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Items: 1 to 20 of 369008

1.

Deciphering ESR1-driven transcription in human endometrial stromal cells via transcriptome, cistrome, and integration with chromatin landscape

(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; Other
Platforms:
GPL24676 GPL18573
29 Samples
Download data: BEDPE, BIGINTERACT, BW
Series
Accession:
GSE295512
ID:
200295512
2.

Genome-binding/occupancy profiling of TNKS/PARP-inhibitor Regulated Naïve (TIRN) cells.

(Submitter supplied) Proteogenomic Reprogramming to a Functional Human Blastomere-like Stem Cell State via a PARP-DUX4 Regulatory Axis; Zimmerlin et al, 2024. PARP1 (ARTD1) and Tankyrases (TNKS1/TNKS2; PARP5a/5b) are poly-ADP-ribose polymerases (PARPs) with catalytic and non-catalytic functions that regulate both the genome and proteome during zygotic genome activation (ZGA) and pluripotent embryonic stages. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
35 Samples
Download data: BED, BROADPEAK, BW, NARROWPEAK, TXT
Series
Accession:
GSE291713
ID:
200291713
3.

CXCR4-LASP1-G9a-SNAIL Axis Drives NEPC Transdifferentiation via Induction of EMT and Downregulation of REST

(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 GPL28337
12 Samples
Download data
Series
Accession:
GSE296570
ID:
200296570
4.

CXCR4-LASP1-G9a-SNAIL Axis Drives NEPC Transdifferentiation via Induction of EMT and Downregulation of REST [331R]

(Submitter supplied) Neuroendocrine prostate cancer (NEPC) is a lethal subtype of prostate cancer that can develop from prostate cancer following aggressive hormonal therapy. Unfortunately, there are few treatment options available and new therapeutic targets and more effective treatments are urgently needed to improve management of the disease. There is now little doubt that the majority of NEPC is derived from prostatic adenocarcinoma cells via “NE transdifferentiation” that is driven at least in part by AR-axis interference and lineage plasticity. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: TXT
Series
Accession:
GSE296569
ID:
200296569
5.

Mineralocorticoid Receptor Antagonism by Finerenone Attenuates Established Pulmonary Hypertension in Rats

(Submitter supplied) We studied the ability of the non-steroidal Mineralocorticoid Receptor (MR) antagonist finerenone to attenuate vascular remodeling and pulmonary hypertension (PH) using two complementary preclinical models [the monocrotaline (MCT) and Sugen
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TSV
Series
Accession:
GSE202698
ID:
200202698
6.

m6A is decoded by modified tRNAs to coordinate mRNA decay [Quant-seq]

(Submitter supplied) Chemically modified mRNA nucleotides are emerging as key regulators of gene expression. Their effects are typically thought to be mediated through reader proteins that selectively bind to RNA molecules containing these modifications. Here, we present a new mechanism by which N6 methyladenosine (m6A) couples the translation of messenger RNA (mRNA) to its decay. m6A-modified codons are decoded inefficiently by the ribosome, rendering them “non-optimal”. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
18 Samples
Download data: TXT
Series
Accession:
GSE291842
ID:
200291842
7.

Recording the activity of protein kinases with chemical labeling for post hoc analysis

(Submitter supplied) Protein kinases control most cellular processes and aberrant kinase activity is involved in numerous diseases. To investigate the link between specific kinase activities and cellular phenotypes in heterogenous cell populations and in vivo, we introduce a new class of biosensors that record kinase activities for post hoc analysis . Based on split-HaloTag and a phosphorylation-dependent molecular switch, our recorders become rapidly labeled in the presence of a specific kinase activity and a fluorescent HaloTag substrate. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
32 Samples
Download data: TXT
Series
Accession:
GSE277987
ID:
200277987
8.

m6A is decoded by modified tRNAs to coordinate mRNA decay.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Other; Expression profiling by high throughput sequencing
Platforms:
GPL16791 GPL18573 GPL19057
89 Samples
Download data: BED, TXT
Series
Accession:
GSE248279
ID:
200248279
9.

m6A is decoded by modified tRNAs to coordinate mRNA decay [SLAM-Seq]

(Submitter supplied) Chemically modified mRNA nucleotides are emerging as key regulators of gene expression. Their effects are typically thought to be mediated through reader proteins that selectively bind to RNA molecules containing these modifications. Here, we present a new mechanism by which N6 methyladenosine (m6A) couples the translation of messenger RNA (mRNA) to its decay. m6A-modified codons are decoded inefficiently by the ribosome, rendering them “non-optimal”. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL18573
18 Samples
Download data: TSV
Series
Accession:
GSE247664
ID:
200247664
10.

m6A is decoded by modified tRNAs to coordinate mRNA decay [ribosome profiling]

(Submitter supplied) In eukaryotes, the genetic code is transcribed into messenger RNA (mRNA) in the nucleus and decoded by transfer RNA (tRNA) in the cytosol.  Nuclear mRNA processing events that do not affect the nucleotide sequence of an mRNA are thought to be invisible to tRNAs during protein translation in the cytosol.  Here, we report a mechanism by which the modified mRNA nucleotide N6‑methyladenosine (m6A) connects nuclear mRNA processing to tRNA decoding. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
28 Samples
Download data: TXT
Series
Accession:
GSE173971
ID:
200173971
11.

Differences between human male and female neutrophils with respect to which RNAs are present in polysomes

(Submitter supplied) Human males and females show differences in the incidence of neutrophil-associated diseases such as systemic lupus erythematosus, rheumatoid arthritis, and multiple sclerosis, and differences in neutrophil physiological responses such as responses to infection, tissue damage, and chemotactic factors. However, little is known about the basis of sex-based differences in human neutrophils. Starting with human neutrophils from healthy donors, we used RNA-seq to examine total RNA profiles, RNAs not associated with ribosomes and thus not being translated, RNAs in monosomes, and RNAs in polysomes and thus heavily translated. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
34 Samples
Download data: CSV
Series
Accession:
GSE288976
ID:
200288976
12.

RNA-binding activity plays an important role in MYC function

(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:
GPL18573 GPL24676
50 Samples
Download data
Series
Accession:
GSE252698
ID:
200252698
13.

Enhanced CLIP-Seq (eCLIP-Seq) of endogenous MYC in different cell lines

(Submitter supplied) MYC binds to thousands of gene regulatory elements in the genome such as promoters and enhancers and exerts an amplification effect on the expression of most genes, regardless of the E-box motif existence. In this study, we discovered that MYC is an RNA-binding protein with a high affinity to guanosine-rich RNAs. RNAs binding to MYC enhance its chromatin occupancy. This process helps on MYC-mediated regulation of gene expression. more...
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL18573 GPL24676
18 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE252697
ID:
200252697
14.

RNA-dependent ChIP-Seq (rChIP-Seq) of MYC and TBP in MCF-7 cells

(Submitter supplied) MYC binds to thousands of gene regulatory elements in the genome such as promoters and enhancers and exerts an amplification effect on the expression of most genes, regardless of the E-box motif existence. In this study, we discovered that MYC is an RNA-binding protein with a high affinity to guanosine-rich RNAs. RNAs binding to MYC enhance its chromatin occupancy. This process helps on MYC-mediated regulation of gene expression. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
10 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE252695
ID:
200252695
15.

Impact of temozolomide on gene expression of LN-229 cells

(Submitter supplied) Transcriptomic gene expression analysis of LN-229 cells stimulated for 48 h or 144 h with temozolomide is compared to unexposed cells for the characterisation of the glioblastoma senescence phenotype
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
9 Samples
Download data: BW
Series
Accession:
GSE276693
ID:
200276693
16.

Targeted Degradation of CDK9 Potently Disrupts MYC Network

(Submitter supplied) Cyclin-dependent kinase 9 (CDK9) coordinates signaling events that regulate RNA polymerase II (Pol II) pause-release states. It is an important co-factor for transcription factors, such as MYC, that drive aberrant cell proliferation when their expression is deregulated. CDK9 modulation offers an approach for attenuating dysregulation in such transcriptional programs. As a result, numerous drug development campaigns to inhibit CDK9 kinase activity have been pursued. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
91 Samples
Download data: TXT
Series
Accession:
GSE263153
ID:
200263153
17.

In vivo CRISPR activation screen identifies a lipid metabolism regulator as a driver of bone metastasis

(Submitter supplied) The role of lipid metabolism in bone metastasis has not been documented. Here, by using an in vivo CRISPR activation screening system coupled with positive selection, we identify acyl-CoA binding protein (ACBP) as a previously undescribed bone metastasis driver. In non-metastatic cancer cells, overexpression of wild-type ACBP, but not the acyl-CoA binding deficient mutant, stimulates fatty acid oxidation (FAO) and bone metastasis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: CSV, TXT
Series
Accession:
GSE250240
ID:
200250240
18.

Efficient profiling of total RNA in single cells with STORM-seq

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
4 related Platforms
89 Samples
Download data: TXT
Series
Accession:
GSE296406
ID:
200296406
19.

Efficient profiling of total RNA in single cells with STORM-seq [cell lines]

(Submitter supplied) Despite significant advances, current single-cell RNA sequencing (scRNA-seq) technologies often struggle with accurately detecting non-coding transcripts, achieving full-length RNA coverage, and/or resolving transcript-level complexity. Many are also difficult to implement or inaccessible without specialized liquid handlers, further limiting their utility. We present Single-cell TOtal RNA-seq Miniaturized (STORM-seq), a random-hexamer primed, ribo-reduced single-cell total RNA sequencing (sc-total-RNA-seq) protocol using standard laboratory equipment. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL24676 GPL30173
7 Samples
Download data: TSV, TXT
Series
Accession:
GSE296405
ID:
200296405
20.

Glycosaminoglycan-driven lipoprotein uptake protects tumours from ferroptosis

(Submitter supplied) Lipids are essential components of cancer cells due to their structural and signaling roles. To meet metabolic demands, many cancers take up extracellular lipids; however, how these lipids contribute to cancer growth and progression remains poorly understood. Here, using functional genetic screens, we identify lipoprotein uptake—the primary mechanism for lipid transport in circulation—as a key determinant of ferroptosis sensitivity in cancer. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
36 Samples
Download data: TXT
Series
Accession:
GSE296260
ID:
200296260
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