mRNA expression in iPS cells generated by a synthetic self-replicative RNA

ChEBI2014-04-25 更新2026-07-21 收录

干细胞重编程

合成RNA技术

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-38265 数据链接链接失效反馈

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mRNA expression in iPS cells generated by a synthetic self-replicative RNA

创建时间：

2014-04-25

Self-Renewing Presomitic Mesoderm Progenitor Lines Reprogrammed from human urine cells [xxx scRNA-seq]. Self-Renewing Presomitic Mesoderm Progenitor Lines Reprogrammed from human urine cells [xxx scRNA-seq]

干细胞重编程

肌肉骨骼再生

Vertebrae formation is the defining feature of all vertebrates1,2. Yet, each vertebrate species appears to have a unique timing mechanism for forming somites along the vertebral column3-5. Human verte

NIAID Data Ecosystem60

Chromatin Accessibility Dynamics during Chemical Induction of Pluripotency [RNA-seq]. Chromatin Accessibility Dynamics during Chemical Induction of Pluripotency [RNA-seq]

干细胞重编程

染色质可及性调控

Chemical induction of pluripotency (CIP) is an ideal way to reprogram cell fate, but remains poorly understood. Here we report the development of an efficient CIP protocol and the chromatin accessibil

NIAID Data Ecosystem40

Reprogramming to pluripotency through a somatic stem cell intermediate

干细胞重编程

细胞多能性诱导

Reprogramming to pluripotency through a somatic stem cell intermediate

ChEBI2014-03-28 更新00

BMP4 Resets Primed to Naive Pluripotency by Reprogramming Chromatin Accessibility [RNA-Seq]

干细胞重编程

染色质可及性分析

Mouse naive and primed pluripotent stem cells, ESC and EpiSC, represent two distinct stages of pluripotency. Here we report that BMP4 drives primed to naive transition or PNT by reprogramming chromati

NIAID Data Ecosystem40

Time course of the miR-203 effect during reprogramming from somatic cells to pluripotent cells. Mus musculus

干细胞重编程

MicroRNA功能研究

The balance between pluripotency and differentiation is critical during development and regeneration. miR-203 is a microRNA previously involved in differentiation of different tissues as well as in tu

NIAID Data Ecosystem30

mRNA expression in iPS cells generated by a synthetic self-replicative RNA

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