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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-86

Papers associated with tail region (and nodal3.1)

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Blastomere derivation and domains of gene expression in the Spemann Organizer of Xenopus laevis., Vodicka MA., Development. November 1, 1995; 121 (11): 3505-18.                  


The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.                


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


XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.                  


Antagonist activity of DWnt-4 and wingless in the Drosophila embryonic ventral ectoderm and in heterologous Xenopus assays., Gieseler K., Mech Dev. July 1, 1999; 85 (1-2): 123-31.    


Regulation of Wnt signaling by Sox proteins: XSox17 alpha/beta and XSox3 physically interact with beta-catenin., Zorn AM., Mol Cell. October 1, 1999; 4 (4): 487-98.                


The putative wnt receptor Xenopus frizzled-7 functions upstream of beta-catenin in vertebrate dorsoventral mesoderm patterning., Sumanas S., Development. May 1, 2000; 127 (9): 1981-90.    


Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach., Heasman J., Dev Biol. June 1, 2000; 222 (1): 124-34.        


Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.                  


The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.              


FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.            


foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.            


The role of maternal axin in patterning the Xenopus embryo., Kofron M., Dev Biol. September 1, 2001; 237 (1): 183-201.


The IGF pathway regulates head formation by inhibiting Wnt signaling in Xenopus., Richard-Parpaillon L., Dev Biol. April 15, 2002; 244 (2): 407-17.                    


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.                  


Nodal signaling in Xenopus gastrulae is cell-autonomous and patterned by beta-catenin., Hashimoto-Partyka MK., Dev Biol. January 1, 2003; 253 (1): 125-38.                    


Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.                    


Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.              


Xenopus tropicalis nodal-related gene 3 regulates BMP signaling: an essential role for the pro-region., Haramoto Y., Dev Biol. January 1, 2004; 265 (1): 155-68.              


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                


XSENP1, a novel sumo-specific protease in Xenopus, inhibits normal head formation by down-regulation of Wnt/beta-catenin signalling., Yukita A., Genes Cells. August 1, 2004; 9 (8): 723-36.              


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


Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo., Pera EM., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.                                  


Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos., Tao Q, Tao Q., Cell. March 25, 2005; 120 (6): 857-71.            


Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.          


Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A., Dev Biol. January 1, 2006; 289 (1): 166-78.                                  


Maternal XTcf1 and XTcf4 have distinct roles in regulating Wnt target genes., Standley HJ., Dev Biol. January 15, 2006; 289 (2): 318-28.  


Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.                    


Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.                                    


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.                  


Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.      


Beta-arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo., Bryja V., Proc Natl Acad Sci U S A. April 17, 2007; 104 (16): 6690-5.  


R-spondin1 is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling., Wei Q., J Biol Chem. May 25, 2007; 282 (21): 15903-11.  


Retinoic acid-inducible G protein-coupled receptors bind to frizzled receptors and may activate non-canonical Wnt signaling., Harada Y., Biochem Biophys Res Commun. July 13, 2007; 358 (4): 968-75.        


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


The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.            


Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation., Cha SW., Development. November 1, 2008; 135 (22): 3719-29.        


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.                    


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA., Dev Cell. August 17, 2010; 19 (2): 220-31.      


Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.                                                


Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.        


Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H., Development. June 1, 2011; 138 (12): 2567-79.                          


HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ., Genes Dev. August 1, 2011; 25 (15): 1654-61.            


Differential role of Axin RGS domain function in Wnt signaling during anteroposterior patterning and maternal axis formation., Schneider PN., PLoS One. January 1, 2012; 7 (9): e44096.                


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Toward an unbiased evolutionary platform for unraveling Xenopus developmental gene networks., Beer R., Genesis. March 1, 2012; 50 (3): 186-91.        


Whole-genome microRNA screening identifies let-7 and mir-18 as regulators of germ layer formation during early embryogenesis., Colas AR., Genes Dev. December 1, 2012; 26 (23): 2567-79.      


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

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