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Links from GEO DataSets

Items: 20

1.

FoxP3 scanning mutagenesis reveals functional variegation and mild mutations with atypical autoimmune phenotypes [nanostring]

(Submitter supplied) Nanostring profiles of CD4+ T cells transduced with EV, WT or FoxP3 mutants
Organism:
Mus musculus
Type:
Other
Platform:
GPL24057
144 Samples
Download data: RCC
Series
Accession:
GSE104344
ID:
200104344
2.

FoxP3 scanning mutagenesis reveals functional variegation and mild mutations with atypical autoimmune phenotypes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Other
Platforms:
GPL24057 GPL6246
156 Samples
Download data: CEL, RCC
Series
Accession:
GSE104346
ID:
200104346
3.

FoxP3 scanning mutagenesis reveals functional variegation and mild mutations with atypical autoimmune phenotypes [microarray]

(Submitter supplied) Microarray profiles of M176, M354 and WT FoxP3 -transdued (in vitro) and -Treg from mice
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE104345
ID:
200104345
4.

Different molecular complexes that mediate transcriptional induction and repression by FoxP3

(Submitter supplied) ChIP-seq profile of WT or mutant FoxP3 in CD4+ T cells
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
11 Samples
Download data: BIGWIG
Series
Accession:
GSE102281
ID:
200102281
5.

Loss of Foxp3-driven epigenetic modification leads to regulatory T cell insufficiency

(Submitter supplied) Regulatory T cells (Tregs) are responsible for limiting autoimmunity and chronic inflammation. Foxp3 is a transcription factor that acts as a master regulator of Treg development and function. A serendipitous observation led to the realization that a well-characterized Foxp3gfp reporter mouse, which expresses an N-terminal GFP-Foxp3 fusion protein, is a hypomorph that causes profoundly accelerated autoimmune diabetes on a NOD background. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
16 Samples
Download data: CEL
Series
Accession:
GSE35164
ID:
200035164
6.

Mutations from IPEX patients elicit a range of phenotypes in mice

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24247 GPL19057
182 Samples
Download data: MTX, TBI, TSV, TXT
Series
Accession:
GSE237199
ID:
200237199
7.

Mutations from IPEX patients elicit a range of phenotypes in mice [scATAC-Seq]

(Submitter supplied) scATAC analysis of mouse Treg from Foxp3 missense mutant mice heterozygous females : R51Q, K199del, R51Q, WT
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
1 Sample
Download data: MTX, TBI, TSV, TXT
Series
Accession:
GSE237198
ID:
200237198
8.

Mutations from IPEX patients elicit a range of phenotypes in mice [RNAseq]

(Submitter supplied) RNAseq analysis of mouse Treg from Foxp3 missense mutant mice hemizygous male and heterozygous female : R51Q, C168Y, K199del, R309Q, F324L, R337Q
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
181 Samples
Download data: TSV
Series
Accession:
GSE225891
ID:
200225891
9.

Analyses of a mutant FoxP3 allele reveal BATF as a critical transcription factor in the differentiation and accumulation of tissue regulatory T cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL1261 GPL18480
47 Samples
Download data: CEL, TXT
Series
Accession:
GSE89744
ID:
200089744
10.

Genome-wide maps of FoxP3 binding in FoxP3WT and FoxP3A384T Treg cells

(Submitter supplied) FoxP3 binding sites in Treg cells expressing WT or A384T mutant FoxP3 were examined.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18480
12 Samples
Download data: TXT
Series
Accession:
GSE89743
ID:
200089743
11.

Expression data from BATF-deficient Treg cells

(Submitter supplied) FoxP3 is a central regulator of immunological tolerance, controlling the development and function of regulatory T (Treg) cells. To dissect the complex processes orchestrated by FoxP3, we investigated impacts of three autoimmune disease-associated missense FoxP3 mutations in mice. The I363V and R397W mutations were loss-of-function mutations, causing multi-organ inflammation by globally compromising Treg cell physiology. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE89656
ID:
200089656
12.

Expression data from Treg cells expressing mutant FoxP3

(Submitter supplied) FoxP3 is a central regulator of immunological tolerance, controlling the development and function of regulatory T (Treg) cells. To dissect the complex processes orchestrated by FoxP3, we investigated impacts of three autoimmune disease-associated missense FoxP3 mutations (i.e., I363V, A384T, R397W) through knock-in mutagenesis in mice. We investigated the impacts of these mutations on Treg cell transcriptome by microarray analysis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE89654
ID:
200089654
13.

Expression data from mutant FoxP3-transduced CD4 T cells

(Submitter supplied) FoxP3 is a central regulator of immunological tolerance, controlling the development and function of regulatory T (Treg) cells. To dissect the complex processes orchestrated by FoxP3, we investigated impacts of three autoimmune disease-associated missense FoxP3 mutations in mice. As a initial approach, we retrovirally transduced naïve conventional T (Tconv) cells with WT or mutant (A384T and R397W) FoxP3 and analyzed the gene expression profiles of the transduced T cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
11 Samples
Download data: CEL
Series
Accession:
GSE89645
ID:
200089645
14.

Transcriptional profiling of LNGFR.FOXP3-expressing scurfy CD4+ T cells

(Submitter supplied) We reported transcriptional characterization of LNGFR.FOXP3-expressing scurfy CD4+ T cells from lymph nodes, at day 35 after transfer in scurfy males, where they were able to rescue mice from scurfy autoimmune disease.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
22 Samples
Download data: TSV
Series
Accession:
GSE166017
ID:
200166017
15.

Contribution of histone methylation to the plasticity of human FOXP3+ Treg cells

(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
Platform:
GPL11154
6 Samples
Download data: TXT, WIG
Series
Accession:
GSE47747
ID:
200047747
16.

Transcriptional profiling of FOXP3+ Treg cells and corresponding FOXP3-losing cells

(Submitter supplied) Natural CD4+FOXP3+ regulatory T (Treg) cells constitute a unique T-cell lineage that plays a pivotal role in maintaining immune homeostasis and immune tolerance. Recent studies provide evidence for the heterogeneity and plasticity of the Treg cell lineage. However, the fate of human Treg cells after loss of FOXP3 expression and the underlying epigenetic mechanisms remain to be fully elucidated. Here, we compared gene expression profiles and histone methylation status on two histone H3 lysine residues (H3K4me3 and H3K27me3) of expanded FOXP3+ and corresponding FOXP3-losing Treg cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: TXT
Series
Accession:
GSE47636
ID:
200047636
17.

Genome-wide maps of H3K4me3 and H3K27me3 in human FOXP3+ Treg cells and the corresponding FOXP3-losing cells

(Submitter supplied) Natural CD4+FOXP3+ regulatory T (Treg) cells constitute a unique T-cell lineage that plays a pivotal role in maintaining immune homeostasis and immune tolerance. Recent studies provide evidence for the heterogeneity and plasticity of the Treg cell lineage. However, the fate of human Treg cells after loss of FOXP3 expression and the underlying epigenetic mechanisms remain to be fully elucidated. Here, we compared gene expression profiles and histone methylation status on two histone H3 lysine residues (H3K4me3 and H3K27me3) of expanded FOXP3+ and corresponding FOXP3-losing Treg cells. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: WIG
Series
Accession:
GSE47510
ID:
200047510
18.

FoxP3 associates with enhancer-promoter loops to regulate Treg-specific gene expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL24247
15 Samples
Download data: BED, HIC, MTX, TBI, TSV, TXT
Series
Accession:
GSE190057
ID:
200190057
19.

FoxP3 associates with enhancer-promoter loops to regulate Treg-specific gene expression [HiChIP]

(Submitter supplied) We applied proximity-ligation with chromatin immunoprecipitation (HiChIP) in Treg and closely related conventional CD4+ T cells (Tconv) to map the H3K27Ac, FoxP3 and Yy1 chromatin structures.
Organism:
Mus musculus
Type:
Other
Platform:
GPL19057
14 Samples
Download data: HIC
Series
Accession:
GSE189442
ID:
200189442
20.

Inflammation induced repression of Foxp3-bound chromatin in regulatory T cells [sequencing]

(Submitter supplied) The transcription factor Foxp3 is indispensable for the ability of regulatory T (Treg) cells to suppress fatal inflammation. Here, we characterized the role of Foxp3 in chromatin remodeling and regulation of gene expression in actively suppressing Treg cells in an inflammatory setting. Although genome-wide Foxp3 occupancy of DNA regulatory elements was similar in resting and in vivo activated Treg cells, Foxp3-bound enhancers were poised for repression only in activated Treg cells. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL9250
18 Samples
Download data: TXT
Series
Accession:
GSE55773
ID:
200055773
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