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Links from GEO DataSets

Items: 20

1.

FLT3+/CD11b+ Dendritic cell (DC) progenitor

(Submitter supplied) FLT3+/CD11b+ Dendritic cell (DC) progenitor was amplified in vitro from mouse bone marrow. Keywords: repeat sample
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
5 Samples
Download data
Series
Accession:
GSE692
ID:
200000692
2.

Antigen Presenting Dendritic Cells

(Submitter supplied) Assessing the gene expression repertoire of antigen presenting dendritic cells Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
7 Samples
Download data
Series
Accession:
GSE702
ID:
200000702
3.

Lin-c-kit+Sca1+ hematopoetic stem cells

(Submitter supplied) sorted hematopoetic stem cells from bone marrow; with two rounds of amplification Keywords: repeat sample
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
2 Samples
Download data
Series
Accession:
GSE693
ID:
200000693
4.

DC differentiation from DC progenitor in vitro

(Submitter supplied) FLT3+CD11b+ DC progenitor was amplified in vitro from mouse bone marrow. DC were differentiated using GM-CSF and analyzed at day 7 and day 10 of differentiation and after 16h TNFalpha stimulation at day 10 Keywords: time-course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2440
Platform:
GPL32
4 Samples
Download data
Series
Accession:
GSE575
ID:
200000575
5.
Full record GDS2440

Dendritic cell development in vitro

Analysis of dendritic cell (DC) development from Flt3(+)CD11b(+) DC progenitors. DC progenitors treated with GM-CSF for 7 and 10 days to induce differentiation. DCs differentiated for 10 days were subsequently treated with TNFalpha to induce maturation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 protocol sets
Platform:
GPL32
Series:
GSE575
4 Samples
Download data
DataSet
Accession:
GDS2440
ID:
2440
6.

TGF-β1 Accelerates Dendritic Cell Differentiation from Common Dendritic Cell Progenitors (CDPs) and Directs Subset Specification Towards Conventional Dendritic Cells

(Submitter supplied) Dendritic cells (DCs) in lymphoid tissue comprise conventional DCs (cDCs) and plasmacytoid DCs (pDCs) that develop from common DC progenitors (CDPs). CDPs are Flt3+c-kitintM-CSFR+ and reside in bone marrow. Here we describe a two-step culture system that recapitulates DC development from c-kithiFlt3-/lo multipotent progenitors (MPPs) into CDPs and further into cDC and pDC subsets. MPPs and CDPs are amplified in vitro with Flt3 ligand, stem cell factor, hyper-IL-6 and insulin- like growth factor-1. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
20 Samples
Download data: CEL
Series
Accession:
GSE22432
ID:
200022432
7.

Transcription profile of CD103- vs CD103+ dendritic cells derived from CX3CR1+c-kit+- bone marrow cells (M1993 M2067)

(Submitter supplied) We hypothesize that under homeostatic as well as inflammatory conditions circulating monocytes and/or their bone marrow-derived progenitors might contribute to the replenishment of CD103+ and CD103- DC in lymphoid and non-lymphoid compartments. To that end, bone marrow cells from CX3CR1+/gfp C57BL/6 mice were sorted as follows: lineage negative (CD3, CD19, NK1.1, Ter119, Ly6G and CD11c) CX3CR1+c-kit+. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
2 Samples
Download data: TXT
Series
Accession:
GSE10882
ID:
200010882
8.

Gene expression of distinct lung dendritic cell subsets

(Submitter supplied) Pulmonary dendritic cells are heterogenous cells comprise four distinct subsets including two conventional dendritic cell subsets, CD103+ and CD11bhiCD14lo cells, and two monocyte-derived dendritic cell subsets. Their functions in terms of migration and T cell activation are distinct, but genes regulating their features are to be determined. We used microarrays to identify a select set of genes that are expressed in conventinal dendritic cells and in monocyte-derived dendriti cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5663
Platform:
GPL1261
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE64896
ID:
200064896
9.
Full record GDS5663

Pulmonary dendritic cell subsets

Analysis of four dendritic cell (DC) subsets purified from the lungs of C57BL/6 males following inhalation of LPS/OVA. The four subsets represent conventional DCs (cDCs) and monocyte-derived DCs (moDCs). Results provide insight into molecular profiles that would discriminate between cDCs and moDCs.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 cell type, 2 other sets
Platform:
GPL1261
Series:
GSE64896
12 Samples
Download data: CEL, CHP
10.

Bcl11a controls Flt3 expression in early hematopoietic progenitors and is required for pDC development in vivo

(Submitter supplied) Bcl11a is a transcription factor known to regulate lymphoid and erythroid development. Recent bioinformatic analysis of global gene expression patterns has suggested a role for Bcl11a in the development of dendritic cell (DC) lineages. We tested this hypothesis by analyzing the development of DC and other lineages in Bcl11a(-/-) mice. We show that Bcl11a is required for expression of IL-7 receptor (IL-7R) and Flt3 in early hematopoietic progenitor cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL
Series
Accession:
GSE46270
ID:
200046270
11.

Altered compensatory cytokine signaling underlies the discrepancy between Flt3-/- and Flt3l-/- mice

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
16 Samples
Download data: CEL
Series
Accession:
GSE110812
ID:
200110812
12.

Gene expression in WT and Flt3 KO pDCs

(Submitter supplied) The goal of this study was to determine whether there are any gene expression changes in pDCs from WT and Flt3 KO mice. Specifically whether developing in the absence of Flt3 signaling had any effects on the gene expression of the pDCs
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL
Series
Accession:
GSE110790
ID:
200110790
13.

Gene expression in WT, Flt3 KO, and Flt3L KO cDC1s and cDC2s

(Submitter supplied) The goal of this study was to determine whether there are any gene expression changes in cDC1s and cDC2s from WT, Flt3 KO, or Flt3L KO mice. Specifically whether developing in the absence of Flt3 signaling had any effects on the gene expression of the cDCs
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE110789
ID:
200110789
14.

Gene expression analysis of Cbfb-deficient LSK and GMP

(Submitter supplied) Runx/Cbfb heterodimers play important roles in the development of hematopoietic cells in mouse embryos and adults. In order to identify genes that are regulated by Runx/Cbfb, we purified Lin– c-kit+ Sca1+ (LSK) cells and Lin– c-kit+ Sca1– CD16/32+ (GMP) cells from Vav1-iCre x Cbfb(F/F) and Vav1-iCre x Cbfb(F/+) mice and profiled gene expression using microarray.
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS5413 GDS5414
Platform:
GPL6246
8 Samples
Download data: CEL
Series
Accession:
GSE55227
ID:
200055227
15.
Full record GDS5414

Core binding factor β deficiency effect on bone marrow derived-granulocyte macrophage progenitor cells

Analysis of purified Lin-c-kit+Sca1-CD16/32+ GMP cells from Cbfβ-conditional knockout mice. Runx/Cbfb heterodimers play important roles in hematopoietic cell development. Results provide insight into molecular mechanisms by which Cbfβ regulates cell fate decisions in bone marrow progenitors.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE55227
4 Samples
Download data: CEL
16.
Full record GDS5413

Core binding factor β deficiency effect on bone marrow derived-LSK hematopoietic stem cells

Analysis of purified Lin-c-kit+Sca1+ LSK cells from Cbfβ- conditional knockout mice. Runx/Cbfb heterodimers play important roles in hematopoietic cell development. Results provide insight into molecular mechanisms by which Cbfβ regulates cell fate decisions in bone marrow progenitors.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE55227
4 Samples
Download data: CEL
17.

Molecular Events Initiating B Cell Fate Specification

(Submitter supplied) Functional genomics comparison of EBFko, Pax5ko, and RAG2ko cell lines. Identify gene signatures associated with specfication and commitment to the B cell fate.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL, CHP, XLS
Series
Accession:
GSE16002
ID:
200016002
18.

Gene expression comparison among spleen dendritic cells, brain microglia, brain dendritic cells and bone marrow monocytes

(Submitter supplied) To understand the functional relationship between brain dendritic cells (brain DCs) and other myeloid cells, we compared the gene expression profile of m/chDCs to that of bone marrow monocytes, brain microglia and classical spleen CD8+ and CD8- DCs. In order to obtain enough brain DCs for mRNA extraction, we expanded brain DCs with in vivo Flt3L treatment before purification.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE29949
ID:
200029949
19.

Retinoic acid determines the in vivo fate-commitment of splenic pre-dendritic cells

(Submitter supplied) Comparison of gene expression changes of FACS sorted splenic CD11b+CD8a- and CD11b-CD8a+ cDC subsets reconstituted in vivo following total body irradiation in combination with exogenous retinoic acid or vehicle control.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
16 Samples
Download data: CEL
Series
Accession:
GSE41021
ID:
200041021
20.

Notch2 receptor signaling controls functional differentiation of dendritic cells in the spleen and intestine

(Submitter supplied) Dendritic cells (DCs) in tissues and lymphoid organs comprise distinct functional subsets that differentiate in situ from circulating progenitors. Tissue-specific signals that regulate DC subset differentiation are poorly understood. We report that DC-specific deletion of the Notch2 receptor caused a reduction of DC populations in the spleen. Within the splenic CD11b+ DCs, Notch signaling blockade ablated a distinct population marked by high expression of adhesion molecule Esam. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
3 Samples
Download data: CEL, CHP
Series
Accession:
GSE31551
ID:
200031551
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