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Links from GEO DataSets

Items: 20

1.

Altered expression of genes in WDR5 knockdown

(Submitter supplied) WDR5 (WD repeat domain 5) plays an important role in the epigenetic regulation of gene transcription, involing in regulation of embryonic stem cell and cancer cell.Bladder cancer is one of the most common cancers that cause approximately 150,000 deaths per year worldwide.The goal of this study is to identify the target genes of WDR5 in bladder cancer.Our results inditcate that the genes regulated by WDR5 involved in a variety of biological functions, such as proliferation and anti-apoptosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
3 Samples
Download data: CEL
Series
Accession:
GSE59132
ID:
200059132
2.

Altered expression of long noncoding RNAs in LNCaP castration resistant prostate cancer cell lines

(Submitter supplied) Castration-resistant prostate cancer (CRPC) that arise after the failure of androgen deprivation therapy is a leading cause of deaths in prostate cancer patients.However, its underlying mechanism is not fully understood. Long noncoding RNAs (lncRNAs) act as crucial regulators in a lot of human cancers, yet their potential roles and molecular mechanisms in CRPC are poorly understood.The goal of this study is to identify the differentially expressed lncRNAs in LNCaP cells and its two castration resistant sublines. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL20115
3 Samples
Download data: TXT
Series
Accession:
GSE93929
ID:
200093929
3.

Altered expression of genes in HOXD-AS1 knockdown prostate cancer cells

(Submitter supplied) Castration-resistant prostate cancer (CRPC) that arise after the failure of androgen deprivation therapy is a leading cause of deaths in prostate cancer patients. HOXD-AS1 is reported to play a role in bladder cancer and neuroblastoma. However, its function and underlying mechanism in CRPC remains unknown. The goal of this study is to identify the target genes of HOXD-AS1 in prostate cancer. Our results inditcate that the genes regulated by HOXD-S1 involved in a variety of biological functions, such as proliferation and and Androgen Receptor signaling.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
3 Samples
Download data: CEL
Series
Accession:
GSE93928
ID:
200093928
4.

Altered expression of genes in WDR5 inhibited (by OICR-9429) bladder cancer cells

(Submitter supplied) To explore the molecular mechanism underlying OICR-9429-induced WDR5 inhibition in BCa cells, a genome-wide RNA-sequencing was conducted to compare gene expression profiles between OICR-9429 treated T24, UM-UC-3 cells and their control cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
4 Samples
Download data: XLSX
5.

Expression profile of lncRNAs in CSCs and non-CSCs of bladder cancer cell line

(Submitter supplied) Bladder cancer stem cells (CSCs) contribute to tumorigenesis, recurrence and chemoresistance of bladder cancer. However, the molecular mechanisms underlying their self-renewal are poorly unknown. Long noncoding RNAs (lncRNAs) act as crucial regulators in a lot of human cancers, yet their potential roles and molecular mechanisms in bladder CSCs are poorly understood. The goal of this study is to identify the differentially expressed lncRNAs in bladder CSCs (UM-UC-3 4th spheres), its two differentiation sublines and bladder non-CSCs (UM-UC-3). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL19748
4 Samples
Download data: TXT
Series
Accession:
GSE107857
ID:
200107857
6.

ChIP-seq and RNA-seq in BGC823 cells after downregulation of GAS1 expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL11154
15 Samples
Download data: TDF
Series
Accession:
GSE63765
ID:
200063765
7.

A novel lncRNA GAS1 promotes gastric carcinogenesis and acts as a modular scaffold of WDR5 and KAT2A complexes to specify the histone modification pattern [RNA-seq]

(Submitter supplied) To elucidate whether GAS1 plays a role in gastric cancer tumorigenesis, a RNA-seq analysis was performed to compare the gene expression profiles of GAS1 shRNA and control shRNA transfectants.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
Series
Accession:
GSE63764
ID:
200063764
8.

Genome-wide maps of chromatin state of WDR5 and KAT2A in gastric cancer BGC823 cells [ChIP-seq]

(Submitter supplied) we performed ChIP coupled with high-throughput sequencing (ChIP-seq) for WDR5 and KAT2A in BGC823 cells. WDR5 and KAT2A ChIP-Seq data analysis revealed 5449 and 6485 called peaks, respectively in BGC823 cells with control shRNA transfection.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
9 Samples
Download data: TDF
Series
Accession:
GSE63763
ID:
200063763
9.

LncRNA/mRNA expression profiling for 20 human samples

(Submitter supplied) Transcriptional profiling of comparing human gatric cancerous tissue with noncancerous tissue. Goal was to determine the different gene expression between gastric cancer and noncancerous tissue.(reference manuscript titled"Long non-coding RNA GAPLINC regulates CD44-dependent cell invasiveness and associates with poor prognosis of gastric cancer" submitted to Cancer Research)
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL13825
20 Samples
Download data: TXT
Series
Accession:
GSE50710
ID:
200050710
10.

A Role for WDR5 in Integrating Threonine 11 Phosphorylation to Lysine 4 Methylationon Histone H3 and in Prostate Cancer

(Submitter supplied) Upon androgen stimulation, PKN1-mediated histone H3 threonine 11 phosphorylation (H3T11P) promotes AR target genes activation. However, the underlying mechanism is not completely understood. Here, we show that WDR5, a subunit of the SET1/MLL complex, interacts with H3T11P and this interaction facilitates the recruitment of the SET1/MLL complex and subsequent H3K4 trimethylation (H3K4me3). Using ChIP-seq, we find that androgen stimulation results in a six-fold increase in the number of H3T11P-marked regions and induces WDR5 colocalization to one third of H3T11P-enriched promoters, thus establishing a genome-wide relationship between H3T11P and recruitment of WDR5. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE55279
ID:
200055279
11.

WDR5 high expression and its effect on tumorigenesis in leukemia

(Submitter supplied) WD repeat domain 5 (WDR5) plays an important role in various biological functions through the epigenetic regulation of gene transcription. However, the oncogenic effect of WDR5 in leukemia remains largely unknown. Here, we found WDR5 expression is increased in leukemia patients. High expression of WDR5 is associated with high risk leukemia; Patients with WDR5 and MLL1 high expression have poor complete remission rate. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
4 Samples
Download data: TXT
Series
Accession:
GSE72864
ID:
200072864
12.

PMP22 Regulates Self-Renewal and Chemoresistance of Gastric Cancer Cells

(Submitter supplied) Cancer stem cells (CSCs) possess self-renewal and chemoresistance activities. However, the manner in which these features are maintained remains obscure. We sought to identify cell surface protein(s) that mark self-renewing and chemoresistant gastric cancer cells using the Explorer Antibody Microarray. We identified PMP22, a target gene of the Wnt/β-catenin pathway, as the most upregulated cell surface protein in gastric cancer xenografts exposed to cisplatin (DDP). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13497
6 Samples
Download data: TXT
Series
Accession:
GSE94714
ID:
200094714
13.

Wdr5

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL24247
43 Samples
Download data: BED, BIGWIG, BW, GTF, NARROWPEAK
Series
Accession:
GSE178556
ID:
200178556
14.

Transcriptome of Wdr5 and (or) p53 double knockout ESCs and embryoid bodies

(Submitter supplied) This study describes the transcriptome profiling of day 6 SFEBq embryonic bodies (EBs): 1) WT; 2) Wdr5 KO ; 3) Wdr5 KO with T12h hWDR5 rescue; 4) Wdr5 KO with T48h hWDR5 rescue
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
18 Samples
Download data: GTF
Series
Accession:
GSE178555
ID:
200178555
15.

Genome profiling of MAX binding in mouse embryonic bodies using SFEBq differentiation methods

(Submitter supplied) This study describes the binding profile of MAX in mouse embryonic bodies at day 2 (WT, Wdr5 KO, Wdr5 and p53 double knockout)
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
3 Samples
Download data: NARROWPEAK
Series
Accession:
GSE178554
ID:
200178554
16.

Genome profiling of WDR5 and H3K4me3 binding in mouse embryonic stem cells

(Submitter supplied) This study describes the binding profile of WDR5 and H3K4me3 in Wdr5 and p53 double knockout ESC rescued with WDR5WT or WDR5S91KY191F
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
6 Samples
Download data: BIGWIG, NARROWPEAK
Series
Accession:
GSE178552
ID:
200178552
17.

Chromatin accessibility profiling of mouse embryonic stem cells and embryonic bodies using SFEBq differentiation methods upon Wdr5 and P53 deletion with or without WT or mutant hWDR5 rescue

(Submitter supplied) This study describes time-course chromatin accessibility profiling of mouse ESC and embryonic bodies n Wdr5 and p53 knockout (with or without WT or mutant hWDR5 rescue)
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
16 Samples
Download data: BED, BW, NARROWPEAK
Series
Accession:
GSE178551
ID:
200178551
18.

Altered expression of genes in lncRNA-LBCS, hnRNPK and PTBP1 knockdown

(Submitter supplied) We identify a lncRNA which low expresses and regulates self-renewal of bladder cancer stem cell. So we named it lncRNA-LBCS (low expresses in bladder cancer stem cell). Further study finds that lncRNA-LBCS bind to hnRNPK and PTBP1. To investigate the genes regulated by these, we knockdown lncRNA-LBCS, hnRNPK and PTBP1 by siRNA, respectively, and perform high-throughput sequence. So we identify a series of genes regulated by lncRNA-LBCS, hnRNPK and PTBP1, respectively.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: TXT
Series
Accession:
GSE79832
ID:
200079832
19.

Next generation sequencing analysis of potential target genes of lncRNA BLACAT2

(Submitter supplied) Next generation sequencing analysis was performed to identify potential target genes of lncRNA BLACAT2. Purified total RNA (3 μg) was used to deplete ribosomal RNA with Ribo-Zero rRNA Removal Kits (MRZMB126,Epicentre). Poly(A)+ RNA was purified with oligo(dT) magnetic beads and fragmented into short sequences. The library was prepared with TruSeq Stranded mRNA LT Sample Prep Kit (Cat. No.15032612,Illumina) according to manufacturer’s instructions. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
3 Samples
Download data: TXT
20.

Gene expression signatures for bladder cancer tissues and normal adjacent tissues.

(Submitter supplied) To identify aberrantly expressed long intergenic noncoding RNAs (lincRNAs) in muscle-invasive bladder cancer tissues compared with normal adjacent tissues, we have employed microarray expression profiling as a discovery platform to identify lincRNAs that may play important roles in bladder cancer progression. Samples of fresh frozen cancer tissues, together with normal adjacent tissues (3 cm away from the tumor), were obtained during surgical resection, and total RNA was extracted for microarray analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14550
6 Samples
Download data: TXT
Series
Accession:
GSE100926
ID:
200100926
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