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Regulation of gene expression downstream of a novel Fgf/Erk pathway during Xenopus development. , Cowell LM., PLoS One. January 1, 2023; 18 (10): e0286040.
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.
HMCES modulates the transcriptional regulation of nodal/activin and BMP signaling in mESCs. , Liang T., Cell Rep. July 12, 2022; 40 (2): 111038.
Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage. , Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
Transcription factors Mix1 and VegT, relocalization of vegt mRNA, and conserved endoderm and dorsal specification in frogs. , Sudou N ., Proc Natl Acad Sci U S A. May 17, 2016; 113 (20): 5628-33.
Genome-wide view of TGFβ/ Foxh1 regulation of the early mesendoderm program. , Chiu WT ., Development. December 1, 2014; 141 (23): 4537-47.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis. , Cao Q., Development. November 1, 2012; 139 (21): 3950-61.
Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer. , Sudou N ., Development. May 1, 2012; 139 (9): 1651-61.
KDEL tagging: a method for generating dominant-negative inhibitors of the secretion of TGF-beta superfamily proteins. , Matsukawa S ., Int J Dev Biol. January 1, 2012; 56 (5): 351-6.
Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis. , Suzawa K ., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase. , Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos. , Callery EM ., Dev Biol. February 15, 2005; 278 (2): 542-59.
Patterning and tissue movements in a novel explant preparation of the marginal zone of Xenopus laevis. , Davidson LA ., Gene Expr Patterns. July 1, 2004; 4 (4): 457-66.
Selective degradation of excess Ldb1 by Rnf12/ RLIM confers proper Ldb1 expression levels and Xlim-1/ Ldb1 stoichiometry in Xenopus organizer functions. , Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus. , Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.
Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function. , Kato Y ., J Neurosci. November 1, 1999; 19 (21): 9364-73.
The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins. , Latinkić BV., Genes Dev. December 1, 1997; 11 (23): 3265-76.