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Links from GEO DataSets

Items: 20

1.

Expression profiling of skeletal muscle following acute β2-adrenergic stimulation

(Submitter supplied) Systemic administration of β-adrenoceptor (β-AR) agonists has been found to induce skeletal muscle hypertrophy and significant metabolic changes. In the context of energy homeostasis, the importance of β-AR signaling has been highlighted by the inability of β1–3-AR-deficient mice to regulate energy expenditure and susceptibility to diet induced obesity. However, the molecular pathways and gene expression changes that initiate and maintain these phenotypic modulations are poorly understood. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6333
16 Samples
Download data: TXT
Series
Accession:
GSE15793
ID:
200015793
2.

Clenbuterol administration in mouse muscle

(Submitter supplied) Background: Beta-adrenergic receptor agonists (BA) induce skeletal muscle hypertrophy, yet specific mechanisms that lead to this effect are not well understood. The objective of this research was to identify novel genes and physiological pathways that potentially facilitate BA induced skeletal muscle growth. We chose to evaluate global changes in gene expression by utilizing the Affymetrix platform to identify gene expression changes in mouse skeletal muscle. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL339 GPL340
18 Samples
Download data
Series
Accession:
GSE4490
ID:
200004490
3.

Role of PDK1 in Skeletal Muscle Hypertrophy Induced by Exercise Load

(Submitter supplied) Skeletal muscle mass is an important determinant of whole-body glucose disposal. We here show that mice (M-PDK1KO mice) with skeletal muscle–specific deficiency of 3'-phosphoinositide–dependent kinase 1 (PDK1), a key component of the phosphatidylinositol 3-kinase (PI3K) signaling pathway, manifest a reduced skeletal muscle mass under the static condition as well as impairment of exercise load–induced muscle hypertrophy. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
4 Samples
Download data: CEL
Series
Accession:
GSE150464
ID:
200150464
4.

Equine skeletal muscle: pre versus post-exercise

(Submitter supplied) Unconditioned thoroughbred geldings were exercised to maximal heart rate or fatigue on an equine high-speed treadmill. Skeletal muscle biopsies were taken from the middle gluteal muscle before, immediately after and four hours after exercise. 
Organism:
Equus caballus
Type:
Expression profiling by array
Platform:
GPL8582
32 Samples
Download data: GPR
Series
Accession:
GSE16235
ID:
200016235
5.

Gene expression analysis of normal primary human bronchial epithelial cells (pHBEC) stimulated by glucocorticoid, long-acting β2-adrenoceptor agonist or both combined.

(Submitter supplied) In 2019, the Global Initiative for Asthma treatment guidelines were updated to recommend that inhaled corticosteroid (ICS)/long-acting β2-adrenoceptor agonist (LABA) combination therapy should be a first-in-line treatment option for asthma. Although clinically superior to ICS, mechanisms underlying the efficacy of this combination therapy remain unclear. We hypothesised the existence of transcriptomic interactions, an effect that was tested in primary human bronchial epithelial cells (pHBECs) using formoterol and budesonide as representative LABA and ICS, respectively. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
24 Samples
Download data: CEL, CHP
Series
Accession:
GSE161805
ID:
200161805
6.

Gene expression analysis of human bronchial airway epithelial BEAS-2B cells stimulated by glucocorticoid, long-acting β2-adrenoceptor agonist or both combined.

(Submitter supplied) In asthma, the clinical efficacy of inhaled corticosteroids (ICSs) is enhanced by long-acting β2-adrenoceptor agonists (LABAs). ICSs, or more accurately, glucocorticoids, promote therapeutically-relevant changes in gene expression and this genomic effect can be enhanced by a LABA. To investigate the gene expression changes by each condition, transcriptomic analysis was performed on RNA extracted from BEAS-2B cells treated with budesonide, formoterol, or both combined.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
64 Samples
Download data: CEL, CHP
Series
Accession:
GSE115830
ID:
200115830
7.

Circadian rhythm in clock mutants

(Submitter supplied) One hundred ninety wildtype male C57BL/6J mice age 7-10 weeks were purchased from Jackson Laboratory and entrained to a 12:12 light:dark cycle for 2 weeks. Mice were placed in light-tight boxes on a 12:12 LD cycle for 4 weeks, then released into constant darkness. Starting 30 hours after entry into DD (CT18), tissues from 5 (skeletal muscle) or 10 (liver or SCN) wildtype mice were collected every 4 hours for 48 hours, for a total of 12 timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1073
76 Samples
Download data: CEL
Series
Accession:
GSE3751
ID:
200003751
8.

Circadian skeletal muscle_wt and Clock mutants

(Submitter supplied) One hundred ninety wildtype male C57BL/6J mice age 7-10 weeks were purchased from Jackson Laboratory and entrained to a 12:12 light:dark cycle for 2 weeks. Mice were placed in light-tight boxes on a 12:12 LD cycle for 4 weeks, then released into constant darkness. Starting 30 hours after entry into DD (CT18), the left leg muscle from 5 wildtype mice, and the right leg muscle from the same wildtype mice were collected every 4 hours for 48 hours, for a total of 12 timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1073
38 Samples
Download data: CEL
Series
Accession:
GSE3746
ID:
200003746
9.

Identification of target genes of myostatin loss-of-function in the muscle of bovine fetuses

(Submitter supplied) Myostatin is a highly conserved Transforming Growth Factor beta family member which negatively regulates muscle development. Double-muscled (DM) cattle have a loss-of-function mutation in their myostatin gene responsible for a hypermuscular phenotype mainly due to hyperplasia. Thus these animals represent a good model for understanding the mechanisms at the origin of muscular hypertrophy. In order to identify individual genes or networks that may be myostatin targets, we looked for genes differentially expressed between DM and normal (NM) animals (n=3 per group) in the semitendinosus muscle (a hypertrophied muscle in DM animals) at 260 days of fetal development (intensive muscle biochemical differentiation). more...
Organism:
Bos taurus; Mus musculus
Type:
Expression profiling by array
Platform:
GPL4049
24 Samples
Download data
Series
Accession:
GSE5456
ID:
200005456
10.

Time and Exercise effects on Human Skeletal Muscle

(Submitter supplied) Four healthy human volunteers underwent an acute bout of resistance exercise with the right leg at 2 pm. Biopsies were removed from the Vastus Lateralis muscle 6 h (8 pm) and 18 h (8 am) after exericise Keywords = Human skeletal muscle Keywords = resistance exerise Keywords = diurnal Keywords = circadian Keywords: time-course
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS894
Platform:
GPL8300
15 Samples
Download data: CEL
Series
Accession:
GSE1832
ID:
200001832
11.
Full record GDS894

Skeletal muscle response to exercise and circadian rhythms

Analysis of effects of resistance exercise (RE) and time of day in skeletal muscle. Biopsies of male vastus lateralis muscle obtained 6 and 18 hours after acute RE, or no RE. Results suggest that RE may directly modulate circadian rhythms in skeletal muscle.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 stress, 2 time sets
Platform:
GPL8300
Series:
GSE1832
15 Samples
Download data: CEL
12.

The effect of age on the skeletal muscle transcriptome during hypertrophy

(Submitter supplied) Transcriptome analysis of skeletal muscle during hypertrophic growth in aged mice Global gene expression patterns were determined from microarray results on day 1, 3, 5, 7, 10 and 14 during plantaris muscle hypertrophy induced by synergist ablation in old adult mice (25 months).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
14 Samples
Download data: CEL, CHP
Series
Accession:
GSE67160
ID:
200067160
13.

Expression data during plantaris muscle hypertrophy induced by synergist ablation in young adult mice

(Submitter supplied) Global gene expression patterns were determined from microarray results on day 1, 3, 5, 7, 10 and 14 during plantaris muscle hypertrophy induced by synergist ablation in young adult mice (5 months).
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4932
Platform:
GPL6246
14 Samples
Download data: CEL
Series
Accession:
GSE47098
ID:
200047098
14.
Full record GDS4932

Synergist ablation effect on young adult plantaris muscle: time course

Analysis of right and left plantaris muscle from young males (5 months old) subjected to 1, 3, 5, 7, 10 and 14 days of synergist ablation surgery to induce hypertrophy. Results provide insight into the molecular response of young skeletal muscle to mechanical overload induced by synergist ablation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 stress, 7 time, 2 tissue sets
Platform:
GPL6246
Series:
GSE47098
14 Samples
Download data: CEL
15.

Effect of formoterol and tumor necrosis factor (TNFα) alone and in combination on gene expression changes in human primary bronchial epithelial cells: a comparison with forskolin treatment

(Submitter supplied) RNA sequencing was performed to study the genomic effects of formoterol, a long acting β2-adrenoceptor agonist, alone and in combination with the pro-inflammatory cytokine, TNFα in human primary bronchial epithelial cells, and to compare its effect to forskolin. Our results show that formoterol promoted a profound genomic response alone and on background of an inflammatory stimulus. Moreover, formoterol and forskolin regulated transcriptomes were highly rank order correlated which suggests that formoterol-mediated gene expression changes are cAMP dependent
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
100 Samples
Download data: TXT
Series
Accession:
GSE202436
ID:
200202436
16.

Skeletal muscle gene expression after myostatin knockout in mature mice

(Submitter supplied) RNA from 5 mice with postdevelopmental knockout of myostatin and 5 mice with normal myostatin expression was analyzed with comprehensive oligonucleotide microarrays. Myostatin depletion affected the expression of several hundred genes at nominal P < 0.01, but fewer than a hundred effects were statistically significant according to a more stringent criterion (false discovery rate < 5%). Most of the effects were less than 1.5-fold in magnitude. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3637
Platform:
GPL1261
10 Samples
Download data: CEL
Series
Accession:
GSE15349
ID:
200015349
17.
Full record GDS3637

Myostatin depletion effect on mature skeletal muscle

Analysis of mature skeletal muscle depleted for the TBFb protein myostatin (MSTN). MSTN inhibits muscle differentiation and growth. MSTN deficiency during development results in muscle hypertrophy. Results provide insight into the effect of reducing MSTN activity after normal muscle development.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL1261
Series:
GSE15349
10 Samples
Download data: CEL
18.

Liver transcriptome comparison of divergently selected Lean and Fat mouse lines in cholesterol homeostasis, bile acids, glucose and lipoprotein metabolism

(Submitter supplied) This study aimed to identify molecular basis of obesity-resistant mechanisms in the Lean line with the emphasis on lipid homeostasis. Expression profiling using custom Steroltalk v2 microarray demonstrated that Lean mice exhibit a higher hepatic expression of cholesterol synthesis genes compared to the Fat line. A significant difference between the strains was also found in the bile acid metabolism. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7190
17 Samples
Download data: TXT
Series
Accession:
GSE24967
ID:
200024967
19.

Leucine differentially regulates gene-specific translation in mouse skeletal muscle

(Submitter supplied) Mice received an oral gavage of either leucine or vehicle, and quadriceps muscle were harvested for ribosome profiling or RNA-Seq analysis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
22 Samples
Download data: XLSX
Series
Accession:
GSE99585
ID:
200099585
20.

Expression data from neonatal pig skeletal muscle

(Submitter supplied) Muscle development and growth is an economically important process in the pig.The neonatal period is another important stage for the pig when the most rapid gain occurring in skeletal muscle.Gene expresseion changes during fetal and postnatal skeletal muscle development that can be used to enhance pig production efficiency, as well as for comparative developmental biology using the pig as a model for other mammalian species. more...
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL3533
12 Samples
Download data: CEL
Series
Accession:
GSE22487
ID:
200022487
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