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Renal failure is characterized by important biological changes resulting in profound pleomorphic physiological effects termed “uremia”, whose molecular causation is not well understood. The data was used to study gene expression changes in uremia using whole genome microarray analysis of peripheral ...
ORGANISM(S): Homo sapiens 
Single-cell assay examining chromatin accessibility reveals transcriptional regulatory variation in the proinflammatory milieu of uremia
A single-cell assay for transposase-accessible chromatin with high-throughput sequencing (scATAC-seq) was applied to compare the single-cell chromatin accessibility profiles of peripheral blood mononuclear cells (PBMCs) that were obtained from healthy volunteers and uremia patients. Besides, we furt...
ORGANISM(S): Homo sapiens 
2022-04-27 | GSE158280 | GEO
Identification of differential gene expression in blood vessels from patients with uremia
ORGANISM(S): Homo sapiens 
2020-09-11 | GSE38751 | GEO
Identification of differential gene expression in blood vessels from patients with uremia
ORGANISM(S): Homo sapiens 
2020-09-11 | GSE38750 | GEO
Cardiovascular disease (CVD) is exceedingly severe in patients with chronic kidney disease (CKD) and further aggravated by peritoneal dialysis (PD), exposing the patients to excessive amounts of intraperitoneal glucose. Children are devoid of pre-existing CVD and give insight into specific uremia an...
ORGANISM(S): Homo sapiens (Human) 
2019-11-08 | PXD006298 | Pride
Effect of chronic uremia on the transcriptional profile of the calcified aorta analyzed by RNA sequencing.
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