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Items: 1 to 20 of 36152

1.

A DGCR8/FLII-dominated on-off switch for immediate-early genes governs embryo implantation in mouse and human

(Submitter supplied) As an essential checkpoint for successful pregnancy, mammalian embryo implantation initiates fetal-maternal communication. However, the underlying transcriptional regulation governing such a fast transition is still unknown. Here, we identify a DGCR8/FLII-dominated on-off switch for immediate-early genes (IEGs) governing pluripotency transition and morphogenesis of epiblasts upon embryo implantation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
5 Samples
Download data
Series
Accession:
GSE264445
ID:
200264445
2.

Investigating the cross-talk between circRNAs and PKR and its implication in the immune response in MS

(Submitter supplied) Circular RNAs (circRNAs) have emerged as a new type of endogenous non-coding RNA characterized by their covalently closed circular structure and a backspliced junction (BSJ) resulting from a back-splicing process. In the last years, several studies have shown that circRNAs are important modulators in the immune system, activation of inflammation, antibacterial and antiviral responses as well as autoimmune diseases, such as multiple sclerosis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
16 Samples
Download data: CSV
Series
Accession:
GSE253443
ID:
200253443
3.

CD161 expression of TRM cells counteracts the HPV-associated clinical benefit in oropharyngeal cancer immunotherapy

(Submitter supplied) Oropharyngeal squamous cell carcinoma (OPSCC), a distinct head and neck cancer subtype that develops in the oropharynx, is well known to be categorized into human papillomavirus induced (HPV+) and non-HPV induced (HPV-). While HPV+ OPSCC is reported to be clinically advantageous compared to HPV- OPSCC, the heterogeneous responses in HPV+ OPSCC during immunotherapy treatment have not been well characterized at the molecular level. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL20795
30 Samples
Download data: MTX, RDS, TSV
Series
Accession:
GSE226620
ID:
200226620
4.

Capturing totipotency in human cells through spliceosomal repression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
112 Samples
Download data: BW, NARROWPEAK, TXT
Series
Accession:
GSE226231
ID:
200226231
5.

Capturing totipotency in human cells through spliceosomal repression [ATAC-seq]

(Submitter supplied) Supplemented with splicing inhibitor PlaB, we realize in vitro culturing of human totipotent stem cells comparable to 2-4-cell blastomeres Assay for transposase accessible chromatin with high-throughput sequencing in hESC sand hTBLCs
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
2 Samples
Download data: NARROWPEAK
Series
Accession:
GSE226229
ID:
200226229
6.

Capturing totipotency in human cells through spliceosomal repression [scRNA-seq]

(Submitter supplied) Supplemented with splicing inhibitor PlaB, we realize in vitro culturing of human totipotent stem cells comparable to 2-4-cell blastomeres
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
14 Samples
Download data: TXT
Series
Accession:
GSE226228
ID:
200226228
7.

Capturing totipotency in human cells through spliceosomal repression [ChIP-seq]

(Submitter supplied) Supplemented with splicing inhibitor PlaB, we realize in vitro culturing of human totipotent stem cells comparable to 2-4-cell blastomeres Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for h3k4me3 and h3k27me3 in hESC sand hTBLCs
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
4 Samples
Download data: BW
Series
Accession:
GSE226227
ID:
200226227
8.

Capturing totipotency in human cells through spliceosomal repression [RNA-Seq]

(Submitter supplied) Supplemented with splicing inhibitor PlaB, we realize in vitro culturing of human totipotent stem cells comparable to 2-4-cellb blastomeres Poly(A) RNA-seq is performed on hESCs cultured in MYCP medium
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
92 Samples
Download data: CSV
Series
Accession:
GSE224794
ID:
200224794
9.

Mis-splicing of mitotic regulators sensitizes SF3B1-mutated human HSCs to CHK1 inhibition [RNA-seq]

(Submitter supplied) Splicing factor SF3B1 mutations are frequent somatic lesions in myeloid neoplasms that transform hematopoietic stem cells (HSCs) by inducing mis-splicing of target genes. However, the molecular and functional consequences of SF3B1 mutations in human HSCs remain unclear. Here, we identify the mis-splicing program in human HSCs as a targetable vulnerability by precise gene editing of SF3B1 K700E mutations in primary CD34+ cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
10 Samples
Download data: CSV
Series
Accession:
GSE263299
ID:
200263299
10.

Differential gene expression analysis of wild type and heterozygous RB1 mutant human iPSC derived retinal organoids.

(Submitter supplied) Recent in vitro studies using RB1+/- fibroblasts and MSCs have shown molecular and functional disruptions without the need for biallelic loss of RB1. However, this was not reflected in the recent in vitro studies employing RB1+/- retinal organoids. To gain further insights into the molecular disruptions in the RB1+/- retinal organoids we performed a high throughput RNA-sequencing analysis.iPSCs were generated from RB1+/+ and RB1+/- Orbital adipose mesenchymal stem cells (OAMSCs) derived from retinoblastoma patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
8 Samples
Download data: TXT
Series
Accession:
GSE255268
ID:
200255268
11.

TWEAK/Fn14 signalling in Breast Cancer [p52_ChIP]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
2 Samples
Download data: BED, BW
Series
Accession:
GSE252381
ID:
200252381
12.

TWEAK/Fn14 signalling in Breast Cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL20795 GPL24676
64 Samples
Download data: BED, BW
Series
Accession:
GSE231483
ID:
200231483
13.

TWEAK/Fn14 signalling in Breast Cancer [patient K27 ChIP]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
24 Samples
Download data: BED, BW
Series
Accession:
GSE231482
ID:
200231482
14.

TWEAK/Fn14 signalling in Breast Cancer [patient ATAC-seq]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
12 Samples
Download data: BED, BW
Series
Accession:
GSE231481
ID:
200231481
15.

TWEAK/Fn14 signalling in Breast Cancer [cell line RNA-seq]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
24 Samples
Download data: TXT
Series
Accession:
GSE231480
ID:
200231480
16.

TWEAK/Fn14 signalling in Breast Cancer [cell line K27 ChIP]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
24 Samples
Download data: BED, BW
Series
Accession:
GSE231479
ID:
200231479
17.

TWEAK/Fn14 signalling in Breast Cancer [cell line hiChIP]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
4 Samples
Download data: COOL
Series
Accession:
GSE231478
ID:
200231478
18.

TWEAK/Fn14 signalling in Breast Cancer [cell line ATAC-seq]

(Submitter supplied) This study explores the transcriptiomic and epigenetic roles of TWEAK/Fn14 signalling in Breast Cancer
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
14 Samples
Download data: BED, BW
Series
Accession:
GSE231477
ID:
200231477
19.

Single-cell multi-omics analysis revealing immune features of inactivated SARS-CoV-2 vaccination in systemic lupus erythematosus patients

(Submitter supplied) The COVID-19 vaccine-induced immunity has been widely reported in the general population, but the protective immune response of COVID-19 vaccines in SLE patients (SLEs) remains largely unknown. Here, we performed a comprehensive and time-series investigation of immunological alterations induced by inactivated COVID-19 vaccines in SLEs and healthy controls using single-cell multi-omics methods. Compared with healthy controls (HCs), the lower titres of neutralizing antibodies and global transcriptomic and epigenomic changes in peripheral immune cells were detected in SLEs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
26 Samples
Download data: CSV, MTX, TSV
Series
Accession:
GSE224198
ID:
200224198
20.

Hepatocyte-macrophage crosstalk via the PGRN-EGFR axis modulates ADAR1-mediated immunity in the liver -HCC scRNAseq

(Submitter supplied) ADAR1 is thought to be an immune suppressor maintaining self-tolerance to endogenous nucleic acids. ADAR1 is often overexpressed in hepatocellular carcinoma tumors, and might contribute to immunosuppression and immune evasion of cancer cells. We performed single cell RNA sequencing on non-tumor and tumor HCC samples. Constructed libraries were sequenced on the HiSeq X platform. Over 150 million pairs of mappable reads for each sample were obtained.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
2 Samples
Download data: MTX, TSV
Series
Accession:
GSE223204
ID:
200223204
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