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Summary Anatomy Item Literature (2231) Expression Attributions Wiki
XB-ANAT-3282

Papers associated with posterior hypothalamus (and fgf2)

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Cold-inducible RNA binding protein is required for the expression of adhesion molecules and embryonic cell movement in Xenopus laevis., Peng Y., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 416-24.        


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.                  


Differential expression of two TEF-1 (TEAD) genes during Xenopus laevis development and in response to inducing factors., Naye F., Int J Dev Biol. January 1, 2007; 51 (8): 745-52.                  


Mouse homologues of Shisa antagonistic to Wnt and Fgf signalings., Furushima K., Dev Biol. June 15, 2007; 306 (2): 480-92.  


Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.                            


FoxM1-driven cell division is required for neuronal differentiation in early Xenopus embryos., Ueno H., Development. June 1, 2008; 135 (11): 2023-30.          


A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways., Kuriyama S., Development. February 1, 2009; 136 (4): 575-84.                    


Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.                                                                                                        


Xmc mediates Xctr1-independent morphogenesis in Xenopus laevis., Haremaki T., Dev Dyn. September 1, 2009; 238 (9): 2382-7.            


BMP inhibition initiates neural induction via FGF signaling and Zic genes., Marchal L., Proc Natl Acad Sci U S A. October 13, 2009; 106 (41): 17437-42.        


RNA helicase Ddx39 is expressed in the developing central nervous system, limb, otic vesicle, branchial arches and facial mesenchyme of Xenopus laevis., Wilson JM., Gene Expr Patterns. January 1, 2010; 10 (1): 44-52.          


Vestigial like gene family expression in Xenopus: common and divergent features with other vertebrates., Faucheux C., Int J Dev Biol. January 1, 2010; 54 (8-9): 1375-82.                            


Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.                  


Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network., de Crozé N., Proc Natl Acad Sci U S A. January 4, 2011; 108 (1): 155-60.        


Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos., Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.                    


TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.                  


The endocytic adapter E-Syt2 recruits the p21 GTPase activated kinase PAK1 to mediate actin dynamics and FGF signalling., Jean S., Biol Open. August 15, 2012; 1 (8): 731-8.          


Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.                          


MRAS GTPase is a novel stemness marker that impacts mouse embryonic stem cell plasticity and Xenopus embryonic cell fate., Mathieu ME., Development. August 1, 2013; 140 (16): 3311-22.              


TBX3 Directs Cell-Fate Decision toward Mesendoderm., Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.                


Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.                              


PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos., Yoon J., BMB Rep. December 1, 2014; 47 (12): 673-8.        


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  

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