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Links from GEO DataSets

Items: 20

1.
Full record GDS4185

Systemic Lupus Erythematosus: mononuclear cells

Analysis of freshly isolated lymphocyte (CD4+ T cells and CD19+ B cells) and CD33+ myeloid subsets from the blood of Systemic Lupus Erythematosus (SLE) patients. Results provide insight into the molecular mechanisms underlying SLE pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 cell type, 2 disease state sets
Platform:
GPL96
Series:
GSE10325
67 Samples
Download data: CEL
2.

Expression data from human peripheral blood subsets

(Submitter supplied) Gene expression profile studies have identified an interferon signature in whole blood or mononuclear cell samples from patients with systemic lupus erythematosus. This study was designed to determine whether specific lymphocyte and myeloid subsets freshly isolated from the blood of systemic lupus erythematosus patients demonstrated unique gene expression profiles compared to subsets isolated from healthy controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4185
Platform:
GPL96
67 Samples
Download data: CEL
Series
Accession:
GSE10325
ID:
200010325
3.

Expression analysis of the gene in microRNA-155 knockout mice and wildtype mice

(Submitter supplied) Investigation of whole genome gene expression level changes in four microRNA-155 knockout mice comparing with 4 wildtype mice We found some gene expression level are different in two groups.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15887
8 Samples
Download data: CALLS, PAIR
Series
Accession:
GSE66815
ID:
200066815
4.

RNA-Seq analysis of the WEHI-231-derived stable cell lines WEHI-control and WEHI-miR-148a

(Submitter supplied) miRNAs regulate the expression of its targets genes by promoting mRNA degradation and translational repression. The goal of this study is to perform RNA-Seq in control or miR-148a-expressing WEHI-231 cell lines for the identification of miR-148a target genes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: TXT
Series
Accession:
GSE75809
ID:
200075809
5.

T helper lymphocyte- and monocyte-specific type I interferon (IFN) signatures in autoimmunity and viral infection.

(Submitter supplied) This study demonstrates quantitative and qualitative differences between type I IFN signatures in autoimmunity and viral infection using purified CD4pos T cells and CD16pos- and CD16neg-monocyte subsets. We were able to discriminate between cell-specific viral response signatures and the pathogenically amplified IFN signatures observed in autoimmunity. The differences were of both a qualitative and quantitative nature, as the signatures in the patients with SLE were characterized by much more complexly compiled gene patterns with increased absolute gene expression levels.
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4888 GDS4889 GDS4890
Platform:
GPL570
36 Samples
Download data: CEL, CHP
Series
Accession:
GSE51997
ID:
200051997
6.
Full record GDS4890

Systemic lupus erythematosus patients and yellow fever vaccine-immunized healthy donors: CD16+ monocytes

Analysis of CD16+ monocytes from SLE patients and YFV-immunized healthy donors. The YFV immunization can be regarded as a real viral infection, based on clinical/serological manifestations. Results provide insight into differences in type I interferon responses in autoimmunity and viral infection.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 7 individual, 3 protocol sets
Platform:
GPL570
Series:
GSE51997
10 Samples
Download data: CEL, CHP
7.
Full record GDS4889

Systemic lupus erythematosus patients and yellow fever vaccine-immunized healthy donors: CD16- monocytes

Analysis of CD16- monocytes from SLE patients and YFV-immunized healthy donors. The YFV immunization can be regarded as a real viral infection, based on clinical/serological manifestations. Results provide insight into differences in type I interferon responses in autoimmunity and viral infection.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 8 individual, 3 protocol sets
Platform:
GPL570
Series:
GSE51997
12 Samples
Download data: CEL, CHP
8.
Full record GDS4888

Systemic lupus erythematosus patients and yellow fever vaccine-immunized healthy donors: CD4 T+ lymphocytes

Analysis of CD4+ T cells from SLE patients and YFV-immunized healthy donors. The YFV immunization can be regarded as a real viral infection, based on clinical/serological manifestations. Results provide insight into differences in type I interferon responses in autoimmunity and viral infection.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 10 individual, 3 protocol sets
Platform:
GPL570
Series:
GSE51997
14 Samples
Download data: CEL, CHP
9.

Gene expression profile of B cells from OPN-competent and deficient Faslpr autoimmune mice

(Submitter supplied) We performed gene expression profile on splenic CD19+ cells from autoimmune Faslpr/lpr and OPN-/-Faslpr/lpr mice to investigate the dynamics at the basis of the more incident transformation characterizing OPN-deficient animals. GEP on splenic CD19+ from BALB/c and OPN-/- mice was performed as control.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21810
14 Samples
Download data: TXT
Series
Accession:
GSE193790
ID:
200193790
10.

Gene expression profilings of naive B cell, memory B cell and plasmablast of healthy donors and SLE patients

(Submitter supplied) Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by production of various pathogenic autoantibodies. Increased type I interferon signature is suggested as a trigger of the disease. Previous studies identify increased plasmablasts in peripheral blood of SLE patients. In spite of the unique cellular properties of the plasmablasts compared with other B cell subsets and plasma cells, the biological characteristics of SLE plasmblast remain unknown and few therapeutic strategies targeting SLE plasmablasts have been applicated. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17077
24 Samples
Download data: TXT
Series
Accession:
GSE156751
ID:
200156751
11.

RNA-seq study reveals unique transcriptome expression in systemic lupus erythematosus patients with distinct autoantibody profile

(Submitter supplied) Systemic lupus erythematosus patients exhibit remarkable heterogeneity in clinical manifestations and autoantibody repertoires. This complexity poses major barrier in diagnosis and effective treatment of SLE. To address this we studied the SLE patients in groups categorized on the basis of distinct sera autoantibodies. SLE patients were segregated into three group based on the presence of autoantibodies against i) dsDNA only ii) ENA (extractable nuclear antigens) only or iii) both.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
16 Samples
Download data: XLSX
12.

The cGAS/STING pathway suppresses TLR-dependent systemic autoimmunity in TMPD-mediated SLE

(Submitter supplied) The purpose of the study was to identify differentially regulated genes between WT MRL/Lpr strain and cGAS deficeint MRL/Lpr strain. We utilized Nanostring technology to analze RNA obtained from spleen of these mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL29935
11 Samples
Download data: RCC
Series
Accession:
GSE169655
ID:
200169655
13.

Analysis of gene expression profiles from alloreactive TCR-Tg CD8 T cells during activation and induction of tolerance

(Submitter supplied) RNA-seq was used to evaluate transcriptional changes in alloreactive TCR-Tg CD8 T cells during activation and tolerance induction. CBA mice were exposed to a low dose whole body irradiation and then injected with bone marrow from TCR-Tg KB5 mice to generate synchimeric mice. The KB5 TCR recognizes alloantigens from H2b MHC molecules, specifically Kb, that are expressed by C57BL/6 mice. The injection of bone marrow from KB5 mice into CBA mice enables the development of small and traceable population of TCR-Tg KB5 CD8 T cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE89030
ID:
200089030
14.

Twin DNA methylation profiling reveals flare-dependent interferon signature and B-cell promoter hypermethylation in systemic lupus erythematosus

(Submitter supplied) Objective: Systemic lupus erythematosus (SLE) has limited monozygotic (MZ) twin concordance, implying a role for other pathogenic factors than genetic variation, such as epigenetic changes. Using the disease discordant twin model, we investigated genome-wide DNA methylation changes in sorted CD4+ T-cells, monocytes, granulocytes and B-cells in twin pairs with at least one SLE-affected twin. Methods: Peripheral blood from 15 SLE twin pairs (six MZ, nine dizygotic (DZ)) was processed using gradient density centrifugation for the granulocyte fraction. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
104 Samples
Download data: CSV, IDAT
Series
Accession:
GSE110607
ID:
200110607
15.

Whole genome transcription and DNA methylation analysis of peripheral blood mononuclear cells identified aberrant gene regulation pathways in systemic lupus erythematosus

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by genome tiling array
Platforms:
GPL13534 GPL10558
110 Samples
Download data
Series
Accession:
GSE82221
ID:
200082221
16.

Whole genome transcription and DNA methylation analysis of peripheral blood mononuclear cells identified aberrant gene regulation pathways in systemic lupus erythematosus [expression]

(Submitter supplied) Our study has demonstrated that significant number of differential genes in SLE was involved in IFN, TLR signaling pathways and inflammatory cytokines. The enrichment of differential genes has been associated with aberrant DNA methylation, which may be relevant to the pathogenesis of SLE. Our observations laid the groundwork for further diagnostic and mechanistic studies of SLE and LN.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
55 Samples
Download data: TXT
Series
Accession:
GSE81622
ID:
200081622
17.

Divergent genome wide transcriptional profiles from immune cell subsets isolated from SLE patients with different ancestral backgrounds

(Submitter supplied) Background/Purpose: Systemic lupus erythematosus (SLE) is a complex multi-system autoimmune disease of uncertain etiology. Patients from different ancestral backgrounds demonstrate differences in clinical manifestations and autoantibody profiles. In this study we examined genome-wide transcriptional patterns in major immune cell subsets across different ancestral backgrounds. Methods: Peripheral blood was collected from 21 African-American (AA) and 21 European-American (EA) SLE patients, 5 AA controls, and 5 EA controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
208 Samples
Download data: TXT
Series
Accession:
GSE55447
ID:
200055447
18.

Interactions of cytokines in peripheral blood cells from Systemic Lupus Erythematosus

(Submitter supplied) SLE patients are always with various disease manifestation. Various cytokines are pointed interacting and playing pathological roles in SLE although the etiopathology is still obscure. In this study, we aimed to investigate the effects of cytokine interactions in the immune response of SLE patients. Overexpressed interferon-inducible(IFI) genes were confirmed in peripheral blood from SLE patients. Using network-based analysis on the immune response-related genes, several networks including cytokines such as TNF and IFN-γ, or beta-estradiol(E2), were constructed. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1291
17 Samples
Download data: TXT
Series
Accession:
GSE12374
ID:
200012374
19.

Expression data from purified human platelets

(Submitter supplied) Patients with systemic lupus erythematosus (SLE) have a markedly increased risk to develop cardiovascular disease, and traditional cardiovascular risk factors fail to account for this increased risk. We used microarray to probe the platelet transcriptome in individuals with SLE and healthy controls, and the gene and protein expression of a subset of differentially expressed genes was further investigated and correlated to platelet activation status. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
2 Samples
Download data: CEL, CHP, XLS
Series
Accession:
GSE22132
ID:
200022132
20.

Inflammatory Expression Profiles in Monocyte to Macrophage Differentiation amongst Patients with Systemic Lupus Erythematosus and Healthy Controls with and without an Atherosclerosis Phenotype

(Submitter supplied) To examine mononuclear cell gene expression profiles in patients with and without SLE and subsets with and without atherosclerosis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
72 Samples
Download data: TXT
Series
Accession:
GSE37356
ID:
200037356
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