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Links from GEO DataSets

Items: 20

1.

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
2.

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
3.

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
4.

The clinical and genomic significance of donor-specific antibody (DSA) positive/C4d negative and DSA negative/C4d negative transplant glomerulopathy

(Submitter supplied) We investigated the clinical, histopathologic and genomic features of donor-specific antibody (DSA) +/C4d- and DSA-/C4d- transplant glomerulopathy (TGP) using microarrays. Comparison of the gene expression profiles of DSA-/C4d- TGP biopsies with ptc+g score > 1 to normal and IFTA (Interstitial Fibrosis and Tubular Atrophy) biopsies by microarrays revealed increased expression of quantitative cytotoxic T cell--associated transcripts (QCAT). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
57 Samples
Download data: CEL
Series
Accession:
GSE44131
ID:
200044131
5.

Expression data from biopsies of TGP patients

(Submitter supplied) We study the global gene expression profiles of TGP patients with or without graft loss to determine if a clinical and/or gene expression profile can predict allograft survival. Transplant glomerulopathy (TGP) carries a poor prognosis and is associated with decreased allograft survival. In a large series of kidney transplant recipients, graft loss was observed in 38% of TGP patients at 5 years compared to 5% in patients without TGP. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
28 Samples
Download data: CEL, TXT
Series
Accession:
GSE58601
ID:
200058601
6.

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
7.
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
8.
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
9.
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
10.

Real-time quantitative PCR analysis of human renal biopsies

(Submitter supplied) Human biopsies were collected from kidney transplant recipients in 4 different european centers in the context of BIOMARGIN study. We used TaqMan™ Advanced miRNA Human A and B Cards to quantitate 754 miRNAs expression according to patient outcome ; ie patient presenting Microvascular Inflammation (MVI) or No MVI .
Organism:
Homo sapiens
Type:
Other
Platform:
GPL30379
88 Samples
Download data: TXT
Series
Accession:
GSE179772
ID:
200179772
11.

miRNA expression profiling in PBMCs from kidney patiens with or without donor specific antibody

(Submitter supplied) Investigation whether PBMCs miRNAs could be a predictable biomarker for chronic AMR (CAMR). A validation study (Study I) based on microarray profiling of total 435 mature human miRNAs using pooled samples of Group I-1 (Stable: n=11), Group I-2 (DSA: n=11) and Group I-3 (clinical CAMR: n=6)
Organism:
Homo sapiens; Mus musculus; Human alphaherpesvirus 1; Human betaherpesvirus 5; Murid betaherpesvirus 1; Human immunodeficiency virus 1; Rattus norvegicus; Human alphaherpesvirus 2; Merkel cell polyomavirus; Mus musculus cytomegalovirus 2; Murid gammaherpesvirus 4; Betapolyomavirus hominis; human gammaherpesvirus 4; JC polyomavirus; Human gammaherpesvirus 8; Betapolyomavirus macacae
Type:
Non-coding RNA profiling by array
Platform:
GPL11434
3 Samples
Download data: TXT
Series
Accession:
GSE59014
ID:
200059014
12.

Transcriptome patterns for Acute Cellular Rejection in Recipients with Recurrent Hepatitis C after Liver Transplantation

(Submitter supplied) The histological evaluation of liver via biopsy remains as the standard for the diagnosis of both acute cellular rejection (ACR) and recurrent hepatitis C (RHC) after liver transplantation. Nevertheless, it is often difficult to diagnose ACR in HCV-positive recipients because of common co-existing and overlapping morphological changes with RHC. The aim of the study was to identify potential target genes for ACR in recipients with RHC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1291
22 Samples
Download data: TXT
Series
Accession:
GSE13440
ID:
200013440
13.

A peripheral blood gene expression signature diagnoses subclinical acute rejection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL11154 GPL5175
153 Samples
Download data: CEL, TXT
Series
Accession:
GSE120398
ID:
200120398
14.

A peripheral blood gene expression signature diagnoses subclinical acute rejection [validation]

(Submitter supplied) Histological features of acute rejection can be detected in surveillance biopsies despite stable graft function and can negatively impact graft outcomes. However, routine surveillance biopsies for detection of subclinical rejection are not generally performed due to potential risks and costs associated with repeated biopsies. Noninvasive biomarkers are required to facilitate early detection of acute rejection and borderline changes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
65 Samples
Download data: CEL
Series
Accession:
GSE120397
ID:
200120397
15.

A peripheral blood gene expression signature diagnoses subclinical acute rejection [discovery]

(Submitter supplied) Histological features of acute rejection can be detected in surveillance biopsies despite stable graft function and can negatively impact graft outcomes. However, routine surveillance biopsies for detection of subclinical rejection are not generally performed due to potential risks and costs associated with repeated biopsies. Noninvasive biomarkers are required to facilitate early detection of acute rejection and borderline changes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
88 Samples
Download data: TXT
16.

Landscape of innate immune system transcriptome and acute T-cell mediated rejection of human kidney allografts

(Submitter supplied) Acute rejection of human allografts has been viewed mostly through the lens of adaptive immunity, and the intragraft landscape of innate immunity genes has not been characterized in an unbiased fashion. We did RNA sequencing of 34 kidney allograft biopsy specimens from 34 adult recipients; 16 were categorized as Banff acute T-cell mediated rejection (TCMR) and 18 as normal. Computational analysis of intragraft mRNA transcriptome identified significantly higher abundance of mRNA for pattern recognition receptors in TCMR compared to normal biopsies, as well as increased expression of mRNAs for cytokines, chemokines, interferons, and caspases. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
34 Samples
Download data: TXT
17.

Molecular analysis identifies a specific role for memory effector T cells in kidney chronic T-cell mediated rejection

(Submitter supplied) Chronic T-cell mediated rejection (TCMR) is characterized by the reduction of vessel lumen with marked intimal thickening, fibrous hyperplasia and a strong component of leukocyte infiltrate. Aim of our work was the study of gene expression profile in renal TCMR biopsies. We performed transcriptomics study using RNA extracted from archival formalin-fixed and paraffin-embedded (FFPE) renal biopsies obtained from patients with chronic and acute TCMR. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14951
76 Samples
Download data: TXT
Series
Accession:
GSE69677
ID:
200069677
18.

The Regulation of IFN Type I Pathway Related Genes RSAD2 and ETV7 Specifically Indicate Antibody-Mediated Rejection After Kidney Transplantation

(Submitter supplied) We performed total RNA-Seq and compared expression levels of genes of whole blood cells isolated from patients after kidney transplantation with stable graft function, antibody mediated- and t cell mediated graft rejection.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
16 Samples
Download data: TXT
Series
Accession:
GSE120649
ID:
200120649
19.

Transcriptome signature in early biopsies of stably functioning kidney allografts identify patients at risk for chronic injury

(Submitter supplied) Chronic injury in kidney transplants remains a major cause of graft loss. The aim of this study was to identify a predictive gene set capable of classifying renal grafts at risk for progressive injury due to fibrosis.The Genomics of Chronic Allograft Rejection (GoCAR) study is a prospective, multicenter study. Biopsies obtained prospectively 3 months after transplantation from renal allograft recipients (n=159) with stable renal function were analyzed for gene expression by microarray. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
159 Samples
Download data: CEL
Series
Accession:
GSE57387
ID:
200057387
20.

An integrated transcriptomic approach to identify molecular markers of calcineurin inhibitor nephrotoxicity in pediatric kidney transplant recipients

(Submitter supplied) Calcineurin inhibitor nephrotoxicity (CNIT) has been associated with the development of chronic renal allograft dysfunction and decreased graft survival. This study evaluated 37 formalin-fixed paraffin-embedded biopsies from pediatric kidney transplant recipients using gene expression profiling. Oxidative phosphorylation and mitochondrial dysfunction were the top molecular pathways as-sociated with overexpressed genes in CNIT samples. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
37 Samples
Download data: CEL
Series
Accession:
GSE174020
ID:
200174020
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