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Items: 1 to 20 of 48

1.

Postnatal development of Cardiomyocyte

(Submitter supplied) Postnatal heart maturation is the basis of normal cardiac function and provides critical insights into heart repair and regenerative medicine. While static snapshots of the maturing heart have provided much insight into its molecular signatures, few key events during postnatal cardiomyocyte maturation have been uncovered.Here we processed bulkRNASeq and ChIPSeq of Cardiomyocyte at different postnatal time points.
Organism:
Mus musculus; Rattus rattus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL28964 GPL19057
115 Samples
Download data: BEDGRAPH, TXT, XLSX
Series
Accession:
GSE155658
ID:
200155658
2.

Small-Molecule-Driven Direct Reprogramming of Fibroblasts into functional Sertoli-like cells as a model for male reproductive toxicology

(Submitter supplied) We report the generation of functional Sertoli-like cells from mice fibroblasts using only chemical cocktails, I-bet151 and Riluzole (IR). CiSCs possess similar gene expression profiles and biological functions to endogenous Sertoli cells and are highly sensitive to reproductive toxicants.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
6 Samples
Download data: TXT
Series
Accession:
GSE192401
ID:
200192401
3.

Conversion of fibroblasts to functional Leydig like cells using defined small molecules

(Submitter supplied) we report that fibroblasts can be efficiently and directly reprogrammed into Leydig-like cells by exposing to a combination of small molecules, Forskolin, 20α-hydroxycholesterol, luteinizing hormone (LH), and SB431542. The chemical compounds induced Leydig-like cells (CiLCs) expressed steroidogenic genes, had a global gene expression profile similar to that of Leydig cell, and acquired androgen synthesis capabilities.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
6 Samples
Download data: TXT
Series
Accession:
GSE145797
ID:
200145797
4.

Hemicastration induced spermatogenesis related DNA methylation and gene expression changes in mice testis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL13112 GPL21103
10 Samples
Download data: TXT
Series
Accession:
GSE95694
ID:
200095694
5.

Hemicastration induced spermatogenesis related DNA methylation and gene expression changes in mice testis

(Submitter supplied) Hemicastration is unilateral orchiectomy to remove an injured testis, and may influence spermatogenesis. However, the underlying molecular mechanisms are poorly understood. Here, we monitored hemicastrated mice and found no significant difference of growth or testosterone (P > 0.05) compared with control. The genome-wide DNA methylation pattern of remaining testis were investigated by RRBS. Substantial genes harbored differentially methylated regions in gene bodies, and were enriched in process of protein binding and cell adhesion. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL21103
6 Samples
Download data: TXT
Series
Accession:
GSE95693
ID:
200095693
6.

Hemicastration induced spermatogenesis-related DNA methylation and gene expression changes in mice testis

(Submitter supplied) Hemicastration is unilateral orchiectomy to remove an injured testis, and may influence spermatogenesis. However, the underlying molecular mechanisms are poorly understood. Here, we monitored hemicastrated mice and found no significant difference of growth or testosterone (P > 0.05) compared with control. The genome-wide DNA methylation pattern of remaining testis were investigated by RRBS. Substantial genes harbored differentially methylated regions in gene bodies, and were enriched in process of protein binding and cell adhesion. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE95692
ID:
200095692
7.

Anti-obesity effect of radix Angelica sinensis and candidate causative genes in transcriptome analyses of adipose tissues in high-fat diet-induced mice

(Submitter supplied) We have previously reported that radix Angelica sinensis (RAS) suppressed body weight and altered FTO expression in mice with high fat diet (HFD)-induced obesity. In the present study we performed RNA sequencing-mediated transcriptome analysis to elucidate the molecular mechanisms underlying the anti-obesogenic effects of RAS in mice. The results revealed that 36 differentially-expressed genes (DEGs) were identified between the RAS supplementation group (DH) and control group (HC). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9185
6 Samples
Download data: TXT
Series
Accession:
GSE89454
ID:
200089454
8.

Artemisinin mimics calorie restriction to trigger mitochondrial biogenesis and compromise telomere shortening in mice

(Submitter supplied) Calorie restriction is known to extend lifespan among organisms by a debating mechanism underlying nitric oxide-driven mitochondrial biogenesis. We report here that nitric oxide generators including artemisinin, sodium nitroprusside, and L-arginine mimics calorie restriction and resembles hydrogen peroxide to initiate the nitric oxide signaling cascades and to elicit the global antioxidative responses in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL19794
6 Samples
Download data: TXT
Series
Accession:
GSE65993
ID:
200065993
9.

KM_p21_2

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709673
ID:
304709673
10.

KM_p21_1

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709672
ID:
304709672
11.

KM_p7_2

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709671
ID:
304709671
12.

KM_p7_1

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709670
ID:
304709670
13.

KM_p1_2

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709669
ID:
304709669
14.

KM_p1_1

Organism:
Mus musculus
Source name:
cardiomyocytes
Platform:
GPL19057
Series:
GSE155658
Download data
Sample
Accession:
GSM4709668
ID:
304709668
15.

MSCs2

Organism:
Mus musculus
Source name:
Sertoli Cells
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746359
ID:
305746359
16.

MSCs1

Organism:
Mus musculus
Source name:
Sertoli Cells
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746358
ID:
305746358
17.

CiSCs2

Organism:
Mus musculus
Source name:
Embryonic Fibroblasts
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746357
ID:
305746357
18.

CiSCs1

Organism:
Mus musculus
Source name:
Embryonic Fibroblasts
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746356
ID:
305746356
19.

MEFs2

Organism:
Mus musculus
Source name:
Embryonic Fibroblasts
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746355
ID:
305746355
20.

MEFs1

Organism:
Mus musculus
Source name:
Embryonic Fibroblasts
Platform:
GPL23479
Series:
GSE192401
Download data: TXT
Sample
Accession:
GSM5746354
ID:
305746354
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Supplemental Content

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