Dynamic changes in Sox2 spatio-temporal expression promote the second cell fate decision through Fgf4/Fgfr2 signaling in preimplantation mouse embryos

• Main Authors: Mistri, T.K, Arindrarto, W, Ng, W.P, Wang, C, Lim, L.H, Sun, L, Chambers, I, Wohland, T, Robson, P
• Other Authors: BIOLOGICAL SCIENCES
• Format: Article
• Published: 2020
• Subjects: fibroblast growth factor 4; fibroblast growth factor receptor 2; octamer transcription factor 4; transcription factor Sox2; Fgf4 protein, mouse; Fgfr2 protein, mouse; Sox2 protein, mouse; transcription factor Sox; animal cell; Article; cell fate; CHO cell line; controlled study; embryo; female; fluorescence correlation spectroscopy; inner cell mass; mouse; mouse embryo; nonhuman; preimplantation embryo; priority journal; protein expression; spatiotemporal analysis; animal; blastocyst; cell culture; cell differentiation; cell lineage; Cricetulus; embryology; endoderm; gene expression regulation; genetics; hamster; mammalian embryo; metabolism; pregnancy; signal transduction; Animals; Blastocyst; Cell Differentiation; Cell Lineage; Cells, Cultured; CHO Cells; Cricetinae; Embryo, Mammalian; Endoderm; Female; Fibroblast Growth Factor 4; Gene Expression Regulation, Developmental; Mice; Pregnancy; Receptor, Fibroblast Growth Factor, Type 2; Signal Transduction; SOXB1 Transcription Factors
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/174664
• Institution: National University of Singapore

10.1042/BCJ20170418