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Links from GEO DataSets

Items: 5

1.

CRISPR screens are feasible in TP53 wild-type cells

(Submitter supplied) CRISPR-Cas9 genome-wide screens were performed in retinal pigment epithelial cells (RPE1) with either wild-type TP53 gene, or a TP53-null background. Results show wild-type TP53 has minimal impact on the efficiency of CRISPR dropout screens.
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL16791 GPL18573
25 Samples
Download data: TXT
Series
Accession:
GSE128210
ID:
200128210
2.

MDM2 and MDM4 are Therapeutic Vulnerabilities in Malignant Rhabdoid Tumors

(Submitter supplied) Malignant rhabdoid tumors (MRT) are highly aggressive pediatric cancers that respond poorly to current therapies. We screened several MRT cell lines each with large-scale RNAi, CRISPR-Cas9, and small-molecule libraries to identify potential drug targets specific for these cancers. We discovered MDM2 and MDM4, the canonical negative regulators of p53, as significant vulnerabilities. Using two compounds currently in clinical development, idasanutlin and ATSP-7041, we show that MRT cells are more sensitive than other p53 wild-type cancer cell lines to MDM2 and dual MDM2/4 inhibition in vitro. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
3.

Analysis of PDCD4 knockdown effects by high throughput sequencing of a human epithelial cell line

(Submitter supplied) Purpose: examination of gene expression and translation changes in immortalized human epithelial cells (hTERT-RPE-1) induced by PDCD4 siRNA-knockdown.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL15456
12 Samples
Download data: TXT
4.

Dissecting the signalling pathways underlying cellular senescence

(Submitter supplied) Cellular senescence is a program of irreversible cell cycle arrest that normal cells undergo in response to progressive shortening of telomeres, changes in telomeric structure, oncogene activation or oxidative stress. The underlying signalling pathways, potentially of major clinicopathological relevance, are unknown. A major stumbling block to studying senescence has been the absence of suitable model systems because of the asynchrony of this process in heterogeneous cell populations. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
48 Samples
Download data: CEL
Series
Accession:
GSE24810
ID:
200024810
5.

Initial characterization of WDR5B reveals a role in the proliferation of retinal pigment epithelial cells

(Submitter supplied) The chromatin-associated protein WDR5 has been widely studied due to its role in histone modification and its potential as a pharmacological target for the treatment of cancer. In humans, the protein with highest sequence homology to WDR5 is encoded by the retrogene WDR5B, which remains unexplored. Here, we used CRISPR-Cas9 genome editing to generate WDR5B knockout and WDR5B-FLAG knock-in cell lines for further characterization. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL24676
14 Samples
Download data: NARROWPEAK
Series
Accession:
GSE244882
ID:
200244882
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