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Temporal transcriptomic profiling reveals dynamic changes in gene expression of Xenopus animal cap upon activin treatment. , Satou-Kobayashi Y., Sci Rep. July 15, 2021; 11 (1): 14537.
Coordinated regulation of the dorsal- ventral and anterior- posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14. , Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.
A gene regulatory program controlling early Xenopus mesendoderm formation: Network conservation and motifs. , Charney RM ., Semin Cell Dev Biol. June 1, 2017; 66 12-24.
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.
Genome-wide view of TGFβ/ Foxh1 regulation of the early mesendoderm program. , Chiu WT ., Development. December 1, 2014; 141 (23): 4537-47.
Developmental enhancers are marked independently of zygotic Nodal signals in Xenopus. , Gupta R ., Dev Biol. November 1, 2014; 395 (1): 38-49.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis. , Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
Signaling crosstalk between TGFβ and Dishevelled/ Par1b. , Mamidi A., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.
HEB and E2A function as SMAD/FOXH1 cofactors. , Yoon SJ ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus. , Smith SJ ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
The function of heterodimeric AP-1 comprised of c- Jun and c- Fos in activin mediated Spemann organizer gene expression. , Lee SY., PLoS One. January 1, 2011; 6 (7): e21796.
High-sensitivity real-time imaging of dual protein-protein interactions in living subjects using multicolor luciferases. , Hida N., PLoS One. June 12, 2009; 4 (6): e5868.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides. , Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
deltaEF1 and SIP1 are differentially expressed and have overlapping activities during Xenopus embryogenesis. , van Grunsven LA., Dev Dyn. June 1, 2006; 235 (6): 1491-500.
The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo. , Collart C ., Development. October 1, 2005; 132 (20): 4575-86.
Molecular regulation of vertebrate early endoderm development. , Shivdasani RA ., Dev Biol. September 15, 2002; 249 (2): 191-203.
The role of a Williams-Beuren syndrome-associated helix-loop-helix domain-containing transcription factor in activin/ nodal signaling. , Ring C., Genes Dev. April 1, 2002; 16 (7): 820-35.
TGF-beta signalling pathways in early Xenopus development. , Hill CS ., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.
Nodal signaling uses activin and transforming growth factor-beta receptor-regulated Smads. , Kumar A., J Biol Chem. January 5, 2001; 276 (1): 656-61.
The C-terminal domain of Mad-like signal transducers is sufficient for biological activity in the Xenopus embryo and transcriptional activation. , Meersseman G., Mech Dev. January 1, 1997; 61 (1-2): 127-40.