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Links from GEO DataSets

Items: 20

1.

Global gene expression profiling using total RNA [BMM, MPI and SPG]

(Submitter supplied) Differentiation of myeloid progenitor cells leads to distinct populations of mononuclear phagocytes.Various macrophages exhibit distinct biological properties. Here wanted to delineate and characterize gene expression patterns in bone marrow derived macrophages Here wanted to delineate and characterize gene expression patterns in two newly established, self-renewing, in vitro grown non-transformed lines (MPI cells) and in the SP37A3 immature myeloid dendritic cell line. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE47473
ID:
200047473
2.

Capacity of yolk sac macrophages, fetal liver and adult monocytes to colonize an empty niche and develop into functional tissue resident macrophages

(Submitter supplied) Tissue-resident macrophages can derive from yolk sac macrophages, fetal liver monocytes or adult bone marrow monocytes. Whether these precursors can give rise to transcriptionally identical alveolar macrophages is unknown. Here, we transferred traceable yolk sac macrophages, fetal liver monocytes, adult bone marrow monocytes or adult alveolar macrophages as a control, into the empty alveolar macrophage niche of neonatal Csf2rb-/- mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
36 Samples
Download data: CEL
Series
Accession:
GSE76999
ID:
200076999
3.

Identification of PPARG regulated genes in human GM-CSF-primed monocyte-derived macrophages

(Submitter supplied) Identification of PPARG regulated genes in human GM-CSF polarized monocyte-derived macrophages by siRNA knock-down approaches.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL21185
6 Samples
Download data: TXT
Series
Accession:
GSE88768
ID:
200088768
4.

The Cytokines IL-21 and GM-CSF have Opposing Regulatory Roles in the Apoptosis of Conventional Dendritic Cells

(Submitter supplied) Interleukin-21 (IL-21) has broad actions on T- and B-cells, but its actions in innate immunity are poorly understood. Here we show that IL-21 induced apoptosis of conventional dendritic cells (cDCs) via STAT3 and Bim, and this was inhibited by granulocyte-macrophage colony-stimulating factor (GM-CSF). ChIP-Seq analysis revealed genome-wide binding competition between GM-CSF-induced STAT5 and IL-21-induced STAT3. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
6 Samples
Download data: BED
Series
Accession:
GSE27161
ID:
200027161
5.

Human monocyte-derived macrophages polarized by GM-CSF or M-CSF

(Submitter supplied) Identification of genes differentially expressed between human monocyte-macrophages generated in the presence of either GM-CSF (termed M1) or M-CSF (termed M2)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL11010
6 Samples
Download data: TXT
Series
Accession:
GSE27792
ID:
200027792
6.

GM-CSF-mediated granulopoiesis is regulated by the transcription factor STAT5A/B

(Submitter supplied) GM-CSF controls the development of granulocytes but little is known about the contribution of the downstream mediating transcription factor STAT5A/B. To elucidate this pathway, we generated mice lacking the Stat5a and 5b genes in blood cells. Peripheral neutrophils were decreased and administration of 5-FU and GM-CSF failed to induce granulopoiesis in Stat5a/b-mutant mice. GMPs were isolated and cultured with GM-CSF. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE14672
ID:
200014672
7.

Gene expression data from murine M1 and M2 macrophages

(Submitter supplied) Macrophages have distinct characteristics depending on their microenvironment. We performed proteomic analysis between M1 and M2 macrophages and found that cellular metabolism is the key regulator of macrophage function. We used microarray to support proteomic data between M1 and M2 macrophages.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL
Series
Accession:
GSE63245
ID:
200063245
8.

Gene expression and genotype data from human fibroblasts and induced Pluripotent Stem cells from Parkinson's Disease patients

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; SNP genotyping by SNP array
Platforms:
GPL13829 GPL10558
14 Samples
Download data
Series
Accession:
GSE53426
ID:
200053426
9.

SNP data from human fibroblasts and induced Pluripotent Stem cells from Parkinson's Disease patients

(Submitter supplied) We have generated human induced Pluripotent Stem cells (hiPSc) from Parkinson's Disease patients, using retrovirus-mediated delivery of reprogramming factors. hiPSc lines have been screened using SNP array to assess chromosomal stability (alongside the fibroblast lines from which they derived), and validation of the pluripotency of the hiPSc lines is provided by Pluritest assessment of transcriptome datasets, prior to differentiation to dopaminergic neuronal clutures and downstream functional assays. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array
Platform:
GPL13829
9 Samples
Download data: TXT
Series
Accession:
GSE53425
ID:
200053425
10.

Gene expression data from human fibroblasts and induced Pluripotent Stem cells from Parkinson's Disease patients

(Submitter supplied) We have generated human induced Pluripotent Stem cells (hiPSc) from Parkinson's Disease patients, using retrovirus-mediated delivery of reprogramming factors. hiPSc lines have been screened using SNP array to assess chromosomal stability (alongside the fibroblast lines from which they derived), and validation of the pluripotency of the hiPSc lines is provided by Pluritest assessment of transcriptome datasets, prior to differentiation to dopaminergic neuronal clutures and downstream functional assays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
5 Samples
Download data: TXT
Series
Accession:
GSE53424
ID:
200053424
11.

BHLHE40 regulates myeloid cell polarization through IL-10-dependent and independent mechanisms

(Submitter supplied) Better understanding of the host responses to Mycobacterium tuberculosis (Mtb) infections is required to prevent tuberculosis and develop new therapeutic interventions. The host transcription factor BHLHE40 is essential for controlling Mtb infection, in part by repressing Il10 expression, where excess IL-10 contributes to the early susceptibility of Bhlhe40-/- mice to Mtb infection. Deletion of Bhlhe40 in lung macrophages and dendritic cells is sufficient to increase the susceptibility of mice to Mtb infection, but how BHLHE40 impacts macrophage and dendritic cell responses to Mtb is unknown. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
27 Samples
Download data: TXT
Series
Accession:
GSE265840
ID:
200265840
12.

PPARγ controls alveolar macrophage identity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
12 Samples
Download data: CEL
Series
Accession:
GSE60249
ID:
200060249
13.

PPARγ controls alveolar macrophage identity [part2]

(Submitter supplied) Tissue-resident macrophages comprise heterogeneous populations with unique functions and distinct gene expression signatures. While it has been established that they mostly originate from embryonic progenitors, the signals inducing a characteristic tissue-specific differentiation program remain unknown. Here we identify PPARγ as the crucial transcription factor determining perinatal alveolar macrophage (AM) development and identity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
4 Samples
Download data: CEL
Series
Accession:
GSE60248
ID:
200060248
14.

PPARγ controls alveolar macrophage identity [part1]

(Submitter supplied) Tissue-resident macrophages comprise heterogeneous populations with unique functions and distinct gene expression signatures. While it has been established that they mostly originate from embryonic progenitors, the signals inducing a characteristic tissue-specific differentiation program remain unknown. Here we identify PPARγ as the crucial transcription factor determining perinatal alveolar macrophage (AM) development and identity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
8 Samples
Download data: CEL
Series
Accession:
GSE60247
ID:
200060247
15.

The impact of breed genotype and tissue compartment on the response of pig macrophages to lipopolysaccharide

(Submitter supplied) The domestic pig (Sus scrofa) provides a large animal model for human innate immune responses and inflammation that is also economically important in its own right. Results: We demonstrate that macrophages can be harvested from 3 different compartments of the pig (lungs, blood and bone-marrow), cryopreserved and subsequently recovered and differentiated in CSF-1. We have performed surface marker analysis and gene expression profiling on macrophages from these compartments, comparing 25 animals from 5 different breeds and their response to lipopolysaccharide. more...
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL16569
140 Samples
Download data: CEL
Series
Accession:
GSE45145
ID:
200045145
16.

Expression data from human alveolar macrophages (AMs)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24539
17 Samples
Download data: CEL, CHP
Series
Accession:
GSE190259
ID:
200190259
17.

Expression data from human alveolar macrophages (AMs) of fetal versus adult origin

(Submitter supplied) The impact of cell origin on human lung macrophage identity and function remains unknown. In this study we characterized human alveolar macrophages of fetal versus adult origin. We used microarray to define the gene signatures of human alveolar macrophages derived from CD116+CD64+ fetal monocytes, CD116+CD64- fetal precursors, and CD34+ HSPCs in MISTRG humanized mice.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24539
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE190257
ID:
200190257
18.

Expression data from different types of human alveolar macrophage (AM) precursors

(Submitter supplied) Despite their importance in lung health and disease, it remains unknown how human alveolar macrophages develop early in life. In this study we identified the fetal progenitor of human alveolar macrophages. We used microarray to define the gene signatures of human CD14+ blood monocytes (adult AM precursors), CD116+CD64+ fetal liver monocytes, and CD116+CD64- fetal AM precursors.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24539
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE190256
ID:
200190256
19.

IL-4 stimulation of Dicer deficient bone-marrow derived macrophages in vitro

(Submitter supplied) Macrophages were derived from the bone-marrow of 3 x fl/+ Dicer LysCre +/- (wild-type) and 3 x fl/fl Dicer LysCre +/- mice and stimulated with IL-4 (50ng/mL) for 72h. Total RNA was isolated and analyzed by gene array.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13712
6 Samples
Download data: CEL
Series
Accession:
GSE36585
ID:
200036585
20.

Identification of a nerve-associated, lung-resident interstitial macrophage subset with distinct localization and immunoregulatory properties

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL24247
12 Samples
Download data
Series
Accession:
GSE146683
ID:
200146683
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