Similar studies for GEO DataSets (Select 2982) - GEO DataSets

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Items: 12

Select item 29821.

CD11b-plus CD11c-minus macrophages of the intestinal lamina propria

Comparison of CD11b+ CD11c- macrophages of the small intestinal lamina propria and the spleen. The intestinal immune system responds robustly to pathogens yet remains tolerant to commensals and food antigens. Results provide insight into the role of intestinal macrophages in immune tolerance.

Organism:: Mus musculus

Type:: Expression profiling by array, count, 2 cell type sets

Platform:: GPL1261
Series:: GSE8868
4 Samples

Download data: CEL, CHP

DataSet

Accession:: GDS2982

ID:: 2982

Select item 2000088682.

Comparison of splenic and small intestine lamina propria macrophages

(Submitter supplied) The intestinal immune system must elicit robust immunity against harmful pathogens but restrain immune responses directed against commensal microbes and dietary antigens. The mechanisms that maintain this dichotomy are poorly understood. Here we describe a population of CD11b+F4/80+CD11c– macrophages in the lamina propria (LP) that express several anti-inflammatory molecules including interleukin 10 (IL-10), but little or no pro-inflammatory cytokines, even upon stimulation with Toll-like receptor (TLR) ligands. more...

Organism:: Mus musculus

Type:: Expression profiling by array

Dataset:: GDS2982
Platform:: GPL1261
4 Samples

Download data: CEL, CHP

Series

Accession:: GSE8868

ID:: 200008868

Select item 2000051193.

Gene expression induced by flagellin stimulation in IECs and CD11c+ LPCs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:: Mus musculus

Type:: Expression profiling by array

Platform:: GPL1261
8 Samples

Download data

Series

Accession:: GSE5119

ID:: 200005119

Select item 2000051134.

Gene expression induced by flagellin stimulation in CD11c+ LPCs

(Submitter supplied) Microarray analysis of IECs from Tlr5+/+ and Tlr5-/- mice stimulated with either medium alone or flagellin (1 µg/ml); to elucidate TLR5-mediated immune responses in CD11c+ LPCs Keywords: ordered

Organism:: Mus musculus

Type:: Expression profiling by array

Dataset:: GDS2212
Platform:: GPL1261
4 Samples

Download data

Series

Accession:: GSE5113

ID:: 200005113

Select item 2000051125.

Gene expression induced by flagellin stimulation in IECs

(Submitter supplied) Microarray analysis of IECs from Tlr5+/+ and Tlr5–/– mice stimulated with either medium alone or flagellin (1 µg/ml); to elucidate TLR5-mediated immune responses in IECs. Keywords: ordered

Organism:: Mus musculus

Type:: Expression profiling by array

Dataset:: GDS2211
Platform:: GPL1261
4 Samples

Download data

Series

Accession:: GSE5112

ID:: 200005112

Select item 22126.

Flagellin effect on toll-like receptor 5 deficient intestinal lamina propria cells

Analysis of CD11c positive intestinal lamina propria cells (LPC) from toll-like receptor 5 (TLR5) null animals stimulated with flagellin. TLR5 mediates the immune response to flagellin. Results provide insight into the role of CD11c positive LPCs in the innate immune response mediated by TLR5.

Organism:: Mus musculus

Type:: Expression profiling by array, count, 2 agent, 2 genotype/variation sets

Platform:: GPL1261
Series:: GSE5113
4 Samples

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DataSet

Accession:: GDS2212

ID:: 2212

Select item 22117.

Flagellin effect on toll-like receptor 5 deficient intestinal epithelial cells

Analysis of intestinal epithelial cells (IECs) from toll-like receptor 5 (TLR5) null animals stimulated with flagellin. TLR5 mediates the immune response to flagellin. Results provide insight into the role of IECs in the innate immune response mediated by TLR5.

Organism:: Mus musculus

Type:: Expression profiling by array, count, 2 agent, 2 genotype/variation sets

Platform:: GPL1261
Series:: GSE5112
4 Samples

Download data

DataSet

Accession:: GDS2211

ID:: 2211

Select item 2002006458.

TLE3 CUT&Tag-Seq to characterize TLE3-binding sites in colonic macrophages

(Submitter supplied) We found that TLE3 in colonic macrophages mainly occupied distal intergenic regions (48%) and gene body regions (47%) with limited occupancy at the gene proximal regions (5%).