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Transcription profiling of mouse multipotent adult progenitor cells (MAPCs), 2 different clones

ChEBI2008-06-14 更新2026-07-21 收录

干细胞转录组学

小鼠多能祖细胞

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-6291 数据链接链接失效反馈

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资源简介：

Transcription profiling of mouse multipotent adult progenitor cells (MAPCs), 2 different clones

应用场景：

创建时间：

2008-06-14

干细胞转录组学

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This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

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Gene expressions of H9s in different culture systems

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H9s were cultued in 2D, static 3D and dynamic 3D suspension and in the microspace cell culture system for 3 days. mRNAs were sequenced. RNA deep sequencing

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Comprehensive transcriptome analysis of pig induced pluripotent stem cells by high-throughput sequencing. Comprehensive transcriptome analysis of pig induced pluripotent stem cells by high-throughput sequencing

干细胞转录组学

猪多能性调控机制

The wide application of pig disease model has caused a surge of interest in the study ofderivation of pig induced pluripotent cells (iPSCs). Here we performed genome-wide analysis of gene expression p

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mRNA sequencing

干细胞转录组学

基因表达分析

To explore the changes of late-passage OM-MSCs under different culture methods.

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Transcriptome analysis of Human Trophoblast Stem cell (HTS) and TEAD4 knock down HTS cells by next generation sequencing

干细胞转录组学

TEAD4基因功能

mRNA profiles of control Human Trophoblast Stem cell (HTS) and TEAD4 knock down HTS cells were generated by deep sequencing, in triplicate, using Illumina NovaSeq 6000 platform. TEAD4 Knock down in HT

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Transcription profiling of mouse multipotent adult progenitor cells (MAPCs), 2 different clones

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