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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.
Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm. , Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
Conservation and evolutionary divergence in the activity of receptor-regulated smads. , Sorrentino GM ., Evodevo. October 1, 2012; 3 (1): 22.
HEB and E2A function as SMAD/FOXH1 cofactors. , Yoon SJ ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
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.
The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo. , Collart C ., Development. October 1, 2005; 132 (20): 4575-86.
Drosophila dSmad2 and Atr-I transmit activin/ TGFbeta signals. , Das P., Genes Cells. February 1, 1999; 4 (2): 123-34.