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Links from GEO DataSets

Items: 18

1.
Full record GDS5352

Long noncoding MALAT1 RNA deficiency effect on normal diploid fibroblasts W138

Analysis of WI38 fibroblasts transfected with MALAT1 antisense oligonucleotides (AS-1, AS-2). MALAT1 RNA is upregulated in cancer tissues and its elevated expression associated with hyper-proliferation. Results provide mechanistic insights on the role of MALAT1 in regulating cellular proliferation.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 protocol sets
Platform:
GPL10558
Series:
GSE44240
9 Samples
Download data
2.

Long Noncoding RNA MALAT1 Controls Cell Cycle Progression by Regulating the Expression of Oncogenic Transcription Factor B-MYB

(Submitter supplied) The long noncoding MALAT1 RNA is upregulated in cancer tissues and its elevated expression is associated with hyper-proliferation, but the underlying mechanism is poorly understood. We demonstrate that MALAT1 levels are regulated during normal cell cycle progression. Genome-wide transcriptome analyses in normal human diploid fibroblasts reveal that MALAT1 modulates the expression of cell cycle genes, and is required for G1/S and mitotic progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5352
Platform:
GPL10558
9 Samples
Download data: TXT
Series
Accession:
GSE44240
ID:
200044240
3.

Long Noncoding RNA MALAT1 Controls Cell Cycle Progression by Regulating the Expression of Oncogenic Transcription Factor B-MYB

(Submitter supplied) Transcriptome analysis of control and MALAT1 lncRNA-depleted RNA samples from human diploid lung fibroblasts [WI38] The long noncoding MALAT1 RNA is upregulated in cancer tissues and its elevated expression is associated with hyper-proliferation, but the underlying mechanism is poorly understood. We demonstrate that MALAT1 levels are regulated during normal cell cycle progression. Genome-wide transcriptome analyses in normal human diploid fibroblasts reveal that MALAT1 modulates the expression of cell cycle genes, and is required for G1/S and mitotic progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5188
6 Samples
Download data: CEL
Series
Accession:
GSE43830
ID:
200043830
4.

The long non-coding RNA GAS5 differentially regulates cell cycle arrest and apoptosis in human neuroblastoma

(Submitter supplied) Comparison of the global transcriptional profiles of the neurblastoma cell line IMR-32 48 hours after transfection with a Negative Control siRNA compared to an siRNA for the lncRNA GAS5.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18460
2 Samples
Download data: TXT
5.

Human endothelial polyA+ RNA expression analysis

(Submitter supplied) The human genome harbors a large number of sequences encoding for RNAs that are not translated but control cellular functions by distinct mechanisms. The expression and function of the longer transcripts namely the long non-coding RNAs (lncRNAs) in the vasculature is largely unknown. Here, we characterized the expression of lncRNAs in human endothelial cells and elucidated the function of the highly expressed metastasis-associated lung adenocarcinoma transcript 1 (MALAT1; also known as MALAT-1 or NEAT2). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: TXT
Series
Accession:
GSE54384
ID:
200054384
6.

Effect of Malat1 ASO on Neuro2 neuroblastoma cells transcriptome

(Submitter supplied) We investigated the effects of transfecting Malat1 antisense oligonucleotides on the whole Neuro2 neuroblastoma transcriptome. In this work, global transcription analyses were combined with detailed analyses of some synaptic genes. Our results provide insight on Malat1 effect on the regulation of gene expression in a mouse neuroblastoma cell line. Keywords: Comparative transcriptome analysis from Mus Musculus Neuro2 neuroblastoma cells transfected by Malat1 or Scamble oligodeoxynucleotides.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
6 Samples
Download data: GPR
Series
Accession:
GSE19928
ID:
200019928
7.

The Nuclear-retained non-coding RNA MALAT1 regulates alternative splicing by modulating SR splicing factor phosphorylation

(Submitter supplied) Alternative splicing (AS) of pre-mRNA is utilized by higher eukaryotes to achieve increased transcriptome and proteomic complexity. The serine/arginine (SR) splicing factors regulate tissue- or cell type-specific AS in a concentration and phosphorylation dependent manner. However, the mechanisms that modulate the cellular levels of active SR proteins remain to be elucidated. In the present study, we provide evidence for a role for the long nuclear-retained regulatory RNA (nrRNA), MALAT1 in AS regulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10691
2 Samples
Download data: TXT
Series
Accession:
GSE22963
ID:
200022963
8.

Effects of the long noncoding RNA Malat1 on gene expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL6096
6 Samples
Download data: CEL
Series
Accession:
GSE37707
ID:
200037707
9.

Effects of the long noncoding RNA Malat1 on gene expression [MoEx-1_0-st]

(Submitter supplied) Malat1 is an abundant long noncoding RNA that localizes to nuclear bodies known as nuclear speckles, which contain a distinct set of pre-mRNA processing factors. Previous in vitro studies have demonstrated that Malat1 interacts with pre-mRNA splicing factors, including the serine- and arginine-rich (SR) family of proteins, and regulates a variety of biological processes, including cancer cell migration, synapse formation, cell cycle progression, and responses to serum stimulation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
4 Samples
Download data: CEL
Series
Accession:
GSE37706
ID:
200037706
10.

Effects of the long noncoding RNA Malat1 on gene expression [Mouse430_2]

(Submitter supplied) Malat1 is an abundant long noncoding RNA that localizes to nuclear bodies known as nuclear speckles, which contain a distinct set of pre-mRNA processing factors. Previous in vitro studies have demonstrated that Malat1 interacts with pre-mRNA splicing factors, including the serine- and arginine-rich (SR) family of proteins, and regulates a variety of biological processes, including cancer cell migration, synapse formation, cell cycle progression, and responses to serum stimulation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL
Series
Accession:
GSE37705
ID:
200037705
11.

Context-dependent function of long noncoding RNA PURPL in transcriptome regulation during p53 activation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24676 GPL28352
28 Samples
Download data: BW, RESULTS, XLSX
Series
Accession:
GSE206702
ID:
200206702
12.

Context-dependent function of long noncoding RNA PURPL in transcriptome regulation during p53 activation (Iso-Seq)

(Submitter supplied) The goal of our study is to investigate the role of the p53-induced lncRNA PURPL in the context of liver cancer. To achieve this, we identified transcript variants of PURPL expressed in liver cancer cells and assayed for the transcriptome changes caused by PURPL knockdown after p53 induction.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28352
2 Samples
Download data: XLSX
Series
Accession:
GSE206701
ID:
200206701
13.

Context-dependent function of long noncoding RNA PURPL in transcriptome regulation during p53 activation (RNA-Seq II)

(Submitter supplied) The goal of our study is to investigate the role of the p53-induced lncRNA PURPL in the context of liver cancer. To achieve this, we identified transcript variants of PURPL expressed in liver cancer cells and assayed for the transcriptome changes caused by PURPL knockdown after p53 induction.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
2 Samples
Download data: BW, RESULTS
Series
Accession:
GSE206699
ID:
200206699
14.

Context-dependent function of long noncoding RNA PURPL in transcriptome regulation during p53 activation (RNA-Seq I)

(Submitter supplied) The goal of our study is to investigate the role of the p53-induced lncRNA PURPL in the context of liver cancer. To achieve this, we identified transcript variants of PURPL expressed in liver cancer cells and assayed for the transcriptome changes caused by PURPL knockdown after p53 induction.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
24 Samples
Download data: BW, TXT
Series
Accession:
GSE206698
ID:
200206698
15.

Long non-coding RNA Expression Profiling in Lung Cancer = Lung Adenocarcinoma (Lu-T) and in normal lung tissue (Lu-N)

(Submitter supplied) The expression of long non-coding RNAs - lncRNAs - was profiled in the lung adenocarcinoma patient samples (LUAD, Lu-T) and in normal lung tissues adjacent to tumors (Lu-N) using the Invitrogen NCode Human lncRNA Array Platform. will be published in: Anna Roth et al., Restoring LINC00673 expression triggers cellular senescence in lung cancer
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL16847
54 Samples
Download data: TXT
Series
Accession:
GSE113852
ID:
200113852
16.

Identification of long noncoding RNAs regulated by p53

(Submitter supplied) Analyize the transcriptpme regulated by p53 in 3 pairs of isogenic p53WT and p53KO colorectal cancer cell lines untreated or treated with Doxorubicin. The hypothsis of this study is that p53 can regulate the expression of subset of lncRNAs to mediate its biological functions.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
14 Samples
Download data: FPKM_TRACKING
17.

Identification of PURPL regulated genes in HCT116 cells

(Submitter supplied) Analysis of changes in gene expression profile upon depletion of PURPL in HCT116 cells. The hypothesis in this study is that PURPL regulates gene expression in the p53 pathway.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE79053
ID:
200079053
18.

The long non-coding RNA MALAT1 contributes to the pathogenesis of multiple sclerosis through alternative splicing and backsplicing regulation

(Submitter supplied) Since we found an upregulation of the long non coding RNA MALAT1 in Multiple Sclerosis (MS) patients, we decided to explore the global effect of MALAT1 modulation on transcriptome. We hence performed high-coverage RNA-seq experiments of MALAT1 knockdown in Jurkat E6-1 T cells to analyze gene expression, alternative splicing (AS), and backsplicing profiles. We found 107 differentially expressed genes, 1114 dysregulated AS events, and 49 circular RNAs that were modulated by MALAT1. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
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