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Differential expression of miRNAs in HGF treated HTR-8/SVneo versus untreated control by next generation sequencing

ABSTRACT: Differential expression of miRNAs in HGF treated HTR-8/SVneo versus untreated control by next generation sequencing

PROVIDER: PRJNA517471 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR8496520.fastq.gz	Fastqsanger.gz
	SRR8496521.fastq.gz	Fastqsanger.gz
	SRR8496522.fastq.gz	Fastqsanger.gz
	SRR8496523.fastq.gz	Fastqsanger.gz
	SRR8496524.fastq.gz	Fastqsanger.gz

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Differential expression of miRNAs in HGF treated HTR-8/SVneo versus untreated control by next generation sequencing

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Differential expression of miRNAs in EGF treated HTR-8/SVneo versus untreated control by next generation sequencing

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Differential expression of miRNAs in IFN-gamma treated HTR-8/SVneo versus untreated control by next generation sequencing

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Differential expression of mRNAs in IFN-gamma treated HTR-8/SVneo versus untreated control by next generation sequencing

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Effect of LIF and IL-6 on gene expression in JEG-3 and HTR-8/SVneo trophoblastic cells

Project description:Both leukemia inhibitory factor (LIF) and interleukin-6 (IL-6) increase the invasiveness of JEG-3 and HTR-8/SVneo cells. This study examines the effect of LIF and IL-6 on gene expression in trophoblastic cell models viz. JEG-3 and HTR-8/SVneo cells to decipher the molecular basis of the increase in invasiveness. JEG-3 and HTR-8/Svneo cells were stimulated with LIF (50 ng/ml) and IL-6 (100 ng/ml) for 24 h in plain medium keeping untreated cells as a control. After 24 h of stimulation, total RNA was isolated from these cells and used for microarray experiments. These experiments were performed once.

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Effect of IL-11 on gene expression in JEG-3 and HTR-8/SVneo trophoblastic cells

Project description:IL-11 increases the invasiveness of JEG-3 cells while, reduces the invasiveness of HTR-8/SVneo cells. This study examines the effect of IL-11 on gene expression in trophobalstic cell models viz. JEG-3 and HTR-8/SVneo cells to resolve the controversies associated with the IL-11 mediated regulation of the invasiveness of these two cell lines. JEG-3 and HTR-8/Svneo cells were stimulated with IL-11 (200 ng/ml) for 24 h in pain medium keeping un-treated cells as control. After 24 h of stimulation, total RNA was isolated from these cells and used for the microarray experiments. These experiments were performed once.

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Differential expression of miRNAs in EGF treated HTR-8/SVneo versus untreated control by next generation sequencing

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Gene expression in HTR-8/SVneo cells exposed to hypoxia or treated with sodium L-lactate

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