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Links from GEO DataSets

Items: 20

1.

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
2.

Shroom3-Fyn interaction determines nephrin phosphorylation and Albuminuria in allografts

(Submitter supplied) Glomerular RNA-sequencing: Shroom3 knockdown adult mice vs controls
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
7 Samples
Download data: TXT
Series
Accession:
GSE110092
ID:
200110092
3.

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
4.

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
5.

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
6.

Progressive Decline of Function in Renal Allografts with Normal One Year Biopsies

(Submitter supplied) Histologic findings on 1-year biopsies such as inflammation with fibrosis and transplant glomerulopathy predict renal allograft loss by 5 years. However, almost half of the patients with graft loss have a 1-year biopsy that is either normal or has only interstitial fibrosis. The goal of this study was to determine if there was a gene expression profile in these relatively normal 1-year biopsies that predicted subsequent decline in renal function. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
440 Samples
Download data: CSV
Series
Accession:
GSE181757
ID:
200181757
7.

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
8.

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
9.

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
10.

Mining the Human Urine Proteome for Monitoring Renal Transplant Injury

(Submitter supplied) Gene expression data was analyzed to map with urine proteomics data gene expression data from kidney biopsies from kidney transplant patients with and without acute rejection, chronic allograft nephropathy and BK virus nephritis was used to study gene expression changes during acute rejection, chronic allograft nephropathy and bk virus nephropathy. Samples labeled STA16, STA22, STA14, and STA18 were included in the CAN vs no-CAN analysis as no-CAN samples as they also qualified as non-CAN samples.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
79 Samples
Download data: CEL
Series
Accession:
GSE75693
ID:
200075693
11.

Innate and adaptive immune responses associate with progressive histological damage of renal allografts

(Submitter supplied) CONTEXT Slowly progressive chronic tubulo-interstitial damage jeopardizes long-term renal allograft survival. Both immune and non-immune mechanisms are thought to contribute, but the most promising targets for timely intervention have not been identified. OBJECTIVE In the current study we seek to determine the driving force behind progressive histological damage of renal allografts, without the interference of donor pathology, delayed graft function and acute graft rejection. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
120 Samples
Download data: CEL
Series
Accession:
GSE25902
ID:
200025902
12.

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
13.

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
14.

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
15.

Fibrosis with Inflammation at One Year Predicts Transplant Functional Decline

(Submitter supplied) We previously observed reduced graft survival for kidney transplants having interstitial fibrosis with subclinical inflammation, but not fibrosis alone, on 1-year protocol biopsy. The current study aimed to determine whether fibrosis with inflammation at 1 year is associated with renal functional decline in a low-risk transplant cohort and to characterize the nature of the inflammation. Subjects were living-donor, tacrolimus/mycophenolate-treated transplant recipients without overt risk factors for reduced graft survival (n=151). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
65 Samples
Download data: CEL, CHP
Series
Accession:
GSE22459
ID:
200022459
16.

Development of gene expression profiles in human chronic kidney disease

(Submitter supplied) A microarray analysis with renal biopsy specimens from CKD patients was conducted in order to identify the responsible genes associated with tubulointerstitial fibrosis and tubular cell injury in CKD. This study showed microarray profiles in total 53 biopsy specimens of CKD patients. In the discovery set, 554 down-regulated and 226 up-regulated signatures were identified. Then, the expressional changes of these genes were examined in the validation set.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
61 Samples
Download data: TXT
Series
Accession:
GSE66494
ID:
200066494
17.

Single nucleus inDrops to profile adult human kidney

(Submitter supplied) Single nucleus inDrops to profile adult human kidney
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
1 Sample
Download data: TXT
Series
Accession:
GSE114156
ID:
200114156
18.

Inflammatory Response and Host-Donor Chimerism Defined by Single Cell RNA-Seq of Allograft Biopsy

(Submitter supplied) Kidney transplantation offers the best survival and quality of life for patients’ with end-stage kidney disease. The major barrier to successful long-term transplantation is the host’s immune response to alloantigens’ causing rejection of the transplant. The complexity of this immune response in kidney transplantation is still not fully understood and effective treatment strategies are needed. To better understand rejection at the molecular and cellular level we characterized 4,487 cells from a single biopsy core from a kidney transplant undergoing mixed rejection using single cell RNA sequencing.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL16791
7 Samples
Download data: TXT
Series
Accession:
GSE109564
ID:
200109564
19.

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
20.

Analyses of heterogeneous renal allograft biopsies reveal conserved rejection signatures and molecular pathways I, partB

(Submitter supplied) Specific early diagnosis of renal allograft rejection is gaining importance in the current trend to minimize and individualize immunosuppression. Gene expression analyses could contribute significantly by defining “molecular Banff” signatures. Several previous studies have applied transcriptomics to distinguish different classes of kidney biopsies. However, the heterogeneity of microarray platforms, clinical samples and data analysis methods complicates the identification of robust signatures for the different types and grades of rejection. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
16 Samples
Download data: CEL, CHP
Series
Accession:
GSE17861
ID:
200017861
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