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Links from GEO DataSets

Items: 7

1.
Full record GDS4785

Steroid receptor coactivator-2 deficiency effect on the liver

Analysis of livers from C57 females lacking Steroid receptor coactivator-2 (SRC-2). SRC-2 is a mediator of steroid receptor action. Results provide insight into the role of steroid receptor coactivators in hepatic metabolism.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE55002
6 Samples
Download data: CEL
DataSet
Accession:
GDS4785
ID:
4785
2.

Transcription array by profiling in WT and SRC-2 null mouse liver

(Submitter supplied) The molecular targets of SRC-2 regulation in the murine liver stimulate fatty acid degradation and glycolytic pathway while fatty acid, cholesterol, and steroid biosynthetic pathways are down-regulated.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4785
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE55002
ID:
200055002
3.

Steroid Receptor Coactivator 1 is an Integrator of Glucose and NAD(+)/NADH Homeostasis

(Submitter supplied) SRC-1 affects the expression of complex I of the mitochondrial electron transport chain, a set of enzymes responsible for the conversion of NADH to NAD(+). NAD(+) and NADH were subsequently identified as metabolites that underlie SRC-1's response to glucose deprivation. Knockdown of SRC-1 in glycolytic cancer cells abrogated their ability to grow in the absence of glucose consistent with SRC-1's role in promoting cellular adaptation to reduced glucose availability
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5418
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE56843
ID:
200056843
4.
Full record GDS5418

Glucose effect on steroid receptor coactivator 1 deficient-A549 lung cancer epithelial cell line

Analysis of highly glycolytic A549 lung cancer cells depleted for steroid receptor coactivator SRC-1 and grown in the absence of glucose. SRC-1 promotes gluconeogenesis and glycemia. Results provide insight into the role of SRC-1 in glycolytic cancer cells undergoing glucose deprivation.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 genotype/variation, 2 protocol sets
Platform:
GPL570
Series:
GSE56843
8 Samples
Download data: CEL
5.

Defining the mammalian coactivation of hepatic 12-hour clock and lipid metabolism

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
43 Samples
Download data: BIGWIG
Series
Accession:
GSE175598
ID:
200175598
6.

Time course hepatic RNA-Seq in the SRC-3 WT versus KO mice

(Submitter supplied) We report the hepatic total gene expression (starting at ZT0 and proceeding every four hours for two complete 12-hour cycles) in the liver of SRC-3 WT and KO mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
12 Samples
Download data: BIGWIG
Series
Accession:
GSE175560
ID:
200175560
7.

Time course SRC-3 ChIP-Seq and XBP1s ChIP-Seq in the C57BJ/L6 WT, SRC-3 WT versus KO, and Xbp1 WT versus LKO mice under chow and fasting conditions

(Submitter supplied) We report the hepatic SRC-3 and XBP1s cistrome at 4-hour interval timecourse zeitgeber times (ZTs) in the liver of the C57BJ/L6 WT mice under chow and fasting conditions; we also chose liver samples at CT24, ZT0 and ZT8 for comprehensive SRC-3 and XBP1s ChIP-Seq to interrogate the genomic binding profiles of hepatic SRC-3 and XBP1s in vivo.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
31 Samples
Download data: BIGWIG
Series
Accession:
GSE175559
ID:
200175559
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Supplemental Content

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