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Highly efficient reprogramming to pluripotency and directed differentiation using synthetic mRNA

ChEBI2010-09-30 更新2026-07-21 收录

干细胞重编程

合成mRNA技术

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-23583 数据链接链接失效反馈

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Highly efficient reprogramming to pluripotency and directed differentiation using synthetic mRNA

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创建时间：

2010-09-30

干细胞重编程

细胞分化

Previous research has shown that a subpopulation of cells within cultured human dermal fibroblasts, termed multilineage-differentiating stress enduring (Muse) cells, are preferentially reprogrammed in

DataCite Commons2024-03-24 更新80

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

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

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

Highly efficient reprogramming to pluripotency and directed differentiation using synthetic mRNA

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