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Links from GEO DataSets

Items: 20

1.

Mock and stably infected rKSHV.219 cells (LEC, BEC, HUVEC, and HAEC) [Expt2]

(Submitter supplied) Expression profiling of stably infected primary endothelial cells using a custom tiling microarray. LEC, BEC, HUVEC, and HAEC were infected with rKSHV.219 and selected with puromycin for 2 weeks. Mock infected LEC, BEC, HUVEC, and HAEC served as controls for their infected counterparts. All cells were harvested after 2 weeks of stable infection.
Organism:
Human herpesvirus 8 strain rKSHV.219; Homo sapiens; Human gammaherpesvirus 8
Type:
Expression profiling by genome tiling array
Platform:
GPL16894
8 Samples
Download data: TXT
Series
Accession:
GSE45591
ID:
200045591
2.

A unique herpesviral transcriptional program in KSHV-infected lymphatic endothelial cells leads to mTORC1 activation and rapamycin sensitivity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Human herpesvirus 8 type M; Human herpesvirus 8 strain rKSHV.219; Homo sapiens; Human gammaherpesvirus 8
Type:
Expression profiling by genome tiling array
Platforms:
GPL16894 GPL10083
15 Samples
Download data: TXT
Series
Accession:
GSE45600
ID:
200045600
3.

Mock, latent, and lytic rKSHV.219-infected iSLK cells [Expt3]

(Submitter supplied) Expression profiling of stably infected epithelial cells using a custom tiling microarray. iSLK was infected with rKSHV.219 and selected with puromycin. Mock infected iSLK served as control for iSLK.219. Lytic reactivation of iSLK.219 was induced with 1 ug/mL doxycycline for 48 hours.
Organism:
Human gammaherpesvirus 8; Homo sapiens; Human herpesvirus 8 type M; Human herpesvirus 8 strain rKSHV.219
Type:
Expression profiling by genome tiling array
Platform:
GPL10083
3 Samples
Download data: TXT
Series
Accession:
GSE45599
ID:
200045599
4.

Mock and stably infected rKSHV.219 cells (LEC and BEC) [Expt1]

(Submitter supplied) Expression profiling of stably infected primary endothelial cells using a custom tiling microarray. LEC and BEC were infected with rKSHV.219 and selected with puromycin for 2 weeks. Mock infected LEC and BEC served as controls for their infected counterparts. All cells were harvested after 2 weeks of stable infection.
Organism:
Human gammaherpesvirus 8; Human herpesvirus 8 strain rKSHV.219; Homo sapiens
Type:
Expression profiling by genome tiling array
Platform:
GPL16894
4 Samples
Download data: TXT
Series
Accession:
GSE45590
ID:
200045590
5.

Role of LANA in KSHV latent infection

(Submitter supplied) Gene expression profiling of three PEL cell lines compare to three Burkitt's lymphoma lines to figure out the changed genes under KSHV latent infection. Gene expression profiling of two time points on TIVE cells after infection by KSHV compare to TIVE cell without infection by KSHV to figure out the changed genes on TIVE cell under latent infection of KSHV. Gene expression profiling of four time points after inducing recombinant LANA protein expression when compare to no inducing BJAB/Tet-On/LANA cells to figure out the changed genes under the latency-associate nuclear antigen (LANA) of KSHV expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS988 GDS989
Platforms:
GPL8300 GPL91
23 Samples
Download data: CEL, EXP
Series
Accession:
GSE1880
ID:
200001880
6.
Full record GDS989

Kaposi's sarcoma-associated herpesvirus and Epstein-Barr virus infected cell lines

Expression profiling of cell lines BCBL-1 and BC-3 infected by Kaposi's sarcoma-associated herpesvirus (KSHV), Raji infected by the Epstein-Barr virus (EBV), and BC-1 infected by both viruses. Results identify expression patterns specific to KSHV-infected primary effusion lymphoma derived cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 6 cell line, 4 infection sets
Platform:
GPL91
Series:
GSE1880
6 Samples
Download data: CEL, EXP
7.
Full record GDS988

Kaposi's sarcoma-associated herpesvirus LANA overexpression in B lymphoid cells: time course

Expression profiling of B lymphoid cell lines overexpressing the latency-associated nuclear antigen (LANA) of Kaposi's sarcoma-associated herpesvirus. B cells made to express LANA from a tetracycline inducible promoter. Expression examined at various time points up to 48 hours after induction.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 cell line, 2 protocol, 8 time sets
Platform:
GPL8300
Series:
GSE1880
14 Samples
Download data: CEL, EXP
8.

KSHV vIRF3 promotes angiogenesis of lymphatic endothelial cells (LECs)

(Submitter supplied) Herein, we report viral interferon regulatory factor 3 (vIRF3) as a pro-angiogenic factor together with HDAC5 that coordinates with LEC transcriptome, thus resulting in hyper-sprouting formation and ultimately leading to abnormal lymphangiogenesis. Overexpression of vIRF3 in LECs but not blood endothelial cells (BECs) exhibited a unique KSHV-associated angiogenic effect, evidenced by elongated spindle shape, sprouting, and tube formation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
9.

Transcriptome Analysis of KSHV during de novo primary infection of human B-and endothelial-cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
24 Samples
Download data: CSV
Series
Accession:
GSE62344
ID:
200062344
10.

Transcriptome Analysis of KSHV virions produced from BCBL1 and BAC36 in 293L cells

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles produced from BCBL1 cells as well as virions from 293L cells containing BAC36 BACs
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
3 Samples
Download data: CSV
Series
Accession:
GSE62343
ID:
200062343
11.

Transcriptome Analysis of KSHV during de novo primary infection of endothelial (TIVE) cells

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles and the transcription profiles of the viral genome during early infection, till the virus establishes latent infection in endothelial (TIVE) cells
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
5 Samples
Download data: CSV
Series
Accession:
GSE62342
ID:
200062342
12.

Transcriptome Analysis of KSHV during de novo primary infection of human B cells (PBMCs)

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles and the transcription profiles of the viral genome during early infection, till the virus establishes latent infection in human PBMCs
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
5 Samples
Download data: CSV
Series
Accession:
GSE62341
ID:
200062341
13.

Transcriptome Analysis of KSHV during de novo primary infection of human CD14+ cells

(Submitter supplied) The objective of this study was to identify the viral transcripts packaged into the virion particles and the transcription profiles of the viral genome during early infection, till the virus establishes latent infection in B-cells as well as in endothelial cells
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
5 Samples
Download data: CSV
Series
Accession:
GSE62340
ID:
200062340
14.

Transcriptome Analysis of BAC36 and ORF59 deleted BAC36 during de novo primary infection of human B cells (PBMCs)

(Submitter supplied) The objective of this study was to identify the transcription profiles of wild type KSHV and ORF59 deleted KSHV (Kaposi's sarcoma-associated herpesvirus) genome during early infection, till the virus establishes latent infection in human PBMCs
Organism:
Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17680
6 Samples
Download data: CSV
Series
Accession:
GSE62339
ID:
200062339
15.

RNA sequencing for KSHV circular RNAs

(Submitter supplied) The purpose was to detect viral circular RNAs from infected cells.
Organism:
Homo sapiens; Human gammaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25719
8 Samples
Download data: BED
Series
Accession:
GSE121756
ID:
200121756
16.

Microarray analysis with KSHV infection and enrichment for circular RNAs

(Submitter supplied) The purpose was to measure expression changes in human circular RNAs. Total RNA was harvested from KSHV-infected HUVEC and MC116 cells. A portion of the RNA was digested with RNase R to enrich for circular RNAs.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19977
12 Samples
Download data: GPR
Series
Accession:
GSE120045
ID:
200120045
17.

RNA sequencing with KSHV infection and enrichment for circular RNAs

(Submitter supplied) The purpose was to measure expression changes in human and viral circular RNAs.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16791
20 Samples
Download data: TXT
18.

Modified cross-linking, ligation, and sequencing of hybrids (qCLASH) identifies KSHV microRNA targets in endothelial cells

(Submitter supplied) KS lesions consist of endothelial cells latently infected with KSHV which express the KSHV miRNAs. Identifying the targets of the KSHV miRNAs will help us understand their role in viral oncogenesis. Cross-Linking and Sequencing of Hybrids (CLASH) is a method for unambiguously identifying miRNA targetomes. We developed a streamlined version of CLASH, called quick CLASH (qCLASH). qCLASH requires a lower initial input of cells than its parent protocol. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
9 Samples
Download data: TXT
Series
Accession:
GSE101978
ID:
200101978
19.

KSHV Requires vCyc to Overcome Replicative Senescence in Primary Human Lymphatic Endothelial Cells

(Submitter supplied) We performed high throughput RNA-sequencing on KSHV-infected blood and lymphatic HMVECs at 48hpi as well as WTKSHV- or KSHVDvcyc-infected lymphatic HMVECS at 1wpi to identify differences in gene expression induced by KSHV in these two cell types and gene expression changes that require the KSHV latent gene vcyclin.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: TXT
20.

Global gene expression differences between blood- and lymphatic-specific endothelial colony forming cells

(Submitter supplied) The identification of circulating endothelial progenitor cells has led to speculation regarding their origin as well as their contribution to neovascular development. Two distinct types of endothelium make up the blood and lymphatic vessel system. However, it has yet to be determined whether there are distinct lymphatic-specific circulating endothelial progenitor cells. We isolated circulating endothelial colony forming cells (ECFCs) from whole peripheral blood. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: TXT
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