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Links from GEO DataSets

Items: 20

1.

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
2.

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
3.

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
4.

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
5.

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
6.

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

(Submitter supplied) To gain insight into the mechanisms by which exercise affects muscle stem cell niche, we subjected young and old mice to aerobic exercise and performed whole transcriptome analysis of muscle cells from these animals.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
16 Samples
Download data: TXT
Series
Accession:
GSE193261
ID:
200193261
7.

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
8.

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
9.

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
10.

DNA methylation changes in mice induced by mock parabiosis

(Submitter supplied) Aging is classically conceptualized as an ever-increasing trajectory of damage accumulation and loss of function, leading to increases in morbidity and mortality. However, recent in vitro studies have raised the possibility of age reversal. We characterized several models in which biological age, assessed primarily through analysis of DNA methylation, undergoes reversible changes. Heterochronic parabiosis is one such example.
Organism:
Homo sapiens; Mus musculus; Rattus; Macaca mulatta
Type:
Methylation profiling by array
Platform:
GPL32543
36 Samples
Download data: CSV, IDAT
Series
Accession:
GSE236617
ID:
200236617
11.

DNA methylation and gene expression changes in mice induced by parabiosis and recovery

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca mulatta; Homo sapiens; Mus musculus; Rattus; Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Methylation profiling by array
4 related Platforms
233 Samples
Download data: COV, IDAT, TXT
Series
Accession:
GSE224447
ID:
200224447
12.

DNA methylation changes in mice induced by parabiosis and recovery [RRBS]

(Submitter supplied) Aging is classically conceptualized as an ever-increasing trajectory of damage accumulation and loss of function, leading to increases in morbidity and mortality. However, recent in vitro studies have raised the possibility of age reversal. We characterized several models in which biological age is perturbed. Heterochronic parabiosis and recovery from this procedure is one such example.
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL17021
78 Samples
Download data: COV
Series
Accession:
GSE224442
ID:
200224442
13.

Gene expression changes in mice induced by parabiosis and recovery [RNA-seq]

(Submitter supplied) Aging is classically conceptualized as an ever-increasing trajectory of damage accumulation and loss of function, leading to increases in morbidity and mortality. However, recent in vitro studies have raised the possibility of age reversal. We characterized several models in which biological age is perturbed. Heterochronic parabiosis and recovery from this procedure is one such example.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
39 Samples
Download data: TXT
Series
Accession:
GSE224378
ID:
200224378
14.

DNA methylation changes in mice induced by parabiosis and recovery [HorvathMammalMethylChip40]

(Submitter supplied) Aging is classically conceptualized as an ever-increasing trajectory of damage accumulation and loss of function, leading to increases in morbidity and mortality. However, recent in vitro studies have raised the possibility of age reversal. We characterized several models in which biological age, assessed primarily through analysis of DNA methylation, undergoes reversible changes. Heterochronic parabiosis and recovery from this procedure is one such example.
Organism:
Homo sapiens; Rattus norvegicus; Mus musculus
Type:
Methylation profiling by array
Platform:
GPL28271
119 Samples
Download data: CSV, IDAT
Series
Accession:
GSE224361
ID:
200224361
15.

Global transcriptomic profiling of the bone marrow stromal microenvironment during postnatal development, aging, and inflammation

(Submitter supplied) RNA-sequencing of a longitudinal comparison of four principal mesenchymal and endothelial stromal cell types (CXCL12-abundant reticular cells, PDGFR-α+ Sca-1+, sinusoidal and arterial endothelial cells), isolated from early postnatal, adult and aged mice. Additional transcriptional profiling of the response of CXCL12-abundant reticular cells and sinusoidal endothelial cells to infection-mimicking agents.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
79 Samples
Download data: TXT
Series
Accession:
GSE133922
ID:
200133922
16.

A skeletal-muscle senescence blueprint defines an aged-like inflamed niche that inhibits regeneration over lifetime [scRNA-seq]

(Submitter supplied) A new sorting protocol was used to identify and isolate different senescent cell types from damaged muscles of young and geriatric mice. Analysis revealed conservation of two universal senescence hallmarks (inflammation and fibrosis) across cell type, regeneration time, and aging, while cell identity traits were preserved. Senescent cells create an “aged-like” inflamed niche, mirroring inflammation-associated with aging (inflammaging), that arrests stem cell proliferation and regeneration.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28330
8 Samples
Download data: RDS
Series
Accession:
GSE197017
ID:
200197017
17.

A skeletal-muscle senescence blueprint defines an aged-like inflamed niche that inhibits regeneration over lifetime

(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
Platforms:
GPL17021 GPL24247 GPL28330
179 Samples
Download data
Series
Accession:
GSE196613
ID:
200196613
18.

A skeletal-muscle senescence blueprint defines an aged-like inflamed niche that inhibits regeneration over lifetime [ATAC-seq]

(Submitter supplied) A new sorting protocol was used to identify and isolate different senescent cell types from damaged muscles of young and geriatric mice. Analysis revealed conservation of two universal senescence hallmarks (inflammation and fibrosis) across cell type, regeneration time, and aging, while cell identity traits were preserved. Senescent cells create an “aged-like” inflamed niche, mirroring inflammation-associated with aging (inflammaging), that arrests stem cell proliferation and regeneration.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
69 Samples
Download data: TXT
Series
Accession:
GSE196612
ID:
200196612
19.

A skeletal-muscle senescence blueprint defines an aged-like inflamed niche that inhibits regeneration over lifetime [RNA-seq]

(Submitter supplied) A new sorting protocol was used to identify and isolate different senescent cell types from damaged muscles of young and geriatric mice. Analysis revealed conservation of two universal senescence hallmarks (inflammation and fibrosis) across cell type, regeneration time, and aging, while cell identity traits were preserved. Senescent cells create an “aged-like” inflamed niche, mirroring inflammation-associated with aging (inflammaging), that arrests stem cell proliferation and regeneration.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
102 Samples
Download data: TXT
Series
Accession:
GSE196611
ID:
200196611
20.

Multi-dimensional transcriptome analysis of an intact hematopoietic organ for HSPC expansion

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Danio rerio
Type:
Expression profiling by array
Platforms:
GPL18413 GPL23085 GPL21741
97 Samples
Download data: TXT
Series
Accession:
GSE120581
ID:
200120581
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