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Items: 1 to 20 of 1131

1.

LncRNA adapters determine SWI/SNF complex occupancy at gene regulatory elements

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL30173 GPL18573
79 Samples
Download data: BW
Series
Accession:
GSE262070
ID:
200262070
2.

LncRNA adapters determine SWI/SNF complex occupancy at gene regulatory elements [CutAndRun_siRNA]

(Submitter supplied) The coordination of chromatin remodeling is essential for DNA accessibility and gene expression control. The highly conserved and ubiquitously expressed SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin remodeling complex plays a key role in regulating gene expression in a context-dependent manner. SWI/SNF actively maintains open chromatin states across the genome and responds dynamically to cellular signals. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30173
26 Samples
Download data: BW
Series
Accession:
GSE262061
ID:
200262061
3.

Remodeling of the chromatin landscape in peripheral blood cells in patients with severe Delta COVID-19

(Submitter supplied) COVID-19 is characterized by systemic proinflammatory shifts with development of serious alterations in the functioning of the immune system. Investigations of the gene expression changes accompanying infection state provide insight towards understanding of the molecular and cellular processes depending on the sickness severity and virus variant. Severe Delta COVID-19 have been characterized by the appearance of the monocyte subset enriched for the proinflammatory gene expression signatures and shift of the ligand-receptor interactions. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL30173
39 Samples
Download data: BED, MTX, TSV
Series
Accession:
GSE282769
ID:
200282769
4.

Protein kinase N1 mediates phosphorylation of H3.3 serine 31 for rapid gene activation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL30173
21 Samples
Download data
Series
Accession:
GSE261756
ID:
200261756
5.

Protein kinase N1 mediates phosphorylation of H3.3 serine 31 for rapid gene activation (ATAC-Seq II)

(Submitter supplied) Atherosclerosis, which develops in the inner layer of arteries, is the major cause of myocardial infarction and stroke. Atherosclerotic plaques develop preferentially in arterial regions exposed to disturbed blood flow, such as vessel curvatures, bifurcations and branching points, where endothelial cells develop an inflammatory phenotype. How disturbed flow induces endothelial cell inflammation is incompletely understood. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30173
6 Samples
Download data: TXT
Series
Accession:
GSE261755
ID:
200261755
6.

The translational landscape of HIV-1 1 infected cells reveals novel gene regulatory principles

(Submitter supplied) Human Immunodeficiency Virus-1 (HIV-1) uses a number of strategies to modulate viral and host gene expression during its lifecycle. To characterize the transcriptional and translational landscape of HIV-1 infected cells, we used a combination of ribosome profiling, disome sequencing and RNA sequencing. We show that HIV-1 mRNAs are efficiently translated at all stages of infection, despite evidence for a substantial decrease in translational efficiency of host genes that are implicated in host cell translation. more...
Organism:
Human immunodeficiency virus 1; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
4 related Platforms
32 Samples
Download data: BED, CSV, TXT
Series
Accession:
GSE244468
ID:
200244468
7.

ChIP-DIP maps binding of hundreds of proteins to DNA simultaneously and identifies diverse gene regulatory elements

(Submitter supplied) Gene expression is controlled by dynamic localization of thousands of regulatory proteins to precise genomic regions. Understanding this cell-type specific process has been a longstanding goal yet remains challenging because DNA-protein mapping methods generally study one protein at a time. To address this, we developed ChIP-DIP (ChIP Done In Parallel) to generate genome-wide maps of hundreds of diverse regulatory proteins in a single experiment. more...
Organism:
Homo sapiens; Mus musculus
Type:
Other
4 related Platforms
10 Samples
Download data: BIGWIG, XLSX
Series
Accession:
GSE227773
ID:
200227773
8.

Single-cell transcriptomic analysis of immune responses within a microfluidic skin equivalent

(Submitter supplied) Microfluidic human skin equivalents (HSEs) were constructed by 3D printing and consisted of an endothelial lined vascular microchannel within a 3D dermal matrix embedded with fibroblasts. Keratinocytes were cultured on the surface to mimic the epidermis. Following exposure of the epidermis to lipopolysaccharide (LPS) and nigericin, human monocytes were injected into the vascular channel and migrated into the HSE. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE282014
ID:
200282014
9.

Single-cell analysis of L-MYC expressing neural stem cells and their extracellular vesicles revealed distinct progenitor populations with neurogenic potential [bulk RNA-seq]

(Submitter supplied) Neural stem cell (NSC)-based therapies can exploit the inherent pathotropism of NSCs to deliver neurotrophic factors for cell replacement therapies and to stimulate endogenous neurogenesis to permanently repair damaged brain tissue after brain injury. Despite studies on the protective/restorative functions of NSCs and their extracellular vesicles (EVs), a major impediment to advancing this approach to late-stage preclinical studies and clinical practice has been the lack of molecular characterization of NSCs and NSC-EV cargo composition. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
4 Samples
Download data: CSV
Series
Accession:
GSE281915
ID:
200281915
10.

spatialGE is a User-Friendly Web Application that Facilitates Spatial Transcriptomics Data Analysis

(Submitter supplied) Spatial transcriptomics (ST) is a powerful tool for understanding tissue biology and disease mechanisms. However, the advanced data analysis and programming skills required can hinder researchers from realizing of the full potential of ST. To address this, we developed spatialGE, a web application that simplifies the analysis of ST data. The application spatialGE provided a user-friendly interface that guides users without programming expertise through various analysis pipelines, including quality control, normalization, domain detection, phenotyping, and multiple spatial analyses. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL30173
3 Samples
Download data: CSV, H5, JSON, MTX, PNG, TSV
Series
Accession:
GSE271422
ID:
200271422
11.

Specific tRNAs promote mRNA decay by recruiting the CCR4-NOT complex to translating ribosomes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL30173 GPL18573
28 Samples
Download data
Series
Accession:
GSE268325
ID:
200268325
12.

Specific tRNAs promote mRNA decay by recruiting the CCR4-NOT complex to translating ribosomes (SLAM-Seq)

(Submitter supplied) The CCR4-NOT complex is a major regulator of eukaryotic messenger RNA (mRNA) stability. Slow decoding during translation promotes association of CCR4-NOT with ribosomes, accelerating mRNA degradation. We applied selective ribosome profiling to further investigate the determinants of CCR4-NOT recruitment to ribosomes in mammalian cells. This revealed that specific arginine codons in the P-site are strong signals for ribosomal recruitment of human CNOT3, a CCR4-NOT subunit. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
24 Samples
Download data: XLSX
Series
Accession:
GSE268322
ID:
200268322
13.

Decoding RNA metabolism by RNA-linked CRISPR screening in human cells

(Submitter supplied) RNAs undergo a complex choreography of metabolic processes that are regulated by thousands of RNA-associated proteins. Here we present a massively parallel RNA-linked CRISPR (ReLiC) platform to measure the responses of diverse RNA metabolic events to knockout of 2,092 human genes encoding all known RNA-associated proteins. ReLiC relies on a pooled, virus-free, serine recombinase-based strategy to integrate DNA libraries encoding Cas9, multiple sgRNAs, and barcoded reporters into a defined genomic locus. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
16 Samples
Download data: TAB
Series
Accession:
GSE282328
ID:
200282328
14.

The respective roles of TMPRSS2 and cathepsins for SARS-CoV-2 infection in human respiratory organoids

(Submitter supplied) A critical aspect of the mechanism of SARS-CoV-2 infection is the protease-mediated activation of the viral spike (S) protein. The type II transmembrane serine protease TMPRSS2 is crucial for SARS-CoV-2 infection in lung epithelial Calu-3 cells and murine airways. However, the importance of TMPRSS2 needs to be re-examined because the ability to utilize TMPRSS2 is significantly reduced in the Omicron variants that spread globally. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
6 Samples
Download data: TXT
Series
Accession:
GSE279753
ID:
200279753
15.

m6A sites in the coding region trigger translation-dependent mRNA decay (SLAM-seq)

(Submitter supplied) N6-Methyladenosine (m6A) is the predominant internal RNA modification in eukaryotic messenger RNAs (mRNAs) and plays a crucial role in mRNA stability. In this study, we reveal that m6A sites in the coding sequence (CDS) trigger CDS–m6A decay (CMD), a novel mRNA decay pathway that is distinct from previously reported m6A-dependent degradation mechanisms. Importantly, CDS m6A sites act considerably faster and more efficiently than those in the 3' untranslated region, which to date have been considered the main effectors of m6A-mediated RNA decay. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
18 Samples
Download data: TXT
Series
Accession:
GSE273217
ID:
200273217
16.

Transcriptome profiles characteristics of peripheral immune in Severe Fever with Thrombocytopenia Syndrome patients

(Submitter supplied) To investigate the response mechanisms of Severe fever with thrombocytopenia syndrome (SFTS) patients, we conducted transcriptomic analysis of peripheral immunity in 14 SFTS patients, ranging from modal infection to severe and fatal disease. Our results observed the potential mechanism for the heterogeneity of clinical symptoms, which can further elucidate the interaction between viruses and hosts and contribute to clinical treatment.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
20 Samples
Download data: TXT
Series
Accession:
GSE264635
ID:
200264635
17.

m6A sites in the coding region trigger translation-dependent mRNA decay.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL30173 GPL18573
74 Samples
Download data: BW, TSV
Series
Accession:
GSE248575
ID:
200248575
18.

m6A sites in the coding region trigger translation-dependent mRNA decay (RNA-seq)

(Submitter supplied) N6-Methyladenosine (m6A) is the predominant internal RNA modification in eukaryotic messenger RNAs (mRNAs) and plays a crucial role in mRNA stability. In this study, we reveal that m6A sites in the coding sequence (CDS) trigger CDS–m6A decay (CMD), a novel mRNA decay pathway that is distinct from previously reported m6A-dependent degradation mechanisms. Importantly, CDS m6A sites act considerably faster and more efficiently than those in the 3' untranslated region, which to date have been considered the main effectors of m6A-mediated RNA decay. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL30173 GPL18573
32 Samples
Download data: TSV
Series
Accession:
GSE248571
ID:
200248571
19.

Single-cell transcriptomics of non-functioning and functioning PitNET subtypes reveals differences in the tumor microenvironment and tumor-specific gene expression signatures that correlate with aggressive tumor growth

(Submitter supplied) Pituitary neuroendocrine tumors (PitNET) are among the most common intracranial tumors. Despite a frequently benign course, aggressive behavior occurs for unexplained reasons, especially in functional PitNET. Tumor behavior is known to be under the influence of the tumor microenvironment (TME). However, the relationship between TME cells and aggressive tumor behavior has not been adequately explored in PitNET. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
10 Samples
Download data: MTX, TSV
Series
Accession:
GSE244101
ID:
200244101
20.

Next Generation Thiazolyl Ketone Inhibitors of Cytosolic Phospholipase A2 α: from Synthesis to Chemotherapeutic Mechanism of Action

(Submitter supplied) Eicosanoids participate in the pathologies of inflammation and carcinogenesis and limiting their production by inhibiting group IVA cytosolic phospholipase A2 (cPLA2α) is a potential approach to cancer treatment. Here we report the synthesis of a new generation of thiazolyl ketone inhibitors of cPLA2α starting from compound GK470 (AVX235), and the discovery of a more potent and selective lead, GK420 (AVX420), with significant chemotherapeutic properties. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL30173
24 Samples
Download data: TSV
Series
Accession:
GSE251999
ID:
200251999
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