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Summary Anatomy Item Literature (6278) Expression Attributions Wiki
XB-ANAT-475

Papers associated with primary germ layer (and post)

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Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions., Johnson K., BMC Genomics. October 23, 2022; 23 (1): 723.                                  


Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    


Ubiquitin C-terminal hydrolase37 regulates Tcf7 DNA binding for the activation of Wnt signalling., Han W., Sci Rep. February 15, 2017; 7 42590.                        


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.                


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


The competence of marginal zone cells to become Spemann's organizer is controlled by Xcad2., Levy V., Dev Biol. August 1, 2002; 248 (1): 40-51.              


Difference in XTcf-3 dependency accounts for change in response to beta-catenin-mediated Wnt signalling in Xenopus blastula., Hamilton FS., Development. June 1, 2001; 128 (11): 2063-73.          


HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R., Development. April 1, 2000; 127 (7): 1455-65.    


Spatial and temporal properties of ventral blood island induction in Xenopus laevis., Kumano G., Development. December 1, 1999; 126 (23): 5327-37.                


Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.                                                            


Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN., Development. December 1, 1997; 124 (23): 4739-48.              


Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S., Cell. March 21, 1997; 88 (6): 757-66.              


eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus., Pownall ME., Development. December 1, 1996; 122 (12): 3881-92.                  


Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S., Genes Dev. November 1, 1996; 10 (21): 2805-17.            


Competition between noggin and bone morphogenetic protein 4 activities may regulate dorsalization during Xenopus development., Re'em-Kalma Y., Proc Natl Acad Sci U S A. December 19, 1995; 92 (26): 12141-5.


Tail bud determination in the vertebrate embryo., Tucker AS., Curr Biol. July 1, 1995; 5 (7): 807-13.        


A truncated bone morphogenetic protein receptor affects dorsal-ventral patterning in the early Xenopus embryo., Suzuki A., Proc Natl Acad Sci U S A. October 25, 1994; 91 (22): 10255-9.          


FGF signalling in the early specification of mesoderm in Xenopus., Amaya E., Development. June 1, 1993; 118 (2): 477-87.        


Localized and inducible expression of Xenopus-posterior (Xpo), a novel gene active in early frog embryos, encoding a protein with a 'CCHC' finger domain., Sato SM., Development. July 1, 1991; 112 (3): 747-53.            

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