Transcriptomics

Dataset Information

0

MRNA-seq read counts of peripheral blood mononuclear cells from congenital generalized lipodystrophy patients and their gender/aged-matched controls


ABSTRACT: Congenital generalized lipodystrophy (CGL) is an autosomal recessive disorder characterized by defective adipose tissue, extreme insulin resistance, and early onset of diabetes. There are four types of congenital generalized lipodystrophy based on the causative genetic alterations. The symptoms and the degrees of disease progression are varied among all affected individuals, which might be due to unknown genetic modifiers. To identify potential predictive biomarkers associated with the disease progressions, we recruited 7 patients (cgl2_p1,cgl2_p2,cgl2_p3,cgl2_p4,cgl2_p5,cgl2_p6,cgl2_p7),as well as gender/aged-matched controls (cgl2_c1,cgl2_c2,cgl2_c3,cgl2_c4,cgl2_c5,cgl2_c6,cgl2_c7).The total RNA samples were extracted from the participants' peripheral blood mononuclear cells, followed by RNA-Seq. To find the molecular signatures that might be associated with disease progression, patients were further categorized into sub-groups based on the results of biochemical analysis and their clinical symptoms (e.g. diabetes, metabolic syndrome and metal retardation). DEGs were identified for each sub-groups of patients, and pathway analysis was performed to explore the underlying dysregulated mechanisms.

ORGANISM(S): Homo sapiens

PROVIDER: GSE159337 | GEO | 2021/08/18

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2023-08-08 | GSE214297 | GEO
2023-12-11 | GSE249808 | GEO
2013-08-07 | E-GEOD-39825 | biostudies-arrayexpress
2011-09-14 | E-GEOD-28073 | biostudies-arrayexpress
| PRJNA171811 | ENA
2013-08-07 | GSE39825 | GEO
| PRJNA884841 | ENA
| PRJNA866148 | ENA
| 2084023 | ecrin-mdr-crc
| PRJNA75597 | ENA