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Links from GEO DataSets

Items: 20

1.

Genome-wide expression kinetics of children with T1D-associated autoantibodies compared to healthy matched controls I

(Submitter supplied) To unravel genes and molecular pathways involved in the pathogenesis of type 1 diabetes (T1D), we performed genome-wide gene expression profiling of prospective venous blood samples from children developing T1D-associated autoantibodies or progressing towards clinical diagnosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
63 Samples
Download data: TXT
Series
Accession:
GSE30208
ID:
200030208
2.

Genome-wide expression kinetics of children with Type 1 diabetes (T1D) -associated autoantibodies or progression towards clinical T1D, compared to healthy matched controls .

(Submitter supplied) To unravel genes and molecular pathways involved in the pathogenesis of type 1 diabetes (T1D), we performed genome-wide gene expression profiling of prospective venous blood samples from children developing T1D-associated autoantibodies or progressing towards clinical diagnosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13667
356 Samples
Download data: CEL, TXT
Series
Accession:
GSE43488
ID:
200043488
3.

Gene expression changes during Type 1 diabetes pathogenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below. Due to privacy concerns, the SNP data is not available with unrestricted access.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6947 GPL13667 GPL6102
724 Samples
Download data: CEL
Series
Accession:
GSE30211
ID:
200030211
4.

Genome-wide espression kinetics of children progressing to clinical Type 1 diabetes (T1D).

(Submitter supplied) To unravel genes and molecular pathways involved in the pathogenesis of type 1 diabetes (T1D), we performed genome-wide gene expression profiling of prospective venous blood samples from children developing T1D-associated autoantibodies or progressing towards clinical diagnosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
247 Samples
Download data: TXT
Series
Accession:
GSE30210
ID:
200030210
5.

Genome-wide expression kinetics of children with T1D-associated autoantibodies compared to healthy matched controls II

(Submitter supplied) To unravel genes and molecular pathways involved in the pathogenesis of type 1 diabetes (T1D), we performed genome-wide gene expression profiling of prospective venous blood samples from children developing T1D-associated autoantibodies or progressing towards clinical diagnosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
58 Samples
Download data: TXT
Series
Accession:
GSE30209
ID:
200030209
6.

Reduced Type I Interferon response signature detected in dendritic cells from prediabetic NOD mice compared to C57BL/6.g7 and Rag KO

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
76 Samples
Download data
Series
Accession:
GSE146453
ID:
200146453
7.

Reduced Type I Interferon response signature detected in dendritic cells from prediabetic NOD mice compared to C57BL/6.g7 and Rag KO [stimulated samples]

(Submitter supplied) Investigating type I interferon in prediabetic stage of DCs from NOD mice compared to C57BL/6.g7 and Rag KO mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: CSV
Series
Accession:
GSE146452
ID:
200146452
8.

Innate immune stimulation of whole blood reveals IFN-1 hyper-responsiveness in type 1 diabetes

(Submitter supplied) TruCulture human whole blood ex vivo stimulation was performed on 17 healthy individuals and 17 post-onset type 1 diabetics, then gene expression was analyzed using Nanostring to characterize stimulated innate immune responses. Ex vivo whole blood stimulation revealed higher induced IFN-1 responses in type 1 diabetes as compared to healthy controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18649
204 Samples
Download data: TXT
Series
Accession:
GSE146338
ID:
200146338
9.

Transcriptome profile of peripheral blood mononuclear cells in patients with type I diabetes and their first grade relatives

(Submitter supplied) Type 1 Diabetes (T1D) is considered to be a Th1 autoimmune disease characterised by an absolute lack of insulin caused by an autoimmune destruction of the insulin producing pancreatic beta cells. Th1 lymphocytes are responsible for the infiltration of the islets of Langerhans and for the cytokine release that supports cytotoxic (Tc) lymphocytes to mediate destruction of the beta cells. The preclinical disease stage is characterized by the generation of the self-reactive lymphocytes that infiltrate the pancreas and selectively destroy the insulin-producing beta cells present in the islets. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13507
29 Samples
Download data: GPR
Series
Accession:
GSE29142
ID:
200029142
10.

Molecular signatures differentiate immune states in Type 1 Diabetes families

(Submitter supplied) The complex milieu of inflammatory mediators associated with many diseases is often too dilute to directly measure in the periphery, necessitating development of more sensitive measurements suitable for mechanistic studies, earlier diagnosis, guiding selection of therapy, and monitoring interventions. Previously, we determined that plasma of recent-onset (RO) Type 1 diabetes (T1D) patients induce a proinflammatory transcriptional signature in fresh peripheral blood mononuclear cells (PBMC) relative to that of unrelated healthy controls (HC). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
286 Samples
Download data: CEL
Series
Accession:
GSE52724
ID:
200052724
11.

Transcriptional Signatures as a Disease-Specific and Predictive Inflammatory Biomarker for Type 1 Diabetes [T1D_114]

(Submitter supplied) The complex milieu of inflammatory mediators associated with many diseases is often too dilute to directly measure in the periphery, necessitating development of more sensitive measurements suitable for mechanistic studies, earlier diagnosis, guiding selection of therapy, and monitoring interventions. Previously, we determined that plasma of recent-onset (RO) Type 1 diabetes (T1D) patients induce a proinflammatory transcriptional signature in fresh peripheral blood mononuclear cells (PBMC) relative to that of unrelated healthy controls (HC). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
114 Samples
Download data: CEL
Series
Accession:
GSE35725
ID:
200035725
12.

Abnormal neutrophil signature in the blood and pancreas of pre-symptomatic and symptomatic type 1 diabetes

(Submitter supplied) Analysis of neutrophils purified from peripheral blood of patients with symptomatic and pre-symptomatic type 1 diabetes (T1D), at risk of T1D, and healthy controls.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
42 Samples
Download data: TXT
13.

Gene expression in PBMCs from children with diabetes

(Submitter supplied) Objective: We hypothesized that type 1 diabetes (T1D) is accompanied by changes in gene expression in peripheral blood mononuclear cells (PBMCs) due to dysregulation of adaptive and innate immunity, counterregulatory responses to immune dysregulation, insulin deficiency and hyperglycemia. Research Design and Methods: Microarray analysis was performed on PBMCs from 43 patients with newly diagnosed T1D, 12 patients with newly diagnosed type 2 diabetes (T2D) and 24 healthy controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS3874 GDS3875
Platforms:
GPL96 GPL97
234 Samples
Download data: CEL
Series
Accession:
GSE9006
ID:
200009006
14.
Full record GDS3875

Diabetic children: peripheral blood mononuclear cells (U133B)

Analysis of PBMCs from children (2-18 years) with newly diagnosed type 1 or 2 diabetes (T1D or T2D). One and 4 month samples were obtained from 20 of the T1D patients. Results provide insight into molecular mechanisms that distinguish T1D and T2D and those that are common to both forms of diabetes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state, 2 gender, 4 time sets
Platform:
GPL97
Series:
GSE9006
117 Samples
Download data: CEL
DataSet
Accession:
GDS3875
ID:
3875
15.
Full record GDS3874

Diabetic children: peripheral blood mononuclear cells (U133A)

Analysis of PBMCs from children (2-18 years) with newly diagnosed type 1 or 2 diabetes (T1D or T2D). One and 4 month samples were obtained from 20 of the T1D patients. Results provide insight into molecular mechanisms that distinguish T1D and T2D and those that are common to both forms of diabetes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state, 2 gender, 4 time sets
Platform:
GPL96
Series:
GSE9006
117 Samples
Download data: CEL
DataSet
Accession:
GDS3874
ID:
3874
16.

Molecular characterization of chronic antibody mediated rejection in kidney transplantation (mRNA CD4)

(Submitter supplied) Chronic antibody-mediated rejection (CAMR) represents the main cause of kidney graft loss, but its pathogenesis is unclear. In order to uncover the molecular mechanisms underlying this condition, we characterized the molecular signature of circulating peripheral blood mononuclear cells and, separately, of CD4+ T lymphocytes isolated from CAMR patients compared to kidney transplant recipients with normal graft function and histology. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
10 Samples
Download data: TXT
Series
Accession:
GSE64261
ID:
200064261
17.

Molecular characterization of chronic antibody mediated rejection in kidney transplantation (microRNA)

(Submitter supplied) Chronic antibody-mediated rejection (CAMR) represents the main cause of kidney graft loss, but its pathogenesis is unclear. In order to uncover the molecular mechanisms underlying this condition, we characterized the molecular signature of circulating peripheral blood mononuclear cells and, separately, of CD4+ T lymphocytes isolated from CAMR patients compared to kidney transplant recipients with normal graft function and histology. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL16770
9 Samples
Download data: TXT
Series
Accession:
GSE51676
ID:
200051676
18.

Molecular characterization of chronic antibody mediated rejection in kidney transplantation (mRNA)

(Submitter supplied) Chronic antibody-mediated rejection (CAMR) represents the main cause of kidney graft loss, but its pathogenesis is unclear. In order to uncover the molecular mechanisms underlying this condition, we characterized the molecular signature of circulating peripheral blood mononuclear cells and, separately, of CD4+ T lymphocytes isolated from CAMR patients compared to kidney transplant recipients with normal graft function and histology. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
18 Samples
Download data: TXT
Series
Accession:
GSE51675
ID:
200051675
19.

Different microRNA Alterations Contribute to Diverse Outcomes Following EV71 and CA16 Infections: Insights from High-Throughput Sequencing in Peripheral Blood Mononuclear Cells of Rhesus Monkey

(Submitter supplied) Enterovirus 71 (EV71) and Coxsackievirus A16 (CA16) are the predominant etiological agents of hand, foot, and mouth disease (HFMD) and both belong to the human enterovirus A species of the Picornaviridae family. These viruses share similar genetic homology, although the clinical manifestations of HFMD caused by the two viruses have some discrepancies. Furthermore, the underlying mechanisms leading to these differences remain unclear. more...
Organism:
Macaca mulatta
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL14954
6 Samples
Download data: XLSX
Series
Accession:
GSE85820
ID:
200085820
20.

gene expression Fulminant type 1 diabetes vs classical type 1A diabetes vs healthy controls

(Submitter supplied) We determined the genes that were differentially expressed between fulminant type 1 diabetes and classical type 1A diabetes or healthy control using gene expression microarray in peripheral blood cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
16 Samples
Download data: TXT
Series
Accession:
GSE44314
ID:
200044314
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