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Summary Anatomy Item Literature (1495) Expression Attributions Wiki
XB-ANAT-20

Papers associated with spinal cord (and cdx4)

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Evo-engineering and the cellular and molecular origins of the vertebrate spinal cord., Steventon B., Dev Biol. December 1, 2017; 432 (1): 3-13.


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.        


Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.                                          


Molecular insights into the origin of the Hox-TALE patterning system., Hudry B., Elife. March 18, 2014; 3 e01939.                                    


Identification and characterization of Xenopus kctd15, an ectodermal gene repressed by the FGF pathway., Takahashi C., Int J Dev Biol. January 1, 2012; 56 (5): 393-402.                  


Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.                


Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.                              


The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.                


Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.                                


Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.            


Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians., Iglesias M., Development. April 1, 2008; 135 (7): 1215-21.  


FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.            


Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.                          


A developmental pathway controlling outgrowth of the Xenopus tail bud., Beck CW., Development. April 1, 1999; 126 (8): 1611-20.                


Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth., Beck CW., Mech Dev. March 1, 1998; 72 (1-2): 41-52.                                                                


Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.              


Polycomb and bmi-1 homologs are expressed in overlapping patterns in Xenopus embryos and are able to interact with each other., Reijnen MJ., Mech Dev. September 1, 1995; 53 (1): 35-46.        

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