Project description:miRNA-sequencing of grapefruit-derived extracellular vesicles and fusion nanovesicles derived from grapefruit-derived extracellular vesicles and gingival mesenchymal stem cell-derived vesicles. We then performed gene expression profiling analysis to explore the miRNAs derived from grapefruit-derived extracellular vesicles, and the retention rate of miRNAs after membrane fusion
2023-10-26 | GSE223353 | GEO
Project description:miRNA sequencing of human mesenchymal stem cell-derived extracellular vesicles
| PRJNA814986 | ENA
Project description:human Bone marrow mesenchymal stem cell-derived small extracellular vesicles miRNA sequencing
Project description:miRNA-sequencing of cell membrane-based vesicles derived from gingiva-derived mesenchymal stem cells and fusion nanovesicles. We then performed gene expression profiling analysis to explore the miRNAs of cell membrane-based vesicles derived from gingiva-derived mesenchymal stem cells , and the retention rate of miRNAs after membrane fusion
2023-10-26 | GSE223577 | GEO
Project description:miRNA sequencing of human Dental Pulp stem cell-derived extracellular vesicles
Project description:To gain insight into the microRNA expression profile of small extracellular vesicles derived from bone metabolism related cell types and to verify their mechanism, we utilized the miRNA sequencing technology to analyze the miRNA profiles of different mouse osteoblast and osteoclast cell derived small extracellular vesicles.
Project description:We report small RNA sequencing technology for high-throughput profiling of microRNA content within small extracellular vesicles isolated from nonsenescent and senescent human umbilical cord mesenchymal stem cells (hUCMSCs)
Project description:Matrix-bound extracellular vesicles were isolated from the left ventricle tissue of de-identified patients with non-failing (healthy) hearts or with non-ischemi heart failure. mIRNA sequencing was performed on the miRNA cargo sequestered within the extracellular vesicles. Differences in the miRNA signature of healthy versus failing-tissue derived extracellular vesicles suggests that disease progression to heart failure is associated with dynamic changes in vesicular cargo.
