by rss feed | Jan 15, 2021 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
We utilized robust parameter design (RPD) for establishing human induced pluripotent stem cell differentiation protocols, which led to the four distinctive endodermal cell induction, while increasing the efficiency of the multifactorial screening in 243‐fold (18 vs...
by rss feed | Jan 14, 2021 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
In order to investigate the role of insulin growth factor binding proteins (IGFBPs) in retinal organoids, human embryonic stem cells (hESCs) were differentiated to retinal organoids using three different conditions: with IGF‐1 individually or in combination with...
by rss feed | Jan 11, 2021 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
ERG1 binds with Integrin β1 to activate the AKT pathway by recruiting and phosphorylating PI3K p85 and FAK, which promotes rat cardiomyocyte differentiation through mediating phosphorylation of GSK3β to upregulate the expression of both β‐catenin and Gata4, and...
by rss feed | Dec 2, 2020 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
Inhibition of the miR‐183/96/182 cluster in human pluripotent stem cells leads to the generation of abnormal retinal organoids. Abstract MicroRNAs (miRNAs), a class of small, noncoding RNA molecules, represent important regulators of gene expression. Recent reports...
by rss feed | Dec 2, 2020 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
MiR‐184 is critical for the differentiation of ES cells by directly targeting Wnt3, thereby inhibits the differentiation of ES cells into cardiac mesoderm, and finally affects the differentiation of cardiac mesoderm into cardiomyocytes. These findings not only...
by rss feed | Nov 26, 2020 | EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS, News Feeds
We generated human induced pluripotent stem cell‐derived alveolar type I (iAT1) cells in alveolar organoids (AOs) and showed that the transcriptomes of iAT1 cells were similar to those of primary AT1 cells. We generated iAT1 cells by inhibiting canonical Wnt signaling...