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Summary Anatomy Item Literature (1054) Expression Attributions Wiki
XB-ANAT-200

Papers associated with animal hemisphere (and cdx4)

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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.                                    


Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.                        


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


An essential role for LPA signalling in telencephalon development., Geach TJ., Development. February 1, 2014; 141 (4): 940-9.                            


Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.                


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.                  


XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.            


Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification., Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.        


Xwnt8 directly initiates expression of labial Hox genes., In der Rieden PM., Dev Dyn. January 1, 2010; 239 (1): 126-39.          


Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.              


Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis., Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.                                


Characterisation of the fibroblast growth factor dependent transcriptome in early development., Branney PA., PLoS One. January 1, 2009; 4 (3): e4951.            


Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.                


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


A consensus Oct1 binding site is required for the activity of the Xenopus Cdx4 promoter., Reece-Hoyes JS., Dev Biol. June 15, 2005; 282 (2): 509-23.              


Microarray-based identification of VegT targets in Xenopus., Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.                                          


Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.                                                                                                                      


Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.                    


Cloning and expression of the Cdx family from the frog Xenopus tropicalis., Reece-Hoyes JS., Dev Dyn. January 1, 2002; 223 (1): 134-40.      


FGF signaling and the anterior neural induction in Xenopus., Hongo I., Dev Biol. December 15, 1999; 216 (2): 561-81.                            


derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.                    


Two phases of Hox gene regulation during early Xenopus development., Pownall ME., Curr Biol. May 21, 1998; 8 (11): 673-6.              


Dorsal-ventral differences in Xcad-3 expression in response to FGF-mediated induction in Xenopus., Northrop JL., Dev Biol. February 1, 1994; 161 (2): 490-503.                

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