Investigate the effect of jhdm1b on Oct4 mediated reprogramming
The histone demethylases Jhdm1a/1b enhance somatic cell reprogramming in a vitamin-C-dependent manner.
Specimen part, Treatment
View SamplesTo identify RA regulated genes in endoderm, we did microarray analysis comparing gene expression levels between wild-type and RA-deficient embryos, which were treated with BMS453 at the beginning of gastrulation and were collected at stages 23.
No associated publication
Sex, Age, Compound
View SamplesThis SuperSeries is composed of the SubSeries listed below.
Vitamin C enhances the generation of mouse and human induced pluripotent stem cells.
Specimen part, Treatment, Time
View SamplesFBS and BMP influence the somatic reprogramming induced by Oct4/Sox2/Klf4/c-Myc similarly. Bone morphogenetic proteins (BMPs) are abundant in serum and activate Smad1/5/8 to regulated target genes.
H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs.
Cell line
View SamplesIn order to understand the global gene expression changes resulting from the addition of vitamin C (Vc) to SKO (sox2, klf4 and oct4)-transduced mouse embryonic fibroblasts (MEFs), we used microarray to compare the gene expression profile at different time points with or without Vc.
Vitamin C enhances the generation of mouse and human induced pluripotent stem cells.
Specimen part, Treatment, Time
View SamplesOverexpression HDAC7 can enhance iPS efficiency in SKO by supressing MEF2 factors
No associated publication
Specimen part, Time
View SamplesTreatment with MicroRNA cluster B and C increase the iPS efficiency
MicroRNA cluster 302-367 enhances somatic cell reprogramming by accelerating a mesenchymal-to-epithelial transition.
Specimen part, Treatment, Time
View SamplesThis SuperSeries is composed of the SubSeries listed below.
A mesenchymal-to-epithelial transition initiates and is required for the nuclear reprogramming of mouse fibroblasts.
Cell line
View SamplesWe present a robust serum-free system for the rapid and efficient reprogramming of mouse somatic cells by Oct4, Sox2 and Klf4. The elimination of fetal bovine serum and oncogene c-Myc allowed reprogramming cells to be detected as early as Day 2 and reached greater than 10% of the population at Day 7 post retroviral transduction. The resulting iPS colonies were isolated with high efficiency to establish pluripotent cell lines. Based on this method, we further developed iPS-SF1 as a dedicated reprogramming medium for chemical screening and mechanistic investigations.
Towards an optimized culture medium for the generation of mouse induced pluripotent stem cells.
Specimen part
View SamplesTreatment with vitamin C (Vc) on MaF pre-induced pluripotent stem cells (pre-iPSCs) induced a rapid conversion into full-iPSCs within a few passages. We used microarrays to identify changes induced by Vc in the MaF pre-iPSC clone.
Vitamin C enhances the generation of mouse and human induced pluripotent stem cells.
Specimen part, Treatment, Time
View Samples