (CFU-GEMM), but not CFU-granulocyte/macrophages (CFU-GM). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL, XLSX
Series
Accession:
GSE95017
ID:
200095017
9.

An essential cell cycle regulator drives chromatin condensation in maturing erythroblasts

(Submitter supplied) We report that Setd8 is essential for murine erythropoeisis. Setd8 null erythroblasts have severe defects in cell cycle progression, chromatin condensation,and heterochromatin integrity. They also have dysregulated gene expression.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TXT
Series
Accession:
GSE83809
ID:
200083809
10.

Expression profiling of mouse fetal liver late erythroblasts after knockdown of Xpo7

(Submitter supplied) To determine the transcriptional function (if any) of the presumed nuclear export protein Xpo7 or RanBP16 Murine fetal liver erythroid precursors (Ter119-negative cells) were isolated from C57Bl6 E14.5 embryos by magnetic depletion and infected with retroviruses containing shRNA constructs against Xpo7. They were then cultured in Epo-containing media (2U/mL) for 36hrs until they were fully differentiated and then sorted by FACS for GFP+ (infected) cells in order to isolate total RNA to be used for the profiling.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
1 Sample
Download data: TXT
Series
Accession:
GSE54457
ID:
200054457
11.

Single cell RNA-seq analysis for spleen tissue under steady state, phenohydrazine (PHZ) and bleeding treatment.

(Submitter supplied) Single cell RNA-seq analysis for spleen tissue isolated from mice under steady state, and subjected to phenohydrazine (PHZ) and bleeding treatment respectively. Single cell RNA-seq analysis for bone marrow cells isolated from mice under steady state.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
4 Samples
Download data: RDS, TSV
Series
Accession:
GSE230331
ID:
200230331
12.

Single cell RNA-seq analysis for early erythroblasts in spleen and bone marrow (BM) with or without mitochondria transfer

(Submitter supplied) Single cell RNA-seq analysis for early erythroblasts in spleen and BM with or without mito-Dendra2 fluorescence signal after macrophage infusion upon PHZ treatment
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
4 Samples
Download data: H5, TSV
Series
Accession:
GSE185267
ID:
200185267
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