U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.
Full record GDS568

Erythroid differentiation: G1E model

Analysis of erythroid differentiation using G1E ER4 clone cells. Estradiol addition induces Gata-1 triggering synchronous differentiation. 30 hour time course corresponds to late burst-forming unit-erythroid stage through orthochromatic erythroblast stage.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 6 time sets
Platform:
GPL81
Series:
GSE628
18 Samples
Download data: CEL
DataSet
Accession:
GDS568
ID:
568
2.

Erythroid Differentiation: G1E Model

(Submitter supplied) G1E cells are a Gata-1 erythroid-committed cell line derived from targeted disruption of Gata-1 in embryonic stem cells. The ER4 subclone contains an inducible form of Gata-1 (Gata-1-ER, Gata-1 fused to the estradiol receptor ligand binding domain). We performed transcriptome analysis using this cell line. Estradiol was added to culture medium triggering synchronous and homogenous differentiation. At various time points, RNA was sampled and analyzed using the Affymetrix MG-U74Av2 platform. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS568
Platform:
GPL81
18 Samples
Download data: CEL
Series
Accession:
GSE628
ID:
200000628
3.

FOG-1-independent transcripition by GATA-1(V205G) in G1E cells

(Submitter supplied) Identification of genes regulated by GATA-1 independent of the cofactor FOG-1. Keywords: cell treatment comparison
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL
Series
Accession:
GSE6958
ID:
200006958
4.

Expression data from normal and MDS erythroids cell cutlures ex vivo

(Submitter supplied) CD34 positive cells of bone marrow samples from normal and MDS samples were cultured ex vivo into erythroid conditions. We used microarrays to detail the gene expression programm of erythroid cells between normal and pathological (MDS) samples
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
26 Samples
Download data: CEL
Series
Accession:
GSE34268
ID:
200034268
5.

Genome-wide maps of GATA1 occupany in induced G1E ER4 cell line.

(Submitter supplied) we mapped the locations of DNA segments occupied by GATA1 using chromatin immunoprecipitation (ChIP). We have produced genome-wide GATA1 ChIP datasets after restoration and activation in G1E-ER4 cells. we employed the sequence census methodology of ChIP-seq , using Illumina GA2 technology to produce 23 million reads (36 nucleotides long) uniquely mapped to the mouse genome (mm8 assembly) for the GATA1 ChIP DNA and 15 million mapped reads for the input DNA
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9250
2 Samples
Download data: TXT
Series
Accession:
GSE18164
ID:
200018164
6.

Erythroid differentiation: G1E model

(Submitter supplied) Analysis of erythroid differentiation using Gata1 gene-disrupted G1E ER4 clone cells. Estradiol addition activates an ectopically expressed Gata-1-estrogen receptor fusion protein, triggering synchronous differentiation. 30 hour time course corresponds roughly to late burst-forming unit-erythroid stage (t=0 hrs) through orthochromatic erythroblast stage (t=30 hrs).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE18042
ID:
200018042
7.

HRI Protects Erythroid Precursors in iron deficiency and beta-Thalassemia by Maintaining GATA-1 and Fog-1 Expression

(Submitter supplied) Heme-regulated eIF2α kinase (HRI) is essential for the survival of erythroid precursors in iron and heme deficiency and it also plays a protective role in red blood cell diseases of erythroid protoporphyria and β-thalassemia. In this study, we demonstrated for the first time the impairment of GATA-1 and Fog-1 expressions in iron deficiency and the impairment of GATA-1 expression in β-thalassemia. Furthermore, HRI is necessary to maintain the GATA-1/Fog-1 induced functions in erythroid differentiation, cell cycle and cell survival by sustaining both expressions of GATA-1 and Fog-1 in iron deficiency and in β-thalassemia. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL96 GPL339
24 Samples
Download data: CEL
Series
Accession:
GSE6808
ID:
200006808
8.

HEXIM1 Overexpression Alters GATA1 Activity and Promotes Fetal Globin Expression

(Submitter supplied) Erythropoiesis is a highly organized process whereby multipotent HSCs become committed to the erythroid linage and mature into enucleate erythrocytes. Recent work from our lab demonstrated that HEXIM1 is essential in the regulation of erythroid proliferation, viability and gene expression, and also promotes the expression of GATA1 target genes. New analyses of HEXIM1 overexpression (OE) in HUDEP2 cells revealed a significant increase of gamma globin production, with a higher proportion of cells expressing fetal hemoglobin. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
45 Samples
Download data: BW
Series
Accession:
GSE213220
ID:
200213220
9.

Foxo3 Regulated Genes in G1E-ER-GATA-1 Cells

(Submitter supplied) The ensemble of Foxo3-regulated genes in the erythroid G1E-ER-GATA-1 cell line was determined by knocking down Foxo3 using siRNA, and measuring genome wide transcription by microarray analysis
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE60137
ID:
200060137
10.

Exosc8-Regulated Genes in Fetal Liver-Derived Erythroid Progenitor Cells

(Submitter supplied) Exosc8 and Exosc9 are components of the exosome that establish a barricade to erythroid maturation. Here, we knocked down Exosc8 in fetal liver-derived erythroid progenitor cells to determine the cohort of Exosc8-regulated genes in erythroid cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE60136
ID:
200060136
11.

SetD8 Knockdown in ß-estradiol-treated (24 h) G1E-ER-GATA-1 cells

(Submitter supplied) The establishment and maintenance of cell type-specific transcriptional programs require an ensemble of broadly expressed chromatin remodeling and modifying enzymes. Many questions remain unanswered regarding the contributions of these enzymes to specialized genetic networks that control critical processes such as lineage commitment and cellular differentiation. We have been addressing this problem in the context of erythrocyte development driven by the transcription factor GATA-1 and its coregulator Friend of GATA-1 (FOG-1). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE49174
ID:
200049174
12.

Autophagy driven by a master regulator of hematopoiesis

(Submitter supplied) Developmental and homeostatic remodeling of cellular organelles is mediated by a complex process termed autophagy. The cohort of proteins that constitute the autophagy machinery function in a multistep biochemical pathway. Though components of the autophagy machinery are broadly expressed, autophagy can occur in specialized cellular contexts, and mechanisms underlying cell type-specific autophagy are poorly understood. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10999
4 Samples
Download data: TXT
Series
Accession:
GSE32491
ID:
200032491
13.

GATA-1-regulated erythroid microRNAs

(Submitter supplied) We employed a gene complementation strategy combined with microarray screening to identify miRNAs involved in the formation of erythroid (red blood) cells. To search for GATA-1-regulated erythroid miRNAs, we used the Gata-1– erythroblast line G1E. These cells proliferate in culture as immature erythroid precursors and undergo terminal maturation when GATA-1 activity is restored. G1E-ER4 is a sub-line stably expressing an estrogen-activated form of GATA-1 (GATA-1 fused to the ligand binding domain of the estrogen receptor). more...
Organism:
Homo sapiens; Mus musculus; Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL5531
6 Samples
Download data: TXT, XLS
Series
Accession:
GSE10134
ID:
200010134
14.

Cpeb4-mediated Translational Regulatory Circuitry Controls Terminal Erythroid Differentiation

(Submitter supplied) Erythropoiesis is essential to mammals and is regulated at multiple steps by both extracellular and intracellular factors. Many transcriptional regulatory networks in erythroid differentiation have been well characterized. However, our understanding of post-transcriptional regulatory circuitries in this developmental process is still limited. Using genomic approaches, we identified a sequence-specific RNA-binding protein, Cpeb4, which is dramatically induced in terminal erythroid differentiation (TED) by two erythroid important transcription factors, Gata1/Tal1. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17791
4 Samples
Download data: CEL
Series
Accession:
GSE57004
ID:
200057004
15.

Genome-wide map of MAZ transcription factor in primary human erythroid cells

(Submitter supplied) We report the distribution of binding sites of Myc-associated zinc finger (MAZ) transcription factor in primary human erythroid cells
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: BED, BW
Series
Accession:
GSE139281
ID:
200139281
16.

Transcriptome of the maturing erythroblast

(Submitter supplied) Understanding the pattern of gene expression and identifying the specific genes expressed during erythropoiesis is crucial for a synthesis of erythroid developmental biology. Here we have isolated four distinct populations of erythroblasts at successive erythropoietin-dependent stages of erythropoiesis including the terminal, pyknotic stage. The transcriptome has been determined using Affymetrix arrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3860
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE22552
ID:
200022552
17.
Full record GDS3860

Erythropoiesis: PBMC-derived, FACS-sorted erythroid progenitors

Analysis of 4 discrete populations of erythroid progenitors at successive erythropoietin-dependent stages of erythropoiesis: CFU-E, Pro-E, Int-E and Late-E. Unsorted erythroid cells at each stage also examined. Results provide insight into the molecular mechanisms underlying erythroblast maturation.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 4 development stage, 2 protocol sets
Platform:
GPL570
Series:
GSE22552
16 Samples
Download data: CEL
DataSet
Accession:
GDS3860
ID:
3860
18.

Global Transcriptome Analyses of Mammalian Terminal Erythroid Differentiation

(Submitter supplied) Purpose:The purpose of this study is to create unbiased, stage-specific transcriptomes by RNA-seq analyses of pure populations of both murine and human erythroblasts at distinct developmental stages. Methods: Recently developed FACS-based methods (Chen et al, PNAS, Liu et al, Blood, Hu et al Blood) were employed to purify morphologically and functionally discrete populations of cells, each representing specific stages of terminal erythroid differentiation. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL13112 GPL11154
27 Samples
Download data: TXT
Series
Accession:
GSE53983
ID:
200053983
19.

Long noncoding RNA expression in several hematopoietic progenitor and differentiated cell populations

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Third-party reanalysis; Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL17864
19 Samples
Download data: TXT
Series
Accession:
GSE52555
ID:
200052555
20.

Long noncoding RNA expression in several hematopoietic progenitor and differentiated cell populations using a custom Agilent microarray

(Submitter supplied) Mammals express thousands of long noncoding (lnc) RNAs, a few of which are shown to function in tissue development. However, the entire repertoire of lncRNAs and the extent to which they regulate biological processes in different tissues and species are not defined. Indeed, most lncRNAs are not conserved between species, raising questions about function. We used RNA-Seq to identify lncRNAs in primary murine fetal liver erythroblasts expressing the lineage marker TER119, megakaryocytes (CD41+) cultured from embryonic day (E) 14.5 murine fetal liver and megakaryocyte erythroid progenitors (MEPs) isolated from mouse bone marrow. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL17864
19 Samples
Download data: TXT
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=46|qty=4|blobid=MCID_672db1309a2d0f71cf6d6df9|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center