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Summary Anatomy Item Literature (1230) Expression Attributions Wiki
XB-ANAT-736

Papers associated with neural tube (and smad1)

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ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.                                          


Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.        


ZC4H2 stabilizes Smads to enhance BMP signalling, which is involved in neural development in Xenopus., Ma P., Open Biol. August 1, 2017; 7 (8):                           


Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development., Schille C., BMC Dev Biol. January 19, 2016; 16 1.                          


The Proto-oncogene Transcription Factor Ets1 Regulates Neural Crest Development through Histone Deacetylase 1 to Mediate Output of Bone Morphogenetic Protein Signaling., Wang C., J Biol Chem. September 4, 2015; 290 (36): 21925-38.                  


Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.                            


Current perspectives of the signaling pathways directing neural crest induction., Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.          


Sizzled-tolloid interactions maintain foregut progenitors by regulating fibronectin-dependent BMP signaling., Kenny AP., Dev Cell. August 14, 2012; 23 (2): 292-304.                                


Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.                


Rab3d is required for Xenopus anterior neurulation by regulating Noggin secretion., Kim H., Dev Dyn. June 1, 2011; 240 (6): 1430-9.              


The role and regulation of GDF11 in Smad2 activation during tailbud formation in the Xenopus embryo., Ho DM., Mech Dev. January 1, 2010; 127 (9-12): 485-95.                  


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.                    


Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning., Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.                            


TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.                  


Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.                


Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.                      


Eye and neural defects associated with loss of GDF6., Hanel ML., BMC Dev Biol. June 6, 2006; 6 43.          


Temporal analysis of the early BMP functions identifies distinct anti-organizer and mesoderm patterning phases., Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.              


MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.              


Neural induction requires BMP inhibition only as a late step, and involves signals other than FGF and Wnt antagonists., Linker C., Development. November 1, 2004; 131 (22): 5671-81.      


Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.              


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.                  


Endogenous patterns of BMP signaling during early chick development., Faure S., Dev Biol. April 1, 2002; 244 (1): 44-65.


Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.                                                                                                      


The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.              


BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.          


OAZ uses distinct DNA- and protein-binding zinc fingers in separate BMP-Smad and Olf signaling pathways., Hata A., Cell. January 21, 2000; 100 (2): 229-40.      


Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.              


Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis., Nakayama T., Genes Cells. June 1, 1998; 3 (6): 387-94.                


Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.                


Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.                  

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