8 Transcriptional Regulation during Somitogenesis
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Cited by (14)
Early transcriptional targets of MyoD link myogenesis and somitogenesis
2012, Developmental BiologyCitation Excerpt :The timing of the analysis in the zebrafish study was at somite stages, while our work analysed gene expression at gastrula stages and it is possible that the regulatory relationships among the MRFs are different at earlier stages. A single element upstream of Xmyf5, containing the E-box identified in Fig. 5, has been shown to be necessary and sufficient for correct Xmyf5 expression during gastrula stages in Xenopus (Polli and Amaya, 2002), while in mouse there are multiple interdigitated control sequences required for myf5 expression during somite stages (Summerbell and Rigby, 2000). Another gene we found to require MyoD for its expression is Seb4, which has previously been recognised as having a role in myogenesis (Li et al., 2010).
Early Embryonic Mesoderm Development
2004, Handbook of Stem CellsThe protocadherin PAPC establishes segmental boundaries during somitogenesis in Xenopus embryos
2000, Current BiologyCitation Excerpt :How cells are assigned to segments in the paraxial mesoderm and how this information is used to generate distinct morphological structures are unanswered questions in developmental biology. Recent studies over the last several years indicate that segmental patterning of the PSM is mediated by components of the Notch signaling pathway, by the Hairy-like WRPW–bHLH proteins, and by bHLH transcription factors of the Mesp family (reviewed in [2–4]). These genes are expressed within the PSM in dynamic patterns that prefigure the subsequent morphological changes associated with segmentation.
In Vitro Embryogenesis and Gastrulation Using Stem Cells in Mice and Humans
2023, International Journal of Molecular SciencesEMT imparts cancer stemness and plasticity: new perspectives and therapeutic potential
2021, Frontiers in Bioscience - LandmarkEpigenetics in skeletal muscle development
2011, Cancer Epigenetics: Biomolecular Therapeutics in Human Cancer