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Items: 1 to 20 of 5807891

1.

Spatial transcriptomics reveal topological immune landscapes of Asian head and neck angiosarcoma

(Submitter supplied) Angiosarcomas are rare malignant tumors of the endothelium, arising commonly from the head and neck region (AS-HN) and recently associated with ultraviolet (UV) exposure and human herpesvirus-7 (HHV-7) infection. We examined 81 cases of angiosarcomas, including 47 cases of AS-HN, integrating information from whole genome sequencing, gene expression profiling and spatial transcriptomics (10X Visium). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24676
4 Samples
Download data
Series
Accession:
GSE227469
ID:
200227469
2.

Effect of the lysphosphatidylcholine analogue edelfosine on gene expression in Saccharomyces cerevisiae

(Submitter supplied) To investigate the impact of a lysolipid burden in the nuclear envelope on the regulation of gene expression, particularly in tethered nuclear domains, we treated cells with edelfosine.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19756
6 Samples
Download data: TXT
Series
Accession:
GSE227381
ID:
200227381
3.

Genome-wide mapping of NRF1 (NFE2L1) binding in HCT116 cells upon proteasome inhibition.

(Submitter supplied) The maintenance of protein homeostasis is an essential characteristic of life. Transcription factor NRF1 (NFE2L1) has been reported to be activated by proteasome dysfunction, although the genome-wide target genes are poorly understood. Using ChIP-seq analysis, we found a potential association between NRF1 and autophagy. Our findings highlight the new activation mechanism of autophagy through gene regulation under proteasome dysfunction.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data
Series
Accession:
GSE227357
ID:
200227357
4.

Pre-weaning heat stress alters liver DNA methylation in dairy calves

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL23295 GPL26012
23 Samples
Download data
Series
Accession:
GSE227325
ID:
200227325
5.

Pre-weaning heat stress alters liver transcriptome in dairy calves [RNA-Seq]

(Submitter supplied) The impact of postnatal heat stress exposure in neonatal calves is not well-understood, and adequate heat abatement methods during the pre-weaning phase are lacking. This study aimed to investigate the impact of pre-weaning heat stress on liver gene expression profiles.
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26012
12 Samples
Download data
Series
Accession:
GSE227323
ID:
200227323
6.

Pre-weaning heat stress alters liver DNA methylation in dairy calves [Bisulfite-Seq]

(Submitter supplied) The impact of postnatal heat stress exposure in neonatal calves is not well-understood, and adequate heat abatement methods during the pre-weaning phase are lacking. This study aimed to investigate the impact of pre-weaning heat stress on liver DNA methylation profiles.
Organism:
Bos taurus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL23295
11 Samples
Download data
Series
Accession:
GSE227249
ID:
200227249
7.

Lipid engulfed macrophages interfere with protective T cell immunity and favor tumor progression in human colon carcinogenesis

(Submitter supplied) Obesity and altered lipid metabolism is associated with colorectal cancer (CRC). In this context, the presence of colonic lipid-engulfed macrophages (foam cells, FC) may be involved in hindering protective T cell immunity, thus favoring gut carcinogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
14 Samples
Download data
Series
Accession:
GSE227206
ID:
200227206
8.

The study of SOX2 deposition in asynchronous and mitotic E14TG2a cells

(Submitter supplied) We executed ChIPseq for SOX2 a different mouse strain E14TG2a.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data
Series
Accession:
GSE216663
ID:
200216663
9.

Transcription profiling of Smarce1- MD (R42A) and Smarce1- MD mouse embryonic body

(Submitter supplied) To evaluate the differential potential affected by SMARCE1 -MD/MD(R42A) , we performed RNA-sequencing (RNA-seq) of Smarce1-MD and control Smarce1-MD (R42A) embrynoic body.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data
Series
Accession:
GSE216662
ID:
200216662
10.

The study of chromatin occupancy other mitotically bound factors upon the mitotic depletion of SMARCE1 in mouse ES cells.

(Submitter supplied) We executed CUT&RUN-seq for SOX2, ESRRB, and EZH2 upon the mitotic depletion of SMARCE1 in mouse ES cells.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
20 Samples
Download data
Series
Accession:
GSE216661
ID:
200216661
11.

The study of SOX2 deposition in asynchronous and mitotic E14TG2a mouse ES cells.

(Submitter supplied) We executed CUT&RUN-seq for SOX2 a different mouse strain E14TG2a
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data
Series
Accession:
GSE216659
ID:
200216659
12.

The study of SMARCE1 and SOX2 deposition in DMSO or BRM014 treated Smarce1-MD(R42A) and Smarce1-MD cells at 90 min after releasing from mitosis.

(Submitter supplied) We executed CUT&RUN-seq for SMARCE1 and SOX2 in BRG1 inhibitor BRM014 treated ,in MD or MD mutatnt mouse embryonic stem cells at 90 min from mitotic release.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
24 Samples
Download data
Series
Accession:
GSE216657
ID:
200216657
13.

Transcription profiling of Smarce1- MD (R42A) and Smarce1- MD mESCs with BMP4 rescue.

(Submitter supplied) To evaluate the effects of mitotic degradation of SMARCE1 upon gene expression, we performed RNA-sequencing (RNA-seq) of cultures of four independent subclones each of Smarce1-MD and control Smarce1-MD (R42A) mESCs. We found that transcription of the core pluripotency regulatory network was not disrupted. In contrast, GO analysis showed that neural differentiation-associated terms were enriched among genes upregulated in Smarce1-MD mESCs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
24 Samples
Download data
Series
Accession:
GSE216656
ID:
200216656
14.

The study of SWI/SNF subunits and other transcription factors deposition in asynchronous and mitotic mESCs and cells released from mitosis II

(Submitter supplied) We conduct ATAC-seq in SMARCE1 MD/MD(R42A) after mitotic release 90 min in either DMSO treated or BRG1 inhibitor BRM014 treated conditions
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data
Series
Accession:
GSE216655
ID:
200216655
15.

Transcription profiling of Smarce1- AID mESCs , cultured the cells with IAA treatment from 0min to 7 days.

(Submitter supplied) To evaluate the effects of degradation of SMARCE1 upon gene expression, we performed RNA-sequencing (RNA-seq) of cultures of two Smarce1-AID mESCs. We found that transcription of the core pluripotency regulatory network was disrupted starting from 240min and there is an accumulation till day 7 .
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
16 Samples
Download data
Series
Accession:
GSE216653
ID:
200216653
16.

RNA-seq from mice CD4+CD25+ splenocytes

(Submitter supplied) To better understand the function of CD4+CD25+ splenocytes from different ages, target cells from young(8-week old) aged(18-month old) were sorted with magnetic beads. We then performed gene expression profiling analysis using data obtained from RNA-seq of different cells from different age.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
7 Samples
Download data: TXT
Series
Accession:
GSE208231
ID:
200208231
17.

Comprehensive characterization of hepatic inflammatory changes in a mouse model of alpha-1 antitrypsin deficiency

(Submitter supplied) In this study, we sought to thoroughly characterize the liver pathophysiology of a human transgenic mouse model for alpha-1 antitrypsin deficiency (AATD) with a strong manifestation of AATD-mediated liver disease. Male and female transgenic mice for normal variant human alpha-1 antitrypsin (Pi*M) and mutant human alpha-1 antitrypsin (Pi*Z) at 3 and 6 months of age with a C57BL/6J background were subjected to study. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: TXT
Series
Accession:
GSE206619
ID:
200206619
18.

The study of histone modifications and SOX2 occupancy in asynchronous and mitotic mESCs.

(Submitter supplied) We performed ChIP-seq for H3K4me3, H3K27ac, H3K4me1, H3K27me3, H3K36me3, H3K9me3, and H4K20me3 to characterize chromatin states and investigated SOX2 deposition in asynchronous and mitotic cells.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
86 Samples
Download data
Series
Accession:
GSE189561
ID:
200189561
19.

The study of SWI/SNF subunits and other transcription factors deposition in asynchronous and mitotic mESCs and cells released from mitosis

(Submitter supplied) We executed CUT&RUN-seq for SWI/SNF components ARID1A, BRD9, SMARCA4, SMARCB1, SMARCE1, as well as ESRRB, SOX2, and EZH2 in asynchronous and mitotic cells and reported that, in asynchronous cells, ARID1A localized primarily at enhancer regions and EZH2 preferentially deposited at bivalent promoters and silent enhancer domains. The remaining factors were enriched at both TSS/promoters and to varying degrees at active enhancers. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
104 Samples
Download data
Series
Accession:
GSE189560
ID:
200189560
20.

The study of nascent RNA transcripts in asynchronous cells and cells released from mitosis at the indicated timepoints between Smarce1- MD (R42A) and Smarce1- MD mESCs.

(Submitter supplied) SMARCE1 binding on mitotic chromatin is required for the timely reinitiation of expression of SMARCE1-bookmarked genes and maintaining identity memory in cell division.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
48 Samples
Download data
Series
Accession:
GSE189559
ID:
200189559
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