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Summary Anatomy Item Literature (3921) Expression Attributions Wiki
XB-ANAT-50

Papers associated with mesoderm (and en2)

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Functions of block of proliferation 1 during anterior development in Xenopus laevis., Gärtner C., PLoS One. August 2, 2022; 17 (8): e0273507.                        


Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.                  


Wnt-inducible Lrp6-APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway., Colozza G., Sci Rep. December 9, 2020; 10 (1): 21555.            


TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9                                                                                           


Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis., Ding Y., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.                    


Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.          


Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.                                                          


An atlas of Wnt activity during embryogenesis in Xenopus tropicalis., Borday C., PLoS One. January 1, 2018; 13 (4): e0193606.                


Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                


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.                    


G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.                                          


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.                                    


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.                                          


Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling., Sheng R., Nat Commun. July 15, 2014; 5 4393.              


Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.                                                                


The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.                                                                    


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


FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.                              


Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.                    


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W., PLoS One. July 1, 2013; 8 (7): e69372.              


β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.            


An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.                                      


Xnr3 affects brain patterning via cell migration in the neural-epidermal tissue boundary during early Xenopus embryogenesis., Morita M., Int J Dev Biol. January 1, 2013; 57 (9-10): 779-86.          


Involvement of XZFP36L1, an RNA-binding protein, in Xenopus neural development., Xia YJ., Dongwuxue Yanjiu. December 1, 2012; 33 (E5-6): E82-8.                


ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.                              


Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development., Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.              


The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.              


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


Transmembrane protein 198 promotes LRP6 phosphorylation and Wnt signaling activation., Liang J., Mol Cell Biol. July 1, 2011; 31 (13): 2577-90.


Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              


FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development., Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.                                                              


The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.                                                    


Xenopus skip modulates Wnt/beta-catenin signaling and functions in neural crest induction., Wang Y., J Biol Chem. April 2, 2010; 285 (14): 10890-901.                            


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.                  


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.                


The lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) receptor gene families: cloning and comparative expression analysis in Xenopus laevis., Massé K., Int J Dev Biol. January 1, 2010; 54 (8-9): 1361-74.                                          


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.                            


Direct control of Hoxd1 and Irx3 expression by Wnt/beta-catenin signaling during anteroposterior patterning of the neural axis in Xenopus., Janssens S., Int J Dev Biol. January 1, 2010; 54 (10): 1435-42.    


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.                              


Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.                    


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


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


Complementary expression of HSPG 6-O-endosulfatases and 6-O-sulfotransferase in the hindbrain of Xenopus laevis., Winterbottom EF., Gene Expr Patterns. March 1, 2009; 9 (3): 166-72.              


Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.                


Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation., Inomata H., Cell. September 5, 2008; 134 (5): 854-65.                  


VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.                  


Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.                


The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.                      


The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions., Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.        

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