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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR. , Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus. , Melchert J., Dev Biol. March 15, 2020; 459 (2): 138-148.
High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis. , Michiue T ., Dev Biol. June 15, 2017; 426 (2): 270-290.
Small C-terminal Domain Phosphatase 3 Dephosphorylates the Linker Sites of Receptor-regulated Smads (R-Smads) to Ensure Transforming Growth Factor β (TGFβ)-mediated Germ Layer Induction in Xenopus Embryos. , Sun G ., J Biol Chem. July 10, 2015; 290 (28): 17239-49.
Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo. , Lim JW., Development. January 1, 2011; 138 (1): 33-44.
Sox3 expression is maintained by FGF signaling and restricted to the neural plate by Vent proteins in the Xenopus embryo. , Rogers CD., Dev Biol. January 1, 2008; 313 (1): 307-19.
Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer. , Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis. , Cao Y ., Dev Growth Differ. October 1, 2001; 43 (5): 563-71.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.