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Links from GEO DataSets

Items: 20

1.

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
2.

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
3.

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
4.

Pretransplant transcriptomic signature in peripheral blood predicts acute rejection and renal allograft loss

(Submitter supplied) Early development of acute rejection after kidney transplantation is associated with diminished long-term graft survival. Predicting early acute rejection (EAR) at the time of transplant is important to risk-stratify patients and titrate immunosuppression accordingly. We performed whole-blood RNA sequencing at the time of transplant in 235 kidney transplant recipients enrolled in a prospective-cohort study [one discovery set (N=81), two validation sets (N=74 and N=80)] and evaluated the relationship with EAR and graft loss. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
235 Samples
Download data: TXT
Series
Accession:
GSE112927
ID:
200112927
5.

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
6.

Gene expression profiling in patients with a kidney transplantation

(Submitter supplied) Microarrays were used to analyze the gene expression in peripheral blood and kidney allograft biopsies from patients with a kidney transplantation to get more insight in the molecular mechanisms underlying the different clinical phenotypes of kidney transplant rejection.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
212 Samples
Download data: CEL
Series
Accession:
GSE129166
ID:
200129166
7.

Peripheral blood biomarker signatures for acute kidney transplant rejection

(Submitter supplied) In the present work, we have used whole genome expression profiling of peripheral blood samples from 51 patients with biopsy-proven acute kidney transplant rejection and 24 patients with excellent function and biopsy-proven normal transplant histology. The results demonstrate that there are 1738 probesets on the Affymetrix HG-U133 Plus 2.0 GeneChip representing 1472 unique genes which are differentially expressed in the peripheral blood during an acute kidney transplant rejection. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
75 Samples
Download data: CEL
Series
Accession:
GSE15296
ID:
200015296
8.

Gene expression profiling of subclinical acute kidney rejection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
659 Samples
Download data: CEL
Series
Accession:
GSE107509
ID:
200107509
9.

Gene expression profiling of subclinical acute kidney rejection II

(Submitter supplied) Sub-clinical acute rejection (subAR) in kidney transplant recipients (KTR) leads to chronic rejection and graft loss. Non-invasive biomarkers are needed to detect subAR. 307 KTR were enrolled into a multi-center observational study. Precise clinical phenotypes (CP) were used to define subAR. Differential gene expression (DGE) data from peripheral blood samples paired with surveillance biopsies were used to train a Random Forests (RF) model to develop a gene expression profile (GEP) for subAR. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
129 Samples
Download data: CEL
Series
Accession:
GSE107506
ID:
200107506
10.

Gene expression profiling of subclinical acute kidney rejection I

(Submitter supplied) Sub-clinical acute rejection (subAR) in kidney transplant recipients (KTR) leads to chronic rejection and graft loss. Non-invasive biomarkers are needed to detect subAR. 307 KTR were enrolled into a multi-center observational study. Precise clinical phenotypes (CP) were used to define subAR. Differential gene expression (DGE) data from peripheral blood samples paired with surveillance biopsies were used to train a Random Forests (RF) model to develop a gene expression profile (GEP) for subAR. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
530 Samples
Download data: CEL
Series
Accession:
GSE107503
ID:
200107503
11.

Borderline Changes in Renal Allografts: Molecular Diagnostics Identifies Risks for Graft Dysfunction

(Submitter supplied) The significance of borderline changes (BL) in kidney allograft biopsies is widely debated. We examined differences in gene expression patterns between early clinical biopsy tissue and 3-month protocol biopsy tissue, all of which had histological BL changes and identified specific molecular BL patterns associated with poor graft outcome. The expression profiles were analyzed in training set of patients and next data were validated in validation cohort using RT-qPCR. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
28 Samples
Download data: TXT
Series
Accession:
GSE52694
ID:
200052694
12.

Detection of cardiac allograft rejection and response to immunosuppressive therapy with peripheral blood gene expression

(Submitter supplied) BACKGROUND: Assessment of gene expression in peripheral blood may provide a noninvasive screening test for allograft rejection. We hypothesized that changes in peripheral blood expression profiles would correlate with biopsy-proven rejection and would resolve after treatment of rejection episodes. METHODS AND RESULTS: We performed a case-control study nested within a cohort of 189 cardiac transplant patients who had blood samples obtained during endomyocardial biopsy (EMB). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2386
Platform:
GPL96
21 Samples
Download data: CEL
Series
Accession:
GSE5967
ID:
200005967
13.
Full record GDS2386

Cardiac allograft rejection and response to immunosuppressive therapy: peripheral blood

Analysis of peripheral blood from cardiac transplant patients with allograft rejection and from the same patients after resolution of rejection with augmented immunosuppression. Results provide insight into potential use of peripheral blood profiling for detection of cardiac allograft rejection.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 individual sets
Platform:
GPL96
Series:
GSE5967
21 Samples
Download data: CEL
DataSet
Accession:
GDS2386
ID:
2386
14.

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
15.

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
16.

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
17.

Profiling of Naïve (CD45RA+CD28+), EM (CD45RA-CD28-) and TEMRA (CD45RA+CD28-) CD8+ T cells

(Submitter supplied) RNAseq of 3 CD8 subsets (NAIVE, TEMRA and EM) from 8 paired Healthy Volunteers
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: TXT
18.

Potential impact of microarray diagnosis of T cell-mediated rejection in kidney transplants: the INTERCOM study

(Submitter supplied) The authors report that in INTERCOM, a prospective international study of 300 kidney transplant biopsies, a microarray-based molecular score for T cell-mediated rejection changed the assessment of 26% of all biopsies, illustrating the potential of precision diagnostics to impact practice.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
306 Samples
Download data: CEL
Series
Accession:
GSE48581
ID:
200048581
19.

Molecular diagnosis of T cell-mediated rejection in human kidney transplant biopsies; Molecular diagnosis of antibody-mediated rejection in human kidney transplants

(Submitter supplied) Histologic diagnosis of T cell-mediated rejection in kidney transplant biopsies has limited reproducibility because it is based on non-specific lesions using arbitrary rules that are subject to differing interpretations. We used microarray results from 403 indication biopsies previously given histologic diagnoses to develop a molecular classifier that assigned a molecular T cell-mediated rejection score to each biopsy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
411 Samples
Download data: CEL
Series
Accession:
GSE36059
ID:
200036059
20.

The effect of cortex/medulla proportions on molecular diagnoses in kidney transplant biopsies: rejection and injury can be assessed in medulla

(Submitter supplied) Histologic assessment of kidney transplant biopsies relies on cortex rather than medulla, but for microarray studies, the proportion cortex in a biopsy is typically unknown and could affect the molecular readings. The present study aimed to develop a molecular estimate of proportion cortex in biopsies and examine its effect on molecular diagnoses. Microarrays from 26 kidney transplant biopsies divided into cortex and medulla components and processed separately showed that many of the most significant differences were in glomerular genes e.g. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
154 Samples
Download data: CEL, TXT
Series
Accession:
GSE95611
ID:
200095611
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