Differentially enriched miRNAs in EVs derived from young and aged osteocytes of mice

ChEBI2022-02-15 更新2026-07-12 收录

骨细胞衰老

细胞外囊泡miRNA

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Differentially enriched miRNAs in EVs derived from young and aged osteocytes of mice

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2022-02-15

Isolation and next generation sequencing of epididymal extracellular vesicles reveals segmental patterns of miRNA expression and a potential mechanism for modification of the sperm epigenome.

表观遗传学

细胞外囊泡miRNA

Interest in the sperm epigenome continues to grow in view of the realization that it is vulnerable to dynamic modifications arising from a variety of paternal environment exposures and that this legac

NIAID Data Ecosystem60

miRNA sequencing of yEVs and mEVs

细胞外囊泡miRNA

生物标志物研究

For miRNA sequencing, yEVs and mEVs of mice were collected. Each group had 3 replicates.

NIAID Data Ecosystem40

Real-time quantitative PCR analysis of EV-containing miRNA from human adipocytes SGBS cells. Real-time quantitative PCR analysis of EV-containing miRNA from human adipocytes SGBS cells

细胞外囊泡miRNA

脂肪细胞炎症响应机制

Mature adipocytes were pretreated with VD for 24h and/or treated with TNFα during 24h. EVs released by adipocytes after TNF treatment were isolated and the miRNAs contained in it were extracted for qP

NIAID Data Ecosystem30

Effects of Mettl3 and Alkbh5 knockdown on small RNA export into EVs

RNA修饰调控

细胞外囊泡miRNA

Understanding the functional role of RNA modifications and to what extent they might regulate mature miRNA function and their secretion in extracellular vesicles (EVs) is unknown. Analysis of RNA con

NIAID Data Ecosystem40

Preferential Release of microRNAs via Extracellular Vesicles is Associated with Ductal Carcinoma In Situ to Invasive Breast Cancer Progression [miRNA-Seq]

乳腺癌进展

细胞外囊泡miRNA

Ductal carcinoma in situ (DCIS) is a precancerous condition that increases the risk of invasive breast cancer (IBC), but not all DCIS cases progress to IBC. The molecular factors driving this transiti

NIAID Data Ecosystem30

Differentially enriched miRNAs in EVs derived from young and aged osteocytes of mice

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