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Summary Anatomy Item Literature (2349) Expression Attributions Wiki
XB-ANAT-4083

Papers associated with tadpole (and ventx2.2)

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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.                                            


R-spondins are BMP receptor antagonists in Xenopus early embryonic development., Lee H, Lee H., Nat Commun. November 4, 2020; 11 (1): 5570.                                            


Xvent-2 expression in regenerating Xenopus tails., Pshennikova ES., Stem Cell Investig. July 20, 2020; 7 13.  


Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.                    


BAP1 regulates epigenetic switch from pluripotency to differentiation in developmental lineages giving rise to BAP1-mutant cancers., Kuznetsov JN., Sci Adv. September 18, 2019; 5 (9): eaax1738.        


Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):                                     


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.                        


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.                                  


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.                                    


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


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification., Mei W., Development. June 1, 2013; 140 (11): 2334-44.                          


Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.              


A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus., Szenker E., Cell Rep. June 28, 2012; 1 (6): 730-40.                                      


Xenopus staufen2 is required for anterior endodermal organ formation., Bilogan CK., Genesis. March 1, 2012; 50 (3): 251-9.                      


Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P., PLoS One. January 1, 2012; 7 (5): e36855.              


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.                


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.                                


The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.                                                    


The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              


MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.              


R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.                          


New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.              


Twisted gastrulation loss-of-function analyses support its role as a BMP inhibitor during early Xenopus embryogenesis., Blitz IL., Development. October 1, 2003; 130 (20): 4975-88.              


XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos., Osada S., Development. May 1, 2003; 130 (9): 1783-94.            


Is chordin a long-range- or short-range-acting factor? Roles for BMP1-related metalloproteases in chordin and BMP4 autofeedback loop regulation., Blitz IL., Dev Biol. July 1, 2000; 223 (1): 120-38.                


Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4., Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.              


A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis., Barbieri AM., Proc Natl Acad Sci U S A. September 14, 1999; 96 (19): 10729-34.            


Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.                


The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.                  

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