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Links from GEO DataSets

Items: 20

1.
Full record GDS4892

Age effect on skeletal muscle precursor cells

Analysis of FACS-sorted CD45-Ter119-Sca-1-CD29+Cxcr4+ skeletal muscle precursor (SMP) cells from young, middle-aged, and old C57BL/6 males. Results provide insight into the molecular mechanisms underlying age-related skeletal muscle and stem cell dysfunction.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age sets
Platform:
GPL1261
Series:
GSE50821
14 Samples
Download data: CEL
2.

Restoring Systemic GDF11 Levels Reverses Age-Related Dysfunction in Mouse Skeletal Muscle

(Submitter supplied) In this study, we investigated signaling pathways in Skeletal muscle precursors that are altered with aging and age-related deficits in muscle regenerative potential. We performed fluorescence activated cell sorting (FACS) to obtain highly purified skeletal muscle satellite cells from young, middle-aged and old mice. Parabiosis experiments indicate that impaired regeneration in aged mice is reversible by exposure to a young circulation, suggesting that young blood contains humoral "rejuvenating" factors that can restore regenerative function. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4892
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE50821
ID:
200050821
3.

GDF11 is a myokine that inhibits muscle differentiation and induces atrophy during regeneration

(Submitter supplied) Age-related frailty may in part be due to a decreased competency in skeletal muscle regeneration. The role of the closely related TGFbeta amily molecules myostatin and GDF11 in regeneration is unclear. The commercially available antibody which in a prior report was used to demonstrate an age-related decrease in GDF11 was found to detect both GDF11 and myostatin, and with this reagent it appears that the combination of GDF11 and myostatin increases with age in serum. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
56 Samples
Download data: CEL
Series
Accession:
GSE67326
ID:
200067326
4.

Cell-free microRNAs circulating with blood in young and aged mice

(Submitter supplied) We investigated cell-free miRNAs in the blood of young and aged mice. The results indicated marked difference in the level of certain miRNAs between the mice.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL17678
4 Samples
Download data: TXT
Series
Accession:
GSE141258
ID:
200141258
5.

Young and Old Pre- and Post-Transplantation ATAC Seq

(Submitter supplied) ATAC-sequencing of paired Y and O mouse HSCs pre and 3mo post lethal irradiation and HSC transplantation
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
16 Samples
Download data: NARROWPEAK
Series
Accession:
GSE151665
ID:
200151665
6.

Young and Old Mouse Parabiosis Hematopoietic Stem Cell RNA Sequencing

(Submitter supplied) RNA sequencing of hematopoietic stem cells isolated from young (8-12 week) and old (24-27 month) BL6 mice from experimental groups that are intended to describe the transcriptomic consequences of parabiosis on the function of old hematopoietic stem cells.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
30 Samples
Download data: CSV
Series
Accession:
GSE134417
ID:
200134417
7.

Rejuvenating Age-impaired Fracture Healing

(Submitter supplied) Skeletal aging and disease are associated with a misbalance in the opposing actions of osteoblasts and osteoclasts that are responsible for maintaining the integrity of bone tissues. Here, we show through detailed functional and single-cell genomic studies that intrinsic aging of bona fide mouse skeletal stem cells (SSCs) alters bone marrow niche signaling and skews bone and blood lineage differentiation leading to fragile bones that regenerate poorly. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
2 Samples
Download data: H5, HTML
Series
Accession:
GSE172149
ID:
200172149
8.

Aged skeletal stem cells during fracture healing

(Submitter supplied) Skeletal aging and disease are associated with a misbalance in the opposing actions of osteoblasts and osteoclasts that are responsible for maintaining the integrity of bone tissues. Here, we show through detailed functional and single-cell genomic studies that intrinsic aging of bona fide mouse skeletal stem cells (SSCs) alters bone marrow niche signaling and skews bone and blood lineage differentiation leading to fragile bones that regenerate poorly. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
9 Samples
Download data: XLSX
Series
Accession:
GSE166441
ID:
200166441
9.

Skeletal Stem Cell Aging

(Submitter supplied) Skeletal aging and disease are associated with a misbalance in the opposing actions of osteoblasts and osteoclasts that are responsible for maintaining the integrity of bone tissues. Here, we show through detailed functional and single-cell genomic studies that intrinsic aging of bona fide mouse skeletal stem cells (SSCs) alters bone marrow niche signaling and skews bone and blood lineage differentiation leading to fragile bones that regenerate poorly. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
670 Samples
Download data: CSV, HTML
Series
Accession:
GSE161946
ID:
200161946
10.

Gene Expression Commons: an open platform for absolute gene expression profiling

(Submitter supplied) Gene expression profiling using microarray has been limited to profiling of differentially expressed genes at comparison setting since probesets for different genes have different sensitivities. We overcome this limitation by using a very large number of varied microarray datasets as a common reference, so that statistical attributes of each probeset, such as dynamic range or a threshold between low and high expression can be reliably discovered through meta-analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL1261
101 Samples
Download data: CEL, TXT
Series
Accession:
GSE34723
ID:
200034723
11.

Regulation of aged skeletal muscle regeneration by extracellular

(Submitter supplied) Heterochronic blood exchange (HBE) has demonstrated that circulating factors restore youthful features to aged tissues. However, the systemic mediators of those rejuvenating effects remain poorly defined. We show that the beneficial effect of young blood on aged muscle regeneration was diminished when serum was depleted of extracellular vesicles (EVs). Whereas EVs from young animals rejuvenate aged cell bioenergetics and skeletal muscle regeneration, aging shifts EV subpopulation heterogeneity and compromises downstream benefits on recipient cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
11 Samples
Download data: TXT
Series
Accession:
GSE176478
ID:
200176478
12.

Transcriptional profiles of skeletal muscle stem cells from mice of different ages, exercise status, and Ccnd1 genotypes

(Submitter supplied) Voluntary exercise enhances old skeletal muscle stem cell (MuSC) function in vivo and ex vivo, dependent on upregulation of Ccnd1. To determine the transcriptional changes associated with these phenotypes, RNA-Seq was performed on MuSCs from young and old mice that had exercised or not exercised, and from young mice with MuSC-specific loss-of-function deletions in zero, one, or both alleles of Ccnd1.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
36 Samples
Download data: TXT
Series
Accession:
GSE77178
ID:
200077178
13.

Molecular hallmarks of heterochronic parabiosis at single cell resolution

(Submitter supplied) Single-cell RNA sequencing data of Mus Musculus heterochronic parabionts
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
1 Sample
Download data: H5AD
Series
Accession:
GSE193093
ID:
200193093
14.

Tabula Muris

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
996 Samples
Download data: CSV, H5AD, LOOM, TAR
Series
Accession:
GSE132042
ID:
200132042
15.

Heterochronic parabiosis reprograms the mouse brain transcriptome by shifting aging signatures in multiple cell types

(Submitter supplied) Aging is a complex process involving transcriptomic changes associated with deterioration across multiple tissues and organs, including the brain. Recent studies using heterochronic parabiosis have shown that various aspects of aging-associated decline are modifiable or even reversible. To better understand how this occurs, we performed single-cell transcriptomic profiling of young and old mouse brains following parabiosis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
56 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE222510
ID:
200222510
16.

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21103 GPL24247
78 Samples
Download data
Series
Accession:
GSE196364
ID:
200196364
17.

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging V

(Submitter supplied) To gain insight into the mechanisms by which exercise affects the neural stem cell compartment, we subjected young and old mice to aerobic exercise and performed single cell transcriptome analysis of cells from the subventricular zone of the brain of these animals.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
15 Samples
Download data: RDATA
Series
Accession:
GSE196362
ID:
200196362
18.

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging IV

(Submitter supplied) To gain insight into the mechanisms by which exercise affects the muscle stem cell compartment, we subjected young and old mice to aerobic exercise and performed single cell transcriptome analysis of mononucleated cells from hindlimb muscles of these animals.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
16 Samples
Download data: RDATA
Series
Accession:
GSE196361
ID:
200196361
19.

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging III

(Submitter supplied) To gain insight into the mechanisms by which exercise affects hematopoietic stem cells, we subjected young and old mice to aerobic exercise and performed single cell transcriptome analysis of hematopoietic progenitors in the bone marrow of these animals.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
15 Samples
Download data: RDS
Series
Accession:
GSE196359
ID:
200196359
20.

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging II

(Submitter supplied) To gain insight into the mechanisms by which exercise affects circulating immune cells, we subjected young and old mice to aerobic exercise and performed single cell transcriptome analysis of circulating immune cells from these animals.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
16 Samples
Download data: RDS
Series
Accession:
GSE196358
ID:
200196358
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