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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-3714

Papers associated with right (and smad3)

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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.    


FoxH1 mediates a Grg4 and Smad2 dependent transcriptional switch in Nodal signaling during Xenopus mesoderm development., Reid CD., Dev Biol. June 1, 2016; 414 (1): 34-44.                  


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.                                  


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.                              


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.                                


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Signaling crosstalk between TGFβ and Dishevelled/Par1b., Mamidi A., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.                    


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.                            


TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.                                      


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.            


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.        


Interaction with Smad4 is indispensable for suppression of BMP signaling by c-Ski., Takeda M., Mol Biol Cell. March 1, 2004; 15 (3): 963-72.                


TGF-beta signalling pathways in early Xenopus development., Hill CS., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.    


Regulation of Smad degradation and activity by Smurf2, an E3 ubiquitin ligase., Zhang Y, Zhang Y., Proc Natl Acad Sci U S A. January 30, 2001; 98 (3): 974-9.        


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.    

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