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Links from GEO DataSets

Items: 20

1.

Comparison between cell lines from 9 different cancer tissue (NCI-60) (Affymetrix HuEx 1.0)

(Submitter supplied) Comparison between cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, Renal) from NCI-60 panel
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5188
178 Samples
Download data: CEL
Series
Accession:
GSE29682
ID:
200029682
2.

Comparison between cell lines from 9 different cancer tissue (NCI-60) (Affymetrix U133 Plus 2.0)

(Submitter supplied) Comparison between cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, Renal) from NCI-60 panel.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4296
Platform:
GPL570
174 Samples
Download data: CEL
Series
Accession:
GSE32474
ID:
200032474
3.

Comparison between cell lines from 9 different cancer tissue (NCI-60) (Agilent WG platform)

(Submitter supplied) Comparison between cell lines from 9 different cancer tissue of origin types
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
132 Samples
Download data: TXT
Series
Accession:
GSE29288
ID:
200029288
4.

NCI60 Expression Profiling using the Agilent Whole Human Genome Oligo Microarray

(Submitter supplied) We present here a new expression profiling study of the 60 cell lines of the National Cancer Institute (NCI) Developmental Therapeutics program (DTP) drug screen (NCI-60) using the 41,000-probe Agilent Whole Human Genome Oligo Microarray. The expression levels of ∼21,000 genes were measured.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6848
132 Samples
Download data: TXT
Series
Accession:
GSE22821
ID:
200022821
5.

Comparison between cell lines from 9 different cancer tissue (NCI-60) (U95 platform)

(Submitter supplied) Comparison between cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, Renal) from NCI-60 panel Keywords: cell_type_comparison_design; disease state; cell line; tissue type
Organism:
Homo sapiens
Type:
Expression profiling by array
5 related Platforms
300 Samples
Download data: CEL, EXP
Series
Accession:
GSE5949
ID:
200005949
6.

Comparison between cell lines from 9 different cancer tissue (NCI-60) (U133 platform)

(Submitter supplied) Comparison between cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, Renal) from NCI-60 panel Keywords: cell_type_comparison_design; disease state; cell line; tissue type
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL97 GPL96
120 Samples
Download data: CEL
Series
Accession:
GSE5720
ID:
200005720
7.

Comparison of protein expression profiles in NCI-60 cell panel containing nine difererent cancer tissue types.

(Submitter supplied) Because most potential molecular markers and targets are proteins, proteomic profiling is expected to yield more direct answers to functional and pharmacological questions than does transcriptional profiling. To aid in such studies, we have developed a protocol for making reverse-phase protein lysate microarrays with larger numbers of spots than previously feasible. Our first application of these arrays was to profiling of the 60 human cancer cell lines (NCI-60) used by the National Cancer Institute to screen compounds for anticancer activity. more...
Organism:
Homo sapiens
Type:
Protein profiling by protein array
Platform:
GPL4081
176 Samples
Download data
Series
Accession:
GSE5501
ID:
200005501
8.
Full record GDS4296

NCI-60 cancer cell line panel

Analysis of cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, and Renal) from the NCI-60 panel. Results provide insight into molecular mechanisms underlying the various cancer types.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 59 cell line, 27 disease state, 9 tissue sets
Platform:
GPL570
Series:
GSE32474
174 Samples
Download data: CEL
9.

The NCI-60 Methylome and Its Integration into CellMiner

(Submitter supplied) Methylation assay of cell lines from 9 different cancer tissue of origin types (Breast, Central Nervous System, Colon, Leukemia, Melanoma, Non-Small Cell Lung, Ovarian, Prostate, Renal) from NCI-60 panel
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
61 Samples
Download data: IDAT, TXT
Series
Accession:
GSE79185
ID:
200079185
10.

Non-Classical Functions of Human Topoisomerase I: Genome-wide and Pharmacological Analyses

(Submitter supplied) The biological functions of nuclear topoisomerase I (Top1) have been difficult to study because knocking out TOP1 is lethal in metazoans. To reveal the functions of human Top1, we have generated stable Top1siRNA cell lines from colon and breast carcinomas (HCT116-siTop1 and MCF-7-siTop1, respectively). In those cells, Top2 compensates for Top1 deficiency. A prominent feature of the siTop1 cells is genomic instability, with chromosomal aberrations and histone gamma-H2AX foci associated with replication. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE7161
ID:
200007161
11.

USP7 substrates identified by proteomics analysis reveal the specificity of USP7

(Submitter supplied) To check whether mRNA level change for the changed proteins in protein level.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
18 Samples
Download data: SF
12.

G-quadruplex on Chromosomal DNA Negatively Regulates Topoisomerase 1 Activity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL20795
13 Samples
Download data: BIGWIG
Series
Accession:
GSE239694
ID:
200239694
13.

G-quadruplex on Chromosomal DNA Negatively Regulates Topoisomerase 1 Activity [ChIP-seq]

(Submitter supplied) Human DNA topoisomerase 1 (Top1) is a crucial enzyme responsible for alleviating torsional stress on DNA during transcription and replication, thereby maintaining genome stability. Previous researches had found that non-working Top1 interacted extensively with chromosomal DNA in human cells. However, the reason for its retention on chromosomal DNA remained unclear. In this study, we discovered a close association between Top1 and chromosomal DNA, specifically linked to the presence of G-quadruplex (G4) structures. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
4 Samples
Download data: BIGWIG
Series
Accession:
GSE239692
ID:
200239692
14.

G-quadruplex on Chromosomal DNA Negatively Regulates Topoisomerase 1 Activity [CUT&Tag]

(Submitter supplied) Human DNA topoisomerase 1 (Top1) is a crucial enzyme responsible for alleviating torsional stress on DNA during transcription and replication, thereby maintaining genome stability. Previous researches had found that non-working Top1 interacted extensively with chromosomal DNA in human cells. However, the reason for its retention on chromosomal DNA remained unclear. In this study, we discovered a close association between Top1 and chromosomal DNA, specifically linked to the presence of G-quadruplex (G4) structures. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
9 Samples
Download data: BIGWIG
Series
Accession:
GSE239690
ID:
200239690
15.

Effect of the USP7 inhibitor HBX41,108 on lipopolysaccharide induced gene expression in mouse bone marrow derived macrophages.

(Submitter supplied) USP7 is a deubiquitinase enzyme that removes polyubiquitin chains form a number of substrates including MDM2, p53 and NF-κB. In this study we assessed the impact of the USP7 inhibitor HBX41,108 on lipopolysaccharide (LPS) induded transcriptional responses in murine bone marrow derived macrophages.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE149478
ID:
200149478
16.

Gene expression in epithelial and non-epithelial cells of renal origin

(Submitter supplied) We aimed to define epithelial-specific genes in the kidney. In the developing mouse kidney at E12.5 epithelial cells are restricted to the ureteric bud, while mesenchymal cells surrounding the ureteric bud are non-epithelial. The mouse renal epithelial cell line mIMCD-3 was used to represent kidney epithelia in vitro. Gene expression was analyzed using Affymetrix microarrays in ureteric bud stalks, ureteric bud tips, and mIMCD-3 cells and compared to metanephric mesenchyme.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
7 Samples
Download data: CEL
Series
Accession:
GSE24295
ID:
200024295
17.

RNAseq analysis of impact of PNN on gene expression and alternative splicing in corneal epithelial cells

(Submitter supplied) The specialized corneal epithelium requires differentiated properties, specific for its role at the anterior surface of the eye, thus tight maintenance of the differentiated qualities of the corneal epithelial is essential. Our studies have focused on pinin (PNN), an exon junction component (EJC) that has dramatic implications on corneal epithelial cell differentiation and may act as a stabilizer of the corneal epithelial cell phenotype. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
32 Samples
Download data: XLSX
18.

USP7 cooperates with SCML2 to regulate the activity of PRC1

(Submitter supplied) In this experiment, we sought to identify the distribution of USP7 on chromatin relative to other PRC1 components
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
1 Sample
Download data: BW
Series
Accession:
GSE61048
ID:
200061048
19.

Topoisomerase I cleavage complexes preferentially down-regulate ubiquitin- and RNA degradation-related transcripts in relationship to gene length, exon-intron junctions and p53-dependent up-regulation of miR-142-3p

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL15454 GPL10850
18 Samples
Download data: CEL, TXT
Series
Accession:
GSE37358
ID:
200037358
20.

Transcription poisoning by topoisomerase I is controlled by gene length, splice sites and miR-142-3p

(Submitter supplied) DNA topoisomerase I (Top1) is required for transcription as it relaxes positive and negative supercoils by forming transient Top1 cleavage complexes (Top1cc) up- and down-stream of transcription complexes. However, Top1cc can also be trapped by endogenous DNA lesions and by camptothecin (CPT) and its anticancer derivatives, which results in transcription blocks. Here, we undertook a genome-wide analysis of the effects of CPT on gene expression at exon resolution.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15454
15 Samples
Download data: CEL, TXT
Series
Accession:
GSE37352
ID:
200037352
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