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Links from GEO DataSets

Items: 20

1.
Full record GDS3936

Primary erythroblast culture response to cytokine-induced increase in fetal hemoglobin

Analysis of primary CD34+ hematopoietic progenitor cells, cultured in low-HbF (EPO alone) or high-HbF conditions (EPO, SCF, and TGFbeta-1), on days 7 (proerythroblasts) and 14 (mature erythrocytes). Results provide insight into molecular mechanisms underlying cytokine-induced increases in HbF.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 development stage, 2 growth protocol, 2 time sets
Platform:
GPL570
Series:
GSE7874
15 Samples
Download data: CEL
2.

Effects of EPO and EST on erythroid maturation

(Submitter supplied) Transcriptional profiles of human CD34+ cells cultured in EPO and EST conditions.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3936
Platform:
GPL570
15 Samples
Download data: CEL
Series
Accession:
GSE7874
ID:
200007874
3.

Human Fetal Hemoglobin Expression is Regulated by the Developmental Stage-Specific Repressor BCL11A

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL570
22 Samples
Download data: CEL
Series
Accession:
GSE13285
ID:
200013285
4.

Human CD34-derived erythroid progenitors treated with BCL11A siRNAs

(Submitter supplied) Differences in the amount of fetal hemoglobin (HbF) that persists into adulthood affect the severity of sickle cell disease and the beta-thalassemia syndromes. Genetic association studies have identified sequence variants in the gene BCL11A that influence HbF levels. Here we examine BCL11A as a potential regulator of HbF expression. The high HbF BCL11A genotype is associated with reduced BCL11A expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE13284
ID:
200013284
5.

Mouse Erythroleukemia (MEL) Cells Expressing Tagged Versions of BCL11A

(Submitter supplied) Differences in the amount of fetal hemoglobin (HbF) that persists into adulthood affect the severity of sickle cell disease and the beta-thalassemia syndromes. Genetic association studies have identified sequence variants in the gene BCL11A that influence HbF levels. Here we examine BCL11A as a potential regulator of HbF expression. The high HbF BCL11A genotype is associated with reduced BCL11A expression. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
10 Samples
Download data: CEL
Series
Accession:
GSE13283
ID:
200013283
6.

EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154 GPL16791
78 Samples
Download data
Series
Accession:
GSE71422
ID:
200071422
7.

EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq]

(Submitter supplied) Using UNC0638 and genetic assays to inhibit EHMT1/2 and derepress fetal hemoglobin in adult hematopoietic cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
8.

EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [ChIP-seq]

(Submitter supplied) Using UNC0638 and genetic assays to inhibit EHMT1/2 and derepress fetal hemoglobin in adult hematopoietic cells.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL18573
72 Samples
Download data: TDF
Series
Accession:
GSE69516
ID:
200069516
9.

Disruption of the MBD2-NuRD complex but not MBD3-NuRD induces high level HbF expression in human adult erythroid cells

(Submitter supplied) As high fetal hemoglobin (HbF) levels ameliorate the underlying pathophysiologic defects in sickle cell anemia and β-thalassemia, understanding the mechanisms that enforce silencing of HbF postnatally offers the promise of effective molecular therapy. Depletion of Methyl cytosine Binding Domain protein 2 (MBD2) causes a 10-20 fold increase in γ-globin gene expression in adult β-YAC transgenic mice. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TXT
10.

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL11154
9 Samples
Download data: TDF
Series
Accession:
GSE160603
ID:
200160603
11.

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia [ChIP-seq]

(Submitter supplied) The fetal-to-adult hemoglobin switch is regulated in a developmental stage-specific manner and reactivation of fetal hemoglobin (HbF) has therapeutic potential for β-hemoglobinopathies. Although BCL11A and ZBTB7A interact with their coregulators, reportedly mediating most γ-globin transcriptional silencing in erythroid in trans, and in cis, the molecular mechanism underlying the epigenetic dysregulation of the switch remains largely unclear. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: TDF
Series
Accession:
GSE160602
ID:
200160602
12.

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia [RNA-seq]

(Submitter supplied) The fetal-to-adult hemoglobin switch is regulated in a developmental stage-specific manner and reactivation of fetal hemoglobin (HbF) has therapeutic potential for β-hemoglobinopathies. Although BCL11A and ZBTB7A interact with their coregulators, reportedly mediating most γ-globin transcriptional silencing in erythroid in trans, and in cis, the molecular mechanism underlying the epigenetic dysregulation of the switch remains largely unclear. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
5 Samples
Download data: TXT, XLS
13.

Chemical inhibition of Histone Deacetylases 1 and 2 induces fetal hemoglobin through activation of Gata2

(Submitter supplied) This SuperSeries is composed of the SubSeries GSE60791 and GSE60792.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL15207
11 Samples
Download data: BW, CEL
Series
Accession:
GSE60793
ID:
200060793
14.

ChIP-seq of erythroid progenitors treated with vehicle or the HDAC1/2-selective inhibitor ACY-957

(Submitter supplied) Establish the DNA binding profiles of HDAC1, HDAC2 and Gata2 in erythroid progenitors derived from human CD34+ bone marrow cells. Determine the effects of HDAC1/2 inhibition on the DNA binding profiles of Gata2.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
5 Samples
Download data: BW
Series
Accession:
GSE60792
ID:
200060792
15.

Gene expression profiles of erythroid progenitors treated with vehicle or the HDAC1/2-selective inhibitor ACY-957

(Submitter supplied) Determine the effects of HDAC1/2-selective chemical inhibtion on the gene expression profiles of erythroid progenitors derived from human CD34+ bone marrow cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
6 Samples
Download data: CEL
Series
Accession:
GSE60791
ID:
200060791
16.

Small RNA sequencing reveals distinct miRNA signatures and networks during fetal and adult erythroid differentiation

(Submitter supplied) MicroRNAs (miRNAs) are small non-coding RNAs (sncRNAs) crucial for post-transcriptional and translational regulation of cellular and developmental pathways. Study of miRNAs in erythropoiesis thus elucidates the process and facilitates diagnosis and therapy development for related disorders. Here, we used high-throughput DNA Nanoball small RNA sequencing to characterise sncRNAs, and in particular miRNAs, comprehensively in human erythroid cell cultures. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL23227
18 Samples
Download data: TXT, XLSX
17.

Genome-wide microRNA analysis of reticulocytes isolated from patients with sickle cell disease

(Submitter supplied) MiRNAs are non-protein-coding small RNA molecules negatively regulating gene through inhibition of mRNA. The characteristics of microRNA expression patterns obtained from sickle cell diseases are not clearly elucidated. In this study, we recruited 12 children and adults suffering from sickle cells diseases with high HbF fetal hemoglobin (HbF) group (6 subjects) and lower HbF (6 subjects). The peripheral blood mononuclear cell (PBMN) were processed using a MACS column with magnetic anti-CD71 antibody to isolate reticulocytes according to the manufacturer’s instructions (Miltenyi Biotec, San Diego, CA). more...
Organism:
Rattus norvegicus; Homo sapiens; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL17728
12 Samples
Download data: TXT
Series
Accession:
GSE111356
ID:
200111356
18.

Genome Wide CUT&Tag in Day 7 and Day 10 human terminally maturing erythroblasts

(Submitter supplied) Occupancy of Ser5-Pol2 and Ser2-Pol2
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
12 Samples
Download data: BW
Series
Accession:
GSE171492
ID:
200171492
19.

Terminally maturing erythroblasts have dynamic changes in transcription-related chromatin modifications and RNA Polymerase II occupancy

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20795 GPL11154
30 Samples
Download data: BIGWIG, BW, TXT
Series
Accession:
GSE155849
ID:
200155849
20.

Terminally maturing erythroblasts have dynamic changes in transcription-related chromatin modifications and RNA Polymerase II occupancy (RNA-Seq)

(Submitter supplied) We suggest a novel paradigm for understanding the epigenetic mechanisms that govern terminal erythroid maturation, and underlie inherited and acquired erythroid disease.  
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: TXT
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