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Links from GEO DataSets

Items: 6

1.
Full record GDS5053

Diabetes and Obesity Regulated gene abalation effect on skeletal muscle

Analysis of quadriceps from a muscle-specific, Diabetes and Obesity Regulated gene (DOR; Tp53inp2) knockout line (SKM-KO). Deletion of DOR results in muscle hypertrophy. Results provide insight into the functional role of DOR in skeletal muscle.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL11180
Series:
GSE54917
6 Samples
Download data: CEL
2.

Mus musculus gene expression profiling for Wt, SKM-Tg, C and SKM-KO in Affymetrix 430PM strip arrays

(Submitter supplied) We analyzed the functional role of DOR (Diabetes and Obesity Regulated gene) (also named Tp53inp2) in skeletal muscle. We show that DOR has a direct impact on skeletal muscle mass in vivo. Thus, using different transgenic mouse models, we demonstrate that while muscle-specific DOR gain-of-function results in reduced muscle mass, loss-of-function causes muscle hypertrophy. DOR has been described as a protein with two different functions, i.e., a nuclear coactivator and an autophagy regulator (Baumgartner et. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS5053 GDS5054
Platform:
GPL11180
13 Samples
Download data: CEL
Series
Accession:
GSE54917
ID:
200054917
3.
Full record GDS5054

Diabetes and Obesity Regulated gene gain-of-function effect on skeletal muscle

Analysis of quadriceps from a muscle-specific, Diabetes and Obesity Regulated gene (DOR; also named Tp53inp2) overexpression line (SKM-Tg). DOR gain of function causes a reduction in muscle mass. Results provide insight into the functional role of DOR in skeletal muscle.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL11180
Series:
GSE54917
7 Samples
Download data: CEL
4.

burde-affy-arabi-64764

(Submitter supplied) In skeletal muscle, the pattern of electrical activity regulates the expression of proteins involved in synaptic transmission, contraction and metabolism. Disruptions in electrical activity, resulting from prolonged bed-rest, cast-immobilization or trauma, inevitably lead to muscle atrophy. The mechanisms that regulate muscle atrophy are poorly understood, but it seems likely that changes in gene expression play a key role in initiating and maintaining a muscle atrophy program. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
11 Samples
Download data: CEL
Series
Accession:
GSE4411
ID:
200004411
5.

Differentially expressed genes involved in the regulation of muscle wasting during catabolic conditions

(Submitter supplied) Loss of muscle proteins and the consequent weakness has important clinical consequences in diseases such as cancer, diabetes, chronic heart failure and in ageing. In fact, excessive proteolysis causes cachexia, accelerates disease progression and worsens life expectancy. Muscle atrophy involves a common pattern of transcriptional changes in a small subset of genes named atrophy-related genes or atrogenes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10688
18 Samples
Download data: CSV
Series
Accession:
GSE52676
ID:
200052676
6.

Involvement of miRNAs in the regulation of muscle wasting during catabolic conditions

(Submitter supplied) Loss of muscle proteins and the consequent weakness has important clinical consequences in diseases such as cancer, diabetes, chronic heart failure and in ageing. In fact, excessive proteolysis causes cachexia, accelerates disease progression and worsens life expectancy. Muscle atrophy involves a common pattern of transcriptional changes in a small subset of genes named atrophy-related genes or atrogenes. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL17835
39 Samples
Download data: CSV
Series
Accession:
GSE51648
ID:
200051648
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Supplemental Content

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