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Summary Anatomy Item Literature (1040) Expression Attributions Wiki
XB-ANAT-71

Papers associated with dorsal marginal zone (and hoxc9-like)

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Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.                    


NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.                


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.                                    


Hox collinearity - a new perspective., Durston AJ., Int J Dev Biol. January 1, 2011; 55 (10-12): 899-908.  


BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus., Wills AE., Dev Biol. January 15, 2010; 337 (2): 335-50.                  


Interaction between X-Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis., Peres JN., Mech Dev. April 1, 2006; 123 (4): 321-33.                          


Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.            


xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O., Dev Biol. July 1, 2005; 283 (1): 17-28.              


Timed interactions between the Hox expressing non-organiser mesoderm and the Spemann organiser generate positional information during vertebrate gastrulation., Wacker SA., Dev Biol. April 1, 2004; 268 (1): 207-19.            


The initiation of Hox gene expression in Xenopus laevis is controlled by Brachyury and BMP-4., Wacker SA., Dev Biol. February 1, 2004; 266 (1): 123-37.                  


PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.            


Twisted gastrulation loss-of-function analyses support its role as a BMP inhibitor during early Xenopus embryogenesis., Blitz IL., Development. October 1, 2003; 130 (20): 4975-88.              


Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.                            


Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor., Bell E., Development. April 1, 2003; 130 (7): 1381-9.    


Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.              


Induction and patterning of the telencephalon in Xenopus laevis., Lupo G., Development. December 1, 2002; 129 (23): 5421-36.                            


Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.            


Evidence for non-axial A/P patterning in the nonneural ectoderm of Xenopus and zebrafish pregastrula embryos., Read EM., Int J Dev Biol. September 1, 1998; 42 (6): 763-74.    


The Spemann organizer of Xenopus is patterned along its anteroposterior axis at the earliest gastrula stage., Zoltewicz JS., Dev Biol. December 15, 1997; 192 (2): 482-91.          

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